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Isabelle Meunier

Showing results (31-40 of 148) with videos related to

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Ophthalmic Genetics|March 29, 2022
Natural history of Usher type 2 with the c.2299delG mutation of <i>USH2A</i> in a large cohortAudrey Meunier, Xavier Zanlonghi, Anne-Françoise Roux, et al.
Ophthalmic Genetics|March 29, 2026
A novel case of Heimler syndrome in a young child with compound heterozygous PEX26 mutations: clinical and genetic insights with literature reviewAurore Aziz, Tristan Bernard-Cuisinier, Daniele Denis, 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|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.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 16, 2021
Novel roles for voltage-gated T-type Ca<sup>2+</sup> and ClC-2 channels in phagocytosis and angiogenic factor balance identified in human iPSC-derived RPEDaria Mamaeva, Zhour Jazouli, Mattia L DiFrancesco, et al.
Vaccine|January 8, 2011
Cellular immune response in the presence of protective antibody levels correlates with protection against 1918 influenza in ferretsStéphane Pillet, Darwyn Kobasa, Isabelle Meunier, 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.
Plos Pathogens|April 18, 2013
Type I IFN triggers RIG-I/TLR3/NLRP3-dependent inflammasome activation in influenza A virus infected cellsJulien Pothlichet, Isabelle Meunier, Beckley K Davis, et al.
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.
Molecular Vision|April 27, 2017
Cone dystrophy or macular dystrophy associated with novel autosomal dominant <i>GUCA1A</i> mutationsGaël Manes, Sonia Mamouni, Emilie Hérald, et al.
Pageof 15

Showing results (31-40 of 148) with videos related to

Sort By:
Pageof 15
Ophthalmic Genetics|March 29, 2022
Natural history of Usher type 2 with the c.2299delG mutation of <i>USH2A</i> in a large cohortAudrey Meunier, Xavier Zanlonghi, Anne-Françoise Roux, et al.
Ophthalmic Genetics|March 29, 2026
A novel case of Heimler syndrome in a young child with compound heterozygous PEX26 mutations: clinical and genetic insights with literature reviewAurore Aziz, Tristan Bernard-Cuisinier, Daniele Denis, 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|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.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 16, 2021
Novel roles for voltage-gated T-type Ca<sup>2+</sup> and ClC-2 channels in phagocytosis and angiogenic factor balance identified in human iPSC-derived RPEDaria Mamaeva, Zhour Jazouli, Mattia L DiFrancesco, et al.
Vaccine|January 8, 2011
Cellular immune response in the presence of protective antibody levels correlates with protection against 1918 influenza in ferretsStéphane Pillet, Darwyn Kobasa, Isabelle Meunier, 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.
Plos Pathogens|April 18, 2013
Type I IFN triggers RIG-I/TLR3/NLRP3-dependent inflammasome activation in influenza A virus infected cellsJulien Pothlichet, Isabelle Meunier, Beckley K Davis, et al.
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.
Molecular Vision|April 27, 2017
Cone dystrophy or macular dystrophy associated with novel autosomal dominant <i>GUCA1A</i> mutationsGaël Manes, Sonia Mamouni, Emilie Hérald, et al.
Pageof 15