Patrick Gallagher, MD, BS
Research & Publications
Biography
News
Research Summary
Dr. Gallagher’s research focuses on normal and perturbed hematopoiesis. His primary focus is the genetic basis of inherited disorders of hematopoiesis, with a special interest in disorders of the erythrocyte the erythrocyte and the molecular control of erythropoiesis. Dr. Gallagher’s research is funded by the NIH and private foundations. Dr. Gallagher is co-director of the Yale Cooperative Center for Excellence in Hematology and administrative Director of the Yale Hemophilia Treatment Center/Yale Center for Bleeding and Clotting Disorders. Dr. Gallagher is fully engaged in the Yale scientific community, with joint appointments in Pathology and Genetics, and active membership in the Yale Stem Cell Center. Current extramural activities include Editorial Board service as Editor-In-Chief of the Journal of Perinatology, Associate Editor of Blood Cells, Molecules and Disease, and Editorial Board Member of the American Journal of Hematology and Frontiers in Physiology, as well as grant and abstract reviewing for numerous NIH, private foundations, and academic society meetings including ASH and PAS. He has served as chair of the NIH Erythrocyte and Leukocyte Biology Study Section (now MCH) and as chair of the American Society of Hematology Scientific Subcommittee on Hemoglobin/Red Cell.
Specialized Terms: Neonatal hematology; Erythropoiesis; Inherited abnormalities of the erythrocyte including metabolic, membrane, and hemoglobin disorders; Sickle cell disease; Hereditary spherocytosis; Elliptocytosis; Pyropoikilocytosis; Stomatocytosis.
Extensive Research Description
Dr. Gallagher has trained numerous undergraduate, graduate and medical students, MD and PhD postdoctoral fellows, and sabbatical faculty. Laboratory graduates hold positions throughout the world and trainees have
received awards and honors from local, regional, and national organizations. After serving as the PI on the Yale Neonatal/Perinatal Medicine T32 training grant for many years, he now participates in training grants in Genetics, Medicine, and Laboratory Medicine. He serves on the Department of Pediatrics Scholarship Oversight Committee (SOC). He has served on numerous individual SOCs as member or chair, as well as various medical and graduate school mentoring committees, PhD thesis committees, etc.
Coauthors
Research Interests
Anemia, Sickle Cell; Elliptocytosis, Hereditary; Erythropoiesis; Genetics; Hemoglobinopathies; Information Science; Neonatology; Pathology; Pediatrics; Polycythemia; Pyruvate Kinase; Spherocytosis, Hereditary; Hydrops Fetalis; Genomics; Diseases; Health Care
Research Image
Erythrocytes
Selected Publications
- Developmental Stage-Specific Hematopoietic Failure In Vivo in a Novel Model of Diamond Blackfan AnemiaTang Y, Kahn M, Papoin J, Yan H, Narla A, Palis J, Steiner L, Gallagher P, Lipton J, Narla M, Blanc L. Developmental Stage-Specific Hematopoietic Failure In Vivo in a Novel Model of Diamond Blackfan Anemia. Blood 2022, 140: 2946-2946. DOI: 10.1182/blood-2022-163200.
- BMI1 Regulates Proliferation of Human Late-Stage Erythroid ProgenitorsOlsen J, McGrath K, Murphy K, Schofield T, Getman M, Narla M, Blanc L, Schulz V, Gallagher P, Steiner L, Palis J. BMI1 Regulates Proliferation of Human Late-Stage Erythroid Progenitors. Blood 2022, 140: 8152-8152. DOI: 10.1182/blood-2022-167830.
- Gender analysis of Journal of Perinatology authorship during COVID-19Gadek L, Dammann C, Savich R, Mmuo-Oji C, Barrera L, Gallagher P, Machut K. Gender analysis of Journal of Perinatology authorship during COVID-19. Journal Of Perinatology 2022, 43: 518-522. PMID: 36335276, PMCID: PMC9638437, DOI: 10.1038/s41372-022-01551-x.
- Anemia in the pediatric patientGallagher PG. Anemia in the pediatric patient. Blood 2022, 140: 571-593. PMID: 35213686, PMCID: PMC9373018, DOI: 10.1182/blood.2020006479.
- Extramedullary hematopoietic stem cells.Gallagher PG. Extramedullary hematopoietic stem cells. Blood 2022, 139: 3353-3354. PMID: 35679074, DOI: 10.1182/blood.2022015879.
- HMGB1-mediated restriction of EPO signaling contributes to anemia of inflammation.Dulmovits BM, Tang Y, Papoin J, He M, Li J, Yang H, Addorisio ME, Kennedy L, Khan M, Brindley E, Ashley RJ, Ackert-Bicknell C, Hale J, Kurita R, Nakamura Y, Diamond B, Barnes BJ, Hermine O, Gallagher PG, Steiner LA, Lipton JM, Taylor N, Mohandas N, Andersson U, Al-Abed Y, Tracey KJ, Blanc L. HMGB1-mediated restriction of EPO signaling contributes to anemia of inflammation. Blood 2022, 139: 3181-3193. PMID: 35040907, PMCID: PMC9136881, DOI: 10.1182/blood.2021012048.
- Histone Acetyltransferases p300 and CBP Coordinate Distinct Chromatin Remodeling Programs in Vascular Smooth Muscle PlasticityChakraborty R, Ostriker AC, Xie Y, Dave JM, Gamez-Mendez A, Chatterjee P, Abu Y, Valentine J, Lezon-Geyda K, Greif DM, Schulz VP, Gallagher PG, Sessa WC, Hwa J, Martin KA. Histone Acetyltransferases p300 and CBP Coordinate Distinct Chromatin Remodeling Programs in Vascular Smooth Muscle Plasticity. Circulation 2022, 145: 1720-1737. PMID: 35502657, DOI: 10.1161/circulationaha.121.057599.
- The Journal of Perinatology: looking forwardGallagher PG. The Journal of Perinatology: looking forward. Journal Of Perinatology 2021, 41: 2700-2701. PMID: 34907365, PMCID: PMC8669232, DOI: 10.1038/s41372-021-01291-4.
- Summary of Joint European Hematology Association (EHA) and EuroBloodNet Recommendations on Diagnosis and Treatment of MethemoglobinemiaIolascon A, Andolfo I, Russo R, Barcellini W, Fermo E, Toldi G, Ghirardello S, Rees D, Van Wijk R, Kattamis A, Gallagher PG, Roy N, Taher A, Mohty R, Kulozik A, De Franceschi L, Gambale A, De Montalembert M, Forni GL, Harteveld CL, Prchal J, Bianchi P. Summary of Joint European Hematology Association (EHA) and EuroBloodNet Recommendations on Diagnosis and Treatment of Methemoglobinemia. HemaSphere 2021, 5: e660. PMID: 34805766, PMCID: PMC8598222, DOI: 10.1097/hs9.0000000000000660.
- Regulation of RNA polymerase II activity is essential for terminal erythroid maturation.Murphy ZC, Murphy K, Myers J, Getman M, Couch T, Schulz VP, Lezon-Geyda K, Palumbo C, Yan H, Mohandas N, Gallagher PG, Steiner LA. Regulation of RNA polymerase II activity is essential for terminal erythroid maturation. Blood 2021, 138: 1740-1756. PMID: 34075391, PMCID: PMC8569412, DOI: 10.1182/blood.2020009903.
- Impairment of human terminal erythroid differentiation by histone deacetylase 5 deficiency.Wang Y, Li W, Schulz VP, Zhao H, Qu X, Qi Q, Cheng Y, Guo X, Zhang S, Wei X, Liu D, Yazdanbakhsh K, Hillyer CD, Mohandas N, Chen L, Gallagher PG, An X. Impairment of human terminal erythroid differentiation by histone deacetylase 5 deficiency. Blood 2021, 138: 1615-1627. PMID: 34036344, PMCID: PMC8554652, DOI: 10.1182/blood.2020007401.
- D‐bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemiaWerner KM, Cox AJ, Qian E, Jain P, Ji W, Tikhonova I, Castaldi C, Bilguvar K, Knight J, Ferdinandusse S, Fawaz R, Jiang Y, Gallagher PG, Bizzarro M, Gruen JR, Bale A, Zhang H. D‐bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia. American Journal Of Medical Genetics Part A 2021, 188: 357-363. PMID: 34623748, PMCID: PMC8678290, DOI: 10.1002/ajmg.a.62520.
- Recommendations for diagnosis and treatment of methemoglobinemiaIolascon A, Bianchi P, Andolfo I, Russo R, Barcellini W, Fermo E, Toldi G, Ghirardello S, Rees D, Van Wijk R, Kattamis A, Gallagher PG, Roy N, Taher A, Mohty R, Kulozik A, De Franceschi L, Gambale A, De Montalembert M, Forni GL, Harteveld CL, Prchal J, cell and iron of EHA and EuroBloodNet S. Recommendations for diagnosis and treatment of methemoglobinemia. American Journal Of Hematology 2021, 96: 1666-1678. PMID: 34467556, PMCID: PMC9291883, DOI: 10.1002/ajh.26340.
- Difficulty in Diagnosis of Hereditary Spherocytosis in the NeonateGallagher PG. Difficulty in Diagnosis of Hereditary Spherocytosis in the Neonate. Pediatrics 2021, 148: e2021051100. PMID: 34376531, DOI: 10.1542/peds.2021-051100.
- An Initiative to Decrease Laboratory Testing in a NICUKlunk CJ, Barrett RE, Peterec SM, Blythe E, Brockett R, Kenney M, Natusch A, Thursland C, Gallagher PG, Pando R, Bizzarro MJ. An Initiative to Decrease Laboratory Testing in a NICU. Pediatrics 2021, 148: e2020000570. PMID: 34088759, DOI: 10.1542/peds.2020-000570.
- Comprehensive phenotyping of erythropoiesis in human bone marrow: Evaluation of normal and ineffective erythropoiesisYan H, Ali A, Blanc L, Narla A, Lane JM, Gao E, Papoin J, Hale J, Hillyer CD, Taylor N, Gallagher PG, Raza A, Kinet S, Mohandas N. Comprehensive phenotyping of erythropoiesis in human bone marrow: Evaluation of normal and ineffective erythropoiesis. American Journal Of Hematology 2021, 96: 1064-1076. PMID: 34021930, PMCID: PMC8355124, DOI: 10.1002/ajh.26247.
- Journal of Perinatology Editorial Updates 2021Raju T, Cheng Y, Mimouni FB, Pearlman SA, Ryan RM, Swanson JR, Gallagher PG. Journal of Perinatology Editorial Updates 2021. Journal Of Perinatology 2021, 41: 917-922. PMID: 33850288, PMCID: PMC8042837, DOI: 10.1038/s41372-021-01048-z.
- Quality criteria for randomized controlled studies: obstetrical journal guidelinesAnderson K, Romero R, Odibo AO, Rouse D, Marsh M, Acharya G, Chitty L, Ortmann O, Geary M, Gratacos E, Gallagher PG, Gupta J, Renzo GCD, Maulik D, de Costa C, Saade G, Dudenhausen JW, Berghella V. Quality criteria for randomized controlled studies: obstetrical journal guidelines. American Journal Of Obstetrics & Gynecology MFM 2021, 3: 100334. PMID: 33607321, PMCID: PMC8324065, DOI: 10.1016/j.ajogmf.2021.100334.
- An IDH1-vitamin C crosstalk drives human erythroid development by inhibiting pro-oxidant mitochondrial metabolismGonzalez-Menendez P, Romano M, Yan H, Deshmukh R, Papoin J, Oburoglu L, Daumur M, Dumé AS, Phadke I, Mongellaz C, Qu X, Bories PN, Fontenay M, An X, Dardalhon V, Sitbon M, Zimmermann VS, Gallagher PG, Tardito S, Blanc L, Mohandas N, Taylor N, Kinet S. An IDH1-vitamin C crosstalk drives human erythroid development by inhibiting pro-oxidant mitochondrial metabolism. Cell Reports 2021, 34: 108723. PMID: 33535038, PMCID: PMC9169698, DOI: 10.1016/j.celrep.2021.108723.
- Disparities in perinatal health: what can we do?Forson-Dare Z, Harris LM, Gallagher PG. Disparities in perinatal health: what can we do? Journal Of Perinatology 2021, 41: 363-364. PMID: 33510417, DOI: 10.1038/s41372-021-00920-2.
- Critical disparities in perinatal health—understanding risks and changing the outcomesHarris LM, Forson-Dare Z, Gallagher PG. Critical disparities in perinatal health—understanding risks and changing the outcomes. Journal Of Perinatology 2021, 41: 181-182. PMID: 33462341, DOI: 10.1038/s41372-020-00913-7.
- Functional characterization of a novel SLC40A1 Arg88Ile mutation in a kindred with familial iron overload treated by phlebotomyWomack J, Sukumaran A, Li X, Lozovatsky L, Gallagher PG, Seid JE, Finberg KE. Functional characterization of a novel SLC40A1 Arg88Ile mutation in a kindred with familial iron overload treated by phlebotomy. Blood Cells Molecules And Diseases 2020, 87: 102532. PMID: 33385755, PMCID: PMC8272917, DOI: 10.1016/j.bcmd.2020.102532.
- Vertical Transmission of Severe Acute Respiratory Syndrome Coronavirus 2 From the Mother to the InfantMimouni FB, Gallagher P, Mendlovic J. Vertical Transmission of Severe Acute Respiratory Syndrome Coronavirus 2 From the Mother to the Infant. JAMA Pediatrics 2020, 174: 1006-1006. PMID: 32687567, DOI: 10.1001/jamapediatrics.2020.2144.
- Characterization of circulating and cultured Tfh-like cells in sickle cell disease in relation to red blood cell alloimmunization statusBalbuena-Merle R, Santhanakrishnan M, Devine L, Gibb DR, Tormey CA, Siddon AJ, Curtis SA, Gallagher PG, Weinstein JS, Hendrickson JE. Characterization of circulating and cultured Tfh-like cells in sickle cell disease in relation to red blood cell alloimmunization status. Transfusion And Apheresis Science 2020, 59: 102778. PMID: 32439490, PMCID: PMC7483805, DOI: 10.1016/j.transci.2020.102778.
