Canlyniadau Chwilio - Gisèle Bonne

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  1. 1
    Emery–Dreifuss muscular dystrophy, laminopathies, and other nuclear envelopathies

    Emery–Dreifuss muscular dystrophy, laminopathies, and other nuclear envelopathies gan Gisèle Bonne, Susana Quijano-Roy

    Cyhoeddwyd 2013
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    Revisão
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  2. 2
    “Laminopathies”: A wide spectrum of human diseases

    “Laminopathies”: A wide spectrum of human diseases gan Howard J. Worman, Gisèle Bonne

    Cyhoeddwyd 2007
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    Revisão
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  3. 3
    Emery-Dreifuss muscular dystrophy

    Emery-Dreifuss muscular dystrophy gan A. Leclerc, Gisèle Bonne, Ketty Schwartz

    Cyhoeddwyd 2002
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  4. 4
    The 2018 version of the gene table of monogenic neuromuscular disorders (nuclear genome)

    The 2018 version of the gene table of monogenic neuromuscular disorders (nuclear genome) gan Gisèle Bonne, François Rivier, Dalil Hamroun

    Cyhoeddwyd 2017
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    Artigo
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  5. 5
    Targeted therapies for congenital myasthenic syndromes: systematic review and steps towards a treatabolome

    Targeted therapies for congenital myasthenic syndromes: systematic review and steps towards a treatabolome gan Rachel Thompson, Gisèle Bonne, Paolo Missier, Hanns Lochmüller

    Cyhoeddwyd 2019
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  6. 6
    The 2020 version of the gene table of neuromuscular disorders (nuclear genome)

    The 2020 version of the gene table of neuromuscular disorders (nuclear genome) gan Louise Benarroch, Gisèle Bonne, François Rivier, Dalil Hamroun

    Cyhoeddwyd 2019
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  7. 7
    The 2021 version of the gene table of neuromuscular disorders (nuclear genome)

    The 2021 version of the gene table of neuromuscular disorders (nuclear genome) gan Louise Benarroch, Gisèle Bonne, François Rivier, Dalil Hamroun

    Cyhoeddwyd 2020
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    Artigo
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  8. 8
    The 2022 version of the gene table of neuromuscular disorders (nuclear genome)

    The 2022 version of the gene table of neuromuscular disorders (nuclear genome) gan Enzo Cohen, Gisèle Bonne, François Rivier, Dalil Hamroun

    Cyhoeddwyd 2021
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    Artigo
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  9. 9
    The 2023 version of the gene table of neuromuscular disorders (nuclear genome)

    The 2023 version of the gene table of neuromuscular disorders (nuclear genome) gan Louise Benarroch, Gisèle Bonne, François Rivier, Dalil Hamroun

    Cyhoeddwyd 2022
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  10. 10
    The 2024 version of the gene table of neuromuscular disorders (nuclear genome)

    The 2024 version of the gene table of neuromuscular disorders (nuclear genome) gan Louise Benarroch, Gisèle Bonne, François Rivier, Dalil Hamroun

    Cyhoeddwyd 2023
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    Artigo
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  11. 11
    Expression of human cytochrome <i>c</i>, oxidase subunits during fetal development

    Expression of human cytochrome <i>c</i>, oxidase subunits during fetal development gan Gisèle Bonne, Peter Seibel, Stefanie Possekel, C. Marsac, Bernhard Kadenbach

    Cyhoeddwyd 1993
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  12. 12
    Mitogen-Activated Protein Kinase Inhibitors Improve Heart Function and Prevent Fibrosis in Cardiomyopathy Caused by Mutation in Lamin A/C Gene

    Mitogen-Activated Protein Kinase Inhibitors Improve Heart Function and Prevent Fibrosis in Cardiomyopathy Caused by Mutation in Lamin A/C Gene gan Wei Wu, Antoine Muchir, Jian Shan, Gisèle Bonne, Howard J. Worman

    Cyhoeddwyd 2010
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    Artigo
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  13. 13
    Pharmacological inhibition of c-Jun N-terminal kinase signaling prevents cardiomyopathy caused by mutation in LMNA gene

    Pharmacological inhibition of c-Jun N-terminal kinase signaling prevents cardiomyopathy caused by mutation in LMNA gene gan Wei Wu, Jian Shan, Gisèle Bonne, Howard J. Worman, Antoine Muchir

    Cyhoeddwyd 2010
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  14. 14
    Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant Emery–Dreifuss muscular dystrophy

    Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant Emery–Dreifuss muscular dystrophy gan Antoine Muchir, Paul Pavlidis, Gisèle Bonne, Yukiko Hayashi, Howard J. Worman

    Cyhoeddwyd 2007
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    Artigo
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  15. 15
    Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins

    Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins gan Antoine Muchir, Jing Shan, Gisèle Bonne, Stephan E. Lehnart, Howard J. Worman

    Cyhoeddwyd 2008
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    Artigo
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  16. 16
    ColVI myopathies: where do we stand, where do we go?

    ColVI myopathies: where do we stand, where do we go? gan Valérie Allamand, Laura Briñas, Pascale Richard, Tanya Stojkovic, Susana Quijano‐Roy, Gisèle Bonne

    Cyhoeddwyd 2011
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    Artigo
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  17. 17
    Autophagic degradation of nuclear components in mammalian cells

    Autophagic degradation of nuclear components in mammalian cells gan Young-Eun Park, Yukiko Hayashi, Gisèle Bonne, Takuro Arimura, S. Noguchi, Ikuya Nonaka, Ichizo Nishino

    Cyhoeddwyd 2009
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    Artigo
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  18. 18
    Primary Prevention of Sudden Death in Patients with Lamin A/C Gene Mutations

    Primary Prevention of Sudden Death in Patients with Lamin A/C Gene Mutations gan Christophe Meune, Jop H. van Berlo, Frédéric Anselme, Gisèle Bonne, Yigal M. Pinto, Denis Duboc

    Cyhoeddwyd 2006
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    Carta
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  19. 19
    Targeting the histone demethylase LSD1 prevents cardiomyopathy in a mouse model of laminopathy

    Targeting the histone demethylase LSD1 prevents cardiomyopathy in a mouse model of laminopathy gan Anne-Claire Guénantin, Imen Jebeniani, Julia Leschik, Erwan Watrin, Gisèle Bonne, Nicolas Vignier, Michel Pucéat

    Cyhoeddwyd 2021
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  20. 20
    Treatment with selumetinib preserves cardiac function and improves survival in cardiomyopathy caused by mutation in the lamin A/C gene

    Treatment with selumetinib preserves cardiac function and improves survival in cardiomyopathy caused by mutation in the lamin A/C gene gan Antoine Muchir, Sarah A Reilly, W. Wu, Shinichi Iwata, Shunichi Homma, Gisèle Bonne, Howard J. Worman

    Cyhoeddwyd 2011
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    Artigo
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