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P Hamel

Showing results (181-190 of 205) with videos related to

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Genome Research|October 27, 2010
OPA1 links human mitochondrial genome maintenance to mtDNA replication and distributionGhizlane Elachouri, Sara Vidoni, Claudia Zanna, et al.
Human Molecular Genetics|October 4, 2017
A novel duplication of PRMD13 causes North Carolina macular dystrophy: overexpression of PRDM13 orthologue in drosophila eye reproduces the human phenotypeGaël Manes, Willy Joly, Thomas Guignard, et al.
Journal of Medicinal Chemistry|September 27, 1996
Dioxabicyclooctanyl naphthalenenitriles as nonredox 5-lipoxygenase inhibitors: structure-activity relationship study directed toward the improvement of metabolic stabilityD Delorme, Y Ducharme, C Brideau, et al.
Journal of Medicinal Chemistry|August 29, 1997
Substituted (pyridylmethoxy)naphthalenes as potent and orally active 5-lipoxygenase inhibitors; synthesis, biological profile, and pharmacokinetics of L-739,010P Hamel, D Riendeau, C Brideau, et al.
Human Molecular Genetics|January 9, 2016
A dominant mutation in MAPKAPK3, an actor of p38 signaling pathway, causes a new retinal dystrophy involving Bruch's membrane and retinal pigment epitheliumIsabelle Meunier, Guy Lenaers, Béatrice Bocquet, et al.
Genes|January 11, 2018
Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate GenesGaluh D N Astuti, L Ingeborgh van den Born, M Imran Khan, et al.
Scientific Reports|September 8, 2016
A new autosomal dominant eye and lung syndrome linked to mutations in TIMP3 geneIsabelle Meunier, Béatrice Bocquet, Gilles Labesse, et al.
American Journal of Ophthalmology|October 1, 2018
The Natural History of Inherited Retinal Dystrophy Due to Biallelic Mutations in the RPE65 GeneDaniel C Chung, Mette Bertelsen, Birgit Lorenz, et al.
Plos One|January 15, 2016
Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation SequencingNicole Weisschuh, Anja K Mayer, Tim M Strom, et al.
American Journal of Human Genetics|December 19, 2012
Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindnessChristina Zeitz, Samuel G Jacobson, Christian P Hamel, et al.
Pageof 21

Showing results (181-190 of 205) with videos related to

Sort By:
Pageof 21
Genome Research|October 27, 2010
OPA1 links human mitochondrial genome maintenance to mtDNA replication and distributionGhizlane Elachouri, Sara Vidoni, Claudia Zanna, et al.
Human Molecular Genetics|October 4, 2017
A novel duplication of PRMD13 causes North Carolina macular dystrophy: overexpression of PRDM13 orthologue in drosophila eye reproduces the human phenotypeGaël Manes, Willy Joly, Thomas Guignard, et al.
Journal of Medicinal Chemistry|September 27, 1996
Dioxabicyclooctanyl naphthalenenitriles as nonredox 5-lipoxygenase inhibitors: structure-activity relationship study directed toward the improvement of metabolic stabilityD Delorme, Y Ducharme, C Brideau, et al.
Journal of Medicinal Chemistry|August 29, 1997
Substituted (pyridylmethoxy)naphthalenes as potent and orally active 5-lipoxygenase inhibitors; synthesis, biological profile, and pharmacokinetics of L-739,010P Hamel, D Riendeau, C Brideau, et al.
Human Molecular Genetics|January 9, 2016
A dominant mutation in MAPKAPK3, an actor of p38 signaling pathway, causes a new retinal dystrophy involving Bruch's membrane and retinal pigment epitheliumIsabelle Meunier, Guy Lenaers, Béatrice Bocquet, et al.
Genes|January 11, 2018
Identification of Inherited Retinal Disease-Associated Genetic Variants in 11 Candidate GenesGaluh D N Astuti, L Ingeborgh van den Born, M Imran Khan, et al.
Scientific Reports|September 8, 2016
A new autosomal dominant eye and lung syndrome linked to mutations in TIMP3 geneIsabelle Meunier, Béatrice Bocquet, Gilles Labesse, et al.
American Journal of Ophthalmology|October 1, 2018
The Natural History of Inherited Retinal Dystrophy Due to Biallelic Mutations in the RPE65 GeneDaniel C Chung, Mette Bertelsen, Birgit Lorenz, et al.
Plos One|January 15, 2016
Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation SequencingNicole Weisschuh, Anja K Mayer, Tim M Strom, et al.
American Journal of Human Genetics|December 19, 2012
Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindnessChristina Zeitz, Samuel G Jacobson, Christian P Hamel, et al.
Pageof 21