Canlyniadau Chwilio - Jean‐Claude KAPLAN

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  1. 1
    The 2014 version of the gene table of monogenic neuromuscular disorders (nuclear genome)

    The 2014 version of the gene table of monogenic neuromuscular disorders (nuclear genome) gan Jean‐Claude Kaplan, Dalil Hamroun

    Cyhoeddwyd 2013
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    Artigo
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  2. 2
    The 2015 version of the gene table of monogenic neuromuscular disorders (nuclear genome)

    The 2015 version of the gene table of monogenic neuromuscular disorders (nuclear genome) gan Jean‐Claude Kaplan, Dalil Hamroun

    Cyhoeddwyd 2014
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    Artigo
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  3. 3
    Illegitimate transcription: Its use in the study of inherited disease

    Illegitimate transcription: Its use in the study of inherited disease gan Jean-Claude Kaplan, Axel Kahn, Jamel Chelly

    Cyhoeddwyd 1992
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    Revisão
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  4. 4
    2,3-Diphosphoglycerate Content and Oxygen Affinity as a Function of Red Cell Age in Normal Individuals

    2,3-Diphosphoglycerate Content and Oxygen Affinity as a Function of Red Cell Age in Normal Individuals gan Stavros Haidas, Dominique Labie, Jean‐Claude Kaplan

    Cyhoeddwyd 1971
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  5. 5
    Quantitative estimation of minor mRNAs by cDNA‐polymerase chain reaction

    Quantitative estimation of minor mRNAs by cDNA‐polymerase chain reaction gan Jamel Chelly, Didier Montarras, Christian Pinset, Yoheved Berwald‐Netter, Jean‐Claude KAPLAN, Axel Kahn

    Cyhoeddwyd 1990
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  6. 6
    Rescue of Dystrophic Muscle Through U7 snRNA-Mediated Exon Skipping

    Rescue of Dystrophic Muscle Through U7 snRNA-Mediated Exon Skipping gan Aurélie Goyenvalle, Adeline Vulin, Françoise Fougerousse, France Leturcq, Jean‐Claude Kaplan, Luis Garcı́a, Olivier Danos

    Cyhoeddwyd 2004
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    Artigo
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  7. 7
    Assessment of the structural and functional impact of in-frame mutations of the DMD gene, using the tools included in the eDystrophin online database

    Assessment of the structural and functional impact of in-frame mutations of the DMD gene, using the tools included in the eDystrophin online database gan Aurélie Nicolas, Céline Lucchetti-Miganeh, Rabah Ben Yaou, Jean‐Claude Kaplan, Jamel Chelly, France Leturcq, Frédérique Barloy-Hubler, Élisabeth Le Rumeur

    Cyhoeddwyd 2012
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  8. 8
    Revised spectrum of mutations in sarcoglycanopathies

    Revised spectrum of mutations in sarcoglycanopathies gan Madiha Trabelsi, Niloufar Kavian, Fatma Daoud, Virginie Commere, Nathalie Deburgrave, Caroline Beugnet, S. Llense, Jean Claude Barbot, Aurélie Vasson, Jean Claude Kaplan, France Leturcq, Jamel Chelly

    Cyhoeddwyd 2008
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  9. 9
    Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene

    Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene gan Nathalie Deburgrave, Fatma Daoud, S. Llense, Jean Claude Barbot, Dominique Récan, Cécile Peccate, Arthur H.M. Burghes, Christophe Béroud, Luis Garcı́a, Jean‐Claude Kaplan, Jamel Chelly, France Leturcq

    Cyhoeddwyd 2006
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  10. 10
    Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase

    Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase gan Sylvie Tuffery‐Giraud, Christophe Béroud, France Leturcq, Rabah Ben Yaou, Dalil Hamroun, Laurence Michel‐Calemard, Marie‐Pierre Moizard, Rafaëlle Bernard, Mireille Cossée, Pierre Boisseau, Martine Blayau, Isabelle Creveaux, Anne Guiochon‐Mantel, Bérengère de Martinville, Christophe Philippe, Nicole Monnier, Éric Bieth, Philippe Khau Van Kien, François-Olivier Desmet, Véronique Humbertclaude, Jean‐Claude Kaplan, Jamel Chelly, Mireille Claustres

    Cyhoeddwyd 2009
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    Artigo
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