Angeliki Louvi, PhD

• Abha Gupta
• Charles Duncan
• James Leckman
• Karl Insogna
• Katarzyna Chawarska
• Katsuhito Yasuno
• Ketu Mishra-Gorur
• Matthew Bizzarro
• Murat Gunel
• Richard Bronen
• Sacit Bulent Omay
• Steven Tommasini
• Thomas Fernandez
• Zeynep Erson Omay

Brain; Intracranial Aneurysm; Disease Models, Animal; Microcephaly; Morphogenesis; Nervous System Diseases; Organoids; Hemangioma, Cavernous, Central Nervous System; Lissencephaly; Induced Pluripotent Stem Cells

• Microcephaly-associated protein WDR62 shuttles from the Golgi apparatus to the spindle poles in human neural progenitorsDell'Amico C, Salavarria M, Takeo Y, Saotome I, Dell'Anno M, Galimberti M, Pellegrino E, Cattaneo E, Louvi A, Onorati M. Microcephaly-associated protein WDR62 shuttles from the Golgi apparatus to the spindle poles in human neural progenitors ELife 2023, 12: e81716. PMID: 37272619, PMCID: PMC10241521, DOI: 10.7554/elife.81716.
• Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart diseaseMishra-Gorur K, Barak T, Kaulen L, Henegariu O, Jin S, Aguilera S, Yalbir E, Goles G, Nishimura S, Miyagishima D, Djenoune L, Altinok S, Rai D, Viviano S, Prendergast A, Zerillo C, Ozcan K, Baran B, Sencar L, Goc N, Yarman Y, Ercan-Sencicek A, Bilguvar K, Lifton R, Moliterno J, Louvi A, Yuan S, Deniz E, Brueckner M, Gunel M. Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart disease Proceedings Of The National Academy Of Sciences Of The United States Of America 2023, 120: e2214997120. PMID: 37043537, PMCID: PMC10120005, DOI: 10.1073/pnas.2214997120.
• Altered Expression of Several Molecular Mediators of Cerebrospinal Fluid Production in Hyp MiceKaplan J, Tommasini S, Yao G, Zhu M, Nishimura S, Ghazarian S, Louvi A, Insogna K. Altered Expression of Several Molecular Mediators of Cerebrospinal Fluid Production in Hyp Mice Journal Of The Endocrine Society 2023, 7: bvad022. PMID: 36819458, PMCID: PMC9936957, DOI: 10.1210/jendso/bvad022.
• The Notch pathway in CNS homeostasis and neurodegenerationHo DM, Artavanis‐Tsakonas S, Louvi A. The Notch pathway in CNS homeostasis and neurodegeneration WIREs Mechanisms Of Disease 2019, 9: e358. PMID: 31502763, DOI: 10.1002/wdev.358.
• Id4 Downstream of Notch2 Maintains Neural Stem Cell Quiescence in the Adult HippocampusZhang R, Boareto M, Engler A, Louvi A, Giachino C, Iber D, Taylor V. Id4 Downstream of Notch2 Maintains Neural Stem Cell Quiescence in the Adult Hippocampus Cell Reports 2019, 28: 1485-1498.e6. PMID: 31390563, DOI: 10.1016/j.celrep.2019.07.014.
• Cerebrovascular disorders associated with genetic lesionsKarschnia P, Nishimura S, Louvi A. Cerebrovascular disorders associated with genetic lesions Cellular And Molecular Life Sciences 2018, 76: 283-300. PMID: 30327838, PMCID: PMC6450555, DOI: 10.1007/s00018-018-2934-5.
• Notch2 Signaling Maintains NSC Quiescence in the Murine Ventricular-Subventricular ZoneEngler A, Rolando C, Giachino C, Saotome I, Erni A, Brien C, Zhang R, Zimber-Strobl U, Radtke F, Artavanis-Tsakonas S, Louvi A, Taylor V. Notch2 Signaling Maintains NSC Quiescence in the Murine Ventricular-Subventricular Zone Cell Reports 2018, 22: 992-1002. PMID: 29386140, DOI: 10.1016/j.celrep.2017.12.094.
