Showing 1 - 13 results of 13 for search 'Daniel F Schorderet', query time: 0.05s Refine Results
  1. 1
    Different Phenotypes in Pseudodominant Inherited Retinal Dystrophies

    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
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  2. 2
    Mutations in the DNA-binding domain of NR2E3 affect in vivo dimerization and interaction with CRX.

    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
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  3. 3
    Bax-induced apoptosis in Leber's congenital amaurosis: a dual role in rod and cone degeneration.

    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
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  4. 4
    Acute hypoglycemia induces retinal cell death in mouse.

    Acute hypoglycemia induces retinal cell death in mouse. by Martine Emery, Daniel F Schorderet, Raphaël Roduit

    Published 2011-01-01
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  5. 5
    A dimerized HMX1 inhibits EPHA6/epha4b in mouse and zebrafish retinas.

    A dimerized HMX1 inhibits EPHA6/epha4b in mouse and zebrafish retinas. by Fabienne Marcelli, Gaëlle Boisset, Daniel F Schorderet

    Published 2014-01-01
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  6. 6
    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.

    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
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  7. 7
    Premature Vertebral Mineralization in <i>hmx1</i>-Mutant Zebrafish

    Premature Vertebral Mineralization in <i>hmx1</i>-Mutant Zebrafish by Younes El Fersioui, Gaëtan Pinton, Nathalie Allaman-Pillet, Daniel F. Schorderet

    Published 2022-03-01
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  8. 8
    Hmx1 regulates urfh1 expression in the craniofacial region in zebrafish.

    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
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  9. 9
    Dental phenotype in Jalili syndrome due to a c.1312 dupC homozygous mutation in the CNNM4 gene.

    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
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  10. 10
    Incomplete Recovery of Zebrafish Retina Following Cryoinjury

    Incomplete Recovery of Zebrafish Retina Following Cryoinjury by Denisa Džulová, Dylan Lawless, Gaëtan G. Pinton, Nicole A. Renner, Daniel F. Schorderet

    Published 2022-04-01
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  11. 11
    Correction: Habibi I. et al. “Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)” Genes, 2019, <i>10</i>, 953

    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
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  12. 12
    Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with <i>MFSD8</i> Variants

    Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with <i>MFSD8</i> Variants by Anaïs F. Poncet, Olivier Grunewald, Veronika Vaclavik, Isabelle Meunier, Isabelle Drumare, Valérie Pelletier, Béatrice Bocquet, Margarita G. Todorova, Anne-Gaëlle Le Moing, Aurore Devos, Daniel F. Schorderet, Florence Jobic, Sabine Defoort-Dhellemmes, Hélène Dollfus, Vasily M. Smirnov, Claire-Marie Dhaenens

    Published 2022-04-01
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  13. 13
    A male with unilateral microphthalmia reveals a role for TMX3 in eye development.

    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
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