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Richard Redon

Showing results (41-50 of 131) with videos related to

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European Journal of Human Genetics : EJHG|February 12, 2020
The genetic history of FranceAude Saint Pierre, Joanna Giemza, Isabel Alves, et al.
European Journal of Human Genetics : EJHG|March 13, 2020
Correction: The genetic history of FranceAude Saint Pierre, Joanna Giemza, Isabel Alves, et al.
Stem Cell Research|March 24, 2024
Generation of a patient-specific induced pluripotent stem cell line carrying the DES p.R406W mutation, an isogenic control and a DES p.R406W knock-in lineMichelle Geryk, Robin Canac, Virginie Forest, et al.
Molecular Therapy. Nucleic Acids|October 28, 2015
Advanced Characterization of DNA Molecules in rAAV Vector Preparations by Single-stranded Virus Next-generation SequencingEmilie Lecomte, Benoît Tournaire, Benjamin Cogné, et al.
Journal of the American College of Cardiology|January 1, 2013
Identification of large families in early repolarization syndromeJean-Baptiste Gourraud, Solena Le Scouarnec, Frederic Sacher, et al.
Nature Genetics|September 11, 2007
Diet and the evolution of human amylase gene copy number variationGeorge H Perry, Nathaniel J Dominy, Katrina G Claw, et al.
Journal of Experimental & Clinical Cancer Research : CR|November 28, 2025
In vitro models to mimic tumor endothelial cell-mediated immune cell reprogramming in lung adenocarcinomaMorgane Krejbich, Emilie Navarro, Judith Fresquet, et al.
Genome Biology|October 27, 2007
Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridizationJohn C Marioni, Natalie P Thorne, Armand Valsesia, et al.
Genome Research|July 1, 2006
Copy number variation: new insights in genome diversityJennifer L Freeman, George H Perry, Lars Feuk, et al.
Nature Genetics|March 8, 2011
Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosisBertrand Isidor, Pierre Lindenbaum, Olivier Pichon, et al.
Pageof 14

Showing results (41-50 of 131) with videos related to

Sort By:
Pageof 14
European Journal of Human Genetics : EJHG|February 12, 2020
The genetic history of FranceAude Saint Pierre, Joanna Giemza, Isabel Alves, et al.
European Journal of Human Genetics : EJHG|March 13, 2020
Correction: The genetic history of FranceAude Saint Pierre, Joanna Giemza, Isabel Alves, et al.
Stem Cell Research|March 24, 2024
Generation of a patient-specific induced pluripotent stem cell line carrying the DES p.R406W mutation, an isogenic control and a DES p.R406W knock-in lineMichelle Geryk, Robin Canac, Virginie Forest, et al.
Molecular Therapy. Nucleic Acids|October 28, 2015
Advanced Characterization of DNA Molecules in rAAV Vector Preparations by Single-stranded Virus Next-generation SequencingEmilie Lecomte, Benoît Tournaire, Benjamin Cogné, et al.
Journal of the American College of Cardiology|January 1, 2013
Identification of large families in early repolarization syndromeJean-Baptiste Gourraud, Solena Le Scouarnec, Frederic Sacher, et al.
Nature Genetics|September 11, 2007
Diet and the evolution of human amylase gene copy number variationGeorge H Perry, Nathaniel J Dominy, Katrina G Claw, et al.
Journal of Experimental & Clinical Cancer Research : CR|November 28, 2025
In vitro models to mimic tumor endothelial cell-mediated immune cell reprogramming in lung adenocarcinomaMorgane Krejbich, Emilie Navarro, Judith Fresquet, et al.
Genome Biology|October 27, 2007
Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridizationJohn C Marioni, Natalie P Thorne, Armand Valsesia, et al.
Genome Research|July 1, 2006
Copy number variation: new insights in genome diversityJennifer L Freeman, George H Perry, Lars Feuk, et al.
Nature Genetics|March 8, 2011
Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosisBertrand Isidor, Pierre Lindenbaum, Olivier Pichon, et al.
Pageof 14