• Combined HMG-COA reductase and prenylation inhibition in treatment of CCMNishimura S, Mishra-Gorur K, Park J, Surovtseva YV, Sebti SM, Levchenko A, Louvi A, Gunel M. Combined HMG-COA reductase and prenylation inhibition in treatment of CCM Proceedings Of The National Academy Of Sciences Of The United States Of America 2017, 114: 5503-5508. PMID: 28500274, PMCID: PMC5448170, DOI: 10.1073/pnas.1702942114.
• Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephalySgourdou P, Mishra-Gorur K, Saotome I, Henagariu O, Tuysuz B, Campos C, Ishigame K, Giannikou K, Quon JL, Sestan N, Caglayan AO, Gunel M, Louvi A. Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephaly Scientific Reports 2017, 7: 43708. PMID: 28272472, PMCID: PMC5341122, DOI: 10.1038/srep43708.
• B-Cell Depletion Reduces the Maturation of Cerebral Cavernous Malformations in Murine ModelsShi C, Shenkar R, Zeineddine HA, Girard R, Fam MD, Austin C, Moore T, Lightle R, Zhang L, Wu M, Cao Y, Gunel M, Louvi A, Rorrer A, Gallione C, Marchuk DA, Awad IA. B-Cell Depletion Reduces the Maturation of Cerebral Cavernous Malformations in Murine Models Journal Of Neuroimmune Pharmacology 2016, 11: 369-377. PMID: 27086141, PMCID: PMC6746226, DOI: 10.1007/s11481-016-9670-0.
• Notch1 and Notch2 receptors regulate mouse and human gastric antral epithelial cell homoeostasisGifford GB, Demitrack ES, Keeley TM, Tam A, La Cunza N, Dedhia PH, Spence JR, Simeone DM, Saotome I, Louvi A, Siebel CW, Samuelson LC. Notch1 and Notch2 receptors regulate mouse and human gastric antral epithelial cell homoeostasis Gut 2016, 66: 1001. PMID: 26933171, PMCID: PMC5009003, DOI: 10.1136/gutjnl-2015-310811.
• Integrated genomic characterization of IDH1-mutant glioma malignant progressionBai H, Harmancı AS, Erson-Omay EZ, Li J, Coşkun S, Simon M, Krischek B, Özduman K, Omay SB, Sorensen EA, Turcan Ş, Bakırcığlu M, Carrión-Grant G, Murray PB, Clark VE, Ercan-Sencicek AG, Knight J, Sencar L, Altınok S, Kaulen LD, Gülez B, Timmer M, Schramm J, Mishra-Gorur K, Henegariu O, Moliterno J, Louvi A, Chan TA, Tannheimer SL, Pamir MN, Vortmeyer AO, Bilguvar K, Yasuno K, Günel M. Integrated genomic characterization of IDH1-mutant glioma malignant progression Nature Genetics 2015, 48: 59-66. PMID: 26618343, PMCID: PMC4829945, DOI: 10.1038/ng.3457.
• Structure and vascular function of MEKK3–cerebral cavernous malformations 2 complexFisher OS, Deng H, Liu D, Zhang Y, Wei R, Deng Y, Zhang F, Louvi A, Turk BE, Boggon TJ, Su B. Structure and vascular function of MEKK3–cerebral cavernous malformations 2 complex Nature Communications 2015, 6: 7937. PMID: 26235885, PMCID: PMC4526114, DOI: 10.1038/ncomms8937.
• Functional Synergy between Cholecystokinin Receptors CCKAR and CCKBR in Mammalian Brain DevelopmentNishimura S, Bilgüvar K, Ishigame K, Sestan N, Günel M, Louvi A. Functional Synergy between Cholecystokinin Receptors CCKAR and CCKBR in Mammalian Brain Development PLOS ONE 2015, 10: e0124295. PMID: 25875176, PMCID: PMC4398320, DOI: 10.1371/journal.pone.0124295.
• Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural ProgenitorsMishra-Gorur K, Çağlayan AO, Schaffer AE, Chabu C, Henegariu O, Vonhoff F, Akgümüş GT, Nishimura S, Han W, Tu S, Baran B, Gümüş H, Dilber C, Zaki MS, Hossni HAA, Rivière JB, Kayserili H, Spencer EG, Rosti RÖ, Schroth J, Per H, Çağlar C, Çağlar Ç, Dölen D, Baranoski JF, Kumandaş S, Minja FJ, Erson-Omay EZ, Mane SM, Lifton RP, Xu T, Keshishian H, Dobyns WB, Chi NC, Šestan N, Louvi A, Bilgüvar K, Yasuno K, Gleeson JG, Günel M. Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors Neuron 2015, 85: 228. PMID: 29654772, DOI: 10.1016/j.neuron.2014.12.046.
• Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural ProgenitorsMishra-Gorur K, Çağlayan AO, Schaffer AE, Chabu C, Henegariu O, Vonhoff F, Akgümüş GT, Nishimura S, Han W, Tu S, Baran B, Gümüş H, Dilber C, Zaki MS, Hossni HA, Rivière JB, Kayserili H, Spencer EG, Rosti RÖ, Schroth J, Per H, Çağlar C, Çağlar Ç, Dölen D, Baranoski JF, Kumandaş S, Minja FJ, Erson-Omay EZ, Mane SM, Lifton RP, Xu T, Keshishian H, Dobyns WB, Chi NC, Šestan N, Louvi A, Bilgüvar K, Yasuno K, Gleeson JG, Günel M. Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors Neuron 2014, 84: 1226-1239. PMID: 25521378, PMCID: PMC5024344, DOI: 10.1016/j.neuron.2014.12.014.
• Ccm3, a gene associated with cerebral cavernous malformations, is required for neuronal migrationLouvi A, Nishimura S, Günel M. Ccm3, a gene associated with cerebral cavernous malformations, is required for neuronal migration Journal Of Cell Science 2014, 127: e1-e1. DOI: 10.1242/jcs.152207.
• Ccm3, a gene associated with cerebral cavernous malformations, is required for neuronal migrationLouvi A, Nishimura S, Günel M. Ccm3, a gene associated with cerebral cavernous malformations, is required for neuronal migration Development 2014, 141: 1404-1415. PMID: 24595293, PMCID: PMC3943187, DOI: 10.1242/dev.093526.
• Cerebral Cavernous Malformations and the Neurovascular UnitLouvi A. Cerebral Cavernous Malformations and the Neurovascular Unit The FASEB Journal 2013, 27: 320.3-320.3. DOI: 10.1096/fasebj.27.1_supplement.320.3.
• Recessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressive neurodegenerationBilguvar K, Tyagi NK, Ozkara C, Tuysuz B, Bakircioglu M, Choi M, Delil S, Caglayan AO, Baranoski JF, Erturk O, Yalcinkaya C, Karacorlu M, Dincer A, Johnson MH, Mane S, Chandra SS, Louvi A, Boggon TJ, Lifton RP, Horwich AL, Gunel M. Recessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressive neurodegeneration Proceedings Of The National Academy Of Sciences Of The United States Of America 2013, 110: 3489-3494. PMID: 23359680, PMCID: PMC3587195, DOI: 10.1073/pnas.1222732110.
• Notch and disease: A growing fieldLouvi A, Artavanis-Tsakonas S. Notch and disease: A growing field Seminars In Cell And Developmental Biology 2012, 23: 473-480. PMID: 22373641, PMCID: PMC4369912, DOI: 10.1016/j.semcdb.2012.02.005.
• Notch Lineages and Activity in Intestinal Stem Cells Determined by a New Set of Knock-In MiceFre S, Hannezo E, Sale S, Huyghe M, Lafkas D, Kissel H, Louvi A, Greve J, Louvard D, Artavanis-Tsakonas S. Notch Lineages and Activity in Intestinal Stem Cells Determined by a New Set of Knock-In Mice PLOS ONE 2011, 6: e25785. PMID: 21991352, PMCID: PMC3185035, DOI: 10.1371/journal.pone.0025785.
