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Angeliki Louvi

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Kaya Bilguvar; Titus Boggon; Ahmet O Caglayan; Sreeganga S Chandra; Murim Choi; Sakir Delil; alp dincer; Ozdem Erturk; Arthur L Horwich; Michele H Johnson; Murat Karacorlu; Richard P Lifton; Angeliki Louvi; Shrikant M Mane; Cigdem Ozkara; Beyhan Tuysuz; Navneet K Tyagi; Cengiz Yalcinkaya; Mehmet Bakircioglu; Jacob F Baranoski; Murat Gunel
Recessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressive neurodegeneration.
Angeliki Louvi; Spyros Artavanis-Tsakonas
Notch and disease: a growing field.
Jesse Rinehart; Aaron M Ring; Norma Vázquez; Angeliki Louvi; Norma A Bobadilla; Gerardo Gamba; Erol E Gulcicek; Caleb A Hodson; Kristopher T Kahle; Richard P Lifton
WNK2 kinase is a novel regulator of essential neuronal cation-chloride cotransporters.

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All Publications

2013: Kaya Bilguvar; Titus Boggon; Ahmet O Caglayan; Sreeganga S Chandra; Murim Choi; Sakir Delil; alp dincer; Ozdem Erturk; Arthur L Horwich; Michele H Johnson; Murat Karacorlu; Richard P Lifton; Angeliki Louvi; Shrikant M Mane; Cigdem Ozkara; Beyhan Tuysuz; Navneet K Tyagi; Cengiz Yalcinkaya; Mehmet Bakircioglu; Jacob F Baranoski; Murat Gunel
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(9):3489-94.
2012: Angeliki Louvi; Spyros Artavanis-Tsakonas
Notch and disease: a growing field.
Seminars in cell & developmental biology 2012;23(4):473-80.
2011: Jesse Rinehart; Aaron M Ring; Norma Vázquez; Angeliki Louvi; Norma A Bobadilla; Gerardo Gamba; Erol E Gulcicek; Caleb A Hodson; Kristopher T Kahle; Richard P Lifton
WNK2 kinase is a novel regulator of essential neuronal cation-chloride cotransporters.
The Journal of biological chemistry 2011;286(34):30171-80.
2011: Tanyeri Barak; Kenneth Y Kwan; Angeliki Louvi; Veysi Demirbilek; Serap Saygı; Beyhan Tüysüz; Murim Choi; Hüseyin Boyacı; Katja Doerschner; Ying Zhu; Hande Kaymakçalan; Saliha Yılmaz; Mehmet Bakırcıoğlu; Ahmet Okay Cağlayan; Ali Kemal Oztürk; Katsuhito Yasuno; William J Brunken; Ergin Atalar; Cengiz Yalçınkaya; Alp Dinçer; Richard A Bronen; Shrikant M Mane; Tayfun Ozçelik; Richard P Lifton; Nenad Sestan; Kaya Bilgüvar; Murat Günel
Recessive LAMC3 mutations cause malformations of occipital cortical development.
Nature genetics 2011;43(6):590-4.
2011: Joseph F Arboleda-Velasquez; Jan Manent; Jeong Hyun Lee; Saara Tikka; Carolina Ospina; Charles R Vanderburg; Matthew P Frosch; Manuel Rodríguez-Falcón; Judit Villen; Steven Gygi; Francisco Lopera; Hannu Kalimo; Michael A Moskowitz; Cenk Ayata; Angeliki Louvi; Spyros Artavanis-Tsakonas
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(21):E128-35.
2011: Angeliki Louvi; Elizabeth A Grove
Cilia in the CNS: the quiet organelle claims center stage.
Neuron 2011;69(6):1046-60.
2011: Angeliki Louvi; Leiling Chen; Aimee M Two; Haifeng Zhang; Wang Min; Murat Günel
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(9):3737-42.
2011: Silvia Fre; Jeffrey Greve; Edouard Hannezo; Mathilde Huyghe; Holger Kissel; Daniel Lafkas; Daniel Louvard; Angeliki Louvi; Sanja Sale; Spyros Artavanis-Tsakonas
Notch lineages and activity in intestinal stem cells determined by a new set of knock-in mice.
PloS one 2011;6(10):e25785.
2010: A Gulhan Ercan-Sencicek; Althea A Stillman; Ananda K Ghosh; Kaya Bilguvar; Brian J O'Roak; Christopher E Mason; Thomas Abbott; Abha Gupta; Robert A King; David L Pauls; Jay A Tischfield; Gary A Heiman; Harvey S Singer; Donald L Gilbert; Pieter J Hoekstra; Thomas M Morgan; Erin Loring; Katsuhito Yasuno; Thomas V Fernandez; Stephan Sanders; Angeliki Louvi; Judy H Cho; Shrikant M Mane; Christopher M Colangelo; Thomas Biederer; Richard P Lifton; Murat Gunel; Sate Matthew
L-histidine decarboxylase and Tourette's syndrome.
The New England journal of medicine 2010;362(20):1901-8.
2009: Leiling Chen; Gamze Tanriover; Hiroko Yano; Robert Friedlander; Angeliki Louvi; Murat Gunel
Apoptotic functions of PDCD10/CCM3, the gene mutated in cerebral cavernous malformation 3.
Stroke; a journal of cerebral circulation 2009;40(4):1474-81.
