Patrick Gallagher, MD, BS

• Abhishek Kumar
• Alexa Siddon
• Biff Forbush
• Christopher Tormey
• David Karas
• Demetrios Braddock
• Diane Krause
• Dianqing (Dan) Wu
• E. Jennifer Edelman
• Elena Gracheva
• Ellice Wong
• Fangyong Li
• Farzana Pashankar
• Francesc Lopez-Giraldez
• Hongyu Zhao
• Jeanne Hendrickson
• Jesse Rinehart
• Jin-Young Choi
• John Sinard
• Jon Morrow
• Joseph Craft
• Joshua Copel
• Jun Lu
• Karin Finberg
• Lesley Devine
• Louise-Marie Dembry
• Marco Mastrotto
• Martin Schwartz
• Matthew Bizzarro
• Megan C. King
• Mei Zhong
• Orly Levit
• Paul Stabach
• Peining Li
• Peter M. Glazer
• Ping-Xia Zhang
• Priti Kumar
• Raffaella Morotti
• Raisa Balbuena-Merle
• Richard Lifton
• Robert Baltimore
• Robert LaMotte
• Robert M. Weiss
• Robert Touloukian
• Rong Fan
• Shangqin Guo
• Sherman Weissman
• Shrikant Mane
• Slav Bagriantsev
• Stephanie Halene
• Stephanie Massaro
• Steven Peterec
• Susan Baserga
• Susan Kaech
• Veronika Shabanova
• Vincent Schulz
• Zaneta Forson-Dare

Anemia, Sickle Cell; Elliptocytosis, Hereditary; Erythropoiesis; Genetics; Hemoglobinopathies; Information Science; Neonatology; Pathology; Pediatrics; Polycythemia; Pyruvate Kinase; Spherocytosis, Hereditary; Hydrops Fetalis; Genomics; Diseases; Health Care

• Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65S.Stewart 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:C1325-43.
• 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. The Journal Of Biological Chemistry 2011, 286:39457-65.
• Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis.Zarychanski 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, 120:1908-15.
• A tissue-specific chromatin loop activates the erythroid ankyrin-1 promoter.Yocum 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, 120:3586-93.
• Genetic diagnosis of neuroacanthocytosis disorders using exome sequencing.Walker RH, Schulz VP, Tikhonova IR, Mahajan MC, Mane S, Arroyo Muniz M, Gallagher PG. Genetic diagnosis of neuroacanthocytosis disorders using exome sequencing. Movement Disorders : Official Journal Of The Movement Disorder Society 2012, 27:539-43.
• The common hereditary elliptocytosis-associated α-spectrin L260P mutation perturbs erythrocyte membranes by stabilizing spectrin in the closed dimer conformation.Harper 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, 122:3045-53.
• 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. The Journal Of Biological Chemistry 2013, 288:8433-8444.
• Exclusion of the stomatin, alpha-adducin and beta-adducin loci in a large kindred with dehydrated hereditary stomatocytosis.Innes DS, Sinard JH, Gilligan DM, Snyder LM, Gallagher PG, Morrow JS. Exclusion of the stomatin, alpha-adducin and beta-adducin loci in a large kindred with dehydrated hereditary stomatocytosis. American Journal Of Hematology 1999, 60:72-4.
• Diaphragmatic plication in the extremely low birth weight infant.Gallagher PG, Seashore JH, Touloukian RJ. Diaphragmatic plication in the extremely low birth weight infant. Journal Of Pediatric Surgery 2000, 35:615-6.
• Erythroid expression of the human alpha-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 alpha-spectrin gene promoter is mediated by GATA-1- and NF-E2-binding proteins. The Journal Of Biological Chemistry 2002, 277:41563-70.
• Altered erythrocyte endothelial adherence and membrane phospholipid asymmetry in hereditary hydrocytosis.Gallagher 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, 101:4625-7.
• Regulation of erythrocyte membrane protein gene expression.Gallagher PG. Regulation of erythrocyte membrane protein gene expression. Current Opinion In Hematology 2003, 10:115-22.
• 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 beta-globin 5' HS4 insulator element.Frazar 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 beta-globin 5' HS4 insulator element. Molecular And Cellular Biology 2003, 23:4753-63.
• Mutation of a highly conserved isoleucine disrupts hydrophobic interactions in the alpha beta spectrin self-association binding site.Gallagher PG, Zhang Z, Morrow JS, Forget BG. Mutation of a highly conserved isoleucine disrupts hydrophobic interactions in the alpha beta spectrin self-association binding site. Laboratory Investigation; A Journal Of Technical Methods And Pathology 2004, 84:229-34.
• Sequences downstream of the erythroid promoter are required for high level expression of the human alpha-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 alpha-spectrin gene. The Journal Of Biological Chemistry 2004, 279:55024-33.
• Conjunctival colonization of infants hospitalized in a neonatal intensive care unit: a longitudinal analysis.Raskind 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, 25:216-20.
• 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.
• Hereditary pyropoikilocytosis and the spectrin St. Claude allele.Mootien S, Gallagher PG. Hereditary pyropoikilocytosis and the spectrin St. Claude allele. British Journal Of Haematology 2004, 124:251-2.
• Human potassium chloride cotransporter 1 (SLC12A4) promoter is regulated by AP-2 and contains a functional downstream promoter element.Zhou 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, 103:4302-9.
• Hereditary elliptocytosis: spectrin and protein 4.1R.Gallagher PG. Hereditary elliptocytosis: spectrin and protein 4.1R. Seminars In Hematology 2004, 41:142-64.
• A dinucleotide deletion in the ankyrin promoter alters gene expression, transcription initiation and TFIID complex formation in hereditary spherocytosis.Gallagher 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, 14:2501-9.
• Hematologically important mutations: ankyrin variants in hereditary spherocytosis.Gallagher PG. Hematologically important mutations: ankyrin variants in hereditary spherocytosis. Blood Cells, Molecules & Diseases 2005, 35:345-7.
• Multiple isoforms of the KC1 cotransporter are expressed in sickle and normal erythroid cells.Crable 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, 33:624-31.