- Comprehensive proteomic analysis of murine terminal erythroid differentiationGautier EF, Leduc M, Ladli M, Schulz VP, Lefèvre C, Boussaid I, Fontenay M, Lacombe C, Verdier F, Guillonneau F, Hillyer CD, Mohandas N, Gallagher PG, Mayeux P. Comprehensive proteomic analysis of murine terminal erythroid differentiation. Blood Advances 2020, 4: 1464-1477. PMID: 32282884, PMCID: PMC7160260, DOI: 10.1182/bloodadvances.2020001652.
- Perinatal aspects on the covid-19 pandemic: a practical resource for perinatal–neonatal specialistsMimouni F, Lakshminrusimha S, Pearlman SA, Raju T, Gallagher PG, Mendlovic J. Perinatal aspects on the covid-19 pandemic: a practical resource for perinatal–neonatal specialists. Journal Of Perinatology 2020, 40: 820-826. PMID: 32277162, PMCID: PMC7147357, DOI: 10.1038/s41372-020-0665-6.
- Genotype‐phenotype correlation and molecular heterogeneity in pyruvate kinase deficiencyBianchi P, Fermo E, Lezon‐Geyda K, Beers E, Morton HD, Barcellini W, Glader B, Chonat S, Ravindranath Y, Newburger PE, Kollmar N, Despotovic JM, Verhovsek M, Sharma M, Kwiatkowski JL, Kuo KHM, Wlodarski MW, Yaish HM, Holzhauer S, Wang H, Kunz J, Addonizio K, Al‐Sayegh H, London WB, Andres O, Wijk R, Gallagher PG, Grace RFF. Genotype‐phenotype correlation and molecular heterogeneity in pyruvate kinase deficiency. American Journal Of Hematology 2020, 95: 472-482. PMID: 32043619, PMCID: PMC8127999, DOI: 10.1002/ajh.25753.
- Why so little progress in regionalization of perinatal care when transport of high-risk neonates remains a substantial risk?Bizzarro MJ, Gallagher PG. Why so little progress in regionalization of perinatal care when transport of high-risk neonates remains a substantial risk? Journal Of Perinatology 2020, 40: 357-358. PMID: 31996764, DOI: 10.1038/s41372-020-0600-x.
- The Journal of Perinatology Turns a PageGallagher PG. The Journal of Perinatology Turns a Page. Journal Of Perinatology 2019, 39: 1323-1324. PMID: 31551512, DOI: 10.1038/s41372-019-0477-8.
- A Unique Epigenomic Landscape Defines Human ErythropoiesisSchulz VP, Yan H, Lezon-Geyda K, An X, Hale J, Hillyer CD, Mohandas N, Gallagher PG. A Unique Epigenomic Landscape Defines Human Erythropoiesis. Cell Reports 2019, 28: 2996-3009.e7. PMID: 31509757, PMCID: PMC6863094, DOI: 10.1016/j.celrep.2019.08.020.
- Aberrant splicing contributes to severe α-spectrin-linked congenital hemolytic anemiaGallagher PG, Maksimova Y, Lezon-Geyda K, Newburger PE, Medeiros D, Hanson RD, Rothman J, Israels S, Wall DA, Sidonio RF, Sieff C, Gowans LK, Mittal N, Rivera-Santiago R, Speicher DW, Baserga SJ, Schulz VP. Aberrant splicing contributes to severe α-spectrin-linked congenital hemolytic anemia. Journal Of Clinical Investigation 2019, 129: 2878-2887. PMID: 31038472, PMCID: PMC6597203, DOI: 10.1172/jci127195.
- Identification and transcriptome analysis of erythroblastic island macrophagesLi W, Wang Y, Zhao H, Zhang H, Xu Y, Wang S, Guo X, Huang Y, Zhang S, Han Y, Wu X, Rice CM, Huang G, Gallagher PG, Mendelson A, Yazdanbakhsh K, Liu J, Chen L, An X. Identification and transcriptome analysis of erythroblastic island macrophages. Blood 2019, 134: 480-491. PMID: 31101625, PMCID: PMC6676133, DOI: 10.1182/blood.2019000430.
- MKL1-actin pathway restricts chromatin accessibility and prevents mature pluripotency activationHu X, Liu ZZ, Chen X, Schulz VP, Kumar A, Hartman AA, Weinstein J, Johnston JF, Rodriguez EC, Eastman AE, Cheng J, Min L, Zhong M, Carroll C, Gallagher PG, Lu J, Schwartz M, King MC, Krause DS, Guo S. MKL1-actin pathway restricts chromatin accessibility and prevents mature pluripotency activation. Nature Communications 2019, 10: 1695. PMID: 30979898, PMCID: PMC6461646, DOI: 10.1038/s41467-019-09636-6.
- MRTFA Augments Megakaryocyte Maturation By Enhancing the SRF Regulatory AxisRahman N, Schulz V, Wang L, Gallagher P, Denisenko O, Gualdrini F, Cyril E, Krause D. MRTFA Augments Megakaryocyte Maturation By Enhancing the SRF Regulatory Axis. Blood 2018, 132: 640-640. DOI: 10.1182/blood-2018-99-118954.
- Altered Splicing from a Mutated Alternate Branch Point Is Common in Severe Alpha-Spectrin Linked Inherited AnemiaLezon-Geyda K, Schulz V, Maksimova Y, Gallagher P. Altered Splicing from a Mutated Alternate Branch Point Is Common in Severe Alpha-Spectrin Linked Inherited Anemia. Blood 2018, 132: 503-503. DOI: 10.1182/blood-2018-99-117752.
- Pklr Intron Splicing-Associated Mutations and Alternate Diagnoses Are Common in Pyruvate Kinase Deficient Patients with Single or No Pklr Coding MutationsLezon-Geyda K, Rose M, McNaull M, Knoll C, Yaish H, Pastore Y, Fermi E, Glader B, Bianchi P, Grace R, Gallagher P. Pklr Intron Splicing-Associated Mutations and Alternate Diagnoses Are Common in Pyruvate Kinase Deficient Patients with Single or No Pklr Coding Mutations. Blood 2018, 132: 3607-3607. DOI: 10.1182/blood-2018-99-117805.
- Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiencyBianchi P, Fermo E, Glader B, Kanno H, Agarwal A, Barcellini W, Eber S, Hoyer JD, Kuter DJ, Maia TM, del Mar Mañu‐Pereira M, Kalfa TA, Pissard S, Segovia J, van Beers E, Gallagher PG, Rees DC, van Wijk R, with the endorsement of EuroBloodNet T. Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency. American Journal Of Hematology 2018, 94: 149-161. PMID: 30358897, PMCID: PMC7344868, DOI: 10.1002/ajh.25325.
- MRTFA augments megakaryocyte maturation by enhancing the SRF regulatory axisRahman NT, Schulz VP, Wang L, Gallagher PG, Denisenko O, Gualdrini F, Esnault C, Krause DS. MRTFA augments megakaryocyte maturation by enhancing the SRF regulatory axis. Blood Advances 2018, 2: 2691-2703. PMID: 30337297, PMCID: PMC6199649, DOI: 10.1182/bloodadvances.2018019448.
- Severe nondominant hereditary spherocytosis in an infant with coinheritance of three rare alpha‐spectrin gene defectsBhatt N, Loew JM, Gallagher P, Mittal N. Severe nondominant hereditary spherocytosis in an infant with coinheritance of three rare alpha‐spectrin gene defects. Pediatric Blood & Cancer 2018, 66: e27480. PMID: 30255572, DOI: 10.1002/pbc.27480.
- Human Extrafollicular CD4+ Th Cells Help Memory B Cells Produce Igs.Kim ST, Choi JY, Lainez B, Schulz VP, Karas DE, Baum ED, Setlur J, Gallagher PG, Craft J. Human Extrafollicular CD4+ Th Cells Help Memory B Cells Produce Igs. The Journal Of Immunology 2018, 201: 1359-1372. PMID: 30030323, PMCID: PMC6112860, DOI: 10.4049/jimmunol.1701217.
- KLF1 E325K-associated Congenital Dyserythropoietic Anemia Type IVRavindranath Y, Johnson RM, Goyette G, Buck S, Gadgeel M, Gallagher PG. KLF1 E325K-associated Congenital Dyserythropoietic Anemia Type IV. Journal Of Pediatric Hematology/Oncology 2018, 40: e405-e409. PMID: 29300242, PMCID: PMC6092092, DOI: 10.1097/mph.0000000000001056.
- Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype–phenotype correlationSingh SA, Sarangi S, Appiah‐Kubi A, Hsu P, Smith WB, Gallagher PG, Glader B, Chui DHK. Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype–phenotype correlation. Pediatric Blood & Cancer 2018, 65: e27220. PMID: 29749692, DOI: 10.1002/pbc.27220.
- Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study.Grace RF, Bianchi P, van Beers EJ, Eber SW, Glader B, Yaish HM, Despotovic JM, Rothman JA, Sharma M, McNaull MM, Fermo E, Lezon-Geyda K, Morton DH, Neufeld EJ, Chonat S, Kollmar N, Knoll CM, Kuo K, Kwiatkowski JL, Pospíšilová D, Pastore YD, Thompson AA, Newburger PE, Ravindranath Y, Wang WC, Wlodarski MW, Wang H, Holzhauer S, Breakey VR, Kunz J, Sheth S, Rose MJ, Bradeen HA, Neu N, Guo D, Al-Sayegh H, London WB, Gallagher PG, Zanella A, Barcellini W. Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study. Blood 2018, 131: 2183-2192. PMID: 29549173, DOI: 10.1182/blood-2017-10-810796.
- A Ser725Arg mutation in Band 3 abolishes transport function and leads to anemia and renal tubular acidosisYang E, Seo-Mayer P, Lezon-Geyda K, Badior KE, Li J, Casey JR, Reithmeier RAF, Gallagher PG. A Ser725Arg mutation in Band 3 abolishes transport function and leads to anemia and renal tubular acidosis. Blood 2018, 131: 1759-1763. PMID: 29483102, PMCID: PMC5897869, DOI: 10.1182/blood-2018-01-827725.
- Correction: STAT4 and T-bet control follicular helper T cell development in viral infectionsWeinstein JS, Laidlaw BJ, Lu Y, Wang JK, Schulz VP, Li N, Herman EI, Kaech SM, Gallagher PG, Craft J. Correction: STAT4 and T-bet control follicular helper T cell development in viral infections. Journal Of Experimental Medicine 2018, 215: 999-999. PMID: 29440270, PMCID: PMC5839754, DOI: 10.1084/jem.2017045702062018c.
- Chapter 45 Red Blood Cell Membrane DisordersGallagher P. Chapter 45 Red Blood Cell Membrane Disorders. 2018, 626-647. DOI: 10.1016/b978-0-323-35762-3.00045-7.
- Hereditary xerocytosis: Diagnostic considerationsRisinger M, Glogowska E, Chonat S, Zhang K, Dagaonkar N, Joiner CH, Quinn CT, Kalfa TA, Gallagher PG. Hereditary xerocytosis: Diagnostic considerations. American Journal Of Hematology 2017, 93: e67-e69. PMID: 29210095, PMCID: PMC5807085, DOI: 10.1002/ajh.24996.
- STAT4 and T-bet control follicular helper T cell development in viral infectionsWeinstein JS, Laidlaw BJ, Lu Y, Wang JK, Schulz VP, Li N, Herman EI, Kaech SM, Gallagher PG, Craft J. STAT4 and T-bet control follicular helper T cell development in viral infections. Journal Of Experimental Medicine 2017, 215: 337-355. PMID: 29212666, PMCID: PMC5748849, DOI: 10.1084/jem.20170457.
- Molecular basis of tactile specialization in the duck billSchneider ER, Anderson EO, Mastrotto M, Matson JD, Schulz VP, Gallagher PG, LaMotte RH, Gracheva EO, Bagriantsev SN. Molecular basis of tactile specialization in the duck bill. Proceedings Of The National Academy Of Sciences Of The United States Of America 2017, 114: 13036-13041. PMID: 29109250, PMCID: PMC5724259, DOI: 10.1073/pnas.1708793114.
- Disorders of erythrocyte hydration.Gallagher PG. Disorders of erythrocyte hydration. Blood 2017, 130: 2699-2708. PMID: 29051181, PMCID: PMC5746162, DOI: 10.1182/blood-2017-04-590810.
- Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosisGlogowska E, Schneider ER, Maksimova Y, Schulz VP, Lezon-Geyda K, Wu J, Radhakrishnan K, Keel SB, Mahoney D, Freidmann AM, Altura RA, Gracheva EO, Bagriantsev SN, Kalfa TA, Gallagher PG. Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis. Blood 2017, 130: 1845-1856. PMID: 28716860, PMCID: PMC5649553, DOI: 10.1182/blood-2017-05-786004.
- Hepatic Malignancy in an Infant with Wolf–Hirschhorn SyndromeRutter S, Morotti RA, Peterec S, Gallagher PG. Hepatic Malignancy in an Infant with Wolf–Hirschhorn Syndrome. Fetal And Pediatric Pathology 2017, 36: 256-262. PMID: 28266898, DOI: 10.1080/15513815.2017.1293201.
- A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β0‐thalassaemia homozygotesJiang Z, Luo H, Farrell JJ, Zhang Z, Schulz VP, Albarawi D, Steinberg MH, Al‐Allawi N, Gallagher PG, Forget BG, Chui DHK. A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β0‐thalassaemia homozygotes. British Journal Of Haematology 2017, 180: 755-757. PMID: 28240767, DOI: 10.1111/bjh.14445.
- Distinct roles for TET family proteins in regulating human erythropoiesisYan H, Wang Y, Qu X, Li J, Hale J, Huang Y, An C, Papoin J, Guo X, Chen L, Kang Q, Li W, Schulz VP, Gallagher PG, Hillyer CD, Mohandas N, An X. Distinct roles for TET family proteins in regulating human erythropoiesis. Blood 2017, 129: 2002-2012. PMID: 28167661, PMCID: PMC5383871, DOI: 10.1182/blood-2016-08-736587.