• WNK2 Kinase Is a Novel Regulator of Essential Neuronal Cation-Chloride Cotransporters*Rinehart J, Vázquez N, Kahle KT, Hodson CA, Ring AM, Gulcicek EE, Louvi A, Bobadilla NA, Gamba G, Lifton RP. WNK2 Kinase Is a Novel Regulator of Essential Neuronal Cation-Chloride Cotransporters* Journal Of Biological Chemistry 2011, 286: 30171-30180. PMID: 21733846, PMCID: PMC3191056, DOI: 10.1074/jbc.m111.222893.
• Recessive LAMC3 mutations cause malformations of occipital cortical developmentBarak T, Kwan KY, Louvi A, Demirbilek V, Saygı S, Tüysüz B, Choi M, Boyacı H, Doerschner K, Zhu Y, Kaymakçalan H, Yılmaz S, Bakırcıoğlu M, Çağlayan A, Öztürk A, Yasuno K, Brunken WJ, Atalar E, Yalçınkaya C, Dinçer A, Bronen RA, Mane S, Özçelik T, Lifton RP, Šestan N, Bilgüvar K, Günel M. Recessive LAMC3 mutations cause malformations of occipital cortical development Nature Genetics 2011, 43: 590-594. PMID: 21572413, PMCID: PMC3329933, DOI: 10.1038/ng.836.
• Hypomorphic Notch 3 alleles link Notch signaling to ischemic cerebral small-vessel diseaseArboleda-Velasquez JF, Manent J, Lee JH, Tikka S, Ospina C, Vanderburg CR, Frosch MP, Rodríguez-Falcón M, Villen J, Gygi S, Lopera F, Kalimo H, Moskowitz MA, Ayata C, Louvi A, Artavanis-Tsakonas S. Hypomorphic Notch 3 alleles link Notch signaling to ischemic cerebral small-vessel disease Proceedings Of The National Academy Of Sciences Of The United States Of America 2011, 108: e128-e135. PMID: 21555590, PMCID: PMC3102344, DOI: 10.1073/pnas.1101964108.
• Cilia in the CNS: The Quiet Organelle Claims Center StageLouvi A, Grove EA. Cilia in the CNS: The Quiet Organelle Claims Center Stage Neuron 2011, 69: 1046-1060. PMID: 21435552, PMCID: PMC3070490, DOI: 10.1016/j.neuron.2011.03.002.
• Loss of cerebral cavernous malformation 3 (Ccm3) in neuroglia leads to CCM and vascular pathologyLouvi A, Chen L, Two AM, Zhang H, Min W, Günel M. Loss of cerebral cavernous malformation 3 (Ccm3) in neuroglia leads to CCM and vascular pathology Proceedings Of The National Academy Of Sciences Of The United States Of America 2011, 108: 3737-3742. PMID: 21321212, PMCID: PMC3048113, DOI: 10.1073/pnas.1012617108.
• Chapter 393 Genetics of Cerebral Cavernous MalformationsOzturk A, Louvi A, Günel M. Chapter 393 Genetics of Cerebral Cavernous Malformations 2011, 4127-4133.e2. DOI: 10.1016/b978-1-4160-5316-3.00396-8.
• Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformationsBilgüvar K, Öztürk A, Louvi A, Kwan KY, Choi M, Tatlı B, Yalnızoğlu D, Tüysüz B, Çağlayan A, Gökben S, Kaymakçalan H, Barak T, Bakırcıoğlu M, Yasuno K, Ho W, Sanders S, Zhu Y, Yılmaz S, Dinçer A, Johnson MH, Bronen RA, Koçer N, Per H, Mane S, Pamir MN, Yalçınkaya C, Kumandaş S, Topçu M, Özmen M, Šestan N, Lifton RP, State MW, Günel M. Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations Nature 2010, 467: 207-210. PMID: 20729831, PMCID: PMC3129007, DOI: 10.1038/nature09327.
• L-Histidine Decarboxylase and Tourette's SyndromeErcan-Sencicek AG, Stillman AA, Ghosh AK, Bilguvar K, O'Roak BJ, Mason CE, Abbott T, Gupta A, King RA, Pauls DL, Tischfield JA, Heiman GA, Singer HS, Gilbert DL, Hoekstra PJ, Morgan TM, Loring E, Yasuno K, Fernandez T, Sanders S, Louvi A, Cho JH, Mane S, Colangelo CM, Biederer T, Lifton RP, Gunel M, State MW. L-Histidine Decarboxylase and Tourette's Syndrome New England Journal Of Medicine 2010, 362: 1901-1908. PMID: 20445167, PMCID: PMC2894694, DOI: 10.1056/nejmoa0907006.