• A novel splicing mutation of the alpha-spectrin gene in the original hereditary pyropoikilocytosis kindred.Costa DB, Lozovatsky L, Gallagher PG, Forget BG. A novel splicing mutation of the alpha-spectrin gene in the original hereditary pyropoikilocytosis kindred. Blood 2005, 106:4367-9.
• Vancomycin-resistant enterococcal bacteremia and necrotizing enterocolitis in a preterm neonate.Raskind CH, Dembry LM, Gallagher PG. Vancomycin-resistant enterococcal bacteremia and necrotizing enterocolitis in a preterm neonate. The Pediatric Infectious Disease Journal 2005, 24:943-4.
• GATA-1 and Oct-1 are required for expression of the human alpha-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 alpha-hemoglobin-stabilizing protein gene. The Journal Of Biological Chemistry 2005, 280:39016-23.
• Seventy-five years of neonatal sepsis at Yale: 1928-2003.Bizzarro MJ, Raskind C, Baltimore RS, Gallagher PG. Seventy-five years of neonatal sepsis at Yale: 1928-2003. Pediatrics 2005, 116:595-602.
• Red cell membrane disorders.Gallagher PG. Red cell membrane disorders. Hematology / The Education Program Of The American Society Of Hematology. American Society Of Hematology. Education Program 2005, 13-8.
• Major erythrocyte membrane protein genes in EKLF-deficient mice.Nilson DG, Sabatino DE, Bodine DM, Gallagher PG. Major erythrocyte membrane protein genes in EKLF-deficient mice. Experimental Hematology 2006, 34:705-12.
• Alterations in expression and chromatin configuration of the alpha hemoglobin-stabilizing protein gene in erythroid Kruppel-like factor-deficient mice.Pilon 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 Kruppel-like factor-deficient mice. Molecular And Cellular Biology 2006, 26:4368-77.
• Antibiotic-resistant organisms in the neonatal intensive care unit.Bizzarro MJ, Gallagher PG. Antibiotic-resistant organisms in the neonatal intensive care unit. Seminars In Perinatology 2007, 31:26-32.
• Case-control analysis of endemic Serratia marcescens bacteremia in a neonatal intensive care unit.Bizzarro 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:F120-6.
• A decline in the frequency of neonatal exchange transfusions and its effect on exchange-related morbidity and mortality.Steiner 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.
• A complex splicing defect associated with homozygous ankyrin-deficient hereditary spherocytosis.Edelman EJ, Maksimova Y, Duru F, Altay C, Gallagher PG. A complex splicing defect associated with homozygous ankyrin-deficient hereditary spherocytosis. Blood 2007, 109:5491-3.
• Pathogenic proline mutation in the linker between spectrin repeats: disease caused by spectrin unfolding.Johnson 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 2007, 109:3538-43.
• Erythrocyte disorders in the perinatal period.Steiner LA, Gallagher PG. Erythrocyte disorders in the perinatal period. Seminars In Perinatology 2007, 31:254-61.
• Novel role for EKLF in megakaryocyte lineage commitment.Frontelo P, Manwani D, Galdass M, Karsunky H, Lohmann F, Gallagher PG, Bieker JJ. Novel role for EKLF in megakaryocyte lineage commitment. Blood 2007, 110:3871-80.
• Aplastic crisis revealing the diagnosis of Hb Evans [alpha62(E11)Val-->Met, GTG-->ATG (alpha2)] in a Hispanic kindred: case report and review.Steiner LA, Van Hoff J, Kutlar F, Gallagher PG. Aplastic crisis revealing the diagnosis of Hb Evans [alpha62(E11)Val-->Met, GTG-->ATG (alpha2)] in a Hispanic kindred: case report and review. Hemoglobin 2007, 31:409-16.
• An 11-amino acid beta-hairpin loop in the cytoplasmic domain of band 3 is responsible for ankyrin binding in mouse erythrocytes.Stefanovic M, Markham NO, Parry EM, Garrett-Beal LJ, Cline AP, Gallagher PG, Low PS, Bodine DM. An 11-amino acid beta-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, 104:13972-7.
• 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.
• Changing patterns in neonatal Escherichia coli sepsis and ampicillin resistance in the era of intrapartum antibiotic prophylaxis.Bizzarro 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, 121:689-96.
• Ankyrin-linked hereditary spherocytosis in an African-American kindred.Sangerman 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, 83:789-94.
• Nonsense mutations of the alpha-spectrin gene in hereditary pyropoikilocytosis.Tolpinrud W, Maksimova YD, Forget BG, Gallagher PG. Nonsense mutations of the alpha-spectrin gene in hereditary pyropoikilocytosis. Haematologica 2008, 93:1752-4.
• Matched case-control analysis of polymicrobial bloodstream infection in a neonatal intensive care unit.Bizzarro 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, 29:914-20.
• Hereditary spherocytosis.Perrotta S, Gallagher PG, Mohandas N. Hereditary spherocytosis. Lancet 2008, 372:1411-26.
• Failure of terminal erythroid differentiation in EKLF-deficient mice is associated with cell cycle perturbation and reduced expression of E2F2.Pilon 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, 28:7394-401.
• Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function.dos 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 2008, 83:103-8.
• Red cell membrane: past, present, and future.Mohandas N, Gallagher PG. Red cell membrane: past, present, and future. Blood 2008, 112:3939-48.
• Structural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer site.Gaetani 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, 111:5712-20.
• Sites of regulated phosphorylation that control K-Cl cotransporter activity.Rinehart 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, 138:525-36.
• An insulator with barrier-element activity promotes alpha-spectrin gene expression in erythroid cells.Gallagher PG, Nilson DG, Steiner LA, Maksimova YD, Lin JY, Bodine DM. An insulator with barrier-element activity promotes alpha-spectrin gene expression in erythroid cells. Blood 2009, 113:1547-54.
• Canine elliptocytosis due to a mutant beta-spectrin.Di Terlizzi R, Gallagher PG, Mohandas N, Steiner LA, Dolce KS, Guo X, Wilkerson MJ, Stockham SL. Canine elliptocytosis due to a mutant beta-spectrin. Veterinary Clinical Pathology / American Society For Veterinary Clinical Pathology 2009, 38:52-8.