- Hemoglobin C trait accentuates erythrocyte dehydration in hereditary xerocytosisYang E, Voelkel EB, Lezon‐Geyda K, Schulz VP, Gallagher PG. Hemoglobin C trait accentuates erythrocyte dehydration in hereditary xerocytosis. Pediatric Blood & Cancer 2017, 64: e26444. PMID: 28121068, PMCID: PMC5858911, DOI: 10.1002/pbc.26444.
- In vivo correction of anaemia in β-thalassemic mice by γPNA-mediated gene editing with nanoparticle deliveryBahal R, Ali McNeer N, Quijano E, Liu Y, Sulkowski P, Turchick A, Lu YC, Bhunia DC, Manna A, Greiner DL, Brehm MA, Cheng CJ, López-Giráldez F, Ricciardi A, Beloor J, Krause DS, Kumar P, Gallagher PG, Braddock DT, Mark Saltzman W, Ly DH, Glazer PM. In vivo correction of anaemia in β-thalassemic mice by γPNA-mediated gene editing with nanoparticle delivery. Nature Communications 2016, 7: 13304. PMID: 27782131, PMCID: PMC5095181, DOI: 10.1038/ncomms13304.
- Mutation in a Highly Conserved COOH-Terminal Residue of Krüppel-Like Factor 1 Associated with Elevated Hb F in a Compound Heterozygous β-Thalassemia Patient with a Nontransfusion-Dependent Thalassemia PhenotypeGallagher PG, Maksimova Y, Schulz VP, Forget BG. Mutation in a Highly Conserved COOH-Terminal Residue of Krüppel-Like Factor 1 Associated with Elevated Hb F in a Compound Heterozygous β-Thalassemia Patient with a Nontransfusion-Dependent Thalassemia Phenotype. Hemoglobin 2016, 40: 361-364. PMID: 27821015, DOI: 10.1080/03630269.2016.1214921.
- Allogeneic bone marrow transplantation for treatment of severe hemolytic anemia attributable to hexokinase deficiency.Khazal S, Polishchuk V, Manwani D, Gallagher PG, Prinzing S, Mahadeo KM. Allogeneic bone marrow transplantation for treatment of severe hemolytic anemia attributable to hexokinase deficiency. Blood 2016, 128: 735-7. PMID: 27297791, DOI: 10.1182/blood-2016-03-702860.
- Adult human megakaryocyte-erythroid progenitors are in the CD34+CD38mid fraction.Sanada C, Xavier-Ferrucio J, Lu YC, Min E, Zhang PX, Zou S, Kang E, Zhang M, Zerafati G, Gallagher PG, Krause DS. Adult human megakaryocyte-erythroid progenitors are in the CD34+CD38mid fraction. Blood 2016, 128: 923-33. PMID: 27268089, PMCID: PMC4990855, DOI: 10.1182/blood-2016-01-693705.
- CTCF and CohesinSA-1 Mark Active Promoters and Boundaries of Repressive Chromatin Domains in Primary Human Erythroid CellsSteiner LA, Schulz V, Makismova Y, Lezon-Geyda K, Gallagher PG. CTCF and CohesinSA-1 Mark Active Promoters and Boundaries of Repressive Chromatin Domains in Primary Human Erythroid Cells. PLOS ONE 2016, 11: e0155378. PMID: 27219007, PMCID: PMC4878738, DOI: 10.1371/journal.pone.0155378.
- Setd1a and NURF mediate chromatin dynamics and gene regulation during erythroid lineage commitment and differentiationLi Y, Schulz VP, Deng C, Li G, Shen Y, Tusi BK, Ma G, Stees J, Qiu Y, Steiner LA, Zhou L, Zhao K, Bungert J, Gallagher PG, Huang S. Setd1a and NURF mediate chromatin dynamics and gene regulation during erythroid lineage commitment and differentiation. Nucleic Acids Research 2016, 44: 7173-7188. PMID: 27141965, PMCID: PMC5009724, DOI: 10.1093/nar/gkw327.
- Diagnosis of Pyruvate Kinase DeficiencyGallagher PG, Glader B. Diagnosis of Pyruvate Kinase Deficiency. Pediatric Blood & Cancer 2016, 63: 771-772. PMID: 26836632, DOI: 10.1002/pbc.25922.
- The genetic basis of asymptomatic codon 8 frame‐shift (HBB:c25_26delAA) β0‐thalassaemia homozygotesJiang Z, Luo HY, Huang S, Farrell JJ, Davis L, Théberge R, Benson KA, Riolueang S, Viprakasit V, Al-Allawi NA, Ünal S, Gümrük F, Akar N, Başak AN, Osorio L, Badens C, Pissard S, Joly P, Campbell AD, Gallagher PG, Steinberg MH, Forget BG, Chui DH. The genetic basis of asymptomatic codon 8 frame‐shift (HBB:c25_26delAA) β0‐thalassaemia homozygotes. British Journal Of Haematology 2016, 172: 958-965. PMID: 26771086, DOI: 10.1111/bjh.13909.
- Transporting down the road to dehydrationGallagher PG. Transporting down the road to dehydration. Blood 2015, 126: 2775-2776. PMID: 26705342, DOI: 10.1182/blood-2015-10-675488.
- Pomalidomide reverses γ-globin silencing through the transcriptional reprogramming of adult hematopoietic progenitors.Dulmovits BM, Appiah-Kubi AO, Papoin J, Hale J, He M, Al-Abed Y, Didier S, Gould M, Husain-Krautter S, Singh SA, Chan KW, Vlachos A, Allen SL, Taylor N, Marambaud P, An X, Gallagher PG, Mohandas N, Lipton JM, Liu JM, Blanc L. Pomalidomide reverses γ-globin silencing through the transcriptional reprogramming of adult hematopoietic progenitors. Blood 2015, 127: 1481-92. PMID: 26679864, PMCID: PMC4797024, DOI: 10.1182/blood-2015-09-667923.
- Diagnosis and management of rare congenital nonimmune hemolytic disease.Gallagher PG. Diagnosis and management of rare congenital nonimmune hemolytic disease. Hematology 2015, 2015: 392-9. PMID: 26637748, DOI: 10.1182/asheducation-2015.1.392.
- Identification of a Novel SLC40A1 Arg88Ile Mutation in a Patient with Familial Iron Overload Treated By PhlebotomySeid J, Lozovatsky L, Gallagher P, Finberg K. Identification of a Novel SLC40A1 Arg88Ile Mutation in a Patient with Familial Iron Overload Treated By Phlebotomy. Blood 2015, 126: 954-954. DOI: 10.1182/blood.v126.23.954.954.
- The Histone Methyltransferase Setd8 Is Essential for Mammalian ErythropoiesisMalik J, Getman M, Lillis J, Gallagher P, Steiner L. The Histone Methyltransferase Setd8 Is Essential for Mammalian Erythropoiesis. Blood 2015, 126: 3577-3577. DOI: 10.1182/blood.v126.23.3577.3577.
- Pomalidomide Transcriptionally Reprograms Adult Erythroid Progenitors Independently of Ikaros Proteasomal DegradationDulmovits B, Appiah-Kubi A, Papoin J, Hale J, He M, Al-Abed Y, Allen S, Taylor N, Marambaud P, An X, Gallagher P, Mohandas N, Lipton J, Liu J, Blanc L. Pomalidomide Transcriptionally Reprograms Adult Erythroid Progenitors Independently of Ikaros Proteasomal Degradation. Blood 2015, 126: 160-160. DOI: 10.1182/blood.v126.23.160.160.
- CASE 5—2016Complex Congenital Cardiac Surgery in an Adult Patient With Hereditary Spherocytosis: Avoidance of Massive Hemolysis Associated With Extracorporeal Circulation in the Presence of Red Blood Cell FragilityHargrave JM, Capdeville MJ, Duncan AE, Smith MM, Mauermann WJ, Gallagher PG. CASE 5—2016Complex Congenital Cardiac Surgery in an Adult Patient With Hereditary Spherocytosis: Avoidance of Massive Hemolysis Associated With Extracorporeal Circulation in the Presence of Red Blood Cell Fragility. Journal Of Cardiothoracic And Vascular Anesthesia 2015, 30: 800-808. PMID: 27021177, DOI: 10.1053/j.jvca.2015.11.016.
- Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosisGlogowska E, Lezon-Geyda K, Maksimova Y, Schulz VP, Gallagher PG. Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis. Blood 2015, 126: 1281-1284. PMID: 26198474, PMCID: PMC4566808, DOI: 10.1182/blood-2015-07-657957.
- A Pediatrician’s Practical Guide to Diagnosing and Treating Hereditary Spherocytosis in NeonatesChristensen RD, Yaish HM, Gallagher PG. A Pediatrician’s Practical Guide to Diagnosing and Treating Hereditary Spherocytosis in Neonates. Pediatrics 2015, 135: 1107-1114. PMID: 26009624, PMCID: PMC4444801, DOI: 10.1542/peds.2014-3516.
- Clinical and Molecular Epidemiology of Methicillin-Resistant Staphylococcus aureus in a Neonatal Intensive Care Unit in the Decade following Implementation of an Active Detection and Isolation ProgramNelson MU, Bizzarro MJ, Baltimore RS, Dembry LM, Gallagher PG. Clinical and Molecular Epidemiology of Methicillin-Resistant Staphylococcus aureus in a Neonatal Intensive Care Unit in the Decade following Implementation of an Active Detection and Isolation Program. Journal Of Clinical Microbiology 2015, 53: 2492-2501. PMID: 26019206, PMCID: PMC4508396, DOI: 10.1128/jcm.00470-15.
- Disorders of erythrocyte volume homeostasisGlogowska E, Gallagher PG. Disorders of erythrocyte volume homeostasis. International Journal Of Laboratory Hematology 2015, 37: 85-91. PMID: 25976965, PMCID: PMC4435826, DOI: 10.1111/ijlh.12357.
- Neonatal Sepsis 2004-2013: The Rise and Fall of Coagulase-Negative StaphylococciBizzarro MJ, Shabanova V, Baltimore RS, Dembry LM, Ehrenkranz RA, Gallagher PG. Neonatal Sepsis 2004-2013: The Rise and Fall of Coagulase-Negative Staphylococci. The Journal Of Pediatrics 2015, 166: 1193-1199. PMID: 25919728, PMCID: PMC4413005, DOI: 10.1016/j.jpeds.2015.02.009.
- Human and murine erythropoiesisAn X, Schulz VP, Mohandas N, Gallagher PG. Human and murine erythropoiesis. Current Opinion In Hematology 2015, 22: 206-211. PMID: 25719574, PMCID: PMC4401149, DOI: 10.1097/moh.0000000000000134.
- Sensing Force by Trigeminal Neurons of Acutely Mechanosensitive BirdsSchneider E, Mastrotto M, Laursen W, Schulz V, Goodman J, Funk O, Gallagher P, Gracheva E, Bagriantsev S. Sensing Force by Trigeminal Neurons of Acutely Mechanosensitive Birds. Biophysical Journal 2015, 108: 562a. DOI: 10.1016/j.bpj.2014.11.3080.
- Codanin-1 Binds to Key Erythroid Genes and Its Knockdown Coupled with Ectopic Mutant Expression Recapitulates the Congenital Dyserythropoietic Anemia Type I (CDA I) PhenotypeBosques L, Tang C, Krause D, Weissman S, Gallagher P, Weiss M, Tamary H, Kupfer G. Codanin-1 Binds to Key Erythroid Genes and Its Knockdown Coupled with Ectopic Mutant Expression Recapitulates the Congenital Dyserythropoietic Anemia Type I (CDA I) Phenotype. Blood 2014, 124: 360-360. DOI: 10.1182/blood.v124.21.360.360.
- Pomalidomide Modulates Transcription Networks Regulating Human Erythropoiesis and Globin Switching: Implications for Treatment of HemoglobinopathiesDulmovits B, Appiah-Kubi A, Papoin J, Gould M, An X, Mohandas N, Gallagher P, Lipton J, Liu J, Blanc L. Pomalidomide Modulates Transcription Networks Regulating Human Erythropoiesis and Globin Switching: Implications for Treatment of Hemoglobinopathies. Blood 2014, 124: 1375-1375. DOI: 10.1182/blood.v124.21.1375.1375.
- The Novel PIEZO1 Mutation p.L2023V Is Causal for Hereditary Xerocytosis Resulting in Delayed Channel Inactivation and a Dehydrated Red Blood Cell PhenotypeRisinger M, Glogowska E, Begtrup A, Dagaonkar N, Chonat S, Joiner C, Quinn C, Kalfa T, Gallagher P. The Novel PIEZO1 Mutation p.L2023V Is Causal for Hereditary Xerocytosis Resulting in Delayed Channel Inactivation and a Dehydrated Red Blood Cell Phenotype. Blood 2014, 124: 741-741. DOI: 10.1182/blood.v124.21.741.741.
- Assessment of HbF QTLs Affecting Disease Severity and Genetic Analysis in Patients Homozygous for Codon 8 (–AA) β0-Thalassemia MutationJiang Z, Huang S, Luo H, Akar N, Basak A, Al-Allawi N, Unal S, Gumruk F, Davis L, Morrison T, Campbell A, Gallagher P, Forget B, Steinberg M, Chui D. Assessment of HbF QTLs Affecting Disease Severity and Genetic Analysis in Patients Homozygous for Codon 8 (–AA) β0-Thalassemia Mutation. Blood 2014, 124: 2690-2690. DOI: 10.1182/blood.v124.21.2690.2690.
- Isolation and transcriptome analyses of human erythroid progenitors: BFU-E and CFU-ELi J, Hale J, Bhagia P, Xue F, Chen L, Jaffray J, Yan H, Lane J, Gallagher PG, Mohandas N, Liu J, An X. Isolation and transcriptome analyses of human erythroid progenitors: BFU-E and CFU-E. Blood 2014, 124: 3636-3645. PMID: 25339359, PMCID: PMC4256913, DOI: 10.1182/blood-2014-07-588806.
- Global transcriptome analysis and enhancer landscape of human primary T follicular helper and T effector lymphocytesWeinstein JS, Lezon-Geyda K, Maksimova Y, Craft S, Zhang Y, Su M, Schulz VP, Craft J, Gallagher PG. Global transcriptome analysis and enhancer landscape of human primary T follicular helper and T effector lymphocytes. Blood 2014, 124: 3719-3729. PMID: 25331115, PMCID: PMC4263981, DOI: 10.1182/blood-2014-06-582700.
