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1دورية أكاديمية
المؤلفون: Chau, Jonathan, Kong, Xiangduo, Nguyen, Nam, Williams, Katherine, Ball, Miya, Tawil, Rabi, Kiyono, Tohru, Mortazavi, Ali, Yokomori, Kyoko
المصدر: Human Mutation. 42(4)
مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Rare Diseases, Muscular Dystrophy, Intellectual and Developmental Disabilities (IDD), Brain Disorders, Biotechnology, Facioscapulohumeral Muscular Dystrophy, Cell Nucleus, Gene Expression, Gene Expression Regulation, Homeodomain Proteins, Humans, Muscle Fibers, Skeletal, Muscle, Skeletal, Muscular Dystrophy, Facioscapulohumeral, DUX4, FSHD, KDM4E, LEUTX, RNAScope, skeletal myotubes, Clinical Sciences, Genetics & Heredity, Clinical sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/2z3611rpTest
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2دورية أكاديمية
المؤلفون: Moyle, Louise A, Blanc, Eric, Jaka, Oihane, Prueller, Johanna, Banerji, Christopher Rs, Tedesco, Francesco Saverio, Harridge, Stephen Dr, Knight, Robert D, Zammit, Peter S
المصدر: eLife. 5(NOVEMBER2016)
مصطلحات موضوعية: Muscles, Cells, Cultured, Myoblasts, Satellite Cells, Skeletal Muscle, Animals, Humans, Mice, Muscular Dystrophy, Facioscapulohumeral, Pyrroles, Indoles, Homeodomain Proteins, Enzyme Inhibitors, Cell Differentiation, Cell Proliferation, Gene Expression, Proto-Oncogene Proteins c-ret, Sunitinib, DUX4, FSHD, RET, cell biology, facioscapulohumeral muscular dystrophy, human, human biology, medicine, mouse, therapy, Biochemistry and Cell Biology
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/9n46f1r1Test
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المؤلفون: Julie Dumonceaux, William Duddy, Romain Joubert, Maximilien Bencze, Laura Le Gall, Thomas Voit, Virginie Mariot, Eva Sidlauskaite, Christophe Hourdé
المصدر: Journal of Cachexia, Sarcopenia and Muscle, Vol 12, Iss 6, Pp 2079-2090 (2021)
Journal of Cachexia, Sarcopenia and Muscleمصطلحات موضوعية: Programmed cell death, Necrosis, DUX4, Necroptosis, Muscle Fibers, Skeletal, Diseases of the musculoskeletal system, Facioscapulohumeral dystrophy, Myoblasts, Mice, Physiology (medical), medicine, Animals, Myocyte, Orthopedics and Sports Medicine, Ripk3, Transcription factor, Homeodomain Proteins, FSHD, Cell Death, business.industry, Myogenesis, QM1-695, Dystrophy, Original Articles, Muscular Dystrophy, Facioscapulohumeral, RC925-935, Receptor-Interacting Protein Serine-Threonine Kinases, Human anatomy, Cancer research, Original Article, medicine.symptom, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::075fc9e33c1a08fbd00487bd0e73361dTest
https://doi.org/10.1002/jcsm.12813Test -
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المؤلفون: Rabi Tawil, Leo H. Wang
المصدر: Journal of Neuromuscular Diseases
مصطلحات موضوعية: musculoskeletal diseases, 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, Review, Bioinformatics, outcome measures, 03 medical and health sciences, 0302 clinical medicine, DUX4, Humans, Medicine, Facioscapulohumeral muscular dystrophy, Muscle, Skeletal, Homeodomain Proteins, facioscapulohumeral dystrophy (FSHD), business.industry, Mechanism (biology), Outcome measures, medicine.disease, Muscular Dystrophy, Facioscapulohumeral, nervous system diseases, Clinical trial, 030104 developmental biology, Muscle disease, Neurology, Drug development, Underlying disease, muscle disease, Neurology (clinical), business, 030217 neurology & neurosurgery, All neuromuscular disease
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31ec4b4e0889a0047e4f84df7bfc1646Test
https://doi.org/10.3233/jnd-200554Test -
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المؤلفون: Takako I. Jones, Andreia M Nunes, M. O. Ramírez, Peter L. Jones
المصدر: Disease Models & Mechanisms, Vol 14, Iss 8 (2021)
Disease Models & Mechanisms
