المؤلفون: Sabrina Sacconi, Leonardo Salviati, Claude Desnuelle

المساهمون: Institut de Biologie Valrose (IBV), Université Nice Sophia Antipolis (... - 2019) (UNS), COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Côte d'Azur (UCA)

المصدر: BBA-Biochimica et Biophysica Acta
BBA-Biochimica et Biophysica Acta, Elsevier, 2015, 1852 (4), pp.607-614

مصطلحات موضوعية: DUX4, Chromosomal Proteins, Non-Histone, Apoptosis, Repetitive Sequences, Muscular Dystrophies, Epigenesis, Genetic, 0302 clinical medicine, Facioscapulohumeral muscular dystrophy, [SDV.BDD]Life Sciences [q-bio]/Development Biology, ComputingMilieux_MISCELLANEOUS, Genetics, 0303 health sciences, DNA methylation, Subtelomere, Chromatin, 3. Good health, Chromosomal Proteins, Pair 4, Genetic Diseases, Molecular Medicine, Epigenetics, Chromosomes, Human, Pair 4, Human, musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, Locus (genetics), Biology, Chromosomes, 03 medical and health sciences, Prophase, Genetic, Subtelomeric repeat, medicine, Animals, Humans, Allele, Molecular Biology, Alleles, 030304 developmental biology, Repetitive Sequences, Nucleic Acid, Homeodomain Proteins, Nucleic Acid, SMCHD1, Genetic Diseases, Inborn, Non-Histone, medicine.disease, Chromatin Assembly and Disassembly, Inborn, Genetic Loci, Mutation, 030217 neurology & neurosurgery, Epigenesis

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::732b8f65d06151b4f77d8617ca84e446Test
https://pubmed.ncbi.nlm.nih.gov/24882751Test

المؤلفون: Douglass M. Turnbull, A. Saunières, B. Mousson de Camaret, Véronique Paquis-Flucklinger, B. Vialettes, Claude Desnuelle, H. Narbonne, D. Perucca-Lostanlen, Robert W. Taylor, C Hayes

المصدر: Biochimica et biophysica acta. 1588(3)

مصطلحات موضوعية: Mitochondrial DNA, Genotype, Mutant, Respiratory chain, Biology, Mitochondrion, Deafness, DNA, Mitochondrial, Cell Fusion, Diabetes Complications, 03 medical and health sciences, Diabetes mellitus genetics, Electron Transport Complex III, 0302 clinical medicine, Multienzyme Complexes, Diabetes Mellitus, Humans, Point Mutation, NADH, NADPH Oxidoreductases, Mitochondrial diabetes, Molecular Biology, Transmitochondrial cybrid, 030304 developmental biology, Genetics, 0303 health sciences, Homoplasmy, Electron Transport Complex I, Base Sequence, Point mutation, Electron Transport Complex II, Fibroblasts, Blotting, Northern, Molecular biology, Heteroplasmy, RNA, Transfer, Glu, Clone Cells, Succinate Dehydrogenase, Molecular Medicine, Oxidoreductases, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93d57488e5e143ad1c6b4ea6a8969579Test
https://pubmed.ncbi.nlm.nih.gov/12393175Test