- Piezo Proteins: Regulators of Mechanosensation and Other Cellular Processes*Bagriantsev SN, Gracheva EO, Gallagher PG. Piezo Proteins: Regulators of Mechanosensation and Other Cellular Processes*. Journal Of Biological Chemistry 2014, 289: 31673-31681. PMID: 25305018, PMCID: PMC4231648, DOI: 10.1074/jbc.r114.612697.
- Neuronal mechanism for acute mechanosensitivity in tactile-foraging waterfowlSchneider ER, Mastrotto M, Laursen WJ, Schulz VP, Goodman JB, Funk OH, Gallagher PG, Gracheva EO, Bagriantsev SN. Neuronal mechanism for acute mechanosensitivity in tactile-foraging waterfowl. Proceedings Of The National Academy Of Sciences Of The United States Of America 2014, 111: 14941-14946. PMID: 25246547, PMCID: PMC4205607, DOI: 10.1073/pnas.1413656111.
- One size does not fit all: why universal decolonization strategies to prevent methicillin-resistant Staphylococcus aureus colonization and infection in adult intensive care units may be inappropriate for neonatal intensive care unitsNelson MU, Bizzarro MJ, Dembry LM, Baltimore RS, Gallagher PG. One size does not fit all: why universal decolonization strategies to prevent methicillin-resistant Staphylococcus aureus colonization and infection in adult intensive care units may be inappropriate for neonatal intensive care units. Journal Of Perinatology 2014, 34: 653-655. PMID: 25010223, PMCID: PMC4152419, DOI: 10.1038/jp.2014.125.
- Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locusBogardus H, Schulz VP, Maksimova Y, Miller BA, Li P, Forget BG, Gallagher PG. Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus. Haematologica 2014, 99: e168-e170. PMID: 24895341, PMCID: PMC4562552, DOI: 10.3324/haematol.2014.110312.
- Global transcriptome analyses of human and murine terminal erythroid differentiationAn X, Schulz VP, Li J, Wu K, Liu J, Xue F, Hu J, Mohandas N, Gallagher PG. Global transcriptome analyses of human and murine terminal erythroid differentiation. Blood 2014, 123: 3466-3477. PMID: 24637361, PMCID: PMC4041167, DOI: 10.1182/blood-2014-01-548305.
- Clinical and Laboratory Factors That Predict Death in Very Low Birth Weight Infants Presenting With Late-onset SepsisLevit O, Bhandari V, Li FY, Shabanova V, Gallagher PG, Bizzarro MJ. Clinical and Laboratory Factors That Predict Death in Very Low Birth Weight Infants Presenting With Late-onset Sepsis. The Pediatric Infectious Disease Journal 2014, 33: 143-146. PMID: 24418836, PMCID: PMC3917323, DOI: 10.1097/inf.0000000000000024.
- Nonstochastic Reprogramming from a Privileged Somatic Cell StateGuo S, Zi X, Schulz VP, Cheng J, Zhong M, Koochaki SH, Megyola CM, Pan X, Heydari K, Weissman SM, Gallagher PG, Krause DS, Fan R, Lu J. Nonstochastic Reprogramming from a Privileged Somatic Cell State. Cell 2014, 156: 649-662. PMID: 24486105, PMCID: PMC4318260, DOI: 10.1016/j.cell.2014.01.020.
- Long noncoding RNAs in erythropoiesisGallagher PG. Long noncoding RNAs in erythropoiesis. Blood 2014, 123: 465-466. PMID: 24458276, DOI: 10.1182/blood-2013-12-538306.
- Probing large conformational rearrangements in wild-type and mutant spectrin using structural mass spectrometrySriswasdi S, Harper SL, Tang HY, Gallagher PG, Speicher DW. Probing large conformational rearrangements in wild-type and mutant spectrin using structural mass spectrometry. Proceedings Of The National Academy Of Sciences Of The United States Of America 2014, 111: 1801-1806. PMID: 24453214, PMCID: PMC3918770, DOI: 10.1073/pnas.1317620111.
- Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disabilityXu F, Li L, Schulz VP, Gallagher PG, Xiang B, Zhao H, Li P. Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disability. Molecular Cytogenetics 2014, 7: 4. PMID: 24410907, PMCID: PMC3905969, DOI: 10.1186/1755-8166-7-4.
- Enhancers and Super Enhancers Are Associated With Genes That Control Phenotypic Traits In Primary Human Erythroid CellsSchulz V, Lezon-Geyda K, Maksimova Y, Gallagher P. Enhancers and Super Enhancers Are Associated With Genes That Control Phenotypic Traits In Primary Human Erythroid Cells. Blood 2013, 122: 1200-1200. DOI: 10.1182/blood.v122.21.1200.1200.
- The Patient With Transfusion-Dependent Anemia: Diagnosis and Directed Management With Targeted Next Generation Sequencing and Copy Number AnalysisSchulz V, Maksimova Y, Lezon-Geyda K, Gallagher P. The Patient With Transfusion-Dependent Anemia: Diagnosis and Directed Management With Targeted Next Generation Sequencing and Copy Number Analysis. Blood 2013, 122: 3419-3419. DOI: 10.1182/blood.v122.21.3419.3419.
- Glucose Phosphate Isomerase Deficiency In 2 Patients With Novel Mutations Presenting As Severe Neurologic Abnormalities and Transfusion Dependent Hemolytic AnemiaPuliyel M, Gallagher P, Berdoukas V, Glader B, Coates T. Glucose Phosphate Isomerase Deficiency In 2 Patients With Novel Mutations Presenting As Severe Neurologic Abnormalities and Transfusion Dependent Hemolytic Anemia. Blood 2013, 122: 947-947. DOI: 10.1182/blood.v122.21.947.947.
- Whole-exome sequencing identifies a novel somatic mutation in MMP8 associated with a t(1;22)-acute megakaryoblastic leukemiaKim Y, Schulz VP, Satake N, Gruber TA, Teixeira AM, Halene S, Gallagher PG, Krause DS. Whole-exome sequencing identifies a novel somatic mutation in MMP8 associated with a t(1;22)-acute megakaryoblastic leukemia. Leukemia 2013, 28: 945-948. PMID: 24157583, PMCID: PMC3981934, DOI: 10.1038/leu.2013.314.
- Concurrent Bloodstream Infections in Infants with Necrotizing EnterocolitisBizzarro MJ, Ehrenkranz RA, Gallagher PG. Concurrent Bloodstream Infections in Infants with Necrotizing Enterocolitis. The Journal Of Pediatrics 2013, 164: 61-66. PMID: 24139563, DOI: 10.1016/j.jpeds.2013.09.020.
- Abnormalities of the Erythrocyte MembraneGallagher PG. Abnormalities of the Erythrocyte Membrane. Pediatric Clinics Of North America 2013, 60: 1349-1362. PMID: 24237975, PMCID: PMC4155395, DOI: 10.1016/j.pcl.2013.09.001.
- Applications of high-throughput DNA sequencing to benign hematologySankaran VG, Gallagher PG. Applications of high-throughput DNA sequencing to benign hematology. Blood 2013, 122: 3575-3582. PMID: 24021670, PMCID: PMC3837507, DOI: 10.1182/blood-2013-07-460337.
- Late-onset Leclercia adecarboxylata sepsis in a premature neonateNelson MU, Maksimova Y, Schulz V, Bizzarro MJ, Gallagher PG. Late-onset Leclercia adecarboxylata sepsis in a premature neonate. Journal Of Perinatology 2013, 33: 740-742. PMID: 23986093, DOI: 10.1038/jp.2013.34.
- The common hereditary elliptocytosis-associated α-spectrin L260P mutation perturbs erythrocyte membranes by stabilizing spectrin in the closed dimer conformationHarper SL, Sriswasdi S, Tang HY, Gaetani M, Gallagher PG, Speicher DW. The common hereditary elliptocytosis-associated α-spectrin L260P mutation perturbs erythrocyte membranes by stabilizing spectrin in the closed dimer conformation. Blood 2013, 122: 3045-3053. PMID: 23974198, PMCID: PMC3811177, DOI: 10.1182/blood-2013-02-487702.
- USF1 and hSET1A Mediated Epigenetic Modifications Regulate Lineage Differentiation and HoxB4 TranscriptionDeng C, Li Y, Liang S, Cui K, Salz T, Yang H, Tang Z, Gallagher PG, Qiu Y, Roeder R, Zhao K, Bungert J, Huang S. USF1 and hSET1A Mediated Epigenetic Modifications Regulate Lineage Differentiation and HoxB4 Transcription. PLOS Genetics 2013, 9: e1003524. PMID: 23754954, PMCID: PMC3675019, DOI: 10.1371/journal.pgen.1003524.
- Disorders of red cell volume regulationGallagher PG. Disorders of red cell volume regulation. Current Opinion In Hematology 2013, 20: 201-207. PMID: 23519154, DOI: 10.1097/moh.0b013e32835f6870.
- Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotypeNgo D, Bae H, Steinberg MH, Sebastiani P, Solovieff N, Baldwin CT, Melista E, Safaya S, Farrer LA, Al-Suliman AM, Albuali WH, Bagshi M, Naserullah Z, Akinsheye I, Gallagher P, Luo HY, Chui DH, Farrell JJ, Al-Ali AK, Alsultan A. Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype. Blood Cells Molecules And Diseases 2013, 51: 22-26. PMID: 23465615, PMCID: PMC3647015, DOI: 10.1016/j.bcmd.2012.12.005.
- Identification of Biologically Relevant Enhancers in Human Erythroid Cells*Su MY, Steiner LA, Bogardus H, Mishra T, Schulz VP, Hardison RC, Gallagher PG. Identification of Biologically Relevant Enhancers in Human Erythroid Cells*. Journal Of Biological Chemistry 2013, 288: 8433-8444. PMID: 23341446, PMCID: PMC3605659, DOI: 10.1074/jbc.m112.413260.
- Methicillin-Resistant Staphylococcus aureus in the Neonatal Intensive Care UnitNelson MU, Gallagher PG. Methicillin-Resistant Staphylococcus aureus in the Neonatal Intensive Care Unit. Seminars In Perinatology 2012, 36: 424-430. PMID: 23177801, PMCID: PMC3508470, DOI: 10.1053/j.semperi.2012.06.004.
- Identification of Biologicaly Relevant Enhancers in Human Erythroid CellsSu M, Steiner L, Bogardus H, Schulz V, Hardison R, Gallagher P. Identification of Biologicaly Relevant Enhancers in Human Erythroid Cells. Blood 2012, 120: 368-368. DOI: 10.1182/blood.v120.21.368.368.
- Severe Impairment of γ-Globin Gene Silencing in an Asymptomatic Adult Patient Homozygous for the Codon 8 (–AA) Frame-Shift β0-Thalassemia MutationCampbell A, Luo H, Benson K, Davis L, Gallagher P, Steinberg M, Fraser P, Forget B, Chui D. Severe Impairment of γ-Globin Gene Silencing in an Asymptomatic Adult Patient Homozygous for the Codon 8 (–AA) Frame-Shift β0-Thalassemia Mutation. Blood 2012, 120: 1022-1022. DOI: 10.1182/blood.v120.21.1022.1022.
- A tissue-specific chromatin loop activates the erythroid ankyrin-1 promoterYocum AO, Steiner LA, Seidel NE, Cline AP, Rout ED, Lin JY, Wong C, Garrett LJ, Gallagher PG, Bodine DM. A tissue-specific chromatin loop activates the erythroid ankyrin-1 promoter. Blood 2012, 120: 3586-3593. PMID: 22968456, PMCID: PMC3482866, DOI: 10.1182/blood-2012-08-450262.
- Teleost growth factor independence (gfi) genes differentially regulate successive waves of hematopoiesisCooney JD, Hildick-Smith GJ, Shafizadeh E, McBride PF, Carroll KJ, Anderson H, Shaw GC, Tamplin OJ, Branco DS, Dalton AJ, Shah DI, Wong C, Gallagher PG, Zon LI, North TE, Paw BH. Teleost growth factor independence (gfi) genes differentially regulate successive waves of hematopoiesis. Developmental Biology 2012, 373: 431-441. PMID: 22960038, PMCID: PMC3532562, DOI: 10.1016/j.ydbio.2012.08.015.
- MKL1 and MKL2 play redundant and crucial roles in megakaryocyte maturation and platelet formationSmith EC, Thon JN, Devine MT, Lin S, Schulz VP, Guo Y, Massaro SA, Halene S, Gallagher P, Italiano JE, Krause DS. MKL1 and MKL2 play redundant and crucial roles in megakaryocyte maturation and platelet formation. Blood 2012, 120: 2317-2329. PMID: 22806889, PMCID: PMC3447785, DOI: 10.1182/blood-2012-04-420828.
- Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosisZarychanski R, Schulz VP, Houston BL, Maksimova Y, Houston DS, Smith B, Rinehart J, Gallagher PG. Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis. Blood 2012, 120: 1908-1915. PMID: 22529292, PMCID: PMC3448561, DOI: 10.1182/blood-2012-04-422253.
- Altered subcellular localization of transcription factor TEAD4 regulates first mammalian cell lineage commitmentHome P, Saha B, Ray S, Dutta D, Gunewardena S, Yoo B, Pal A, Vivian JL, Larson M, Petroff M, Gallagher PG, Schulz VP, White KL, Golos TG, Behr B, Paul S. Altered subcellular localization of transcription factor TEAD4 regulates first mammalian cell lineage commitment. Proceedings Of The National Academy Of Sciences Of The United States Of America 2012, 109: 7362-7367. PMID: 22529382, PMCID: PMC3358889, DOI: 10.1073/pnas.1201595109.
- A de novo band 3 mutation in hereditary spherocytosisBogardus HH, Maksimova YD, Forget BG, Gallagher PG. A de novo band 3 mutation in hereditary spherocytosis. Pediatric Blood & Cancer 2011, 58: 1004-1004. PMID: 22170767, DOI: 10.1002/pbc.23400.