article-version (VoR) Version of Recordمصطلحات موضوعية: musculoskeletal diseases, Genetically modified mouse, Neuromuscular Disease Models, congenital, hereditary, and neonatal diseases and abnormalities, Neuroscience (miscellaneous), Medicine (miscellaneous), Biology, Skeletal Myocytes, Bioinformatics, General Biochemistry, Genetics and Molecular Biology, fshd, Mice, Immunology and Microbiology (miscellaneous), DUX4, microRNA, dux4, Pathology, medicine, Animals, Humans, RB1-214, Facioscapulohumeral muscular dystrophy, Muscle, Skeletal, Homeodomain Proteins, Skeletal muscle, medicine.disease, Phenotype, Muscular Dystrophy, Facioscapulohumeral, nervous system diseases, MicroRNAs, medicine.anatomical_structure, biomarker, Medicine, Biomarker (medicine), mir-206, Biomarkers, Research Article, mirna
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc6f431a5b82fa0033d275635b0deaadTest
https://doi.org/10.1242/dmm.049016Test -
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المؤلفون: E. N. Popova, Anna Karpukhina, Ivan I. Galkin, Carla Dib, Olga Pletjushkina, Yinxing Ma, Roman A. Zinovkin, Boris V. Chernyak, Yegor S. Vassetzky
المساهمون: Aspects métaboliques et systémiques de l'oncogénèse pour de nouvelles approches thérapeutiques (METSY), Institut Gustave Roussy (IGR)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Koltzov Institute of Developmental Biology, the Russian Academy of Sciences [Moscow, Russia] (RAS), Lomonosov Moscow State University (MSU), Belozersky Institute of Physico-Chemical Biology
المصدر: Redox Biology, Vol 43, Iss, Pp 102008-(2021)
Redox Biology
Redox Biology, Elsevier, 2021, 43, pp.102008. ⟨10.1016/j.redox.2021.102008⟩مصطلحات موضوعية: 0301 basic medicine, Mitochondrial ROS, Medicine (General), DUX4, QH301-705.5, Short Communication, Clinical Biochemistry, Biology, medicine.disease_cause, Biochemistry, Transcriptome, Myoblasts, 03 medical and health sciences, 0302 clinical medicine, R5-920, Downregulation and upregulation, [SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], medicine, Myocyte, Gene silencing, Humans, Biology (General), PITX1, Muscle differentiation, Homeodomain Proteins, FSHD, Organic Chemistry, Dystrophy, Cell Differentiation, Muscular Dystrophy, Facioscapulohumeral, 3. Good health, Cell biology, 030104 developmental biology, Oxidative stress, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0614c56056daeefe87ccc767ebdd5b62Test
http://www.sciencedirect.com/science/article/pii/S221323172100166XTest -
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المؤلفون: Karpukhina, Anna, Tiukacheva, Eugenia, Dib, Carla, Vassetzky, Yegor, Dokudovskaya, Svetlana
المساهمون: Aspects métaboliques et systémiques de l'oncogénèse pour de nouvelles approches thérapeutiques (METSY), Institut Gustave Roussy (IGR)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)
المصدر: Trends in Molecular Medicine
Trends in Molecular Medicine, Elsevier, 2021, 27 (6), pp.588-601. ⟨10.1016/j.molmed.2021.03.008⟩مصطلحات موضوعية: 0301 basic medicine, musculoskeletal diseases, sarcoma, DUX4, Manuscript Click here to access/download, [SDV]Life Sciences [q-bio], DUX4 regulation R1.docx, medicine.disease_cause, Epigenesis, Genetic, 03 medical and health sciences, 0302 clinical medicine, Neoplasms, medicine, Facioscapulohumeral muscular dystrophy, Humans, Epigenetics, Gene Silencing, Molecular Targeted Therapy, Molecular Biology, Genetics, Regulation of gene expression, Homeodomain Proteins, FSHD, biology, epigenetics, leukemia, DNA Methylation, Subtelomere, medicine.disease, Muscular Dystrophy, Facioscapulohumeral, 3. Good health, Manuscript, 030104 developmental biology, Histone, Gene Expression Regulation, DNA methylation, biology.protein, Molecular Medicine, Carcinogenesis, gene regulation, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb2ed468da373e21f06f184f3ddb2627Test
