UNITÉ DE RECHERCHE Génétique médicale et génomique ...

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Endele S, Rosenberger G, Geider K, Popp B, Tamer C, Stefanova I, Milh M, Kortüm F, Fritsch A,
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von Spiczak S, Tönnies H, Villeneuve N, Villard L, Zabel B, Zenker M, Laube B, Reis A, Wieczorek D,
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NMDA receptors cause variable neurodevelopmental phenotypes. Nat Genet. 2010, 42(11):1021-6.
Cacciagli P, Haddad MR, Mignon-Ravix C, El-Waly B, Moncla A, Missirian C, Chabrol B, Villard L.
Disruption of the ATP8A2 gene in a patient with a t(10;13) de novo balanced translocation and a
severe neurological phenotype. Eur J Hum Genet. 2010, 18(12):1360-3.
Roux JC, Villard L. Biogenic amines in Rett syndrome: the usual suspects. Behav Genet. 2010,
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Thienpont B, Béna F, Breckpot J, Philip N, Menten B, Van Esch H, Scalais E, Salamone JM, Fong CT,
Kussmann JL, Grange DK, Gorski JL, Zahir F, Yong SL, Morris MM, Gimelli S, Fryns JP, Mortier G,
Friedman JM, Villard L, Bottani A, Vermeesch JR, Cheung SW, Devriendt K. Duplications of the
critical Rubinstein-Taybi deletion region on chromosome 16p13.3 cause a novel recognisable
syndrome. J Med Genet. 2010, 47(3):155-61.
Mignon-Ravix C, Cacciagli P, El-Waly B, Moncla A, Milh M, Girard N, Chabrol B, Philip N, Villard L.
Deletion of YWHAE in a patient with periventricular heterotopias and pronounced corpus callosum
hypoplasia.. J Med Genet. 2010, 47(2):132-6.
Ottaviani A, Schluth-Bolard C, Gilson E, Magdinier F. D4Z4 as a prototype of CTCF and laminsdependent
insulator in human cells. Nucleus. 2010, 1(1):30-6.
Ye J, Lenain C, Bauwens S, Rizzo A, Saint-Léger A, Poulet A, Benarroch D, Magdinier F, Morere J,
Amiard S, Verhoeyen E, Britton S, Calsou P, Salles B, Bizard A, Nadal M, Salvati E, Sabatier L, Wu
Y, Biroccio A, Londoño-Vallejo A, Giraud-Panis MJ, Gilson E. TRF2 and apollo cooperate with
topoisomerase 2alpha to protect human telomeres from replicative damage. Cell. 2010,
142(2):230-42.
Arnoult N, Schluth-Bolard C, Letessier A, Drascovic I, Bouarich-Bourimi R, Campisi J, Kim SH,
Boussouar A, Ottaviani A, Magdinier F, Gilson E, Londoño-Vallejo A. Replication timing of human
telomeres is chromosome arm-specific, influenced by subtelomeric structures and connected to
nuclear localization. PLoS Genet. 2010, 6(4):e1000920.
Falandry C, Fourel G, Galy V, Ristriani T, Horard B, Bensimon E, Salles G, Gilson E, Magdinier F.
CLLD8/KMT1F is a lysine methyltransferase that is important for chromosome segregation. J Biol
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Ourliac-Garnier I, Poulet A, Charif R, Amiard S, Magdinier F, Rezaï K, Gilson E, Giraud-Panis MJ,
Bombard S. Platination of telomeric DNA by cisplatin disrupts recognition by TRF2 and TRF1. J Biol
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Medioni C, N Bertrand, K Mesbah, B Hudry, L Dupays, O Wolstein, AJ Washkowitz, VE Papaioannou,
TJ Mohun, RP Harvey and S Zaffran. Expression of Slit and Robo genes in the developing mouse
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Lin SC, P Dolle, L Ryckebusch, M Noseda, S Zaffran, MD Schneider and K Niederreither. (.
Endogenous retinoic acid regulates cardiac progenitor differentiation. Proc Natl Acad Sci U S A.
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Thomas S, F Encha-Razavi, L Devisme, H Etchevers, B Bessieres-Grattagliano, G Goudefroye, N
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Unité de Recherche. Génétique médicale et génomique fonctionnelle (GMGF) 8/14