- A New Case of KLF1 G973A Mutation and Congenital Dyserythropoeitic Anemia (CDA)- Further Definition of Emerging New Syndrome and Possible Association with Gonadal DysgenesisRavindranath Y, Goyette G, Buck S, Gadgeel M, Dombkowski A, Boxer L, Gallagher P, Johnson R. A New Case of KLF1 G973A Mutation and Congenital Dyserythropoeitic Anemia (CDA)- Further Definition of Emerging New Syndrome and Possible Association with Gonadal Dysgenesis. Blood 2011, 118: 2101-2101. DOI: 10.1182/blood.v118.21.2101.2101.
- Unbiased Identification of Functional Barrier Insulators in Primary Human Erythroid Cells,Steiner L, Schulz V, Maksimova Y, Seidel N, Bodine D, Gallagher P. Unbiased Identification of Functional Barrier Insulators in Primary Human Erythroid Cells,. Blood 2011, 118: 3385-3385. DOI: 10.1182/blood.v118.21.3385.3385.
- Transfusion-Dependent Alpha-Spectrin Deficient Hemolytic Anemia Due to Maternal Uniparental DisomyBogardus H, Schulz V, Maksimova Y, Miller B, Forget B, Gallagher P. Transfusion-Dependent Alpha-Spectrin Deficient Hemolytic Anemia Due to Maternal Uniparental Disomy. Blood 2011, 118: 1030-1030. DOI: 10.1182/blood.v118.21.1030.1030.
- Integrated Genome-Wide CTCF and CohesinSA1 Occupancy and Expression Analyses in ErythropoiesisSchulz V, Steiner L, Maksimova Y, Gallagher P. Integrated Genome-Wide CTCF and CohesinSA1 Occupancy and Expression Analyses in Erythropoiesis. Blood 2011, 118: 1305-1305. DOI: 10.1182/blood.v118.21.1305.1305.
- Primitive Erythroid Progenitors Are Regulated by Hypoxia and Display An Aerobic Glycolytic Metabolic Profile,Baron M, Isern J, Fraser S, He Z, Ma'ayan A, Schulz V, Tuck D, Gallagher P. Primitive Erythroid Progenitors Are Regulated by Hypoxia and Display An Aerobic Glycolytic Metabolic Profile,. Blood 2011, 118: 3159-3159. DOI: 10.1182/blood.v118.21.3159.3159.
- Genetic Linkage of the Dehydrated Hereditary Stomatocytosis Locus to Chromosome 16 in Two Kindreds and Refinement of the Candidate Gene Region to 16q24.2 - 16qter,Houston B, Zelinski T, Houston D, Israels S, Coghlan G, Chodirker B, Gallagher P, Zarychanski R. Genetic Linkage of the Dehydrated Hereditary Stomatocytosis Locus to Chromosome 16 in Two Kindreds and Refinement of the Candidate Gene Region to 16q24.2 - 16qter,. Blood 2011, 118: 3170-3170. DOI: 10.1182/blood.v118.21.3170.3170.
- Genetic diagnosis of neuroacanthocytosis disorders using exome sequencingWalker RH, Schulz VP, Tikhonova IR, Mahajan MC, Mane S, Muniz M, Gallagher PG. Genetic diagnosis of neuroacanthocytosis disorders using exome sequencing. Movement Disorders 2011, 27: 539-543. PMID: 22038564, DOI: 10.1002/mds.24020.
- HbA2: at the borderline of the KLFGallagher PG. HbA2: at the borderline of the KLF. Blood 2011, 118: 4301-4302. PMID: 22021451, DOI: 10.1182/blood-2011-08-373324.
- Granulicatella adiacens and Early-Onset Sepsis in Neonate - Volume 17, Number 10—October 2011 - Emerging Infectious Diseases journal - CDCBizzarro MJ, Callan DA, Farrel PA, Dembry LM, Gallagher PG. Granulicatella adiacens and Early-Onset Sepsis in Neonate - Volume 17, Number 10—October 2011 - Emerging Infectious Diseases journal - CDC. Emerging Infectious Diseases 2011, 17: 1971-1973. PMID: 22000391, PMCID: PMC3310662, DOI: 10.3201/eid1710.101967.
- Granulicatella adiacens and Early-Onset Sepsis in NeonateBizzarro M, Callan D, Farrel P, Dembry L, Gallagher P. Granulicatella adiacens and Early-Onset Sepsis in Neonate. Emerging Infectious Diseases 2011 DOI: 10.3201/eid1710.101967_article.htm.
- Refinement of the hereditary xerocytosis locus on chromosome 16q in a large Canadian kindredHouston BL, Zelinski T, Israels SJ, Coghlan G, Chodirker BN, Gallagher PG, Houston DS, Zarychanski R. Refinement of the hereditary xerocytosis locus on chromosome 16q in a large Canadian kindred. Blood Cells Molecules And Diseases 2011, 47: 226-231. PMID: 21944700, DOI: 10.1016/j.bcmd.2011.08.001.
- Patterns of Histone H3 Lysine 27 Monomethylation and Erythroid Cell Type-specific Gene Expression*Steiner LA, Schulz VP, Maksimova Y, Wong C, Gallagher PG. Patterns of Histone H3 Lysine 27 Monomethylation and Erythroid Cell Type-specific Gene Expression*. Journal Of Biological Chemistry 2011, 286: 39457-39465. PMID: 21937433, PMCID: PMC3234769, DOI: 10.1074/jbc.m111.243006.
- Genome-wide ChIP-Seq reveals a dramatic shift in the binding of the transcription factor erythroid Kruppel-like factor during erythrocyte differentiationPilon AM, Ajay SS, Kumar SA, Steiner LA, Cherukuri PF, Wincovitch S, Anderson SM, Center N, Mullikin J, Mullikin JC, Gallagher P, Gallagher PG, Hardison R, Hardison RC, Margulies E, Margulies EH, Bodine D, Bodine DM. Genome-wide ChIP-Seq reveals a dramatic shift in the binding of the transcription factor erythroid Kruppel-like factor during erythrocyte differentiation. Blood 2011, 118: e139-e148. PMID: 21900194, PMCID: PMC3208289, DOI: 10.1182/blood-2011-05-355107.
- Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65SStewart AK, Shmukler BE, Vandorpe DH, Rivera A, Heneghan JF, Li X, Hsu A, Karpatkin M, O'Neill AF, Bauer DE, Heeney MM, John K, Kuypers FA, Gallagher PG, Lux SE, Brugnara C, Westhoff CM, Alper SL. Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65S. American Journal Of Physiology - Cell Physiology 2011, 301: c1325-c1343. PMID: 21849667, PMCID: PMC3233792, DOI: 10.1152/ajpcell.00054.2011.
- Erythrocyte peripheral type benzodiazepine receptor/voltage-dependent anion channels are upregulated by Plasmodium falciparumBouyer G, Cueff A, Egée S, Kmiecik J, Maksimova Y, Glogowska E, Gallagher PG, Thomas SL. Erythrocyte peripheral type benzodiazepine receptor/voltage-dependent anion channels are upregulated by Plasmodium falciparum. Blood 2011, 118: 2305-2312. PMID: 21795748, DOI: 10.1182/blood-2011-01-329300.
- Perinatal Onset Mevalonate Kinase DeficiencySteiner LA, Ehrenkranz RA, Peterec SM, Steiner RD, Reyes-Múgica M, Gallagher PG. Perinatal Onset Mevalonate Kinase Deficiency. Pediatric And Developmental Pathology 2011, 14: 301-306. PMID: 21425920, DOI: 10.2350/11-02-0985-oa.1.
- Chromatin boundaries require functional collaboration between the hSET1 and NURF complexesLi X, Wang S, Li Y, Deng C, Steiner LA, Xiao H, Wu C, Bungert J, Gallagher PG, Felsenfeld G, Qiu Y, Huang S. Chromatin boundaries require functional collaboration between the hSET1 and NURF complexes. Blood 2011, 118: 1386-1394. PMID: 21653943, PMCID: PMC3152501, DOI: 10.1182/blood-2010-11-319111.
- Bi‐allelic deletions within 13q14 and transient trisomy 21 with absence of GATA1s in pediatric acute megakaryoblastic leukemiaMassaro SA, Bajaj R, Pashankar FD, Ornstein D, Gallagher PG, Krause DS, Li P. Bi‐allelic deletions within 13q14 and transient trisomy 21 with absence of GATA1s in pediatric acute megakaryoblastic leukemia. Pediatric Blood & Cancer 2011, 57: 516-519. PMID: 21538823, PMCID: PMC4517576, DOI: 10.1002/pbc.23156.
- Partial Exchange Transfusion for Polycythemia Hyperviscosity SyndromeHopewell B, Steiner L, Ehrenkranz R, Bizzarro M, Gallagher P. Partial Exchange Transfusion for Polycythemia Hyperviscosity Syndrome. American Journal Of Perinatology 2011, 28: 557-564. PMID: 21365533, DOI: 10.1055/s-0031-1274504.
- Single-lineage transcriptome analysis reveals key regulatory pathways in primitive erythroid progenitors in the mouse embryoIsern J, He Z, Fraser ST, Nowotschin S, Ferrer-Vaquer A, Moore R, Hadjantonakis AK, Schulz V, Tuck D, Gallagher PG, Baron MH. Single-lineage transcriptome analysis reveals key regulatory pathways in primitive erythroid progenitors in the mouse embryo. Blood 2011, 117: 4924-4934. PMID: 21263157, PMCID: PMC3100699, DOI: 10.1182/blood-2010-10-313676.
- Mutation of a barrier insulator in the human ankyrin-1 gene is associated with hereditary spherocytosisGallagher PG, Steiner LA, Liem RI, Owen AN, Cline AP, Seidel NE, Garrett LJ, Bodine DM. Mutation of a barrier insulator in the human ankyrin-1 gene is associated with hereditary spherocytosis. Journal Of Clinical Investigation 2010, 120: 4453-4465. PMID: 21099109, PMCID: PMC2993586, DOI: 10.1172/jci42240.
- A Common Regulatory Signature Associated with Barrier Insulators in Human Primary Erythroid CellsSteiner L, Maksimova Y, Schulz V, Gallagher P. A Common Regulatory Signature Associated with Barrier Insulators in Human Primary Erythroid Cells. Blood 2010, 116: 3868-3868. DOI: 10.1182/blood.v116.21.3868.3868.
- Dynamic CO-Localization of GATA1, NFE2, and EKLF and Changes in Gene Expression During HematopoiesisSteiner L, Schulz V, Maksimova Y, Mahajan M, Bodine D, Gallagher P. Dynamic CO-Localization of GATA1, NFE2, and EKLF and Changes in Gene Expression During Hematopoiesis. Blood 2010, 116: 741-741. DOI: 10.1182/blood.v116.21.741.741.
- Genome-wide detection of a TFIID localization element from an initial human disease mutationYang MQ, Laflamme K, Gotea V, Joiner CH, Seidel NE, Wong C, Petrykowska HM, Lichtenberg J, Lee S, Welch L, Gallagher PG, Bodine DM, Elnitski L. Genome-wide detection of a TFIID localization element from an initial human disease mutation. Nucleic Acids Research 2010, 39: 2175-2187. PMID: 21071415, PMCID: PMC3064768, DOI: 10.1093/nar/gkq1035.
- A Comprehensive Model of the Spectrin Divalent Tetramer Binding Region Deduced Using Homology Modeling and Chemical Cross-linking of a Mini-spectrin [S] *Li D, Harper SL, Tang HY, Maksimova Y, Gallagher PG, Speicher DW. A Comprehensive Model of the Spectrin Divalent Tetramer Binding Region Deduced Using Homology Modeling and Chemical Cross-linking of a Mini-spectrin [S] *. Journal Of Biological Chemistry 2010, 285: 29535-29545. PMID: 20610390, PMCID: PMC2937985, DOI: 10.1074/jbc.m110.145573.
- Functional Analysis of a Novel cis-Acting Regulatory Region within the Human Ankyrin Gene (ANK-1) PromoterLaflamme K, Owen AN, Devlin EE, Yang MQ, Wong C, Steiner LA, Garrett LJ, Elnitski L, Gallagher PG, Bodine DM. Functional Analysis of a Novel cis-Acting Regulatory Region within the Human Ankyrin Gene (ANK-1) Promoter. Molecular And Cellular Biology 2010, 30: 3493-3502. PMID: 20479128, PMCID: PMC2897556, DOI: 10.1128/mcb.00119-10.
- A Fused α-β “Mini-spectrin” Mimics the Intact Erythrocyte Spectrin Head-to-head Tetramer*Harper SL, Li D, Maksimova Y, Gallagher PG, Speicher DW. A Fused α-β “Mini-spectrin” Mimics the Intact Erythrocyte Spectrin Head-to-head Tetramer*. Journal Of Biological Chemistry 2010, 285: 11003-11012. PMID: 20139081, PMCID: PMC2856305, DOI: 10.1074/jbc.m109.083048.
- Determinants of erythrocyte hydrationRinehart J, Gulcicek EE, Joiner CH, Lifton RP, Gallagher PG. Determinants of erythrocyte hydration. Current Opinion In Hematology 2010, 17: 191-197. PMID: 20182354, PMCID: PMC4155397, DOI: 10.1097/moh.0b013e32833800d0.
- Patterns of Monomethylation of Histone H3 Lysine 27 Influence Gene Expression in a Cell-Type Specific Manner.Steiner L, Schulz V, Maksimova Y, Wong C, Tuck D, Gallagher P. Patterns of Monomethylation of Histone H3 Lysine 27 Influence Gene Expression in a Cell-Type Specific Manner. Blood 2009, 114: 4585-4585. DOI: 10.1182/blood.v114.22.4585.4585.
- A Modified ANK-1 Promoter Directs Uniform, Copy Number Dependent Gamma Globin Gene Expression at Therapeutic Levels of a in a Lentivirus Vector.Harrow F, Cline A, Seidel N, Persons D, Gallagher P, Bodine D. A Modified ANK-1 Promoter Directs Uniform, Copy Number Dependent Gamma Globin Gene Expression at Therapeutic Levels of a in a Lentivirus Vector. Blood 2009, 114: 3565-3565. DOI: 10.1182/blood.v114.22.3565.3565.