• Imaging of the diffusion of single band 3 molecules on normal and mutant erythrocytes.Kodippili 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, 113:6237-45.
• Chromatin architecture and transcription factor binding regulate expression of erythrocyte membrane protein genes.Steiner 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, 29:5399-412.
• The GPA-dependent, spherostomatocytosis mutant AE1 E758K induces GPA-independent, endogenous cation transport in amphibian oocytes.Stewart 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 2010, 298:C283-97.
• Determinants of erythrocyte hydration.Rinehart J, Gulcicek EE, Joiner CH, Lifton RP, Gallagher PG. Determinants of erythrocyte hydration. Current Opinion In Hematology 2010, 17:191-7.
• A fused alpha-beta "mini-spectrin" mimics the intact erythrocyte spectrin head-to-head tetramer.Harper SL, Li D, Maksimova Y, Gallagher PG, Speicher DW. A fused alpha-beta "mini-spectrin" mimics the intact erythrocyte spectrin head-to-head tetramer. The Journal Of Biological Chemistry 2010, 285:11003-12.
• Functional analysis of a novel cis-acting regulatory region within the human ankyrin gene (ANK-1) promoter.Laflamme 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, 30:3493-502.
• A comprehensive model of the spectrin divalent tetramer binding region deduced using homology modeling and chemical cross-linking of a mini-spectrin.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. The Journal Of Biological Chemistry 2010, 285:29535-45.
• Mutation of a barrier insulator in the human ankyrin-1 gene is associated with hereditary spherocytosis.Gallagher 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. The Journal Of Clinical Investigation 2010, 120:4453-65.
• Perinatal onset mevalonate kinase deficiency.Steiner LA, Ehrenkranz RA, Peterec SM, Steiner RD, Reyes-Múgica M, Gallagher PG. Perinatal onset mevalonate kinase deficiency. Pediatric And Developmental Pathology : The Official Journal Of The Society For Pediatric Pathology And The Paediatric Pathology Society 2011, 14:301-6.
• Partial exchange transfusion for polycythemia hyperviscosity syndrome.Hopewell B, Steiner LA, Ehrenkranz RA, Bizzarro MJ, Gallagher PG. Partial exchange transfusion for polycythemia hyperviscosity syndrome. American Journal Of Perinatology 2011, 28:557-64.
• Bi-allelic deletions within 13q14 and transient trisomy 21 with absence of GATA1s in pediatric acute megakaryoblastic leukemia.Massaro 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, 57:516-9.
• Granulicatella adiacens and early-onset sepsis in neonate.Bizzarro MJ, Callan DA, Farrel PA, Dembry LM, Gallagher PG. Granulicatella adiacens and early-onset sepsis in neonate. Emerging Infectious Diseases 2011, 17:1971-3.
• Single-lineage transcriptome analysis reveals key regulatory pathways in primitive erythroid progenitors in the mouse embryo.Isern 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, 117:4924-34.
• Genome-wide detection of a TFIID localization element from an initial human disease mutation.Yang 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 2011, 39:2175-87.
• Chromatin boundaries require functional collaboration between the hSET1 and NURF complexes.Li 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, 118:1386-94.
• Erythrocyte peripheral type benzodiazepine receptor/voltage-dependent anion channels are upregulated by Plasmodium falciparum.Bouyer 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, 118:2305-12.
• Genome-wide ChIP-Seq reveals a dramatic shift in the binding of the transcription factor erythroid Kruppel-like factor during erythrocyte differentiation.Pilon AM, Ajay SS, Kumar SA, Steiner LA, Cherukuri PF, Wincovitch S, Anderson SM, Mullikin JC, Gallagher PG, Hardison RC, Margulies EH, 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:e139-48.
• HbA(2): at the borderline of the KLF.Gallagher PG. HbA(2): at the borderline of the KLF. Blood 2011, 118:4301-2.
• MKL1 and MKL2 play redundant and crucial roles in megakaryocyte maturation and platelet formation.Smith 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, 120:2317-29.
• A de novo band 3 mutation in hereditary spherocytosis.Bogardus HH, Maksimova YD, Forget BG, Gallagher PG. A de novo band 3 mutation in hereditary spherocytosis. Pediatric Blood & Cancer 2012, 58:1004.
• Altered subcellular localization of transcription factor TEAD4 regulates first mammalian cell lineage commitment.Home 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, 109:7362-7.
• Methicillin-resistant Staphylococcus aureus in the neonatal intensive care unit.Nelson MU, Gallagher PG. Methicillin-resistant Staphylococcus aureus in the neonatal intensive care unit. Seminars In Perinatology 2012, 36:424-30.
• USF1 and hSET1A mediated epigenetic modifications regulate lineage differentiation and HoxB4 transcription.Deng 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.
• Disorders of red cell volume regulation.Gallagher PG. Disorders of red cell volume regulation. Current Opinion In Hematology 2013, 20:201-7.
• Abnormalities of the erythrocyte membrane.Gallagher PG. Abnormalities of the erythrocyte membrane. Pediatric Clinics Of North America 2013, 60:1349-62.
• Teleost growth factor independence (gfi) genes differentially regulate successive waves of hematopoiesis.Cooney 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 2013, 373:431-41.
• Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype.Ngo D, Bae H, Steinberg MH, Sebastiani P, Solovieff N, Baldwin CT, Melista E, Safaya S, Farrer LA, Al-Suliman AM, Albuali WH, Al Bagshi MH, 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 & Diseases 2013, 51:22-6.
• Applications of high-throughput DNA sequencing to benign hematology.Sankaran VG, Gallagher PG. Applications of high-throughput DNA sequencing to benign hematology. Blood 2013, 122:3575-82.
• Clinical and laboratory factors that predict death in very low birth weight infants presenting with late-onset sepsis.Levit 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, 33:143-6.
• Global transcriptome analysis and enhancer landscape of human primary T follicular helper and T effector lymphocytes.Weinstein 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, 124:3719-29.
• Neuronal mechanism for acute mechanosensitivity in tactile-foraging waterfowl.Schneider 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, 111:14941-6.
