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Isabelle Meunier

Showing results (41-50 of 148) with videos related to

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Retina (Philadelphia, Pa.)|December 14, 2020
A ROD-CONE DYSTROPHY IS SYSTEMATICALLY ASSOCIATED TO THE RTN4IP1 RECESSIVE OPTIC ATROPHYIsabelle Meunier, Béatrice Bocquet, Majida Charif, et al.
Investigative Ophthalmology & Visual Science|September 2, 2025
Novel BEST1 Variant Characterization in a Large French Cohort in Light of Updated Bestrophin-1 Structure-Function CorrelationJoan Bitan, Anaïs F Poncet, Claire Lecigne, et al.
BMC Medical Genetics|April 19, 2011
A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1Gaël Manes, Maxime Hebrard, Béatrice Bocquet, et al.
American Journal of Ophthalmology|September 8, 2009
Unilateral retinal pigment epithelium dysgenesisSalomon Y Cohen, Anne E Fung, Ramin Tadayoni, et al.
Ophthalmology|March 20, 2016
Clinical Evaluation and Cone Alterations in ChoroideremiaNicolas Nabholz, Marie-Céline Lorenzini, Béatrice Bocquet, et al.
Virology|November 15, 2011
Virulence differences of closely related pandemic 2009 H1N1 isolates correlate with increased inflammatory responses in ferretsIsabelle Meunier, Carissa Embury-Hyatt, Shane Stebner, et al.
International Journal of Biological Macromolecules|August 28, 2024
Differential pathogenetic mechanisms of mutations in helix 2 and helix 6 of rhodopsinAndrea Bighinati, Sara D'Alessandro, Angelo Felline, et al.
Stem Cell Research|August 27, 2025
Generation of a human iPSC line, INMi007-A, carrying compound heterozygous DCT variants associated with oculocutaneous albinism type 8Daria Mamaeva, Nejla Erkilic, Christel Vaché, et al.
International Journal of Molecular Sciences|July 27, 2022
<i>Casitas B-lineage lymphoma</i> Gene Mutation Ocular PhenotypeChristine Fardeau, Munirah Alafaleq, Marie-Adélaïde Ferchaud, et al.
European Journal of Human Genetics : EJHG|July 28, 2011
Combining gene mapping and phenotype assessment for fast mutation finding in non-consanguineous autosomal recessive retinitis pigmentosa familiesMaxime Hebrard, Gaël Manes, Béatrice Bocquet, et al.
Pageof 15

Showing results (41-50 of 148) with videos related to

Sort By:
Pageof 15
Retina (Philadelphia, Pa.)|December 14, 2020
A ROD-CONE DYSTROPHY IS SYSTEMATICALLY ASSOCIATED TO THE RTN4IP1 RECESSIVE OPTIC ATROPHYIsabelle Meunier, Béatrice Bocquet, Majida Charif, et al.
Investigative Ophthalmology & Visual Science|September 2, 2025
Novel BEST1 Variant Characterization in a Large French Cohort in Light of Updated Bestrophin-1 Structure-Function CorrelationJoan Bitan, Anaïs F Poncet, Claire Lecigne, et al.
BMC Medical Genetics|April 19, 2011
A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1Gaël Manes, Maxime Hebrard, Béatrice Bocquet, et al.
American Journal of Ophthalmology|September 8, 2009
Unilateral retinal pigment epithelium dysgenesisSalomon Y Cohen, Anne E Fung, Ramin Tadayoni, et al.
Ophthalmology|March 20, 2016
Clinical Evaluation and Cone Alterations in ChoroideremiaNicolas Nabholz, Marie-Céline Lorenzini, Béatrice Bocquet, et al.
Virology|November 15, 2011
Virulence differences of closely related pandemic 2009 H1N1 isolates correlate with increased inflammatory responses in ferretsIsabelle Meunier, Carissa Embury-Hyatt, Shane Stebner, et al.
International Journal of Biological Macromolecules|August 28, 2024
Differential pathogenetic mechanisms of mutations in helix 2 and helix 6 of rhodopsinAndrea Bighinati, Sara D'Alessandro, Angelo Felline, et al.
Stem Cell Research|August 27, 2025
Generation of a human iPSC line, INMi007-A, carrying compound heterozygous DCT variants associated with oculocutaneous albinism type 8Daria Mamaeva, Nejla Erkilic, Christel Vaché, et al.
International Journal of Molecular Sciences|July 27, 2022
<i>Casitas B-lineage lymphoma</i> Gene Mutation Ocular PhenotypeChristine Fardeau, Munirah Alafaleq, Marie-Adélaïde Ferchaud, et al.
European Journal of Human Genetics : EJHG|July 28, 2011
Combining gene mapping and phenotype assessment for fast mutation finding in non-consanguineous autosomal recessive retinitis pigmentosa familiesMaxime Hebrard, Gaël Manes, Béatrice Bocquet, et al.
Pageof 15