- Genome-Wide ChIP-Seq Reveals a Dramatic Shift in the EKLF Binding Profile Between Erythroid Progenitors and Erythroblasts.Pilon A, Ajay S, Abaan H, Margulies E, Gallagher P, Bodine D. Genome-Wide ChIP-Seq Reveals a Dramatic Shift in the EKLF Binding Profile Between Erythroid Progenitors and Erythroblasts. Blood 2009, 114: 565-565. DOI: 10.1182/blood.v114.22.565.565.
- The GPA-dependent, spherostomatocytosis mutant AE1 E758K induces GPA-independent, endogenous cation transport in amphibian oocytesStewart AK, Vandorpe DH, Heneghan JF, Chebib F, Stolpe K, Akhavein A, Edelman EJ, Maksimova Y, Gallagher PG, Alper SL. The GPA-dependent, spherostomatocytosis mutant AE1 E758K induces GPA-independent, endogenous cation transport in amphibian oocytes. American Journal Of Physiology - Cell Physiology 2009, 298: c283-c297. PMID: 19907019, PMCID: PMC2822494, DOI: 10.1152/ajpcell.00444.2009.
- Chromatin Architecture and Transcription Factor Binding Regulate Expression of Erythrocyte Membrane Protein GenesSteiner LA, Maksimova Y, Schulz V, Wong C, Raha D, Mahajan MC, Weissman SM, Gallagher PG. Chromatin Architecture and Transcription Factor Binding Regulate Expression of Erythrocyte Membrane Protein Genes. Molecular And Cellular Biology 2009, 29: 5399-5412. PMID: 19687298, PMCID: PMC2756878, DOI: 10.1128/mcb.00777-09.
- Sites of Regulated Phosphorylation that Control K-Cl Cotransporter ActivityRinehart J, Maksimova Y, Tanis J, Stone K, Hodson C, Zhang J, Risinger M, Pan W, Wu D, Colangelo C, Forbush B, Joiner C, Gulcicek E, Gallagher P, Lifton R. Sites of Regulated Phosphorylation that Control K-Cl Cotransporter Activity. Journal Of End-to-End-testing 2009, 138: 525-536. DOI: 10.1016/s9999-9994(09)20441-7.
- Sites of Regulated Phosphorylation that Control K-Cl Cotransporter ActivityRinehart J, Maksimova YD, Tanis JE, Stone KL, Hodson CA, Zhang J, Risinger M, Pan W, Wu D, Colangelo CM, Forbush B, Joiner CH, Gulcicek EE, Gallagher PG, Lifton RP. Sites of Regulated Phosphorylation that Control K-Cl Cotransporter Activity. Cell 2009, 138: 525-536. PMID: 19665974, PMCID: PMC2811214, DOI: 10.1016/j.cell.2009.05.031.
- Imaging of the diffusion of single band 3 molecules on normal and mutant erythrocytesKodippili GC, Spector J, Sullivan C, Kuypers FA, Labotka R, Gallagher PG, Ritchie K, Low PS. Imaging of the diffusion of single band 3 molecules on normal and mutant erythrocytes. Blood 2009, 113: 6237-6245. PMID: 19369229, PMCID: PMC2699255, DOI: 10.1182/blood-2009-02-205450.
- Failure of Terminal Erythroid Differentiation in EKLF-Deficient Mice Is Associated with Cell Cycle Perturbation and Reduced Expression of E2F2Pilon AM, Arcasoy MO, Dressman HK, Vayda SE, Maksimova YD, Sangerman JI, Gallagher PG, Bodine DM. Failure of Terminal Erythroid Differentiation in EKLF-Deficient Mice Is Associated with Cell Cycle Perturbation and Reduced Expression of E2F2. Molecular And Cellular Biology 2008, 28: 7394-7401. PMID: 18852285, PMCID: PMC2593440, DOI: 10.1128/mcb.01087-08.
- Insulator Elements in Erythrocyte Membrane GenesSteiner L, Maksimova Y, Lin J, Owen A, Schulz V, Bodine D, Gallagher P. Insulator Elements in Erythrocyte Membrane Genes. Blood 2008, 112: 3584-3584. DOI: 10.1182/blood.v112.11.3584.3584.
- Structural and Functional Interactions of KCl Cotransport Proteins KCC1 and KCC3 in Sickle and Normal Erythrocyte MembranesRisinger M, Rinehart J, Crable S, Ottlinger A, Winkelmann R, Pan D, Huebner C, Gallagher P, Joiner C. Structural and Functional Interactions of KCl Cotransport Proteins KCC1 and KCC3 in Sickle and Normal Erythrocyte Membranes. Blood 2008, 112: 2474-2474. DOI: 10.1182/blood.v112.11.2474.2474.
- Genome-Wide Analysis of EKLF Occupancy in Erythroid Chromatin Reveals 5′, 3′ and Intragenic Binding Sites in EKLF Target GenesPilon A, Margulies E, Abaan H, Allen A, Townes T, Frederick A, Zhou D, Gallagher P, Bodine D. Genome-Wide Analysis of EKLF Occupancy in Erythroid Chromatin Reveals 5′, 3′ and Intragenic Binding Sites in EKLF Target Genes. Blood 2008, 112: 283-283. DOI: 10.1182/blood.v112.11.283.283.
- Red cell membrane: past, present, and futureMohandas N, Gallagher PG. Red cell membrane: past, present, and future. Blood 2008, 112: 3939-3948. PMID: 18988878, PMCID: PMC2582001, DOI: 10.1182/blood-2008-07-161166.
- An insulator with barrier-element activity promotes α-spectrin gene expression in erythroid cellsGallagher PG, Nilson DG, Steiner LA, Maksimova YD, Lin JY, Bodine DM. An insulator with barrier-element activity promotes α-spectrin gene expression in erythroid cells. Blood 2008, 113: 1547-1554. PMID: 19008453, PMCID: PMC2644083, DOI: 10.1182/blood-2008-06-164954.
- Canine elliptocytosis due to a mutant β‐spectrinDi Terlizzi R, Gallagher PG, Mohandas N, Steiner LA, Dolce KS, Guo X, Wilkerson MJ, Stockham SL. Canine elliptocytosis due to a mutant β‐spectrin. Veterinary Clinical Pathology 2008, 38: 52-58. PMID: 19228356, DOI: 10.1111/j.1939-165x.2008.00092.x.
- Matched Case-Control Analysis of Polymicrobial Bloodstream Infection In A Neonatal Intensive Care UnitBizzarro MJ, Dembry LM, Baltimore RS, Gallagher PG. Matched Case-Control Analysis of Polymicrobial Bloodstream Infection In A Neonatal Intensive Care Unit. Infection Control And Hospital Epidemiology 2008, 29: 914-920. PMID: 18808341, DOI: 10.1086/591323.
- Hereditary spherocytosisPerrotta S, Gallagher PG, Mohandas N. Hereditary spherocytosis. The Lancet 2008, 372: 1411-1426. PMID: 18940465, DOI: 10.1016/s0140-6736(08)61588-3.
- Nonsense mutations of the α-spectrin gene in hereditary pyropoikilocytosisTolpinrud W, Maksimova YD, Forget BG, Gallagher PG. Nonsense mutations of the α-spectrin gene in hereditary pyropoikilocytosis. Haematologica 2008, 93: 1752-1754. PMID: 18815189, DOI: 10.3324/haematol.13639.
- Ankyrin‐linked hereditary spherocytosis in an African–American kindredSangerman J, Maksimova Y, Edelman EJ, Morrow JS, Forget BG, Gallagher PG. Ankyrin‐linked hereditary spherocytosis in an African–American kindred. American Journal Of Hematology 2008, 83: 789-794. PMID: 18704959, DOI: 10.1002/ajh.21254.
- Changing Patterns in Neonatal Escherichia coli Sepsis and Ampicillin Resistance in the Era of Intrapartum Antibiotic ProphylaxisBizzarro MJ, Dembry LM, Baltimore RS, Gallagher PG. Changing Patterns in Neonatal Escherichia coli Sepsis and Ampicillin Resistance in the Era of Intrapartum Antibiotic Prophylaxis. Pediatrics 2008, 121: 689-696. PMID: 18381532, DOI: 10.1542/peds.2007-2171.
- Structural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer siteGaetani M, Mootien S, Harper S, Gallagher PG, Speicher DW. Structural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer site. Blood 2008, 111: 5712-5720. PMID: 18218854, PMCID: PMC2424163, DOI: 10.1182/blood-2007-11-122457.
- Multiple Defects of Both Primitive and Definitive Erythrocytes in EKLF-Deficient Mice.Pilon A, Beaupre J, Bieker J, Gallagher P, Bodine D. Multiple Defects of Both Primitive and Definitive Erythrocytes in EKLF-Deficient Mice. Blood 2007, 110: 1234-1234. DOI: 10.1182/blood.v110.11.1234.1234.
- Identification and Characterization of α-Spectrin Mutations Associated with Inherited Hemolytic Anemia.Tolpinrud W, Gaetani M, Maksimova Y, Mootien S, Harper S, Forget B, Speicher D, Gallagher P. Identification and Characterization of α-Spectrin Mutations Associated with Inherited Hemolytic Anemia. Blood 2007, 110: 1706-1706. DOI: 10.1182/blood.v110.11.1706.1706.
- Alternate Promoters Direct Tissue-Specific Expression of Erythrocyte Ankyrin Transcripts with Novel NH2-Termini.Steiner L, Lin J, Owens A, Sangerman J, Bodine D, Gallagher P. Alternate Promoters Direct Tissue-Specific Expression of Erythrocyte Ankyrin Transcripts with Novel NH2-Termini. Blood 2007, 110: 1710-1710. DOI: 10.1182/blood.v110.11.1710.1710.
- A GC Box Element Is Critical for Transcriptional Regulation of the K-Cl Cotransporter Isoform KCC3a in Hematopoetic Cells.Crable S, Joiner C, Gallagher P. A GC Box Element Is Critical for Transcriptional Regulation of the K-Cl Cotransporter Isoform KCC3a in Hematopoetic Cells. Blood 2007, 110: 1712-1712. DOI: 10.1182/blood.v110.11.1712.1712.
- A Case of HPP with a Novel Combination of α and β Spectrin Mutations.Natarajan K, Kutlar F, Li T, Gallagher P, Kutlar A. A Case of HPP with a Novel Combination of α and β Spectrin Mutations. Blood 2007, 110: 1736-1736. DOI: 10.1182/blood.v110.11.1736.1736.
- Characterization of Regulatory Elements in the Slc4a1 (Band 3) Locus To Create Safe and Effective Vectors for Globin Gene TherapyHarrow F, Battle S, Seidel N, Cline A, Gallagher P, Bodine D. Characterization of Regulatory Elements in the Slc4a1 (Band 3) Locus To Create Safe and Effective Vectors for Globin Gene Therapy. Blood 2007, 110: 3740-3740. DOI: 10.1182/blood.v110.11.3740.3740.
- Identification of a TFIID Binding Sequence That Increases Expression from the Ankyrin-1 Promoter: Application to Globin Gene TherapyLaflamme K, Elnitski L, Wong C, Mary Y, Gallagher P, Bodine D. Identification of a TFIID Binding Sequence That Increases Expression from the Ankyrin-1 Promoter: Application to Globin Gene Therapy. Blood 2007, 110: 3741-3741. DOI: 10.1182/blood.v110.11.3741.3741.
- Picture of the month. Blueberry muffin baby (extramedullary hematopoiesis) due to congenital cytomegalovirus infection.Gaffin JM, Gallagher PG. Picture of the month. Blueberry muffin baby (extramedullary hematopoiesis) due to congenital cytomegalovirus infection. Archives Of Pediatrics & Adolescent Medicine 2007, 161: 1102-3. PMID: 17984414, DOI: 10.1001/archpedi.161.11.1102.
- Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and functiondos Santos CO, Zhou S, Secolin R, Wang X, Cunha AF, Higgs DR, Kwiatkowski JL, Thein SL, Gallagher PG, Costa FF, Weiss MJ. Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function. American Journal Of Hematology 2007, 83: 103-108. PMID: 17874450, DOI: 10.1002/ajh.21041.
- An 11-amino acid β-hairpin loop in the cytoplasmic domain of band 3 is responsible for ankyrin binding in mouse erythrocytesStefanovic M, Markham NO, Parry EM, Garrett-Beal LJ, Cline AP, Gallagher PG, Low PS, Bodine DM. An 11-amino acid β-hairpin loop in the cytoplasmic domain of band 3 is responsible for ankyrin binding in mouse erythrocytes. Proceedings Of The National Academy Of Sciences Of The United States Of America 2007, 104: 13972-13977. PMID: 17715300, PMCID: PMC1950715, DOI: 10.1073/pnas.0706266104.
- Novel role for EKLF in megakaryocyte lineage commitmentFrontelo P, Manwani D, Galdass M, Karsunky H, Lohmann F, Gallagher PG, Bieker JJ. Novel role for EKLF in megakaryocyte lineage commitment. Blood 2007, 110: 3871-3880. PMID: 17715392, PMCID: PMC2190608, DOI: 10.1182/blood-2007-03-082065.
- Erythrocyte Disorders in the Perinatal PeriodSteiner LA, Gallagher PG. Erythrocyte Disorders in the Perinatal Period. Seminars In Perinatology 2007, 31: 254-261. PMID: 17825683, PMCID: PMC2098040, DOI: 10.1053/j.semperi.2007.05.003.
- A Decline in the Frequency of Neonatal Exchange Transfusions and Its Effect on Exchange-Related Morbidity and MortalitySteiner LA, Bizzarro MJ, Ehrenkranz RA, Gallagher PG. A Decline in the Frequency of Neonatal Exchange Transfusions and Its Effect on Exchange-Related Morbidity and Mortality. Pediatrics 2007, 120: 27-32. PMID: 17606558, DOI: 10.1542/peds.2006-2910.
- Failure of definitive erythropoiesis in EKLF-deficient miceGallagher P, Pilon A, Arcasoy M, Vayda S, Dressman H, Bieker J, Bodine D. Failure of definitive erythropoiesis in EKLF-deficient mice. Blood Cells Molecules And Diseases 2007, 38: 140-141. DOI: 10.1016/j.bcmd.2006.10.050.