• Whole-exome sequencing identifies a novel somatic mutation in MMP8 associated with a t(1;22)-acute megakaryoblastic leukemia.Kim 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 2014, 28:945-8.
• Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disability.Xu 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.
• Piezo proteins: regulators of mechanosensation and other cellular processes.Bagriantsev SN, Gracheva EO, Gallagher PG. Piezo proteins: regulators of mechanosensation and other cellular processes. The Journal Of Biological Chemistry 2014, 289:31673-31681.
• Nonstochastic reprogramming from a privileged somatic cell state.Guo 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, 156:649-62.
• Concurrent bloodstream infections in infants with necrotizing enterocolitis.Bizzarro MJ, Ehrenkranz RA, Gallagher PG. Concurrent bloodstream infections in infants with necrotizing enterocolitis. The Journal Of Pediatrics 2014, 164:61-6.
• Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus.Bogardus 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:e168-70.
• Probing large conformational rearrangements in wild-type and mutant spectrin using structural mass spectrometry.Sriswasdi 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, 111:1801-6.
• Long noncoding RNAs in erythropoiesis.Gallagher PG. Long noncoding RNAs in erythropoiesis. Blood 2014, 123:465-6.
• Global transcriptome analyses of human and murine terminal erythroid differentiation.An 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, 123:3466-77.
• Isolation and transcriptome analyses of human erythroid progenitors: BFU-E and CFU-E.Li 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, 124:3636-45.
• Diagnosis and management of rare congenital nonimmune hemolytic disease.Gallagher PG. Diagnosis and management of rare congenital nonimmune hemolytic disease. Hematology / The Education Program Of The American Society Of Hematology. American Society Of Hematology. Education Program 2015, 2015:392-9.
• Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis.Glogowska E, Lezon-Geyda K, Maksimova Y, Schulz VP, Gallagher PG. Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis. Blood 2015, 126:1281-4.
• Transporting down the road to dehydration.Gallagher PG. Transporting down the road to dehydration. Blood 2015, 126:2775-6.
• Neonatal sepsis 2004-2013: the rise and fall of coagulase-negative staphylococci.Bizzarro 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, 166:1193-9.
• 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.Nelson 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, 53:2492-501.
• A pediatrician's practical guide to diagnosing and treating hereditary spherocytosis in neonates.Christensen RD, Yaish HM, Gallagher PG. A pediatrician's practical guide to diagnosing and treating hereditary spherocytosis in neonates. Pediatrics 2015, 135:1107-14.
• Human and murine erythropoiesis.An X, Schulz VP, Mohandas N, Gallagher PG. Human and murine erythropoiesis. Current Opinion In Hematology 2015, 22:206-11.
• CTCF and CohesinSA-1 Mark Active Promoters and Boundaries of Repressive Chromatin Domains in Primary Human Erythroid Cells.Steiner 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.
• 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.
• In vivo correction of anaemia in β-thalassemic mice by γPNA-mediated gene editing with nanoparticle delivery.Bahal 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.
• The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotes.Jiang 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, Basak 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) β(0) -thalassaemia homozygotes. British Journal Of Haematology 2016, 172:958-65.
• Setd1a and NURF mediate chromatin dynamics and gene regulation during erythroid lineage commitment and differentiation.Li 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, 44:7173-88.
• 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.Hargrave 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 2016, 30:800-8.
• Diagnosis of Pyruvate Kinase Deficiency.Gallagher PG, Glader B. Diagnosis of Pyruvate Kinase Deficiency. Pediatric Blood & Cancer 2016, 63:771-2.
• 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 2016, 127:1481-92.
• 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.
• 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.Gallagher 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.
• Hepatic Malignancy in an Infant with Wolf-Hirschhorn Syndrome.Rutter S, Morotti RA, Peterec S, Gallagher PG. Hepatic Malignancy in an Infant with Wolf-Hirschhorn Syndrome. Fetal And Pediatric Pathology 2017, 36:256-262.
• Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis.Glogowska 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.
• Disorders of erythrocyte hydration.Gallagher PG. Disorders of erythrocyte hydration. Blood 2017, 130:2699-2708.
• Hemoglobin C trait accentuates erythrocyte dehydration in hereditary xerocytosis.Yang E, Voelkel EB, Lezon-Geyda K, Schulz VP, Gallagher PG. Hemoglobin C trait accentuates erythrocyte dehydration in hereditary xerocytosis. Pediatric Blood & Cancer 2017, 64.
• Molecular basis of tactile specialization in the duck bill.Schneider 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.
• Distinct roles for TET family proteins in regulating human erythropoiesis.Yan 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.
• A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β0 -thalassaemia homozygotes.Jiang Z, Luo HY, Farrell JJ, Zhang Z, Schulz VP, Albarawi D, Steinberg MH, Al-Allawi NA, Gallagher PG, Forget BG, Chui DH. A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β0 -thalassaemia homozygotes. British Journal Of Haematology 2018, 180:755-757.
• 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, Pospíŝilová 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.
• A Ser725Arg mutation in Band 3 abolishes transport function and leads to anemia and renal tubular acidosis.Yang 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.
• Hereditary xerocytosis: Diagnostic considerations.Risinger 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 2018, 93:E67-E69.
• STAT4 and T-bet control follicular helper T cell development in viral infections.Weinstein 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. The Journal Of Experimental Medicine 2018, 215:337-355.
• Correction: STAT4 and T-bet control follicular helper T cell development in viral infections.Weinstein 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. The Journal Of Experimental Medicine 2018, 215:999.
• KLF1 E325K-associated Congenital Dyserythropoietic Anemia Type IV: Insights Into the Variable Clinical Severity.Ravindranath Y, Johnson RM, Goyette G, Buck S, Gadgeel M, Gallagher PG. KLF1 E325K-associated Congenital Dyserythropoietic Anemia Type IV: Insights Into the Variable Clinical Severity. Journal Of Pediatric Hematology/oncology 2018, 40:e405-e409.
• Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlation.Singh 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.
• 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. Journal Of Immunology (Baltimore, Md. : 1950) 2018, 201:1359-1372.
