Publications 2005
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PDFPubmed
D-TAT transporter as an ocular peptide delivery system.
Schorderet DF, Manzi V, Canola K, Bonny C, Arsenijevic Y, Munier FL, Maurer F.
Clin Experiment Ophthalmol. 2005 Dec;33(6):628-35. -
PDFPubmed
Meesmann corneal dystrophy (MECD): report of 2 families and a novel mutation in the cornea specific keratin 12 (KRT12) gene.
Nichini O, Manzi V, Munier FL, Schorderet DF.
Ophthalmic Genet. 2005 Dec;26(4):169-73. -
PDFPubmed
Association Down syndrome-retinoblastoma: a new observation.
Satge D, Schorderet DF, Balmer A, Beck-Popovic M, Addor MC, Beckmann JS, Munier FL.
Ophthalmic Genet. 2005 Sep;26(3):151-2 -
PDFPubmed
Bmi1 loss produces an increase in astroglial cells and a decrease in neural stem cell population and proliferation.
Zencak D, Lingbeek M, Kostic C, Tekaya M, Tanger E, Hornfeld D, Jaquet M, Munier FL, Schorderet DF, van Lohuizen M, Arsenijevic Y.
J Neurosci. 2005 Jun 15;25(24):5774-83. -
PDFPubmed
Mutations in PIP5K3 are associated with Francois-Neetens mouchetee fleck corneal dystrophy.
Li S, Tiab L, Jiao X, Munier FL, Zografos L, Frueh BE, Sergeev Y, Smith J, Rubin B, Meallet MA, Forster RK, Hejtmancik JF, Schorderet DF.
Am J Hum Genet. 2005 Jul;77(1):54-63. -
PDFPubmed
Morphological, clinical and genetic aspects in a family with a novel LAMP-2 gene mutation (Danon disease).
Lobrinus JA, Schorderet DF, Payot M, Jeanrenaud X, Bottani A, Superti-Furga A, Schlaepfer J, Fromer M, Jeannet PY.
Neuromuscul Disord. 2005 Apr;15(4):293-8. -
PDFPubmed
Hereditary lattice corneal dystrophy is associated with corneal amyloid deposits enclosing C-terminal fragments of keratoepithelin.
Stix B, Leber M, Bingemer P, Gross C, Ruschoff J, Fandrich M, Schorderet DF, Vorwerk CK, Zacharias M, Roessner A, Rocken C.
Invest Ophthalmol Vis Sci. 2005 Apr;46(4):1133-9. -
PDFPubmed
Optical coherence tomography in Malattia Leventinese.
Gaillard MC, Wolfensberger TJ, Uffer S, Mantel I, Pournaras JA, Schorderet DF, Munier FL.
Klin Monatsbl Augenheilkd. 2005 Mar;222(3):180-5 -
PDFPubmed
Lentiviral vector-mediated gene transfer in adult mouse photoreceptors is impaired by the presence of a physical barrier.
Gruter O, Kostic C, Crippa SV, Perez MT, Zografos L, Schorderet DF, Munier FL, Arsenijevic Y.Gruter O, Kostic C, Crippa SV, Perez MT, Zografos L, Schorderet DF, Munier FL, Arsenijevic Y.
Gene Ther. 2005 Jun;12(11):942-7. -
PDFPubmed
Clinical and immunopathological corneal phenotype in homozygotes for the BIGH3 R124H mutation.
Diaper CJ, Schorderet DF, Chaubert P, Munier FL.
Eye. 2005 Jan;19(1):92-6.