- Structure and function of the chromatin surrounding the erythroid ankyrin promoter (ANK-1E)Owen A, Pilon A, Wong C, Seidel N, Cline A, Gallagher P, Bodine D. Structure and function of the chromatin surrounding the erythroid ankyrin promoter (ANK-1E). Blood Cells Molecules And Diseases 2007, 38: 165. DOI: 10.1016/j.bcmd.2006.10.105.
- Erythroid specific activation of the ankyrin-1E promoter by the formation of a chromatin loopBodine D, Owen A, Maksimova Y, Elnitski L, Wong C, Seidel N, Cline A, Gallagher P. Erythroid specific activation of the ankyrin-1E promoter by the formation of a chromatin loop. Blood Cells Molecules And Diseases 2007, 38: 126-127. DOI: 10.1016/j.bcmd.2006.10.018.
- EKLF-deficiency leads to multiple defects in erythropoiesis: Dysregulation of AHSP and E2FPilon A, Arcasoy M, Vayda S, Dressman H, Bieker J, Bodine D, Gallagher P. EKLF-deficiency leads to multiple defects in erythropoiesis: Dysregulation of AHSP and E2F. Blood Cells Molecules And Diseases 2007, 38: 172. DOI: 10.1016/j.bcmd.2006.10.118.
- A complex splicing defect associated with homozygous ankyrin-deficient hereditary spherocytosisEdelman EJ, Maksimova Y, Duru F, Altay C, Gallagher PG. A complex splicing defect associated with homozygous ankyrin-deficient hereditary spherocytosis. Blood 2007, 109: 5491-5493. PMID: 17327413, PMCID: PMC1890827, DOI: 10.1182/blood-2006-09-046573.
- Case-control analysis of endemic Serratia marcescens bacteremia in a neonatal intensive care unitBizzarro MJ, Dembry LM, Baltimore RS, Gallagher PG. Case-control analysis of endemic Serratia marcescens bacteremia in a neonatal intensive care unit. Archives Of Disease In Childhood - Fetal And Neonatal Edition 2007, 92: f120. PMID: 17088342, PMCID: PMC2675455, DOI: 10.1136/adc.2006.102855.
- Antibiotic-Resistant Organisms in the Neonatal Intensive Care UnitBizzarro MJ, Gallagher PG. Antibiotic-Resistant Organisms in the Neonatal Intensive Care Unit. Seminars In Perinatology 2007, 31: 26-32. PMID: 17317424, DOI: 10.1053/j.semperi.2007.01.004.
- Aplastic Crisis Revealing the Diagnosis of Hb Evans [α62(E11)Val→Met, GTG→ATG (α2)] in a Hispanic Kindred: Case Report and ReviewSteiner LA, Van Hoff J, Kutlar F, Gallagher PG. Aplastic Crisis Revealing the Diagnosis of Hb Evans [α62(E11)Val→Met, GTG→ATG (α2)] in a Hispanic Kindred: Case Report and Review. Hemoglobin 2007, 31: 409-416. PMID: 17994374, DOI: 10.1080/03630260701590301.
- Pathogenic proline mutation in the linker between spectrin repeats: disease caused by spectrin unfoldingJohnson CP, Gaetani M, Ortiz V, Bhasin N, Harper S, Gallagher PG, Speicher DW, Discher DE. Pathogenic proline mutation in the linker between spectrin repeats: disease caused by spectrin unfolding. Blood 2006, 109: 3538-3543. PMID: 17192394, PMCID: PMC1852230, DOI: 10.1182/blood-2006-07-038588.
- Alternative Splicing within Exon 1 of the KCl Cotransporter-3 (KCC3) Gene Results in Novel Transcripts in Erythroid Cells.Joiner C, Crable S, Gallagher P. Alternative Splicing within Exon 1 of the KCl Cotransporter-3 (KCC3) Gene Results in Novel Transcripts in Erythroid Cells. Blood 2006, 108: 1564-1564. DOI: 10.1182/blood.v108.11.1564.1564.
- Identification of a Novel Core Promoter Element That Enhances Transcription: Application to Ankyrin Promoters for Globin Gene Therapy.Laflamme K, Elnitski L, Owen A, Gallagher P, Bodine D. Identification of a Novel Core Promoter Element That Enhances Transcription: Application to Ankyrin Promoters for Globin Gene Therapy. Blood 2006, 108: 3261-3261. DOI: 10.1182/blood.v108.11.3261.3261.
- A Transgenic Mouse Assay To Compare the Barrier Activities of the Chicken β-Globin 5′HS4, Human β-Globin 5′HS5 and Mouse 3′HS1.Devlin E, Horton C, Garrett-Beal L, Gallagher P, Bodine D. A Transgenic Mouse Assay To Compare the Barrier Activities of the Chicken β-Globin 5′HS4, Human β-Globin 5′HS5 and Mouse 3′HS1. Blood 2006, 108: 362-362. DOI: 10.1182/blood.v108.11.362.362.
- A 200 kb Survey of Chromatin in the ANK-1 Locus Demonstrates an Erythroid-Specific Chromatin Hub That Activates the Erythrocyte Ankyrin (ANK-1E) Promoter.Owen A, Wolfsberg T, Laflamme K, Wong C, Maksimova Y, Elnitski L, Gallagher P, Bodine D. A 200 kb Survey of Chromatin in the ANK-1 Locus Demonstrates an Erythroid-Specific Chromatin Hub That Activates the Erythrocyte Ankyrin (ANK-1E) Promoter. Blood 2006, 108: 536-536. DOI: 10.1182/blood.v108.11.536.536.
- Novel Role for EKLF in Megakaryocyte-Erythroid Differential Lineage Commitment.Frontelo M, Manwani D, Galdass M, Karsunky H, Gallagher P, Bieker J. Novel Role for EKLF in Megakaryocyte-Erythroid Differential Lineage Commitment. Blood 2006, 108: 4205-4205. DOI: 10.1182/blood.v108.11.4205.4205.
- Defects in E2F1/2 Expression Are Associated with Abnormalities in Cell Cycle and Differentiation in EKLF-Deficient Erythroid Cells.Pilon A, Arcasoy M, Vayda S, Dressman H, Bieker J, Bodine D, Gallagher P. Defects in E2F1/2 Expression Are Associated with Abnormalities in Cell Cycle and Differentiation in EKLF-Deficient Erythroid Cells. Blood 2006, 108: 84-84. DOI: 10.1182/blood.v108.11.84.84.
- Major erythrocyte membrane protein genes in EKLF-deficient miceNilson DG, Sabatino DE, Bodine DM, Gallagher PG. Major erythrocyte membrane protein genes in EKLF-deficient mice. Experimental Hematology 2006, 34: 705-712. PMID: 16728274, DOI: 10.1016/j.exphem.2006.02.018.
- Alterations in Expression and Chromatin Configuration of the Alpha Hemoglobin-Stabilizing Protein Gene in Erythroid Krüppel-Like Factor-Deficient MicePilon AM, Nilson DG, Zhou D, Sangerman J, Townes TM, Bodine DM, Gallagher PG. Alterations in Expression and Chromatin Configuration of the Alpha Hemoglobin-Stabilizing Protein Gene in Erythroid Krüppel-Like Factor-Deficient Mice. Molecular And Cellular Biology 2006, 26: 4368-4377. PMID: 16705186, PMCID: PMC1489081, DOI: 10.1128/mcb.02216-05.
- Hematologically important mutations: Ankyrin variants in hereditary spherocytosisGallagher PG. Hematologically important mutations: Ankyrin variants in hereditary spherocytosis. Blood Cells Molecules And Diseases 2005, 35: 345-347. PMID: 16223590, DOI: 10.1016/j.bcmd.2005.08.008.
- Vancomycin-Resistant Enterococcal Bacteremia and Necrotizing Enterocolitis in a Preterm NeonateRaskind CH, Dembry LM, Gallagher PG. Vancomycin-Resistant Enterococcal Bacteremia and Necrotizing Enterocolitis in a Preterm Neonate. The Pediatric Infectious Disease Journal 2005, 24: 943-944. PMID: 16220106, DOI: 10.1097/01.inf.0000180987.00122.5d.
- GATA-1 and Oct-1 Are Required for Expression of the Human α-Hemoglobin-stabilizing Protein Gene*Gallagher PG, Liem RI, Wong E, Weiss MJ, Bodine DM. GATA-1 and Oct-1 Are Required for Expression of the Human α-Hemoglobin-stabilizing Protein Gene*. Journal Of Biological Chemistry 2005, 280: 39016-39023. PMID: 16186125, DOI: 10.1074/jbc.m506062200.
- A novel splicing mutation of the α-spectrin gene in the original hereditary pyropoikilocytosis kindredCosta DB, Lozovatsky L, Gallagher PG, Forget BG. A novel splicing mutation of the α-spectrin gene in the original hereditary pyropoikilocytosis kindred. Blood 2005, 106: 4367-4369. PMID: 16150946, PMCID: PMC1895230, DOI: 10.1182/blood-2005-05-1813.
- Seventy-Five Years of Neonatal Sepsis at Yale: 1928–2003Bizzarro MJ, Raskind C, Baltimore RS, Gallagher PG. Seventy-Five Years of Neonatal Sepsis at Yale: 1928–2003. Pediatrics 2005, 116: 595-602. PMID: 16140698, DOI: 10.1542/peds.2005-0552.
- A dinucleotide deletion in the ankyrin promoter alters gene expression, transcription initiation and TFIID complex formation in hereditary spherocytosisGallagher PG, Nilson DG, Wong C, Weisbein JL, Garrett-Beal LJ, Eber SW, Bodine DM. A dinucleotide deletion in the ankyrin promoter alters gene expression, transcription initiation and TFIID complex formation in hereditary spherocytosis. Human Molecular Genetics 2005, 14: 2501-2509. PMID: 16037067, DOI: 10.1093/hmg/ddi254.
- Multiple isoforms of the KC1 cotransporter are expressed in sickle and normal erythroid cellsCrable SC, Hammond SM, Papes R, Rettig RK, Zhou GP, Gallagher PG, Joiner CH, Anderson KP. Multiple isoforms of the KC1 cotransporter are expressed in sickle and normal erythroid cells. Experimental Hematology 2005, 33: 624-631. PMID: 15911086, DOI: 10.1016/j.exphem.2005.02.006.
- Red Cell Membrane DisordersGallagher PG. Red Cell Membrane Disorders. Hematology 2005, 2005: 13-18. PMID: 16304353, DOI: 10.1182/asheducation-2005.1.13.
- Sequences Downstream of the Erythroid Promoter Are Required for High Level Expression of the Human α-Spectrin Gene*Wong EY, Lin J, Forget BG, Bodine DM, Gallagher PG. Sequences Downstream of the Erythroid Promoter Are Required for High Level Expression of the Human α-Spectrin Gene*. Journal Of Biological Chemistry 2004, 279: 55024-55033. PMID: 15456760, DOI: 10.1074/jbc.m408886200.
- Hereditary elliptocytosis: spectrin and protein 4.1RGallagher PG. Hereditary elliptocytosis: spectrin and protein 4.1R. Seminars In Hematology 2004, 41: 142-164. PMID: 15071791, DOI: 10.1053/j.seminhematol.2004.01.003.
- Conjunctival Colonization of Infants Hospitalized in a Neonatal Intensive Care Unit: A Longitudinal AnalysisRaskind CH, Sabo BE, Callan DA, Farrel PA, Dembry LM, Gallagher PG. Conjunctival Colonization of Infants Hospitalized in a Neonatal Intensive Care Unit: A Longitudinal Analysis. Infection Control And Hospital Epidemiology 2004, 25: 216-220. PMID: 15061413, DOI: 10.1086/502381.
- Update on the clinical spectrum and genetics of red blood cell membrane disorders.Gallagher PG. Update on the clinical spectrum and genetics of red blood cell membrane disorders. Current Hematology Reports 2004, 3: 85-91. PMID: 14965483.
- Human potassium chloride cotransporter 1 (SLC12A4) promoter is regulated by AP-2 and contains a functional downstream promoter elementZhou GP, Wong C, Su R, Crable SC, Anderson KP, Gallagher PG. Human potassium chloride cotransporter 1 (SLC12A4) promoter is regulated by AP-2 and contains a functional downstream promoter element. Blood 2004, 103: 4302-4309. PMID: 14976052, DOI: 10.1182/blood-2003-01-0107.
- Mutation of a highly conserved isoleucine disrupts hydrophobic interactions in the αβ spectrin self-association binding siteGallagher PG, Zhang Z, Morrow JS, Forget BG. Mutation of a highly conserved isoleucine disrupts hydrophobic interactions in the αβ spectrin self-association binding site. Laboratory Investigation 2004, 84: 229-234. PMID: 14661034, DOI: 10.1038/labinvest.3700029.
- Hereditary pyropoikilocytosis and the spectrinSt. Claude alleleMootien S, Gallagher PG. Hereditary pyropoikilocytosis and the spectrinSt. Claude allele. British Journal Of Haematology 2003, 124: 251-252. PMID: 14687038, DOI: 10.1046/j.1365-2141.2003.04748.x.
- Variegated Expression from the Murine Band 3 (AE1) Promoter in Transgenic Mice Is Associated with mRNA Transcript Initiation at Upstream Start Sites and Can Be Suppressed by the Addition of the Chicken β-Globin 5′ HS4 Insulator ElementFrazar TF, Weisbein JL, Anderson SM, Cline AP, Garrett LJ, Felsenfeld G, Gallagher PG, Bodine DM. Variegated Expression from the Murine Band 3 (AE1) Promoter in Transgenic Mice Is Associated with mRNA Transcript Initiation at Upstream Start Sites and Can Be Suppressed by the Addition of the Chicken β-Globin 5′ HS4 Insulator Element. Molecular And Cellular Biology 2003, 23: 4753-4763. PMID: 12832463, PMCID: PMC162203, DOI: 10.1128/mcb.23.14.4753-4763.2003.
