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Nadine Gigarel

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Journal of Assisted Reproduction and Genetics|April 24, 2025
Scoping review on the embryonic developmental potential of tripronuclear zygotes and their use for clinical and research purposesAnne Mayeur, Khadija Ouaziz, Brian Sperelakis-Beedham, et al.
Human Genetics|December 16, 2003
Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28Nadine Gigarel, Nelly Frydman, Philippe Burlet, et al.
Bulletin De L'Academie Nationale De Medecine|March 2, 2012
[Extending preimplantation genetic diagnosis to HLA typing: the French exception]Julie Steffann, Nelly Frydman, Philippe Burlet, et al.
Human Reproduction (Oxford, England)|April 2, 2025
Profiling mitochondrial DNA variant segregation during human preimplantation development: a prerequisite to preimplantation genetic testing for mitochondrial DNA-related disordersPaula Rubens, Anne Mayeur, Kalliopi Chatzovoulou, et al.
European Journal of Human Genetics : EJHG|November 12, 2009
Single-sperm analysis for recurrence risk assessment of spinal muscular atrophyPhilippe Burlet, Nadine Gigarel, Maryse Magen, et al.
Mitochondrion|February 27, 2021
Mitochondrial DNA mutations do not impact early human embryonic developmentKalliopi Chatzovoulou, Anne Mayeur, Nadine Gigarel, et al.
Molecular Genetics and Metabolism|February 8, 2005
Single cell quantification of the 8993T>G NARP mitochondrial DNA mutation by fluorescent PCRNadine Gigarel, Pierre F Ray, Philippe Burlet, et al.
Fertility and Sterility|September 20, 2005
Improved single-cell protocol for preimplantation genetic diagnosis of spinal muscular atrophyPhilippe Burlet, Nelly Frydman, Nadine Gigarel, et al.
Human Mutation|November 25, 2003
NDP gene mutations in 14 French families with Norrie diseaseGhislaine Royer, Sylvain Hanein, Valérie Raclin, et al.
American Journal of Medical Genetics|January 25, 2002
Osteopathia striata cranial sclerosis: non-random X-inactivation suggestive of X-linked dominant inheritanceGéraldine Viot, Didier Lacombe, Albert David, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Journal of Assisted Reproduction and Genetics|April 24, 2025
Scoping review on the embryonic developmental potential of tripronuclear zygotes and their use for clinical and research purposesAnne Mayeur, Khadija Ouaziz, Brian Sperelakis-Beedham, et al.
Human Genetics|December 16, 2003
Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28Nadine Gigarel, Nelly Frydman, Philippe Burlet, et al.
Bulletin De L'Academie Nationale De Medecine|March 2, 2012
[Extending preimplantation genetic diagnosis to HLA typing: the French exception]Julie Steffann, Nelly Frydman, Philippe Burlet, et al.
Human Reproduction (Oxford, England)|April 2, 2025
Profiling mitochondrial DNA variant segregation during human preimplantation development: a prerequisite to preimplantation genetic testing for mitochondrial DNA-related disordersPaula Rubens, Anne Mayeur, Kalliopi Chatzovoulou, et al.
European Journal of Human Genetics : EJHG|November 12, 2009
Single-sperm analysis for recurrence risk assessment of spinal muscular atrophyPhilippe Burlet, Nadine Gigarel, Maryse Magen, et al.
Mitochondrion|February 27, 2021
Mitochondrial DNA mutations do not impact early human embryonic developmentKalliopi Chatzovoulou, Anne Mayeur, Nadine Gigarel, et al.
Molecular Genetics and Metabolism|February 8, 2005
Single cell quantification of the 8993T>G NARP mitochondrial DNA mutation by fluorescent PCRNadine Gigarel, Pierre F Ray, Philippe Burlet, et al.
Fertility and Sterility|September 20, 2005
Improved single-cell protocol for preimplantation genetic diagnosis of spinal muscular atrophyPhilippe Burlet, Nelly Frydman, Nadine Gigarel, et al.
Human Mutation|November 25, 2003
NDP gene mutations in 14 French families with Norrie diseaseGhislaine Royer, Sylvain Hanein, Valérie Raclin, et al.
American Journal of Medical Genetics|January 25, 2002
Osteopathia striata cranial sclerosis: non-random X-inactivation suggestive of X-linked dominant inheritanceGéraldine Viot, Didier Lacombe, Albert David, et al.
Pageof 2