• MRTFA augments megakaryocyte maturation by enhancing the SRF regulatory axis.Rahman 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.
• Severe nondominant hereditary spherocytosis in an infant with coinheritance of three rare alpha-spectrin gene defects.Bhatt 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 2019, 66:e27480.
• Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency.Bianchi P, Elisa 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 JC, van Beers E, Gallagher PG, Rees DC, van Wijk R. Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency. American Journal Of Hematology 2019, 94:149-161.
• MKL1-actin pathway restricts chromatin accessibility and prevents mature pluripotency activation.Hu 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.
• Aberrant splicing contributes to severe α-spectrin-linked congenital hemolytic anemia.Gallagher PG, Maksimova Y, Lezon-Geyda K, Newburger PE, Medeiros D, Hanson RD, Rothman JA, Israels SJ, 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. The Journal Of Clinical Investigation 2019, 129:2878-2887.
• Identification and transcriptome analysis of erythroblastic island macrophages.Li 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.
• A Unique Epigenomic Landscape Defines Human Erythropoiesis.Schulz 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.
• The Journal of Perinatology Turns a Page.Gallagher PG. The Journal of Perinatology Turns a Page. Journal Of Perinatology : Official Journal Of The California Perinatal Association 2019, 39:1323-1324.
• 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. Transactions Of The Association Of American Physicians 1992, 105:268-77.
• 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.
• 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. The Journal Of Clinical Investigation 1992, 89:892-8.
• 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.
• 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.
• A splice site mutation of the beta-spectrin gene causing exon skipping in hereditary elliptocytosis associated with a truncated beta-spectrin chain.Gallagher 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. The Journal Of Biological Chemistry 1991, 266:15154-9.
• 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. Transactions Of The Association Of American Physicians 1991, 104:32-9.
• Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptide.Floyd PB, Gallagher PG, Valentino LA, Davis M, Marchesi SL, Forget BG. Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptide. Blood 1991, 78:1364-72.
• Sclerotherapy.Gallagher PG. Sclerotherapy. The Journal Of Dermatologic Surgery And Oncology 1991, 17:304.
• 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.
• 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. The Journal Of Clinical Investigation 1991, 88:76-81.
• An insertional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin nice (beta 220/216).Tse WT, Gallagher PG, Pothier B, Costa FF, Scarpa A, Delaunay J, Forget BG. An insertional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin nice (beta 220/216). Blood 1991, 78:517-23.
• 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.
• Facial nerve paralysis and Kawasaki disease.Gallagher PG. Facial nerve paralysis and Kawasaki disease. Reviews Of Infectious Diseases 1990, 12:403-5.
• Enterobacter bacteremia in pediatric patients.Gallagher PG. Enterobacter bacteremia in pediatric patients. Reviews Of Infectious Diseases 1990, 12:808-12.
• Group C streptococcal sinusitis.Gallagher PG, Myer CM, Crone K, Benzing G. Group C streptococcal sinusitis. American Journal Of Otolaryngology 1990, 11:352-4.
• 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.
• Osteomyelitis of the skull after varicella infection.Gallagher PG. Osteomyelitis of the skull after varicella infection. Clinical Pediatrics 1990, 29:29.
• 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.
• 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.
• 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.
• 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.
• 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.
• Group B streptococcal meningitis in adults.Gallagher PG, Watanakunakorn C. Group B streptococcal meningitis in adults. Archives Of Neurology 1985, 42:626-7.
• Blastocystis hominis enteritis.Gallagher PG, Venglarcik JS. Blastocystis hominis enteritis. Pediatric Infectious Disease 1985, 4:556-7.
• cDNA structure, tissue-specific expression, and chromosomal localization of the murine band 7.2b gene.Gallagher PG, Romana M, Lieman JH, Ward DC. cDNA structure, tissue-specific expression, and chromosomal localization of the murine band 7.2b gene. Blood 1995, 86:359-65.
• Structure, organization, and expression of the human band 7.2b gene, a candidate gene for hereditary hydrocytosis.Gallagher PG, Forget BG. Structure, organization, and expression of the human band 7.2b gene, a candidate gene for hereditary hydrocytosis. The Journal Of Biological Chemistry 1995, 270:26358-63.
• Location and PCR-based detection of three polymorphisms of the human erythrocyte beta-spectrin gene (SPTB).Gallagher PG, Lecomte MC, Galand C, Wang YP, Tse WT, Forget BG. Location and PCR-based detection of three polymorphisms of the human erythrocyte beta-spectrin gene (SPTB). British Journal Of Haematology 1994, 88:413-4.
• 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. The Journal Of Clinical Investigation 1995, 95:1174-82.
• Analysis of a PstI polymorphism of the human erythrocyte band 3 gene (EPB3).Jenkins PB, Gallagher PG, Forget BG. Analysis of a PstI polymorphism of the human erythrocyte band 3 gene (EPB3). British Journal Of Haematology 1993, 85:816-8.
• Spectrin St Louis and the alpha LELY allele.Gallagher PG, Forget BG. Spectrin St Louis and the alpha LELY allele. Blood 1994, 84:1686-7.
• Spectrin genes in health and disease.Gallagher PG, Forget BG. Spectrin genes in health and disease. Seminars In Hematology 1993, 30:4-20.
• Localization of the human alpha-fodrin gene (SPTAN1) to 9q33-->q34 by fluorescence in situ hybridization.Upender M, Gallagher PG, Moon RT, Ward DC, Forget BG. Localization of the human alpha-fodrin gene (SPTAN1) to 9q33-->q34 by fluorescence in situ hybridization. Cytogenetics And Cell Genetics 1994, 66:39-41.
• The gene for human erythrocyte membrane protein band 7.2 (EPB72) maps to 9q33-q34 centromeric to the Philadelphia chromosome translocation breakpoint region.Gallagher PG, Upender M, Ward DC, Forget BG. The gene for human erythrocyte membrane protein band 7.2 (EPB72) maps to 9q33-q34 centromeric to the Philadelphia chromosome translocation breakpoint region. Genomics 1993, 18:167-9.
• Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria: an alpha I/50b Kd variant that is caused by a single amino acid deletion.Gallagher PG, Roberts WE, Benoit L, Speicher DW, Marchesi SL, Forget BG. Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria: an alpha I/50b Kd variant that is caused by a single amino acid deletion. Blood 1993, 82:2210-5.
• Erythropoietin therapy for anemia of prematurity.Gallagher PG, Ehrenkranz RA. Erythropoietin therapy for anemia of prematurity. Clinics In Perinatology 1993, 20:169-91.
• Nutritional anemias in infancy.Gallagher PG, Ehrenkranz RA. Nutritional anemias in infancy. Clinics In Perinatology 1995, 22:671-92.
• 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. The Journal Of Clinical Investigation 1996, 97:373-80.
• Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.Eber SW, Gonzalez JM, Lux ML, Scarpa AL, Tse WT, Dornwell M, Herbers J, Kugler W, Ozcan R, Pekrun A, Gallagher PG, Schröter W, Forget BG, Lux SE. Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis. Nature Genetics 1996, 13:214-8.
• 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; A Journal Of Technical Methods And Pathology 1996, 74:1117-29.
• 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.
• Genomic organization and 5'-flanking DNA sequence of the murine stomatin gene (Epb72).Gallagher PG, Turetsky T, Mentzer WC. Genomic organization and 5'-flanking DNA sequence of the murine stomatin gene (Epb72). Genomics 1996, 34:410-2.
• Seminars in perinatology.Gallagher PG. Seminars in perinatology. Seminars In Perinatology 1995, 19:435-6.
• Hematologic disorders and nonimmune hydrops fetalis.Arcasoy MO, Gallagher PG. Hematologic disorders and nonimmune hydrops fetalis. Seminars In Perinatology 1995, 19:502-15.
• Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin.Glele-Kakai C, Garbarz M, Lecomte MC, Leborgne S, Galand C, Bournier O, Devaux I, Gautero H, Zohoun I, Gallagher PG, Forget BG, Dhermy D. Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin. British Journal Of Haematology 1996, 95:57-66.
• 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. The Journal Of Clinical Investigation 1997, 99:267-77.
• Amino-acid substitution in alpha-spectrin commonly coinherited with nondominant hereditary spherocytosis.Tse WT, Gallagher PG, Jenkins PB, Wang Y, Benoit L, Speicher D, Winkelmann JC, Agre P, Forget BG, Marchesi SL. Amino-acid substitution in alpha-spectrin commonly coinherited with nondominant hereditary spherocytosis. American Journal Of Hematology 1997, 54:233-41.
• Hematologically important mutations: spectrin variants in hereditary elliptocytosis and hereditary pyropoikilocytosis.Gallagher PG, Forget BG. Hematologically important mutations: spectrin variants in hereditary elliptocytosis and hereditary pyropoikilocytosis. Blood Cells, Molecules & Diseases 1996, 22:254-8.
• Molecular basis of erythrocyte membrane disorders.Gallagher PG, Ferriera JD. Molecular basis of erythrocyte membrane disorders. Current Opinion In Hematology 1997, 4:128-35.
• Spectrin St Claude, a splicing mutation of the human alpha-spectrin gene associated with severe poikilocytic anemia.Fournier CM, Nicolas G, Gallagher PG, Dhermy D, Grandchamp B, Lecomte MC. Spectrin St Claude, a splicing mutation of the human alpha-spectrin gene associated with severe poikilocytic anemia. Blood 1997, 89:4584-90.
• Structure and organization of the human ankyrin-1 gene. Basis for complexity of pre-mRNA processing.Gallagher PG, Tse WT, Scarpa AL, Lux SE, Forget BG. Structure and organization of the human ankyrin-1 gene. Basis for complexity of pre-mRNA processing. The Journal Of Biological Chemistry 1997, 272:19220-8.
• Genetic basis of the polymorphisms of the alphaI domain of spectrin.Gallagher PG, Romana M, Wong C, Forget BG. Genetic basis of the polymorphisms of the alphaI domain of spectrin. American Journal Of Hematology 1997, 56:107-11.
• Pseudoexstrophy of the bladder: case report and literature review.Swana HS, Gallagher PG, Weiss RM. Pseudoexstrophy of the bladder: case report and literature review. Journal Of Pediatric Surgery 1997, 32:1480-1.
• 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.
• An alternate promoter directs expression of a truncated, muscle-specific isoform of the human ankyrin 1 gene.Gallagher PG, Forget BG. An alternate promoter directs expression of a truncated, muscle-specific isoform of the human ankyrin 1 gene. The Journal Of Biological Chemistry 1998, 273:1339-48.
• Hematologically important mutations: band 3 and protein 4.2 variants in hereditary spherocytosis.Gallagher PG, Forget BG. Hematologically important mutations: band 3 and protein 4.2 variants in hereditary spherocytosis. Blood Cells, Molecules & Diseases 1997, 23:417-21.
• Complications of conjunctivitis caused by Pseudomonas aeruginosa in a newborn intensive care unit.Shah SS, Gallagher PG. Complications of conjunctivitis caused by Pseudomonas aeruginosa in a newborn intensive care unit. The Pediatric Infectious Disease Journal 1998, 17:97-102.
• Atrial flutter complicating neonatal Coxsackie B2 myocarditis.Shah SS, Hellenbrand WE, Gallagher PG. Atrial flutter complicating neonatal Coxsackie B2 myocarditis. Pediatric Cardiology 1998, 19:185-6.
• 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.
• Substitution of the human beta-spectrin promoter for the human agamma-globin promoter prevents silencing of a linked human beta-globin gene in transgenic mice.Sabatino DE, Cline AP, Gallagher PG, Garrett LJ, Stamatoyannopoulos G, Forget BG, Bodine DM. Substitution of the human beta-spectrin promoter for the human agamma-globin promoter prevents silencing of a linked human beta-globin gene in transgenic mice. Molecular And Cellular Biology 1998, 18:6634-40.
• Understanding iron absorption and metabolism.Gallagher PG, Ehrenkranz RA. Understanding iron absorption and metabolism. Journal Of Pediatric Gastroenterology And Nutrition 1998, 27:610-1.
