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P Hamel

Showing results (101-110 of 233) with videos related to

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Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1997
[Feasibility of bilateral sacrospinous ligament vaginal suspension with a stapler. Prospective studies with the 34 first cases]W Febbraro, G Beucher, P Von Theobald, et al.
JMIR Rehabilitation and Assistive Technologies|April 17, 2026
Use of Wearable Devices to Augment Traditional Measurements of Postoperative Outcomes Following Total Joint Arthroplasty: Systematic ReviewRobert Raymond Hall Iii, Alexander P Hamel, Pamela A Chan, et al.
Genomics|April 1, 1994
The gene for the retinal pigment epithelium-specific protein RPE65 is localized to human 1p31 and mouse 3C P Hamel, N A Jenkins, D J Gilbert, et al.
Molecular Microbiology|January 20, 2012
The flavoprotein Cyc2p, a mitochondrial cytochrome c assembly factor, is a NAD(P)H-dependent haem reductaseVincent Corvest, Darren A Murrey, Mazakazu Hirasawa, et al.
Stem Cell Research|November 24, 2018
Generation of a human iPSC line, INMi002-A, carrying the most prevalent USH2A variant associated with Usher syndrome type 2Carla Sanjurjo-Soriano, Nejla Erkilic, Gaël Manes, et al.
Scientific Reports|January 9, 2021
Investigating the influence of physiologically relevant hydrostatic pressure on CHO cell batch cultureMenglin Shang, Taehong Kwon, Jean-Francois P Hamel, et al.
Retinal Cases & Brief Reports|May 21, 2016
LEBER CONGENITAL AMAUROSIS WITH LARGE RETINAL PIGMENT CLUMPS CAUSED BY COMPOUND HETEROZYGOUS MUTATIONS IN KCNJ13Sarah Perez-Roustit, Virginie Marquette, Béatrice Bocquet, et al.
The Journal of Biological Chemistry|July 25, 1993
Molecular cloning and expression of RPE65, a novel retinal pigment epithelium-specific microsomal protein that is post-transcriptionally regulated in vitroC P Hamel, E Tsilou, B A Pfeffer, et al.
Genetics|August 11, 2010
c-type cytochrome assembly in Saccharomyces cerevisiae: a key residue for apocytochrome c1/lyase interactionVincent Corvest, Darren A Murrey, Delphine G Bernard, et al.
Stem Cell Research|November 20, 2018
Generation of an iPSC line, INMi001-A, carrying the two most common USH2A mutations from a compound heterozygote with non-syndromic retinitis pigmentosaCarla Sanjurjo-Soriano, Nejla Erkilic, Gaël Manes, et al.
Pageof 24

Showing results (101-110 of 233) with videos related to

Sort By:
Pageof 24
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1997
[Feasibility of bilateral sacrospinous ligament vaginal suspension with a stapler. Prospective studies with the 34 first cases]W Febbraro, G Beucher, P Von Theobald, et al.
JMIR Rehabilitation and Assistive Technologies|April 17, 2026
Use of Wearable Devices to Augment Traditional Measurements of Postoperative Outcomes Following Total Joint Arthroplasty: Systematic ReviewRobert Raymond Hall Iii, Alexander P Hamel, Pamela A Chan, et al.
Genomics|April 1, 1994
The gene for the retinal pigment epithelium-specific protein RPE65 is localized to human 1p31 and mouse 3C P Hamel, N A Jenkins, D J Gilbert, et al.
Molecular Microbiology|January 20, 2012
The flavoprotein Cyc2p, a mitochondrial cytochrome c assembly factor, is a NAD(P)H-dependent haem reductaseVincent Corvest, Darren A Murrey, Mazakazu Hirasawa, et al.
Stem Cell Research|November 24, 2018
Generation of a human iPSC line, INMi002-A, carrying the most prevalent USH2A variant associated with Usher syndrome type 2Carla Sanjurjo-Soriano, Nejla Erkilic, Gaël Manes, et al.
Scientific Reports|January 9, 2021
Investigating the influence of physiologically relevant hydrostatic pressure on CHO cell batch cultureMenglin Shang, Taehong Kwon, Jean-Francois P Hamel, et al.
Retinal Cases & Brief Reports|May 21, 2016
LEBER CONGENITAL AMAUROSIS WITH LARGE RETINAL PIGMENT CLUMPS CAUSED BY COMPOUND HETEROZYGOUS MUTATIONS IN KCNJ13Sarah Perez-Roustit, Virginie Marquette, Béatrice Bocquet, et al.
The Journal of Biological Chemistry|July 25, 1993
Molecular cloning and expression of RPE65, a novel retinal pigment epithelium-specific microsomal protein that is post-transcriptionally regulated in vitroC P Hamel, E Tsilou, B A Pfeffer, et al.
Genetics|August 11, 2010
c-type cytochrome assembly in Saccharomyces cerevisiae: a key residue for apocytochrome c1/lyase interactionVincent Corvest, Darren A Murrey, Delphine G Bernard, et al.
Stem Cell Research|November 20, 2018
Generation of an iPSC line, INMi001-A, carrying the two most common USH2A mutations from a compound heterozygote with non-syndromic retinitis pigmentosaCarla Sanjurjo-Soriano, Nejla Erkilic, Gaël Manes, et al.
Pageof 24