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ARVO Annual Meeting Abstract May 2006

A Heterozygous Mutation in the NR2E3 Gene Is Associated With an Autosomal Dominant Retinitis Pigmentosa

L. Bouayed–Tiab; T. Delarive; C. Agosti; F.–X. Borruat; F.L. Munier; D.F. Schorderet

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):1033. doi:

ARVO Annual Meeting Abstract May 2006

Concomitant Occurrence of Parasellar and Pineal Tumors in Bilateral Retinoblastoma: A Case of Quadrilateral Retinoblastoma ?

F.L. Munier; M. Beck–Popovic; H. Abouzeid; P. Maeder; A. Balmer; D.F. Schorderet

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):2293. doi:

ARVO Annual Meeting Abstract May 2006

Impaired Viability, Morphology and Cell–Surface Expression of Integrins in the Retinal Pigment Epithelial Cell Line ARPE–19 Showing siRNA–Targeted Silencing of Rpe65 Protein

O. Nichini; S. Cottet; T. Favez; N. Voirol; C. Ruegg; D.F. Schorderet

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):2321. doi:

ARVO Annual Meeting Abstract May 2006

Knockdown of PIP5k3 Fleck Corneal Dystrophy–Linked Gene in Zebrafish

G. Boisset; A. Tasinato; S. Métrailler; D.F. Schorderet

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):2777. doi:

ARVO Annual Meeting Abstract May 2006

Biological Characterization of Gene Response in Rpe65–/– Mouse Model of Leber's Congenital Amaurosis During Progression of the Disease

S. Cottet; L. Michaut; G. Boisset; Y. Arsenijevic; U. Schlecht; F.L. Munier; W. Gehring; D.F. Schorderet

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):4560. doi:

ARVO Annual Meeting Abstract May 2006

Altered Expression of Anti– and Pro–Apoptotic Genes in Rpe65–/– Mouse Model of Leber's Congenital Amaurosis

D.F. Schorderet; G. Boisset; T. Favez; S. Cottet

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):4598. doi:

ARVO Annual Meeting Abstract May 2005

An Additional Locus for Autosomal Dominant Retinitis Pigmentosa (RP) on Chromosome 7p

G. Boisset; L. Tiab; S. Bolay; T. Delarive; S. Métrailler; M. Matter; M.–C. Gaillard; F.X. Borruat; F. Munier; D.F. Schorderet

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):511. doi:

ARVO Annual Meeting Abstract May 2005

Anterior Bipolar Cataract : A Novel Lens Phenotype Associated With CRYGD and L–Ferritin Mutations

T.C. Delarive; W. Ferrini; S. Uffer; E. Héon; P. Othenin–Girard; D. Brooks; D.F. Schorderet; F.L. Munier

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):828. doi:

ARVO Annual Meeting Abstract May 2005

Genotype–Phenotype Correlation in Malattia Leventinese Patients With Homo–Heterozygote R345W Mutation in Fibulin 3

J.–A.C. Pournaras; S. Uffer; A. Kundzewics; G. Niemeyer; D.F. Schorderet; F.L. Munier

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):1836. doi:

ARVO Annual Meeting Abstract May 2005

A Family With Congenital X–Linked Inherited Nystagmus and Mutation in CDR1

D.F. Schorderet; L. Tiab; S. Bolay; C. Agosti; T. Favez; I. Favre; M.–C. Gaillard; F.X. Borruat; F.L. Munier

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):2289. doi:

ARVO Annual Meeting Abstract May 2005

Loss of Bmi1 Prevents Degeneration of Photoreceptors in rd Mice

Y. Arsenijevic; D. Zencak; S.V. Crippa; M. Tekaya; E. Tanger; D.F. Schorderet; M. van Lohuizen; F.L. Munier

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):2298. doi:

ARVO Annual Meeting Abstract May 2005

Neurogenic Potential of Retinal Precursor Cells (Rpcs) Transplanted into a Model of Terminal Stages of Retinitis Pigmentosa

K.B. Canola; B. Angénieux; M. Tekaya; A. Quiambao; M.I. Naash; D.F. Schorderet; F.L. Munier; Y. Arsenijevic

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):4161. doi:

ARVO Annual Meeting Abstract May 2005

First Complete Autopsy of a Patient Affected With BIGH3–related Corneal Dystrophy

I. ElKochairi; I. Letovanec; S. Uffer; F.L. Munier; P. Chaubert; D.F. Schorderet

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):4922. doi:

ARVO Annual Meeting Abstract May 2005

Meesmann Corneal Dystrophy (MECD): Report Of 2 Families and a Novel Mutation in the Cornea Specific Keratin KRT12 Gene

O. Nichini; V. d'Allèves Manzi; L. Tiab; C. Agosti; T. Favez; I. Favre; S. Métrailler; F.L. Munier; D.F. Schorderet

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):4930. doi:

ARVO Annual Meeting Abstract May 2005

Knockdown of TGFBI/BIGH3 Corneal Dystrophy–Linked Gene Leads to Developmental Impairment in Zebrafish

A. Tasinato; D. Belet; F.L. Munier; S. Neuhauss; D.F. Schorderet

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):4934. doi:

ARVO Annual Meeting Abstract May 2005

Analysis of RPE65 Promoter Activity Using Lentiviral Vectors for Gene Transfer in Leber Congenital Amaurosis Mouse Model

C. Kostic; A.–P. Bemelmans; M. Jaquet; M.W. Seeliger; W.W. Hauswirth; J. Lem; D.F. Schorderet; F.L. Munier; A. Wenzel; Y. Arsenijevic

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):5212. doi:

ARVO Annual Meeting Abstract May 2005

Lentiviral Gene Transfer of RPE65 cDNA in Two Knock–Out Mouse Models of Leber Congenital Amaurosis

A. Bemelmans; C. Kostic; D. Hornfeld; W.W. Hauswirth; J. Lem; D.F. Schorderet; F.L. Munier; M. Seeliger; A. Wenzel; Y. Arsenijevic

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):5214. doi:

ARVO Annual Meeting Abstract May 2005

Targeted Silencing of RPE65 in the Retinal Pigment Epithelial Cell Line ARPE–19 Using Lentivirus–Mediated siRNA Delivery

S. Cottet; T. Favez; F. Maurer; C. Bonny; Y. Arsenijevic; F.L. Munier; D.F. Schorderet

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):3054. doi:

ARVO Annual Meeting Abstract May 2005

Risk Assessment of Recurrence in Sporadic Retinoblastoma (Rb) Using a Novel Molecular–Based Algorithm

H.V. Tran; A. Balmer; D.F. Schorderet; F.L. Munier

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):3211. doi:

ARVO Annual Meeting Abstract May 2005

Adult Human Retinal Stem Cells Express Genes Common to Other Stem Cells as Revealed by Microarray Analyses

B.A. Angenieux; L. Michaut; D.F. Schorderet; F.L. Munier; W. Gehring; Y. Arsenijevic

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):3226. doi:

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