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P Hamel

Showing results (141-150 of 233) with videos related to

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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.
Frontiers in Dementia|June 24, 2024
Association Between Acoustic Features and Brain Volumes: the Framingham Heart StudyHuitong Ding, Alexander P Hamel, Cody Karjadi, et al.
Medicine and Science in Sports and Exercise|December 1, 1986
Aerobic performance in brothers, dizygotic and monozygotic twinsC Bouchard, R Lesage, G Lortie, 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.
Ophthalmology|March 20, 2016
Clinical Evaluation and Cone Alterations in ChoroideremiaNicolas Nabholz, Marie-Céline Lorenzini, Béatrice Bocquet, 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.
The Journal of Biological Chemistry|July 15, 2010
CCS5, a thioredoxin-like protein involved in the assembly of plastid c-type cytochromesStéphane T Gabilly, Beth Welty Dreyfuss, Mohamed Karamoko, et al.
Molecular and Cellular Biology|January 6, 2005
Deafness and cochlear fibrocyte alterations in mice deficient for the inner ear protein otospiralinBenjamin Delprat, Jérôme Ruel, Matthieu J Guitton, et al.
Pageof 24

Showing results (141-150 of 233) with videos related to

Sort By:
Pageof 24
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.
Frontiers in Dementia|June 24, 2024
Association Between Acoustic Features and Brain Volumes: the Framingham Heart StudyHuitong Ding, Alexander P Hamel, Cody Karjadi, et al.
Medicine and Science in Sports and Exercise|December 1, 1986
Aerobic performance in brothers, dizygotic and monozygotic twinsC Bouchard, R Lesage, G Lortie, 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.
Ophthalmology|March 20, 2016
Clinical Evaluation and Cone Alterations in ChoroideremiaNicolas Nabholz, Marie-Céline Lorenzini, Béatrice Bocquet, 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.
The Journal of Biological Chemistry|July 15, 2010
CCS5, a thioredoxin-like protein involved in the assembly of plastid c-type cytochromesStéphane T Gabilly, Beth Welty Dreyfuss, Mohamed Karamoko, et al.
Molecular and Cellular Biology|January 6, 2005
Deafness and cochlear fibrocyte alterations in mice deficient for the inner ear protein otospiralinBenjamin Delprat, Jérôme Ruel, Matthieu J Guitton, et al.
Pageof 24