https://hal.archives-ouvertes.fr/hal-03375995Test -
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المؤلفون: Christopher R. S. Banerji, Peter S. Zammit
المصدر: EMBO Molecular Medicine
EMBO Molecular Medicine, Vol 13, Iss 8, Pp n/a-n/a (2021)مصطلحات موضوعية: 0301 basic medicine, musculoskeletal diseases, Medicine (General), congenital, hereditary, and neonatal diseases and abnormalities, DUX4, Gene Expression, Review, QH426-470, Biology, 03 medical and health sciences, R5-920, 0302 clinical medicine, Genetics, medicine, Facioscapulohumeral muscular dystrophy, Humans, Epigenetics, Transcription factor, Musculoskeletal System, Homeodomain Proteins, Myogenesis, PAX7 Transcription Factor, Subtelomere, medicine.disease, Muscular Dystrophy, Facioscapulohumeral, PAX7, 030104 developmental biology, Gene Expression Regulation, facioscapulohumeral muscular dystrophy (FSHD), Molecular Medicine, Biomarker (medicine), biomarker, pathology, Genetics, Gene Therapy & Genetic Disease, 030217 neurology & neurosurgery, Biomarkers
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::803fa659628223e36d078d9fe386c60fTest
https://pubmed.ncbi.nlm.nih.gov/34151531Test -
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المؤلفون: Teresa Schätzl, Lars Kaiser, Hans-Peter Deigner
المساهمون: Publica
المصدر: Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-26 (2021)مصطلحات موضوعية: 0301 basic medicine, musculoskeletal diseases, Transcriptional Activation, Downstream signalling, lcsh:Medicine, Context (language use), Review, Biology, Facioscapulohumeral muscular dystrophy (FSHD), 03 medical and health sciences, 0302 clinical medicine, DUX4, Double Homeobox 4 (DUX4), medicine, Facioscapulohumeral muscular dystrophy, Humans, Pharmacology (medical), Epigenetics, Muscle, Skeletal, Gene, Genetics (clinical), Genetics, Regulation of gene expression, Homeodomain Proteins, lcsh:R, Epigenetic, General Medicine, medicine.disease, Human genetics, Muscular Dystrophy, Facioscapulohumeral, 030104 developmental biology, Ectopic expression, 030217 neurology & neurosurgery, Treatment strategies, Signal Transduction
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ca0b83582d7eab95f54f726e0b16734Test
http://europepmc.org/articles/PMC7953708Test -
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المؤلفون: Aiping Zhang, Jyoti K. Jaiswal, James S. Novak, Yi-Wen Chen, Adam Horn, Adam J. Bittel, Daniel C. Bittel, Sen Chandra Sreetama, Rika Maruyama, Toshifumi Yokota, Kenji Rowel Q. Lim
المصدر: International Journal of Molecular Sciences
Volume 21
Issue 15
International Journal of Molecular Sciences, Vol 21, Iss 5575, p 5575 (2020)مصطلحات موضوعية: Male, 0301 basic medicine, antisense oligonucleotide, antioxidant, DUX4, muscle, Duchenne muscular dystrophy, Muscle Fibers, Skeletal, Antioxidants, Myoblasts, lcsh:Chemistry, Mice, 0302 clinical medicine, Myofibrils, Myocyte, Facioscapulohumeral muscular dystrophy, lcsh:QH301-705.5, membrane, Cells, Cultured, Spectroscopy, gapmer, General Medicine, Middle Aged, Muscular Dystrophy, Facioscapulohumeral, Computer Science Applications, Female, medicine.symptom, Adult, musculoskeletal diseases, Dysferlinopathy, congenital, hereditary, and neonatal diseases and abnormalities, myofiber, Article, Catalysis, Inorganic Chemistry, 03 medical and health sciences, medicine, Animals, Humans, Physical and Theoretical Chemistry, Myopathy, Molecular Biology, MOE, Aged, Homeodomain Proteins, FSHD, Sarcolemma, business.industry, Cell Membrane, Organic Chemistry, Plasma membrane repair, Oligonucleotides, Antisense, medicine.disease, Oxidative Stress, 030104 developmental biology, Gene Expression Regulation, lcsh:Biology (General), lcsh:QD1-999, repair, Cancer research, myoblast, business, 030217 neurology & neurosurgery
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8009681e7d6a248c8bed3e0a237f5308Test