• Elevated blood lead levels in children are associated with lower erythropoietin concentrations.Liebelt EL, Schonfeld DJ, Gallagher P. Elevated blood lead levels in children are associated with lower erythropoietin concentrations. The Journal Of Pediatrics 1999, 134:107-9.
• Hematologically important mutations: spectrin and ankyrin variants in hereditary spherocytosis.Gallagher PG, Forget BG. Hematologically important mutations: spectrin and ankyrin variants in hereditary spherocytosis. Blood Cells, Molecules & Diseases 1998, 24:539-43.
• A human beta-spectrin gene promoter directs high level expression in erythroid but not muscle or neural cells.Gallagher PG, Sabatino DE, Romana M, Cline AP, Garrett LJ, Bodine DM, Forget BG. A human beta-spectrin gene promoter directs high level expression in erythroid but not muscle or neural cells. The Journal Of Biological Chemistry 1999, 274:6062-73.
• Stomatocytosis is absent in "stomatin"-deficient murine red blood cells.Zhu Y, Paszty C, Turetsky T, Tsai S, Kuypers FA, Lee G, Cooper P, Gallagher PG, Stevens ME, Rubin E, Mohandas N, Mentzer WC. Stomatocytosis is absent in "stomatin"-deficient murine red blood cells. Blood 1999, 93:2404-10.
• 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.
• Increasing incidence of gram-negative rod bacteremia in a newborn intensive care unit.Shah SS, Ehrenkranz RA, Gallagher PG. Increasing incidence of gram-negative rod bacteremia in a newborn intensive care unit. The Pediatric Infectious Disease Journal 1999, 18:591-5.
• Neonatal tumors. Introduction.Gallagher PG, Lampkin BC. Neonatal tumors. Introduction. Seminars In Perinatology 1999, 23:261-2.
• Cystic hygroma in the fetus and newborn.Gallagher PG, Mahoney MJ, Gosche JR. Cystic hygroma in the fetus and newborn. Seminars In Perinatology 1999, 23:341-56.
• 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.
• 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.
• Bacteremia, meningitis, and brain abscesses in a hospitalized infant: complications of Pseudomonas aeruginosa conjunctivitis.Shah SS, Gloor P, Gallagher PG. Bacteremia, meningitis, and brain abscesses in a hospitalized infant: complications of Pseudomonas aeruginosa conjunctivitis. Journal Of Perinatology : Official Journal Of The California Perinatal Association 1999, 19:462-5.
• Proton block and voltage gating are potassium-dependent in the cardiac leak channel Kcnk3.Lopes CM, Gallagher PG, Buck ME, Butler MH, Goldstein SA. Proton block and voltage gating are potassium-dependent in the cardiac leak channel Kcnk3. The Journal Of Biological Chemistry 2000, 275:16969-78.
• A minimal ankyrin promoter linked to a human gamma-globin gene demonstrates erythroid specific copy number dependent expression with minimal position or enhancer dependence in transgenic mice.Sabatino DE, Wong C, Cline AP, Pyle L, Garrett LJ, Gallagher PG, Bodine DM. A minimal ankyrin promoter linked to a human gamma-globin gene demonstrates erythroid specific copy number dependent expression with minimal position or enhancer dependence in transgenic mice. The Journal Of Biological Chemistry 2000, 275:28549-54.
• Gene transfer to ankyrin-deficient bone marrow corrects spherocytosis in vitro.Dooner GJ, Barker JE, Gallagher PG, Debatis ME, Brown AH, Forget BG, Becker PS. Gene transfer to ankyrin-deficient bone marrow corrects spherocytosis in vitro. Experimental Hematology 2000, 28:765-74.
• The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter.Gallagher PG, Romana M, Tse WT, Lux SE, Forget BG. The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter. Blood 2000, 96:1136-43.
• Congenital chylothorax.Dubin PJ, King IN, Gallagher PG. Congenital chylothorax. Current Opinion In Pediatrics 2000, 12:505-9.
• Long-term expression of gamma-globin mRNA in mouse erythrocytes from retrovirus vectors containing the human gamma-globin gene fused to the ankyrin-1 promoter.Sabatino DE, Seidel NE, Aviles-Mendoza GJ, Cline AP, Anderson SM, Gallagher PG, Bodine DM. Long-term expression of gamma-globin mRNA in mouse erythrocytes from retrovirus vectors containing the human gamma-globin gene fused to the ankyrin-1 promoter. Proceedings Of The National Academy Of Sciences Of The United States Of America 2000, 97:13294-9.
• Genomic organization and chromosomal localization of the murine 2 P domain potassium channel gene Kcnk8: conservation of gene structure in 2 P domain potassium channels.Bockenhauer D, Nimmakayalu MA, Ward DC, Goldstein SA, Gallagher PG. Genomic organization and chromosomal localization of the murine 2 P domain potassium channel gene Kcnk8: conservation of gene structure in 2 P domain potassium channels. Gene 2000, 261:365-72.
• A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosis.Gallagher PG, Ferreira JD, Costa FF, Saad ST, Forget BG. A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosis. British Journal Of Haematology 2000, 111:1190-3.
• Modification of erythrocyte hydration in the treatment of sickle cell disease.Zhou GP, Anderson KP, Joiner CH, Gallagher PG. Modification of erythrocyte hydration in the treatment of sickle cell disease. Blood Cells, Molecules & Diseases 2001, 27:65-8.
• Spectrin oligomerization is cooperatively coupled to membrane assembly: a linkage targeted by many hereditary hemolytic anemias?Giorgi M, Cianci CD, Gallagher PG, Morrow JS. Spectrin oligomerization is cooperatively coupled to membrane assembly: a linkage targeted by many hereditary hemolytic anemias? Experimental And Molecular Pathology 2001, 70:215-30.
• Development of a stable retrovirus vector capable of long-term expression of gamma-globin mRNA in mouse erythrocytes.Sabatino DE, Seidel NE, Cline AP, Anderson SM, Gallagher PG, Bodine DM. Development of a stable retrovirus vector capable of long-term expression of gamma-globin mRNA in mouse erythrocytes. Annals Of The New York Academy Of Sciences 2001, 938:246-61.
