Schorderet, D.F.

Schorderet, D.F.; Haider, N.; Escher, Pascal (2012). NR2E3-linked retinal degenerations: enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP). In: Traboulsi, E.I. (ed.) Genetic diseases of the eye (pp. 437-447). Oxford: Oxford University Press

Escher, Pascal; Schorderet, D.F. (2011). Exploration of the visual system: Part 1: Dissection of the mouse eye for RNA, protein, and histological analyses. In: Current Protocols in Mouse Biology 1 (pp. 445-462). Wiley 10.1002/9780470942390.mo110129

Tran, H.V.; Escher, Pascal; Vaclavik, V.; Favre, I.; Bajrami, H.; Borruat, F.X.; Schorderet, D.F.; Munier, F.L. (2011). Autofluorescence Study In NR2E3 p.G56R-linked Autosomal Dominant Retinitis Pigmentosa In A Single Kindred. In: ARVO E-Abstract 6604. Fort Lauderdale: Association for Research in Vision and Ophthalmology

Schorderet, D.F.; Polok, B.; Escher, Pascal; Favez, T.; Voirol, N.; Bolay, S.; Ambresin, A.; Hamel, C.; Mégarbane, A.; Munier, F.L. (2009). The metal ion binding protein Cnnm4 is mutated in rod-cone dystrophy/amelogenesis imperfecta syndrome. In: Investigative ophthalmology and visual science 50. ARVO E-Abstract 2324

Roduit, R.; Escher, Pascal; Emery, M.; Voirol, N.; Favez, T.; Schorderet, D.F. (2009). The DNA-binding domain (DBD) is essential for NR2E3 dimerization and interaction with Crx. In: Investigative ophthalmology and visual science 50. ARVO E-Abstract 5459

Escher, Pascal; Voirol, N.; Favez, T.; Roduit, R.; Schorderet, D.F. (2009). Functional analysis of disease-causing NR2E3 mutations. In: Investigative Ophthalmology and Visual Science 50. ARVO E-Abstract 2296

Escher, Pascal; Schorderet, D.F. (2008). Génétique et pathologie vasculaire oculaire. In: Pournaras, C.J. (ed.) Pathologies vasculaires oculaires (pp. 219-228). Paris: Masson