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Alain Lescure

Showing results (11-20 of 25) with videos related to

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Experimental Cell Research|November 25, 2006
Loss of selenoprotein N function causes disruption of muscle architecture in the zebrafish embryoMarzanna Deniziak, Christine Thisse, Mathieu Rederstorff, et al.
Human Molecular Genetics|April 18, 2003
Selenoprotein N: an endoplasmic reticulum glycoprotein with an early developmental expression patternNathalie Petit, Alain Lescure, Mathieu Rederstorff, et al.
BMC Developmental Biology|August 25, 2009
Selenoprotein N is dynamically expressed during mouse development and detected early in muscle precursorsPerrine Castets, Svetlana Maugenre, Corine Gartioux, et al.
EMBO Reports|January 8, 2004
Reconsidering the evolution of eukaryotic selenoproteins: a novel nonmammalian family with scattered phylogenetic distributionSergi Castellano, Sergey V Novoselov, Gregory V Kryukov, et al.
Biochemistry|August 31, 2010
Compartmentalization and regulation of mitochondrial function by methionine sulfoxide reductases in yeastAlaattin Kaya, Ahmet Koc, Byung Cheon Lee, et al.
Gene Expression Patterns : GEP|August 14, 2003
Spatial and temporal expression patterns of selenoprotein genes during embryogenesis in zebrafishChristine Thisse, Agnès Degrave, Gregory V Kryukov, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 2, 2005
Diversity and functional plasticity of eukaryotic selenoproteins: identification and characterization of the SelJ familySergi Castellano, Alexey V Lobanov, Charles Chapple, et al.
EMBO Reports|February 25, 2006
A single homozygous point mutation in a 3'untranslated region motif of selenoprotein N mRNA causes SEPN1-related myopathyValérie Allamand, Pascale Richard, Alain Lescure, et al.
Plos One|August 23, 2011
Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathyMathieu Rederstorff, Perrine Castets, Sandrine Arbogast, et al.
Human Molecular Genetics|December 7, 2010
Satellite cell loss and impaired muscle regeneration in selenoprotein N deficiencyPerrine Castets, Anne T Bertrand, Maud Beuvin, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Experimental Cell Research|November 25, 2006
Loss of selenoprotein N function causes disruption of muscle architecture in the zebrafish embryoMarzanna Deniziak, Christine Thisse, Mathieu Rederstorff, et al.
Human Molecular Genetics|April 18, 2003
Selenoprotein N: an endoplasmic reticulum glycoprotein with an early developmental expression patternNathalie Petit, Alain Lescure, Mathieu Rederstorff, et al.
BMC Developmental Biology|August 25, 2009
Selenoprotein N is dynamically expressed during mouse development and detected early in muscle precursorsPerrine Castets, Svetlana Maugenre, Corine Gartioux, et al.
EMBO Reports|January 8, 2004
Reconsidering the evolution of eukaryotic selenoproteins: a novel nonmammalian family with scattered phylogenetic distributionSergi Castellano, Sergey V Novoselov, Gregory V Kryukov, et al.
Biochemistry|August 31, 2010
Compartmentalization and regulation of mitochondrial function by methionine sulfoxide reductases in yeastAlaattin Kaya, Ahmet Koc, Byung Cheon Lee, et al.
Gene Expression Patterns : GEP|August 14, 2003
Spatial and temporal expression patterns of selenoprotein genes during embryogenesis in zebrafishChristine Thisse, Agnès Degrave, Gregory V Kryukov, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 2, 2005
Diversity and functional plasticity of eukaryotic selenoproteins: identification and characterization of the SelJ familySergi Castellano, Alexey V Lobanov, Charles Chapple, et al.
EMBO Reports|February 25, 2006
A single homozygous point mutation in a 3'untranslated region motif of selenoprotein N mRNA causes SEPN1-related myopathyValérie Allamand, Pascale Richard, Alain Lescure, et al.
Plos One|August 23, 2011
Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathyMathieu Rederstorff, Perrine Castets, Sandrine Arbogast, et al.
Human Molecular Genetics|December 7, 2010
Satellite cell loss and impaired muscle regeneration in selenoprotein N deficiencyPerrine Castets, Anne T Bertrand, Maud Beuvin, et al.
Pageof 3