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P Hamel

Showing results (111-120 of 233) with videos related to

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Human Molecular Genetics|September 16, 2017
Pathogenicity of a novel missense variant associated with choroideremia and its impact on gene replacement therapySimona Torriano, Nejla Erkilic, Valérie Faugère, et al.
Stem Cell Research|June 28, 2019
Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosisNejla Erkilic, Carla Sanjurjo-Soriano, Gaël Manes, et al.
Ophthalmic Research|September 24, 2010
Screening for a canine model of choroideremia exclusively identifies nonpathogenic CHM variantsLorenne Robert, Audrey Sénéchal, Béatrice Bocquet, et al.
Brain Research. Molecular Brain Research|December 28, 1995
Molecular cloning and expression of alpha parvalbumin in the guinea pig cochleaA Soto-Prior, M Cluzel, N Renard, et al.
Molecular Vision|December 17, 2013
Homozygosity mapping in autosomal recessive retinitis pigmentosa families detects novel mutationsBéatrice Bocquet, Nour Al Dain Marzouka, Maxime Hebrard, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
Meaning-based guidance of attention in rhesus monkeys during naturalistic scene viewingOrhan Soyuhos, Taylor R Hayes, Wenqing Hu, et al.
Frontiers in Dementia|June 19, 2024
Prediction of Progression from Mild Cognitive Impairment to Alzheimer's disease with Longitudinal and Multimodal DataHuitong Ding, Biqi Wang, Alexander P Hamel, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|March 22, 2024
Exploring cognitive progression subtypes in the Framingham Heart StudyHuitong Ding, Biqi Wang, Alexander P Hamel, et al.
Journal of Neuroscience Research|March 1, 1993
A developmentally regulated microsomal protein specific for the pigment epithelium of the vertebrate retinaC P Hamel, E Tsilou, E Harris, et al.
Eukaryotic Cell|July 21, 2009
The ARG9 gene encodes the plastid-resident N-acetyl ornithine aminotransferase in the green alga Chlamydomonas reinhardtiiClaire Remacle, Sara Cline, Layla Boutaffala, et al.
Pageof 24

Showing results (111-120 of 233) with videos related to

Sort By:
Pageof 24
Human Molecular Genetics|September 16, 2017
Pathogenicity of a novel missense variant associated with choroideremia and its impact on gene replacement therapySimona Torriano, Nejla Erkilic, Valérie Faugère, et al.
Stem Cell Research|June 28, 2019
Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosisNejla Erkilic, Carla Sanjurjo-Soriano, Gaël Manes, et al.
Ophthalmic Research|September 24, 2010
Screening for a canine model of choroideremia exclusively identifies nonpathogenic CHM variantsLorenne Robert, Audrey Sénéchal, Béatrice Bocquet, et al.
Brain Research. Molecular Brain Research|December 28, 1995
Molecular cloning and expression of alpha parvalbumin in the guinea pig cochleaA Soto-Prior, M Cluzel, N Renard, et al.
Molecular Vision|December 17, 2013
Homozygosity mapping in autosomal recessive retinitis pigmentosa families detects novel mutationsBéatrice Bocquet, Nour Al Dain Marzouka, Maxime Hebrard, et al.
Biorxiv : the Preprint Server for Biology|April 10, 2026
Meaning-based guidance of attention in rhesus monkeys during naturalistic scene viewingOrhan Soyuhos, Taylor R Hayes, Wenqing Hu, et al.
Frontiers in Dementia|June 19, 2024
Prediction of Progression from Mild Cognitive Impairment to Alzheimer's disease with Longitudinal and Multimodal DataHuitong Ding, Biqi Wang, Alexander P Hamel, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|March 22, 2024
Exploring cognitive progression subtypes in the Framingham Heart StudyHuitong Ding, Biqi Wang, Alexander P Hamel, et al.
Journal of Neuroscience Research|March 1, 1993
A developmentally regulated microsomal protein specific for the pigment epithelium of the vertebrate retinaC P Hamel, E Tsilou, E Harris, et al.
Eukaryotic Cell|July 21, 2009
The ARG9 gene encodes the plastid-resident N-acetyl ornithine aminotransferase in the green alga Chlamydomonas reinhardtiiClaire Remacle, Sara Cline, Layla Boutaffala, et al.
Pageof 24