Different Phenotypes in Pseudodominant Inherited Retinal Dystrophies

by Imen Habibi, Yosra Falfoul, Hoai Viet Tran, Khaled El Matri, Ahmed Chebil, Leila El Matri, Daniel F. Schorderet, Daniel F. Schorderet, Daniel F. Schorderet
Published 2021-02-01

Bax-induced apoptosis in Leber's congenital amaurosis: a dual role in rod and cone degeneration.

by Séverine Hamann, Daniel F Schorderet, Sandra Cottet
Published 2009-08-01

Acute hypoglycemia induces retinal cell death in mouse.

by Martine Emery, Daniel F Schorderet, Raphaël Roduit
Published 2011-01-01

A dimerized HMX1 inhibits EPHA6/epha4b in mouse and zebrafish retinas.

by Fabienne Marcelli, Gaëlle Boisset, Daniel F Schorderet
Published 2014-01-01

Mutations in the DNA-binding domain of NR2E3 affect in vivo dimerization and interaction with CRX.

by Raphael Roduit, Pascal Escher, Daniel F Schorderet
Published 2009-10-01

Analysis of the cytoprotective role of α-crystallins in cell survival and implication of the αA-crystallin C-terminal extension domain in preventing Bax-induced apoptosis.

by Séverine Hamann, Sylviane Métrailler, Daniel F Schorderet, Sandra Cottet
Published 2013-01-01

IROme, a New High-Throughput Molecular Tool for the Diagnosis of Inherited Retinal Dystrophies

by Daniel F. Schorderet, Alexandra Iouranova, Tatiana Favez, Leila Tiab, Pascal Escher
Published 2013-01-01

Hmx1 regulates urfh1 expression in the craniofacial region in zebrafish.

by Younes El Fersioui, Gaëtan Pinton, Nathalie Allaman-Pillet, Daniel F Schorderet
Published 2021-01-01

Dental phenotype in Jalili syndrome due to a c.1312 dupC homozygous mutation in the CNNM4 gene.

by Hans U Luder, Christina Gerth-Kahlert, Silke Ostertag-Benzinger, Daniel F Schorderet
Published 2013-01-01

Phenotypic Progression of Stargardt Disease in a Large Consanguineous Tunisian Family Harboring New ABCA4 Mutations

by Yousra Falfoul, Imen Habibi, Ahmed Turki, Ahmed Chebil, Asma Hassairi, Daniel F. Schorderet, Leila El Matri
Published 2018-01-01

Autophagy defect is associated with low glucose-induced apoptosis in 661W photoreceptor cells.

by Delphine Balmer, Martine Emery, Pénélope Andreux, Johan Auwerx, Vanessa Ginet, Julien Puyal, Daniel F Schorderet, Raphaël Roduit
Published 2013-01-01

Genetic spectrum of retinal dystrophies in Tunisia

by Imen Habibi, Yosra Falfoul, Ahmed Turki, Asma Hassairi, Khaled El Matri, Ahmed Chebil, Daniel F. Schorderet, Leila El Matri
Published 2020-07-01

Correction: Habibi I. et al. “Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)” Genes, 2019, <i>10</i>, 953

by Imen Habibi, Yosra Falfoul, Margarita G. Todorova, Stefan Wyrsch, Veronika Vaclavik, Maria Helfenstein, Ahmed Turki, Khaled El Matri, Leila El Matri, Daniel F. Schorderet
Published 2020-05-01

Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)

by Imen Habibi, Yosra Falfoul, Margarita G. Todorova, Stefan Wyrsch, Veronika Vaclavik, Maria Helfenstein, Ahmed Turki, Khaled El Matri, Leila El Matri, Daniel F. Schorderet
Published 2019-11-01

A male with unilateral microphthalmia reveals a role for TMX3 in eye development.

by Ryan Chao, Linda Nevin, Pooja Agarwal, Jan Riemer, Xiaoyang Bai, Allen Delaney, Matthew Akana, Nelson JimenezLopez, Tanya Bardakjian, Adele Schneider, Nicolas Chassaing, Daniel F Schorderet, David FitzPatrick, Pui-yan Kwok, Lars Ellgaard, Douglas B Gould, Yan Zhang, Jarema Malicki, Herwig Baier, Anne Slavotinek
Published 2010-05-01