• Erythrocyte ankyrin promoter mutations associated with recessive hereditary spherocytosis cause significant abnormalities in ankyrin expression.Gallagher PG, Sabatino DE, Basseres DS, Nilson DM, Wong C, Cline AP, Garrett LJ, Bodine DM. Erythrocyte ankyrin promoter mutations associated with recessive hereditary spherocytosis cause significant abnormalities in ankyrin expression. The Journal Of Biological Chemistry 2001, 276:41683-9.
• Dynamic molecular modeling of pathogenic mutations in the spectrin self-association domain.Zhang Z, Weed SA, Gallagher PG, Morrow JS. Dynamic molecular modeling of pathogenic mutations in the spectrin self-association domain. Blood 2001, 98:1645-53.
• 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 : Official Journal Of The American Institute Of Ultrasound In Medicine 2001, 20:1357-63.
• Refinement of the hereditary xerocytosis locus on chromosome 16q in a large Canadian kindred.Houston 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 & Diseases 2011, 47:226-31.
• Late-onset Leclercia adecarboxylata sepsis in a premature neonate.Nelson MU, Maksimova Y, Schulz V, Bizzarro MJ, Gallagher PG. Late-onset Leclercia adecarboxylata sepsis in a premature neonate. Journal Of Perinatology : Official Journal Of The California Perinatal Association 2013, 33:740-2.
• 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.Nelson 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 : Official Journal Of The California Perinatal Association 2014, 34:653-5.
• Disorders of erythrocyte volume homeostasis.Glogowska E, Gallagher PG. Disorders of erythrocyte volume homeostasis. International Journal Of Laboratory Hematology 2015, 37 Suppl 1:85-91.
• 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 : Official Journal Of The California Perinatal Association 2020, 40:357-358.
• Genotype-phenotype correlation and molecular heterogeneity in pyruvate kinase deficiency.Bianchi P, Fermo E, Lezon-Geyda K, van Beers E, Morton DH, Barcellini W, Glader B, Chonat S, Ravindranath Y, Newburger P, Kollmar N, Despotovic J, Verhovsek M, Sharma M, Kwiatkowski JL, Kuo KHM, Wlodarski M, Yaish H, Holzhauer S, Wang H, Kunz J, Addonizio K, Al-Sayegh H, London W, Andres O, van Wijk R, Gallagher PG, Grace R. Genotype-phenotype correlation and molecular heterogeneity in pyruvate kinase deficiency. American Journal Of Hematology 2020, 95:472-482.
• Perinatal aspects on the covid-19 pandemic: a practical resource for perinatal-neonatal specialists.Mimouni 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 : Official Journal Of The California Perinatal Association 2020, 40:820-826.
• Comprehensive proteomic analysis of murine terminal erythroid differentiation.Gautier 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.
• Characterization of circulating and cultured Tfh-like cells in sickle cell disease in relation to red blood cell alloimmunization status.Balbuena-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 : Official Journal Of The World Apheresis Association : Official Journal Of The European Society For Haemapheresis 2020, 59:102778.
• Vertical Transmission of Severe Acute Respiratory Syndrome Coronavirus 2 From the Mother to the Infant.Mimouni 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.
• Functional characterization of a novel SLC40A1 Arg88Ile mutation in a kindred with familial iron overload treated by phlebotomy.Womack 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 & Diseases 2021, 87:102532.
• Critical disparities in perinatal health-understanding risks and changing the outcomes.Harris LM, Forson-Dare Z, Gallagher PG. Critical disparities in perinatal health-understanding risks and changing the outcomes. Journal Of Perinatology : Official Journal Of The California Perinatal Association 2021, 41:181-182.
• 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 : Official Journal Of The California Perinatal Association 2021, 41:363-364.
• An IDH1-vitamin C crosstalk drives human erythroid development by inhibiting pro-oxidant mitochondrial metabolism.Gonzalez-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.
• Quality criteria for randomized controlled studies: obstetrical journal guidelines.Anderson 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.
• Journal of Perinatology Editorial Updates 2021.Raju T, Cheng Y, Mimouni FB, Pearlman SA, Ryan RM, Swanson JR, Gallagher PG. Journal of Perinatology Editorial Updates 2021. Journal Of Perinatology : Official Journal Of The California Perinatal Association 2021, 41:917-922.
• Comprehensive phenotyping of erythropoiesis in human bone marrow: Evaluation of normal and ineffective erythropoiesis.Yan 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.
• Impairment of human terminal erythroid differentiation by histone deacetylase 5 deficiency.Wang Y, Li W, Schulz V, Zhao H, Qu X, Qi Q, Cheng Y, Guo X, Zhang S, Wei X, Liu D, Yazdanbakhsh K, Hillyer CD, Narla M, Chen L, Gallagher PG, An X. Impairment of human terminal erythroid differentiation by histone deacetylase 5 deficiency. Blood 2021.
• Regulation of RNA Polymerase II Activity is Essential for Terminal Erythroid Maturation.Murphy Z, Murphy K, Myers JA, Getman MR, Couch T, Schulz V, Lezon-Geyda K, Palumbo C, Yan H, Narla M, Gallagher PG, Steiner LA. Regulation of RNA Polymerase II Activity is Essential for Terminal Erythroid Maturation. Blood 2021.
• An Initiative to Decrease Laboratory Testing in a NICU.Klunk 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.
• Difficulty in Diagnosis of Hereditary Spherocytosis in the Neonate.Gallagher PG. Difficulty in Diagnosis of Hereditary Spherocytosis in the Neonate. Pediatrics 2021, 148.
• Recommendations for diagnosis and treatment of methemoglobinemia.Iolascon 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. Recommendations for diagnosis and treatment of methemoglobinemia. American Journal Of Hematology 2021.
• D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia.Werner KM, Cox AJ, Qian E, Jain P, Ji W, Tikhonova I, Castaldi C, Bilguvar K, Knight J, Ferdinandusse S, Fawaz R, Jiang YH, 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.