Publications 2008
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PDFPubmed
Differential neuroglycan C expression during retinal degeneration in Rpe65 mice.
Escher P, Cottet S, Aono S, Oohira A, Schorderet DF.
Mol Vis. 2008;14:2126-35. -
PDFPubmed
A novel dominant mutation of the Nav1.4 alpha-subunit domain I leading to sodium channel myotonia.
Petitprez S, Tiab L, Chen L, Kappeler L, Rösler KM, Schorderet D, Abriel H, Burgunder JM.
Neurology. 2008 Nov 18;71(21):1669-75. -
PDFPubmed
PROM1 is mutated in macular degeneration and is essential for photoreceptor disk membrane morphogenesis.
Yang Z et al.
J Clin Invest, 118:2908-2916,2008 -
PDFPubmed
Overexpression of a mutant form of TGFBI/BIGH3 induces retinal degeneration in transgenic mice.
Mauro Bustamante, Andrea Tasinato, Fabienne Maurer, Ilhem Elkochairi, Mario G. Lepore, Yvan Arsenijevic, Thierry Pedrazzini, Francis L. Munier, Schorderet DF
Molecular Vision 14:1131-1139,2008 -
PDFPubmed
Characterization of pip5k3 fleck corneal dystrophy-linked gene in zebrafish.
Boisset G, Polok BK, Schorderet DF.
Gene Expr Patterns. 8(6):404-410,2008 -
PDFPubmed
Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndrome.
Schorderet DF, Nichini O, Boisset G, Polok B, Tiab L, Mayeur H, Raji B, de la Houssaye G, Abitbol MM, Munier FL.
Am J Hum Genet. 2008 May;82(5):1178-84 -
PDFPubmed
Triggering of Bcl-2-related pathway is associated with apoptosis of photoreceptors in Rpe65-/- mouse models of Leber's congenital amaurosis.
Cottet S, Schorderet DF
Apoptosis, 13(3):329-42, 2008 -
PDF
Pubmed
Glucose and leptin induce apoptosis in human ß-cells and impair glucose-stimulated insulin secretion through activation of c-Jun N-terminal kinases
Maedler K, Schulthess FT, Bielman C, Berney T, Bonny C, Prentki M, Donath MY, Roduit R.
FASEB J. 2008 Jun;22(6):1905-13. Epub 2008 Feb 8 -
PDFPubmed
Identification of the minimal promoter region of NKX5-3, a transcription factor implicated in eye development.
Nichini O, Shorderet DF.
Gene, 411(1-2):10-8, 2008 -
PDFPubmed
Role of MAP Kinase pathways in UV-induced Retinal Pigment Epithelium Cells apoptosis.
Roduit R, Schorderet DF.
Apoptosis, 13(3):343-53, 2008 -
PDFPubmed
Deposits of Transforming Growth Factor-beta-Induced Protein in Granular Corneal Dystrophy Type II after LASIK.
Kim TI, Roh MI, Grossniklaus HE, Kang SJ, Hamilton SM, Schorderet DF, Lee WB, Kim EK.
Cornea. 27(1):28-32, 2008. -
PDFPubmed
Genotype-phenotype correlation of age-related macular degeneration: influence of complement factor H polymorphism.
Droz I, Mantel I, Faouzi M, Ambresin A, Schorderet DF, Munier FL.
Br J Ophthalmol, 92(4):513-7, 2008 -
Classification of corneal dystrophies on a molecular genetic basis.
Munier FL, Schorderet DF
In Essentials in Ophthalmology, pp 83-100. T Reinhard & F Karkin Ed. Springer-Verlag, Berlin Heidelberg, 2008 -
Modulation de l'apoptose à l'aide de peptides intracellulaires.
Allaman-Pillet N, Roduit R, Produit-Zengaffinen N, Schorderet DF
In Pathologies vasculaires oculaires. pp 793-796. Rapport de la Société Française d'Ophtalmologie. Ed. C. Pournaras. 2008 -
Génétique et pathologie vasculaire oculaire.
Escher P, Schorderet DF
In Pathologies vasculaires oculaires. pp 219-228. Rapport de la Société Française d'Ophtalmologie. Ed. C. Pournaras. 2008 -
Ischémies et atteintes neuronales - apoptose.
Roduit R, Schorderet DF.
In Pathologies vasculaires oculaires. pp 184-194. Rapport de la Société Française d'Ophtalmologie. Ed. C. Pournaras. 2008 -
Gènes de différentiation vasculaire.
Schorderet DF
In Pathologies vasculaires oculaires. pp 15-19. Rapport de la Société Française d'Ophtalmologie. Ed. C. Pournaras. 2008 -
Anomalie du développement de l'oeil et de l'oreille due à une mutation dans le gène NKX5-3/HMX1 : Épilogue d'une histoire commencée il y a plus de 60 ans.
Schorderet D, Munier F.
Ophta, 4:273-273,2008
