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Pierre Lindenbaum

Showing results (11-20 of 43) with videos related to

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Frontiers in Medicine|May 21, 2025
Corrigendum: Exome sequencing data reanalysis of 200 hypertrophic cardiomyopathy patients: the HYPERGEN French cohort 5 years after the initial analysisHager Jaouadi, Victor Morel, Helene Martel, et al.
Frontiers in Medicine|November 18, 2024
Exome sequencing data reanalysis of 200 hypertrophic cardiomyopathy patients: the HYPERGEN French cohort 5 years after the initial analysisHager Jaouadi, Victor Morel, Helene Martel, et al.
Human Gene Therapy Methods|May 3, 2017
Accurate Identification and Quantification of DNA Species by Next-Generation Sequencing in Adeno-Associated Viral Vectors Produced in Insect CellsMagalie Penaud-Budloo, Emilie Lecomte, Aurélien Guy-Duché, et al.
Plos Computational Biology|November 3, 2011
BioStar: an online question & answer resource for the bioinformatics communityLaurence D Parnell, Pierre Lindenbaum, Khader Shameer, 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.
International Journal of Molecular Sciences|April 23, 2022
<i>APOB</i> CRISPR-Cas9 Engineering in Hypobetalipoproteinemia: A Promising Tool for Functional Studies of Novel VariantsXavier Vanhoye, Alexandre Janin, Amandine Caillaud, 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.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 4, 2026
<i>LDLR</i>-3'UTR Deletions Identified as a Genetic Cause of Hypobetalipoproteinemia: Evidence From Familial and Population-Based StudiesAntoine Lainé, Zoé Begué-Racapé, Pierre Lindenbaum, 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.
European Journal of Human Genetics : EJHG|October 9, 2019
Fryns type mesomelic dysplasia of the upper limbs caused by inverted duplications of the HOXD gene clusterCédric Le Caignec, Olivier Pichon, Annaig Briand, et al.
Pageof 5

Showing results (11-20 of 43) with videos related to

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Pageof 5
Frontiers in Medicine|May 21, 2025
Corrigendum: Exome sequencing data reanalysis of 200 hypertrophic cardiomyopathy patients: the HYPERGEN French cohort 5 years after the initial analysisHager Jaouadi, Victor Morel, Helene Martel, et al.
Frontiers in Medicine|November 18, 2024
Exome sequencing data reanalysis of 200 hypertrophic cardiomyopathy patients: the HYPERGEN French cohort 5 years after the initial analysisHager Jaouadi, Victor Morel, Helene Martel, et al.
Human Gene Therapy Methods|May 3, 2017
Accurate Identification and Quantification of DNA Species by Next-Generation Sequencing in Adeno-Associated Viral Vectors Produced in Insect CellsMagalie Penaud-Budloo, Emilie Lecomte, Aurélien Guy-Duché, et al.
Plos Computational Biology|November 3, 2011
BioStar: an online question & answer resource for the bioinformatics communityLaurence D Parnell, Pierre Lindenbaum, Khader Shameer, 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.
International Journal of Molecular Sciences|April 23, 2022
<i>APOB</i> CRISPR-Cas9 Engineering in Hypobetalipoproteinemia: A Promising Tool for Functional Studies of Novel VariantsXavier Vanhoye, Alexandre Janin, Amandine Caillaud, 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.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 4, 2026
<i>LDLR</i>-3'UTR Deletions Identified as a Genetic Cause of Hypobetalipoproteinemia: Evidence From Familial and Population-Based StudiesAntoine Lainé, Zoé Begué-Racapé, Pierre Lindenbaum, 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.
European Journal of Human Genetics : EJHG|October 9, 2019
Fryns type mesomelic dysplasia of the upper limbs caused by inverted duplications of the HOXD gene clusterCédric Le Caignec, Olivier Pichon, Annaig Briand, et al.
Pageof 5