2009: Althea A Stillman; Zeljka Krsnik; Jinhao Sun; Mladen-Roko Rasin; Sate Matthew; Nenad Sestan; Angeliki Louvi
Developmentally regulated and evolutionarily conserved expression of SLITRK1 in brain circuits implicated in Tourette syndrome.
The Journal of comparative neurology 2009;513(1):21-37.
2008: Sekiya Shibazaki; Zhiheng Yu; Saori Nishio; Xin Tian; R Brent Thomson; Michihiro Mitobe; Angeliki Louvi; Heino Velazquez; Shuta Ishibe; Lloyd G Cantley; Peter Igarashi; Stefan Somlo
Cyst formation and activation of the extracellular regulated kinase pathway after kidney specific inactivation of Pkd1.
Human molecular genetics 2008;17(11):1505-16.
2008: Gamze Tanriover; Arianne J Boylan; Michael L DiLuna; Katie L Pricola; Angeliki Louvi; Murat Gunel
PDCD10, the gene mutated in cerebral cavernous malformation 3, is expressed in the neurovascular unit.
Neurosurgery 2008;62(4):930-8; discussion 938.
2008: Joseph F Arboleda-Velasquez; Zhipeng Zhou; Hwa Kyoung Shin; Angeliki Louvi; Hyung-Hwan Kim; Sean I Savitz; James K Liao; Salvatore Salomone; Cenk Ayata; Michael A Moskowitz; Spyros Artavanis-Tsakonas
Linking Notch signaling to ischemic stroke.
Proceedings of the National Academy of Sciences of the United States of America 2008;105(12):4856-61.
2008: Betul Bakkaloglu; Brian J O'Roak; Angeliki Louvi; Abha R Gupta; Jesse F Abelson; Thomas M Morgan; Katarzyna Chawarska; Ami Klin; A Gulhan Ercan-Sencicek; Althea A Stillman; Gamze Tanriover; Brett S. Abrahams; Jacqueline Duvall; Elissa M Robbins; Daniel Geschwind; Thomas Biederer; Murat Gunel; Richard P Lifton; Sate Matthew
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.
American journal of human genetics 2008;82(1):165-73.
2007: Angeliki Louvi; Michio Yoshida; Elizabeth A Grove
The derivatives of the Wnt3a lineage in the central nervous system.
The Journal of comparative neurology 2007;504(5):550-69.
2006: Angeliki Louvi; Spyros Artavanis-Tsakonas
Notch signalling in vertebrate neural development.
Nature reviews. Neuroscience 2006;7(2):93-102.
2006: Askin Seker; Katie L Pricola; Bulent Guclu; Ali K Ozturk; Angeliki Louvi; Murat Gunel
CCM2 expression parallels that of CCM1.
Stroke; a journal of cerebral circulation 2006;37(2):518-23.
2006: Angeliki Louvi; Joseph F Arboleda-Velasquez; Spyros Artavanis-Tsakonas
CADASIL: a critical look at a Notch disease.
Developmental neuroscience 2006;28(1-2):5-12.
2005: Kristopher T Kahle; Jesse Rinehart; Paola de los Heros; Angeliki Louvi; Patricia Meade; Norma Vazquez; Steven C Hebert; Gerardo Gamba; Ignacio Gimenez; Richard P Lifton
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(46):16783-8.
2005: Jesse F Abelson; Kenneth Y Kwan; Brian J O'Roak; Danielle Y Baek; Althea A Stillman; Thomas M Morgan; Carol A Mathews; David L Pauls; Mladen-Roko Rasin; Murat Gunel; Nicole R Davis; A Gulhan Ercan-Sencicek; Danielle H Guez; John A Spertus; James F Leckman; Leon S Dure; Roger Kurlan; Harvey S Singer; Donald L Gilbert; anita farhi; Angeliki Louvi; Richard P Lifton; Nenad Sestan; Sate Matthew
Sequence variants in SLITRK1 are associated with Tourette's syndrome.
Science (New York, N.Y.) 2005;310(5746):317-20.
2005: Nicolas Narboux-Nême; Angeliki Louvi; Paula Alexandre; Marion Wassef
Regionalization of the isthmic and cerebellar primordia.
Progress in brain research 2005;148():29-36.
2004: Angeliki Louvi; Sangram S Sisodia; Elizabeth A Grove
Presenilin 1 in migration and morphogenesis in the central nervous system.
Development (Cambridge, England) 2004;131(13):3093-105.
2003: Angeliki Louvi; Paula Alexandre; Christine Métin; Wolfgang Wurst; Marion Wassef
The isthmic neuroepithelium is essential for cerebellar midline fusion.
Development (Cambridge, England) 2003;130(22):5319-30.
2003: James M McClintock; C Jozefowicz; Stavroula Assimacopoulos; Elizabeth A Grove; Angeliki Louvi; Victoria E Prince
Conserved expression of Hoxa1 in neurons at the ventral forebrain/midbrain boundary of vertebrates.
Development genes and evolution 2003;213(8):399-406.
2000: Angeliki Louvi; Marion Wassef
Ectopic engrailed 1 expression in the dorsal midline causes cell death, abnormal differentiation of circumventricular organs and errors in axonal pathfinding.
Development (Cambridge, England) 2000;127(18):4061-71.