• Mutations in the Type IV Collagens, COL4A1 and COL4A2 are Associated with Intraventricular Hemorrhage in Preterm Infants: 956.DiLuna ML, Bilguvar K, Louvi A, Bizzarro M, Bayrakli F, Bayri Y, Bydon M, Schneider K, Duncan CC, State M, Lifton RP, Ment LR, Gunel M. Mutations in the Type IV Collagens, COL4A1 and COL4A2 are Associated with Intraventricular Hemorrhage in Preterm Infants: 956. Neurosurgery 2009, 65: 419. PMID: 28173201, DOI: 10.1227/01.neu.0000358727.92507.ea.
• Mutations in the Type IV Collagens, COL4A1 and COL4A2 are Associated with Intraventricular Hemorrhage in Preterm InfantsDiLuna M, Bilguvar K, Louvi A, Bizzarro M, Bayrakli F, Bayri Y, Bydon M, Schneider K, Duncan C, State M, Lifton R, Ment L, Gunel M. Mutations in the Type IV Collagens, COL4A1 and COL4A2 are Associated with Intraventricular Hemorrhage in Preterm Infants Neurosurgery 2009, 65: 419. DOI: 10.1227/01.neu.0000358727.92507.ea.
• Apoptotic Functions of PDCD10/CCM3, the Gene Mutated in Cerebral Cavernous Malformation 3Chen L, Tanriover G, Yano H, Friedlander R, Louvi A, Gunel M. Apoptotic Functions of PDCD10/CCM3, the Gene Mutated in Cerebral Cavernous Malformation 3 Stroke 2009, 40: 1474-1481. PMID: 19246713, PMCID: PMC2709460, DOI: 10.1161/strokeaha.108.527135.
• Developmentally regulated and evolutionarily conserved expression of SLITRK1 in brain circuits implicated in Tourette syndromeStillman AA, Krsnik Ž, Sun J, Rašin M, State MW, šestan N, Louvi A. Developmentally regulated and evolutionarily conserved expression of SLITRK1 in brain circuits implicated in Tourette syndrome The Journal Of Comparative Neurology 2008, 513: 21-37. PMID: 19105198, PMCID: PMC3292218, DOI: 10.1002/cne.21919.
• PDCD10, the gene mutated in cerebral cavernous malformation 3, is expressed in the neurovascular unit.Tanriover G, Boylan AJ, Diluna ML, Pricola KL, Louvi A, Gunel M. PDCD10, the gene mutated in cerebral cavernous malformation 3, is expressed in the neurovascular unit. Neurosurgery 2008, 62: 930-8; discussion 938. PMID: 18496199, DOI: 10.1227/01.neu.0000318179.02912.ca.
• Linking Notch signaling to ischemic strokeArboleda-Velasquez JF, Zhou Z, Shin HK, Louvi A, Kim HH, Savitz SI, Liao JK, Salomone S, Ayata C, Moskowitz MA, Artavanis-Tsakonas S. Linking Notch signaling to ischemic stroke Proceedings Of The National Academy Of Sciences Of The United States Of America 2008, 105: 4856-4861. PMID: 18347334, PMCID: PMC2290794, DOI: 10.1073/pnas.0709867105.
• Cyst formation and activation of the extracellular regulated kinase pathway after kidney specific inactivation of Pkd1Shibazaki S, Yu Z, Nishio S, Tian X, Thomson RB, Mitobe M, Louvi A, Velazquez H, Ishibe S, Cantley LG, Igarashi P, Somlo S. Cyst formation and activation of the extracellular regulated kinase pathway after kidney specific inactivation of Pkd1 Human Molecular Genetics 2008, 17: 1505-1516. PMID: 18263604, PMCID: PMC2902289, DOI: 10.1093/hmg/ddn039.
• Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum DisordersBakkaloglu B, O'Roak BJ, Louvi A, Gupta AR, Abelson JF, Morgan TM, Chawarska K, Klin A, Ercan-Sencicek AG, Stillman AA, Tanriover G, Abrahams BS, Duvall JA, Robbins EM, Geschwind DH, Biederer T, Gunel M, Lifton RP, State MW. Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum Disorders American Journal Of Human Genetics 2008, 82: 165-173. PMID: 18179895, PMCID: PMC2253974, DOI: 10.1016/j.ajhg.2007.09.017.
• The derivatives of the Wnt3a lineage in the central nervous systemLouvi A, Yoshida M, Grove EA. The derivatives of the Wnt3a lineage in the central nervous system The Journal Of Comparative Neurology 2007, 504: 550-569. PMID: 17701978, DOI: 10.1002/cne.21461.
• The dorsal midline as a migration center: Insights from the analysis of the Wnt3a lineageLouvi A, Yoshida M, Grove E. The dorsal midline as a migration center: Insights from the analysis of the Wnt3a lineage Developmental Biology 2006, 295: 396-397. DOI: 10.1016/j.ydbio.2006.04.216.
• CADASIL: A Critical Look at a Notch DiseaseLouvi A, Arboleda-Velasquez JF, Artavanis-Tsakonas S. CADASIL: A Critical Look at a Notch Disease Developmental Neuroscience 2006, 28: 5-12. PMID: 16508299, DOI: 10.1159/000090748.
• Notch signalling in vertebrate neural developmentLouvi A, Artavanis-Tsakonas S. Notch signalling in vertebrate neural development Nature Reviews Neuroscience 2006, 7: 93-102. PMID: 16429119, DOI: 10.1038/nrn1847.
• CCM2 Expression Parallels That of CCM1Seker A, Pricola KL, Guclu B, Ozturk AK, Louvi A, Gunel M. CCM2 Expression Parallels That of CCM1 Stroke 2005, 37: 518-523. PMID: 16373645, DOI: 10.1161/01.str.0000198835.49387.25.
• WNK3 modulates transport of Cl- in and out of cells: Implications for control of cell volume and neuronal excitabilityKahle KT, Rinehart J, de los Heros P, Louvi A, Meade P, Vazquez N, Hebert SC, Gamba G, Gimenez I, Lifton RP. WNK3 modulates transport of Cl- in and out of cells: Implications for control of cell volume and neuronal excitability Proceedings Of The National Academy Of Sciences Of The United States Of America 2005, 102: 16783-16788. PMID: 16275911, PMCID: PMC1283843, DOI: 10.1073/pnas.0508307102.
• Sequence Variants in SLITRK1 Are Associated with Tourette's SyndromeAbelson JF, Kwan KY, O'Roak BJ, Baek DY, Stillman AA, Morgan TM, Mathews CA, Pauls DL, Rašin M, Gunel M, Davis NR, Ercan-Sencicek AG, Guez DH, Spertus JA, Leckman JF, Dure LS, Kurlan R, Singer HS, Gilbert DL, Farhi A, Louvi A, Lifton RP, Šestan N, State MW. Sequence Variants in SLITRK1 Are Associated with Tourette's Syndrome Science 2005, 310: 317-320. PMID: 16224024, DOI: 10.1126/science.1116502.
• Regionalization of the isthmic and cerebellar primordiâme N, Louvi A, Alexandre P, Wassef M. Regionalization of the isthmic and cerebellar primordia 2005, 148: 29-36. PMID: 15856550, DOI: 10.1016/s0079-6123(04)48003-0.
• Presenilin 1 in migration and morphogenesis in the central nervous systemLouvi A, Sisodia SS, Grove EA. Presenilin 1 in migration and morphogenesis in the central nervous system Development 2004, 131: 3093-3105. PMID: 15163631, DOI: 10.1242/dev.01191.
