المؤلفون: Portilho, Débora, Ribeiro Alves, Marcelo, Kratassiouk, Gueorgui, Roche, Stéphane, Magdinier, Frédérique, Corrêa de Santana, Eliane, Polesskaya, Anna, Harel-Bellan, Annick, Mouly, Vincent, Savino, Wilson, Butler-Browne, Gillian, Dumonceaux, Julie

المساهمون: Centre de recherche en myologie, Université Pierre et Marie Curie - Paris 6 (UPMC)-Association française contre les myopathies (AFM-Téléthon)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Laboratory on Thymus Research - Department of Immunology / Laboratório de Pesquisas sobre o Timo - Departamento de Imunologia Rio de Janeiro, Instituto Oswaldo Cruz = Oswaldo Cruz Institute Rio de Janeiro (IOC), Fundação Oswaldo Cruz / Oswaldo Cruz Foundation (FIOCRUZ), Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Fundação Oswaldo Cruz / Oswaldo Cruz Foundation (FIOCRUZ), Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Laboratório de Pesquisa Clínica em DST e AIDS Rio de Janeiro, Instituto Nacional de Infectologia Evandro Chagas Rio de Janeiro (INI), Génétique moléculaire et destin cellulaire (FRE 3377), Université Paris-Sud - Paris 11 (UP11)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Centre National de la Recherche Scientifique (CNRS), Génétique Médicale et Génomique Fonctionnelle (GMGF), Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)-Hôpital de la Timone CHU - APHM (TIMONE)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)

المصدر: ISSN: 1932-6203.

مصطلحات موضوعية: FSHD, D4Z4, Differentiation, Target genes, Skeletal muscle, Hypertrophy, Disease, MicroRNA, Location, Myoblast, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, [SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology, [SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN]

العلاقة: hal-01219803; https://amu.hal.science/hal-01219803Test; https://amu.hal.science/hal-01219803/documentTest; https://amu.hal.science/hal-01219803/file/fetchObject.pdfTest

الإتاحة: https://doi.org/10.1371/journal.pone.0116853Test
https://amu.hal.science/hal-01219803Test
https://amu.hal.science/hal-01219803/documentTest
https://amu.hal.science/hal-01219803/file/fetchObject.pdfTest

المؤلفون: Caruso, Nathalie, Herberth, Balàzs, Bartoli, Marc, Puppo, Francesca, Dumonceaux, Julie, Zimmermann, Angela, Denadai, Simon, Lebossé, Marie, Roche, Stephane, Geng, Linda, Magdinier, Frédérique, Attarian, Shahram, Bernard, Rafaelle, Maina, Flavio, Lévy, Nicolas, Helmbacher, Françoise

المساهمون: Institut de Biologie du Développement de Marseille (IBDM), Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS), Génétique Médicale et Génomique Fonctionnelle (GMGF), Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone CHU - APHM (TIMONE)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Thérapie des maladies du muscle strié, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)

المصدر: ISSN: 1553-7390.

مصطلحات موضوعية: FAT1-protocadherin, Facioscapulohumeral dystrophy, Development, FSHD, MESH: Adult, MESH: Animals, MESH: Organ Specificity, MESH: Cadherins, MESH: Cell Differentiation, MESH: Cells, Cultured, MESH: Humans, MESH: Mice, MESH: Muscle Development, MESH: Muscles, MESH: Muscular Dystrophy, Facioscapulohumeral, MESH: Myoblasts, MESH: Oligonucleotide Array Sequence Analysis, [SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN]

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23785297; hal-00862092; https://hal.science/hal-00862092Test; https://hal.science/hal-00862092/documentTest; https://hal.science/hal-00862092/file/journal.pgen.1003550.PDFTest; PUBMED: 23785297

الإتاحة: https://doi.org/10.1371/journal.pgen.1003550Test
https://hal.science/hal-00862092Test
https://hal.science/hal-00862092/documentTest
https://hal.science/hal-00862092/file/journal.pgen.1003550.PDFTest

المؤلفون: Absorn Sriratana, Christina Anne Mitchell, Stefan M. Gehrig, Colleen Elizabeth D'Arcy, Gordon S. Lynch, Meagan Jane Mcgrath, Sandra J Feeney, Catriona McLean, Rossella Tupler, John T. Price

المصدر: PLoS ONE
PLoS ONE, Vol 10, Iss 2, p e0117665 (2015)

مصطلحات موضوعية: muscular dystrophy, Male, FSHD region gene 1, FHL1, mouse model, Science, Gene Expression, Muscle Proteins, Mice, Transgenic, Biology, Muscle Development, Myotonic dystrophy, Cell Line, Myoblasts, Myoblast fusion, Mice, DUX4, medicine, Facioscapulohumeral muscular dystrophy, Animals, Humans, Muscular dystrophy, Muscle, Skeletal, Genetics, Multidisciplinary, Microfilament Proteins, Intracellular Signaling Peptides and Proteins, Dystrophy, Nuclear Proteins, RNA-Binding Proteins, LIM Domain Proteins, medicine.disease, musculoskeletal system, Fibrosis, Muscular Dystrophy, Facioscapulohumeral, Cell biology, transgenic mouse, Medicine, Female, C2C12, muscular dystrophy, mouse model, FSHD region gene 1, FHL1, transgenic mouse, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::972362df3395f9a9c97edf79ad832872Test
http://europepmc.org/articles/PMC4335040Test