- Regulation of erythrocyte membrane protein gene expressionGallagher PG. Regulation of erythrocyte membrane protein gene expression. Current Opinion In Hematology 2003, 10: 115-122. PMID: 12579036, DOI: 10.1097/00062752-200303000-00003.
- Altered erythrocyte endothelial adherence and membrane phospholipid asymmetry in hereditary hydrocytosisGallagher PG, Chang SH, Rettig MP, Neely JE, Hillery CA, Smith BD, Low PS. Altered erythrocyte endothelial adherence and membrane phospholipid asymmetry in hereditary hydrocytosis. Blood 2003, 101: 4625-4627. PMID: 12560240, DOI: 10.1182/blood-2001-12-0329.
- Erythroid Expression of the Human α-Spectrin Gene Promoter Is Mediated by GATA-1- and NF-E2-binding Proteins*Boulanger L, Sabatino DE, Wong EY, Cline AP, Garrett LJ, Garbarz M, Dhermy D, Bodine DM, Gallagher PG. Erythroid Expression of the Human α-Spectrin Gene Promoter Is Mediated by GATA-1- and NF-E2-binding Proteins*. Journal Of Biological Chemistry 2002, 277: 41563-41570. PMID: 12196550, DOI: 10.1074/jbc.m208184200.
- Three‐dimensional sonographic imaging of a highly developed fetus in fetu with spontaneous movement of the extremities.Jones DC, Reyes-Múgica M, Gallagher PG, Fricks P, Touloukian RJ, Copel JA. Three‐dimensional sonographic imaging of a highly developed fetus in fetu with spontaneous movement of the extremities. Journal Of Ultrasound In Medicine 2001, 20: 1357-1363. PMID: 11762548, DOI: 10.7863/jum.2001.20.12.1357.
- Molecular diagnosis of hemoglobinopathies and other red blood cell disorders.Arcasoy MO, Gallagher PG. Molecular diagnosis of hemoglobinopathies and other red blood cell disorders. Seminars In Hematology 1999, 36: 328-39. PMID: 10530715.
- Neonatal tumors. Introduction.Gallagher PG, Lampkin BC. Neonatal tumors. Introduction. Seminars In Perinatology 1999, 23: 261-2. PMID: 10475539.
- Dehydrated hereditary stomatocytosis is not linked to the hlK1 locus, a Gardos channel candidate, on chromosome 19q13.2.Gallagher PG, Smith BD. Dehydrated hereditary stomatocytosis is not linked to the hlK1 locus, a Gardos channel candidate, on chromosome 19q13.2. Blood 1999, 93: 2134-5. PMID: 10189206.
- Assignment of the 2P domain, acid-sensitive potassium channel OAT1 gene KCNK3 to human chromosome bands 2p24.1-->p23.3 and murine 5B by in situ hybridization.Manjunath NA, Bray-Ward P, Goldstein SA, Gallagher PG. Assignment of the 2P domain, acid-sensitive potassium channel OAT1 gene KCNK3 to human chromosome bands 2p24.1-->p23.3 and murine 5B by in situ hybridization. Cytogenetics And Cell Genetics 1999, 86: 242-3. PMID: 10575216, DOI: 10.1159/000015349.
- Understanding iron absorption and metabolism.Gallagher PG, Ehrenkranz RA. Understanding iron absorption and metabolism. Journal Of Pediatric Gastroenterology And Nutrition 1998, 27: 610-1. PMID: 9822334, DOI: 10.1097/00005176-199811000-00023.
- Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?Jonsson JJ, Renieri A, Gallagher PG, Kashtan CE, Cherniske EM, Bruttini M, Piccini M, Vitelli F, Ballabio A, Pober BR. Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome? Journal Of Medical Genetics 1998, 35: 273-8. PMID: 9598718, PMCID: PMC1051272, DOI: 10.1136/jmg.35.4.273.
- Atrial Flutter Complicating Neonatal Coxsackie B2 MyocarditisShah SS, Hellenbrand WE, Gallagher PG. Atrial Flutter Complicating Neonatal Coxsackie B2 Myocarditis. Pediatric Cardiology 1998, 19: 185-186. PMID: 9565516, DOI: 10.1007/s002469900277.
- Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia.Gallagher PG, Petruzzi MJ, Weed SA, Zhang Z, Marchesi SL, Mohandas N, Morrow JS, Forget BG. Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia. Journal Of Clinical Investigation 1997, 99: 267-277. PMID: 9005995, PMCID: PMC507794, DOI: 10.1172/jci119155.
- Neonatal sepsis due to echovirus 18 infection.Shah SS, Gallagher PG. Neonatal sepsis due to echovirus 18 infection. Journal Of Perinatal Medicine 1997, 25: 381-4. PMID: 9350610, DOI: 10.1515/jpme.1997.25.4.381.
- Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis.Gallagher PG, Kotula L, Wang Y, Marchesi SL, Curtis PJ, Speicher DW, Forget BG. Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis. American Journal Of Human Genetics 1996, 59: 351-9. PMID: 8755921, PMCID: PMC1914747.
- The lethal hemolytic mutation in beta I sigma 2 spectrin Providence yields a null phenotype in neonatal skeletal muscle.Weed SA, Stabach PR, Oyer CE, Gallagher PG, Morrow JS. The lethal hemolytic mutation in beta I sigma 2 spectrin Providence yields a null phenotype in neonatal skeletal muscle. Laboratory Investigation 1996, 74: 1117-29. PMID: 8667615.
- A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis.Jenkins PB, Abou-Alfa GK, Dhermy D, Bursaux E, Féo C, Scarpa AL, Lux SE, Garbarz M, Forget BG, Gallagher PG. A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis. Journal Of Clinical Investigation 1996, 97: 373-380. PMID: 8567957, PMCID: PMC507027, DOI: 10.1172/jci118425.
- Seminars in perinatology.Gallagher PG. Seminars in perinatology. Seminars In Perinatology 1995, 19: 435-6. PMID: 8822327.
- Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene.Gallagher PG, Weed SA, Tse WT, Benoit L, Morrow JS, Marchesi SL, Mohandas N, Forget BG. Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene. Journal Of Clinical Investigation 1995, 95: 1174-1182. PMID: 7883966, PMCID: PMC441455, DOI: 10.1172/jci117766.
- Spectrin St Louis and the αLELV AlleleGallagher P, Forget B. Spectrin St Louis and the αLELV Allele. Blood 1994, 84: 1686-1687. PMID: 8068958, DOI: 10.1182/blood.v84.5.1686.1686.
- Localization of the human α-fodrin gene (SPTAN1) to 9q33→q34 by fluorescence in situ hybridizationUpender M, Gallagher PG, Moon RT, Ward DC, Forget BG. Localization of the human α-fodrin gene (SPTAN1) to 9q33→q34 by fluorescence in situ hybridization. Cytogenetic And Genome Research 1994, 66: 39-41. PMID: 8275706, DOI: 10.1159/000133660.
- Spectrin genes in health and disease.Gallagher PG, Forget BG. Spectrin genes in health and disease. Seminars In Hematology 1993, 30: 4-20. PMID: 8094577.
- Polymerase chain reaction analysis of an NcoI polymorphism of the human erythrocyte ankyrin gene.Gallagher PG, Tse WT, Forget BG. Polymerase chain reaction analysis of an NcoI polymorphism of the human erythrocyte ankyrin gene. Blood 1992, 80: 1856-7. PMID: 1356512.
- A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrin.Gallagher PG, Tse WT, Coetzer T, Lecomte MC, Garbarz M, Zarkowsky HS, Baruchel A, Ballas SK, Dhermy D, Palek J. A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrin. Journal Of Clinical Investigation 1992, 89: 892-898. PMID: 1541680, PMCID: PMC442935, DOI: 10.1172/jci115669.
- Large numbers of alternatively spliced isoforms of the regulatory region of human erythrocyte ankyrin.Gallagher PG, Tse WT, Scarpa AL, Lux SE, Forget BG. Large numbers of alternatively spliced isoforms of the regulatory region of human erythrocyte ankyrin. Proceedings Of The Association Of American Physicians 1992, 105: 268-77. PMID: 1309004.
- Varicose veins--primary treatment with sclerotherapy. A personal appraisal.Gallagher PG. Varicose veins--primary treatment with sclerotherapy. A personal appraisal. The Journal Of Dermatologic Surgery And Oncology 1992, 18: 39-42. PMID: 1740566, DOI: 10.1111/j.1524-4725.1992.tb03299.x.
- An approach to the diagnosis and treatment of membranous laryngotracheobronchitis in infants and children.Gallagher PG, Myer CM. An approach to the diagnosis and treatment of membranous laryngotracheobronchitis in infants and children. Pediatric Emergency Care 1991, 7: 337-42. PMID: 1788120, DOI: 10.1097/00006565-199112000-00004.
- A splice site mutation of the beta-spectrin gene causing exon skipping in hereditary elliptocytosis associated with a truncated beta-spectrin chainGallagher PG, Tse WT, Costa F, Scarpa A, Boivin P, Delaunay J, Forget BG. A splice site mutation of the beta-spectrin gene causing exon skipping in hereditary elliptocytosis associated with a truncated beta-spectrin chain. Journal Of Biological Chemistry 1991, 266: 15154-15159. PMID: 1840591, DOI: 10.1016/s0021-9258(18)98598-4.
- Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutation.Garbarz M, Tse WT, Gallagher PG, Picat C, Lecomte MC, Galibert F, Dhermy D, Forget BG. Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutation. Journal Of Clinical Investigation 1991, 88: 76-81. PMID: 2056132, PMCID: PMC296005, DOI: 10.1172/jci115307.
- Sclerotherapy.Gallagher PG. Sclerotherapy. The Journal Of Dermatologic Surgery And Oncology 1991, 17: 304. PMID: 2005255, DOI: 10.1111/j.1524-4725.1991.tb03648.x.
- A defect in alpha-spectrin mRNA accumulation in hereditary pyropoikilocytosis.Gallagher PG, Tse WT, Marchesi SL, Zarkowsky HS, Forget BG. A defect in alpha-spectrin mRNA accumulation in hereditary pyropoikilocytosis. Proceedings Of The Association Of American Physicians 1991, 104: 32-9. PMID: 1845156.
- Cerebral infarctions due to CNS infection with Enterobacter sakazakii.Gallagher PG, Ball WS. Cerebral infarctions due to CNS infection with Enterobacter sakazakii. Pediatric Radiology 1991, 21: 135-6. PMID: 2027718, DOI: 10.1007/bf02015629.
- Clinical and molecular aspects of disorders of the erythrocyte membrane skeleton.Gallagher PG, Tse WT, Forget BG. Clinical and molecular aspects of disorders of the erythrocyte membrane skeleton. Seminars In Perinatology 1990, 14: 351-67. PMID: 2287951.
- Enterobacter bacteremia in pediatric patients.Gallagher PG. Enterobacter bacteremia in pediatric patients. Reviews Of Infectious Diseases 1990, 12: 808-12. PMID: 2237121, DOI: 10.1093/clinids/12.5.808.
- Group C streptococcal sinusitis.Gallagher PG, Myer CM, Crone K, Benzing G. Group C streptococcal sinusitis. American Journal Of Otolaryngology 1990, 11: 352-4. PMID: 2264588, DOI: 10.1016/0196-0709(90)90067-6.
- Radiological case of the month. Mesenteric cyst with hemorrhage.Gallagher PG, Kirks D, Wood BP. Radiological case of the month. Mesenteric cyst with hemorrhage. American Journal Of Diseases Of Children (1960) 1990, 144: 793-4. PMID: 2192543, DOI: 10.1001/archpedi.1990.02150310061028.
- Facial nerve paralysis and Kawasaki disease.Gallagher PG. Facial nerve paralysis and Kawasaki disease. Reviews Of Infectious Diseases 1990, 12: 403-5. PMID: 2193347, DOI: 10.1093/clinids/12.3.403.
- Osteomyelitis of the Skull after Varicella InfectionGallagher PG. Osteomyelitis of the Skull after Varicella Infection. Clinical Pediatrics 1990, 29: 29-29. PMID: 2293949, DOI: 10.1177/000992289002900104.
- Pseudomonas bacteremia in a community teaching hospital, 1980-1984.Gallagher PG, Watanakunakorn C. Pseudomonas bacteremia in a community teaching hospital, 1980-1984. Reviews Of Infectious Diseases 1989, 11: 846-52. PMID: 2602775, DOI: 10.1093/clinids/11.6.846.
- Listeria monocytogenes endocarditis: a review of the literature 1950-1986.Gallagher PG, Watanakunakorn C. Listeria monocytogenes endocarditis: a review of the literature 1950-1986. Scandinavian Journal Of Infectious Diseases 1988, 20: 359-68. PMID: 3057615, DOI: 10.3109/00365548809032469.
- Listeria monocytogenes endocarditis in a patient on chronic hemodialysis, successfully treated with vancomycin-gentamicin.Gallagher PG, Amedia CA, Watanakunakorn C. Listeria monocytogenes endocarditis in a patient on chronic hemodialysis, successfully treated with vancomycin-gentamicin. Infection 1986, 14: 125-8. PMID: 3733226, DOI: 10.1007/bf01643476.
- Group B streptococcal endocarditis: report of seven cases and review of the literature, 1962-1985.Gallagher PG, Watanakunakorn C. Group B streptococcal endocarditis: report of seven cases and review of the literature, 1962-1985. Reviews Of Infectious Diseases 1986, 8: 175-88. PMID: 3518020, DOI: 10.1093/clinids/8.2.175.
- Blastocystis hominis enteritis.Gallagher PG, Venglarcik JS. Blastocystis hominis enteritis. Pediatric Infectious Disease 1985, 4: 556-7. PMID: 4047965.
- Group B streptococcal meningitis in adults.Gallagher PG, Watanakunakorn C. Group B streptococcal meningitis in adults. Archives Of Neurology 1985, 42: 626-7. PMID: 3893397, DOI: 10.1001/archneur.1985.04060070012005.
- Group B streptococcal bacteremia in a community teaching hospital.Gallagher PG, Watanakunakorn C. Group B streptococcal bacteremia in a community teaching hospital. The American Journal Of Medicine 1985, 78: 795-800. PMID: 3887911, DOI: 10.1016/0002-9343(85)90285-2.