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Bernard Jost

Showing results (31-40 of 41) with videos related to

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The Journal of Experimental Medicine|August 30, 2021
Helios represses megakaryocyte priming in hematopoietic stem and progenitor cellsGiovanni Cova, Chiara Taroni, Marie-Céline Deau, et al.
Plos One|July 5, 2013
An integrated diagnosis strategy for congenital myopathiesJohann Böhm, Nasim Vasli, Edoardo Malfatti, et al.
Nature Structural & Molecular Biology|June 21, 2011
Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophyFrédérique Rau, Fernande Freyermuth, Charlotte Fugier, et al.
Genome Biology|June 17, 2017
The Arabidopsis SWI/SNF protein BAF60 mediates seedling growth control by modulating DNA accessibilityTeddy Jégu, Alaguraj Veluchamy, Juan S Ramirez-Prado, et al.
Nucleic Acids Research|July 21, 2006
An open-access long oligonucleotide microarray resource for analysis of the human and mouse transcriptomesKévin Le Brigand, Roslin Russell, Chimène Moreilhon, et al.
European Journal of Human Genetics : EJHG|October 31, 2013
20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognitionAmélie Piton, Hélène Poquet, Claire Redin, et al.
European Journal of Human Genetics : EJHG|February 9, 2017
Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndromeAngélique Quartier, Hélène Poquet, Brigitte Gilbert-Dussardier, et al.
Nature Communications|April 12, 2016
Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophyFernande Freyermuth, Frédérique Rau, Yosuke Kokunai, et al.
Journal of Medical Genetics|August 30, 2014
Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencingClaire Redin, Bénédicte Gérard, Julia Lauer, et al.
Nature Communications|October 31, 2019
Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3Rahel T Florian, Florian Kraft, Elsa Leitão, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
The Journal of Experimental Medicine|August 30, 2021
Helios represses megakaryocyte priming in hematopoietic stem and progenitor cellsGiovanni Cova, Chiara Taroni, Marie-Céline Deau, et al.
Plos One|July 5, 2013
An integrated diagnosis strategy for congenital myopathiesJohann Böhm, Nasim Vasli, Edoardo Malfatti, et al.
Nature Structural & Molecular Biology|June 21, 2011
Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophyFrédérique Rau, Fernande Freyermuth, Charlotte Fugier, et al.
Genome Biology|June 17, 2017
The Arabidopsis SWI/SNF protein BAF60 mediates seedling growth control by modulating DNA accessibilityTeddy Jégu, Alaguraj Veluchamy, Juan S Ramirez-Prado, et al.
Nucleic Acids Research|July 21, 2006
An open-access long oligonucleotide microarray resource for analysis of the human and mouse transcriptomesKévin Le Brigand, Roslin Russell, Chimène Moreilhon, et al.
European Journal of Human Genetics : EJHG|October 31, 2013
20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognitionAmélie Piton, Hélène Poquet, Claire Redin, et al.
European Journal of Human Genetics : EJHG|February 9, 2017
Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndromeAngélique Quartier, Hélène Poquet, Brigitte Gilbert-Dussardier, et al.
Nature Communications|April 12, 2016
Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophyFernande Freyermuth, Frédérique Rau, Yosuke Kokunai, et al.
Journal of Medical Genetics|August 30, 2014
Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencingClaire Redin, Bénédicte Gérard, Julia Lauer, et al.
Nature Communications|October 31, 2019
Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3Rahel T Florian, Florian Kraft, Elsa Leitão, et al.
Pageof 5