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Christian P Hamel

Showing results (21-30 of 101) with videos related to

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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.
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.
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.
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.
Plos One|April 25, 2014
A truncated form of rod photoreceptor PDE6 β-subunit causes autosomal dominant congenital stationary night blindness by interfering with the inhibitory activity of the γ-subunitGaël Manes, Pallavi Cheguru, Anurima Majumder, et al.
Stem Cell Research|June 17, 2019
Generation of a human iPSC line, INMi003-A, with a missense mutation in CRX associated with autosomal dominant cone-rod dystrophyNejla Erkilic, Carla Sanjurjo-Soriano, Michalitsa Diakatou, et al.
Molecular Therapy. Methods & Clinical Development|December 11, 2025
Erratum: Genome Editing in Patient iPSCs Corrects the Most Prevalent <i>USH2A</i> Mutations and Reveals Intriguing Mutant mRNA Expression ProfilesCarla Sanjurjo-Soriano, Nejla Erkilic, David Baux, et al.
Molecular Therapy. Methods & Clinical Development|January 8, 2020
Genome Editing in Patient iPSCs Corrects the Most Prevalent <i>USH2A</i> Mutations and Reveals Intriguing Mutant mRNA Expression ProfilesCarla Sanjurjo-Soriano, Nejla Erkilic, David Baux, et al.
Pageof 11

Showing results (21-30 of 101) with videos related to

Sort By:
Pageof 11
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.
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.
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.
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.
Plos One|April 25, 2014
A truncated form of rod photoreceptor PDE6 β-subunit causes autosomal dominant congenital stationary night blindness by interfering with the inhibitory activity of the γ-subunitGaël Manes, Pallavi Cheguru, Anurima Majumder, et al.
Stem Cell Research|June 17, 2019
Generation of a human iPSC line, INMi003-A, with a missense mutation in CRX associated with autosomal dominant cone-rod dystrophyNejla Erkilic, Carla Sanjurjo-Soriano, Michalitsa Diakatou, et al.
Molecular Therapy. Methods & Clinical Development|December 11, 2025
Erratum: Genome Editing in Patient iPSCs Corrects the Most Prevalent <i>USH2A</i> Mutations and Reveals Intriguing Mutant mRNA Expression ProfilesCarla Sanjurjo-Soriano, Nejla Erkilic, David Baux, et al.
Molecular Therapy. Methods & Clinical Development|January 8, 2020
Genome Editing in Patient iPSCs Corrects the Most Prevalent <i>USH2A</i> Mutations and Reveals Intriguing Mutant mRNA Expression ProfilesCarla Sanjurjo-Soriano, Nejla Erkilic, David Baux, et al.
Pageof 11