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Isabelle Meunier

Showing results (11-20 of 148) with videos related to

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European Journal of Ophthalmology|December 20, 2011
Homozygous mutation in MERTK causes severe autosomal recessive retinitis pigmentosaMohamed Ksantini, Estèle Lafont, Béatrice Bocquet, et al.
Physical Review Letters|November 13, 2003
Cu-Ag (111) polymorphism induced by segregation and advacanciesRobert Tétot, Fabienne Berthier, Jérôme Creuze, et al.
Ophthalmic Research|February 5, 2010
Electrophysiological retinal pigment epithelium changes observed with indocyanine green, trypan blue and triamcinoloneCarl Arndt, Isabelle Meunier, Olivier Rebollo, et al.
International Journal of Molecular Sciences|April 3, 2021
Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3Michalitsa Diakatou, Gregor Dubois, Nejla Erkilic, et al.
Scientific Reports|May 6, 2021
Quantification of the early pupillary dilation kinetic to assess rod and cone activityCorinne Kostic, Sylvain V Crippa, Lorette Leon, et al.
Plos One|September 19, 2015
Infection with a Mouse-Adapted Strain of the 2009 Pandemic Virus Causes a Highly Severe Disease Associated with an Impaired T Cell ResponseIsabelle Meunier, Olivier Morisseau, Émilie Garneau, et al.
Ophthalmic Genetics|November 12, 2010
Screening genes of the visual cycle RGR, RBP1 and RBP3 identifies rare sequence variationsMohamed Ksantini, Audrey Sénéchal, Béatrice Bocquet, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|September 25, 2020
Melanoma-associated retinopathy during pembrolizumab treatment probably controlled by intravitreal injections of dexamethasoneLaura Poujade, Quentin Samaran, Frédéric Mura, et al.
Journal of Clinical Immunology|June 23, 2021
ALPK1 Gene Mutations Drive Autoinflammation with Ectodermal Dysplasia and Progressive Vision LossYvan Jamilloux, Thibaud Mathis, Olivier Grunewald, et al.
Virology|June 20, 2006
Study of a novel hypervariable region in hepatitis C virus (HCV) E2 envelope glycoproteinMyriam Troesch, Isabelle Meunier, Pascal Lapierre, et al.
Pageof 15

Showing results (11-20 of 148) with videos related to

Sort By:
Pageof 15
European Journal of Ophthalmology|December 20, 2011
Homozygous mutation in MERTK causes severe autosomal recessive retinitis pigmentosaMohamed Ksantini, Estèle Lafont, Béatrice Bocquet, et al.
Physical Review Letters|November 13, 2003
Cu-Ag (111) polymorphism induced by segregation and advacanciesRobert Tétot, Fabienne Berthier, Jérôme Creuze, et al.
Ophthalmic Research|February 5, 2010
Electrophysiological retinal pigment epithelium changes observed with indocyanine green, trypan blue and triamcinoloneCarl Arndt, Isabelle Meunier, Olivier Rebollo, et al.
International Journal of Molecular Sciences|April 3, 2021
Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3Michalitsa Diakatou, Gregor Dubois, Nejla Erkilic, et al.
Scientific Reports|May 6, 2021
Quantification of the early pupillary dilation kinetic to assess rod and cone activityCorinne Kostic, Sylvain V Crippa, Lorette Leon, et al.
Plos One|September 19, 2015
Infection with a Mouse-Adapted Strain of the 2009 Pandemic Virus Causes a Highly Severe Disease Associated with an Impaired T Cell ResponseIsabelle Meunier, Olivier Morisseau, Émilie Garneau, et al.
Ophthalmic Genetics|November 12, 2010
Screening genes of the visual cycle RGR, RBP1 and RBP3 identifies rare sequence variationsMohamed Ksantini, Audrey Sénéchal, Béatrice Bocquet, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|September 25, 2020
Melanoma-associated retinopathy during pembrolizumab treatment probably controlled by intravitreal injections of dexamethasoneLaura Poujade, Quentin Samaran, Frédéric Mura, et al.
Journal of Clinical Immunology|June 23, 2021
ALPK1 Gene Mutations Drive Autoinflammation with Ectodermal Dysplasia and Progressive Vision LossYvan Jamilloux, Thibaud Mathis, Olivier Grunewald, et al.
Virology|June 20, 2006
Study of a novel hypervariable region in hepatitis C virus (HCV) E2 envelope glycoproteinMyriam Troesch, Isabelle Meunier, Pascal Lapierre, et al.
Pageof 15