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Christian P Hamel

Showing results (31-40 of 101) with videos related to

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Investigative Ophthalmology & Visual Science|October 27, 2006
Homozygous deletion related to Alu repeats in RLBP1 causes retinitis punctata albescensGhyslaine Humbert, Cécile Delettre, Audrey Sénéchal, et al.
Neurogenetics|April 11, 2003
Gene structure, chromosomal localization, and mutation screening of the human gene for the inner ear protein otospiralinMireille Lavigne-Rebillard, Benjamin Delprat, Marie-Odile Surget, et al.
Molecular Vision|April 27, 2017
Cone dystrophy or macular dystrophy associated with novel autosomal dominant <i>GUCA1A</i> mutationsGaël Manes, Sonia Mamouni, Emilie Hérald, et al.
Yeast (Chichester, England)|September 19, 2002
What similarity between human and fission yeast proteins is required for orthology?Guy Lenaers, Laetitia Pelloquin, Aurélien Olichon, et al.
Molecular Vision|March 31, 2017
Novel splice-site mutation in TTLL5 causes cone dystrophy in a consanguineous familyMiguel de Sousa Dias, Christian P Hamel, Isabelle Meunier, et al.
Ophthalmology|March 20, 2016
Clinical Evaluation and Cone Alterations in ChoroideremiaNicolas Nabholz, Marie-Céline Lorenzini, Béatrice Bocquet, et al.
American Journal of Ophthalmology|April 11, 2008
Novel KCNV2 mutations in cone dystrophy with supernormal rod electroretinogramSafouane Ben Salah, Satomi Kamei, Audrey Sénéćhal, et al.
BMC Medical Genetics|April 19, 2011
A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1Gaël Manes, Maxime Hebrard, Béatrice Bocquet, et al.
Journal of Cellular and Molecular Medicine|April 14, 2016
Phloroglucinol protects retinal pigment epithelium and photoreceptor against all-trans-retinal-induced toxicity and inhibits A2E formationDavid Cia, Aurélie Cubizolle, Céline Crauste, et al.
American Journal of Ophthalmology|April 30, 2003
A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindnessFelix Karl Jacobi, Christian P Hamel, Bernard Arnaud, et al.
Pageof 11

Showing results (31-40 of 101) with videos related to

Sort By:
Pageof 11
Investigative Ophthalmology & Visual Science|October 27, 2006
Homozygous deletion related to Alu repeats in RLBP1 causes retinitis punctata albescensGhyslaine Humbert, Cécile Delettre, Audrey Sénéchal, et al.
Neurogenetics|April 11, 2003
Gene structure, chromosomal localization, and mutation screening of the human gene for the inner ear protein otospiralinMireille Lavigne-Rebillard, Benjamin Delprat, Marie-Odile Surget, et al.
Molecular Vision|April 27, 2017
Cone dystrophy or macular dystrophy associated with novel autosomal dominant <i>GUCA1A</i> mutationsGaël Manes, Sonia Mamouni, Emilie Hérald, et al.
Yeast (Chichester, England)|September 19, 2002
What similarity between human and fission yeast proteins is required for orthology?Guy Lenaers, Laetitia Pelloquin, Aurélien Olichon, et al.
Molecular Vision|March 31, 2017
Novel splice-site mutation in TTLL5 causes cone dystrophy in a consanguineous familyMiguel de Sousa Dias, Christian P Hamel, Isabelle Meunier, et al.
Ophthalmology|March 20, 2016
Clinical Evaluation and Cone Alterations in ChoroideremiaNicolas Nabholz, Marie-Céline Lorenzini, Béatrice Bocquet, et al.
American Journal of Ophthalmology|April 11, 2008
Novel KCNV2 mutations in cone dystrophy with supernormal rod electroretinogramSafouane Ben Salah, Satomi Kamei, Audrey Sénéćhal, et al.
BMC Medical Genetics|April 19, 2011
A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1Gaël Manes, Maxime Hebrard, Béatrice Bocquet, et al.
Journal of Cellular and Molecular Medicine|April 14, 2016
Phloroglucinol protects retinal pigment epithelium and photoreceptor against all-trans-retinal-induced toxicity and inhibits A2E formationDavid Cia, Aurélie Cubizolle, Céline Crauste, et al.
American Journal of Ophthalmology|April 30, 2003
A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindnessFelix Karl Jacobi, Christian P Hamel, Bernard Arnaud, et al.
Pageof 11