• Creating Coordination in the Cerebellum Catania, 2–4 October 2003Andjus P, Zhu L, Strata P, Arata A, Ito M, Bearzatto B, Servais L, Baba-Aïssa F, de Kerchove d’Exaerde A, Schurmans S, Cheron G, Schiffmann S, Bower J, Devor A, Burguière E, Rutteman M, De Zeeuw C, Berthoz A, Wiener S, Rondi-Reig L, Campana A, Dusart I, Wherlé R, Weitzman J, Yaniv M, Sotelo C, Mariani J, Cavallari P, Esposti R, Cerri G, Cerminara N, Apps R, Marple-Horvat D, Wagstaff J, Dan B, Chorev E, Manor Y, Sohl G, Willecke K, Yarom Y, Philipona D, Dognin E, Coenen O, Sola E, Prestori F, Rossi P, Taglietti V, D’Angelo E, De Filippi G, Baldwinson T, Sher E, Ekerot C, Jorntell H, Fernández G, Martínez S, Gall D, Roussel C, Forti L, Schiffmann S, Gruol D, Netzeband J, Quina L, Blakely Gonzalez P, Hoebeek F, Van Alphen A, Schonewille M, Frens M, Goossens H, Stahl J, Ango F, di Cristo G, Hagashiyama H, Bennett V, Huang Z, Jörntell H, Ekerot C, Launey T, Endo S, Sakai R, Harano J, Lohof A, Sherrard R, Lu H, Huang C, Hartmann M, Marshall S, Lang E, Michikawa T, Mikoshiba K, Nitschke M, Erdmann C, Melchert U, Arp T, Sprenger A, Petersen D, Kömpf D, Binkofski F, Heide W, Pedroarena C, Schwarz C, Parsons L, Schmahmann J, Grill S, Walker M, Petacchi A, Rokni D, Saito S, Kato K, Sajdel-Sulkowska E, Nguon K, Selimi F, Wang Q, Cristea I, Chait B, Heintz N, Serapide M, Cicirata F, De Saedeleer C, Schwaller B, Swinny J, Ijkema-Paassen J, Metzger F, Kalicharan D, Gramsbergen A, van der Want J, Slemmer J, Weber J, Winkelman B, Chédotal A, De Schutter E, Maex R, Koekkoek S, Bouslama L, Ghoumari A, Ebner T, Häusser M, Hawkes R, Herrup K, Lisberger S, Mugnaini E, Nunzi M, Russo M, Ptak K, Orr H, Zoghbi H, Rossi F, Ruigrok T, Sabel-Goedknegt E, Simpson J, Morando L, Cesa R, Dumoulin A, Dieudonné S, Dugué G, Triller A, Louvi A, Alexandre P, Wurst W, Wassef M. Creating Coordination in the Cerebellum Catania, 2–4 October 2003 The Cerebellum 2004, 3: 39-64. DOI: 10.1080/14734220310020164.
• The isthmic neuroepithelium is essential for cerebellar midline fusionLouvi A, Alexandre P, Métin C, Wurst W, Wassef M. The isthmic neuroepithelium is essential for cerebellar midline fusion Development 2003, 130: 5319-5330. PMID: 14507778, DOI: 10.1242/dev.00736.
• Growth-Promoting Interaction of IGF-II with the Insulin Receptor during Mouse Embryonic DevelopmentLouvi A, Accili D, Efstratiadis A. Growth-Promoting Interaction of IGF-II with the Insulin Receptor during Mouse Embryonic Development Developmental Biology 1997, 189: 33-48. PMID: 9281335, DOI: 10.1006/dbio.1997.8666.
• Insulin-like growth factor II stimulates cell proliferation through the insulin receptorMorrione A, Valentinis B, Xu S, Yumet G, Louvi A, Efstratiadis A, Baserga R. Insulin-like growth factor II stimulates cell proliferation through the insulin receptor Proceedings Of The National Academy Of Sciences Of The United States Of America 1997, 94: 3777-3782. PMID: 9108054, PMCID: PMC20517, DOI: 10.1073/pnas.94.8.3777.
• A cDNA clone encoding the ADP/ATP translocase of Drosophila melanogaster shows a high degree of similarity with the mammalian ADP/ATP translocasesLouvi A, Tsitilou S. A cDNA clone encoding the ADP/ATP translocase of Drosophila melanogaster shows a high degree of similarity with the mammalian ADP/ATP translocases Journal Of Molecular Evolution 1992, 35: 44-50. PMID: 1387687, DOI: 10.1007/bf00160259.