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المؤلفون: Camille Laberthonnière, Marie-Cécile Gaillard, Natacha Broucqsault, Cherif Badja, Stéphane Roche, Jérôme D. Robin, Julia Morere, Karine Nguyen, Frédérique Magdinier, Camille Dion
المساهمون: Marseille medical genetics - Centre de génétique médicale de Marseille (MMG), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM)
المصدر: Scientific Reports
Scientific Reports, Nature Publishing Group, 2019, ⟨10.1038/s41598-019-46861-x⟩
Scientific Reports, 2019, 1, ⟨10.1038/s41598-019-46861-x⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-15 (2019)مصطلحات موضوعية: Male, Chromosomal Proteins, Non-Histone, [SDV.NEU.NB]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology, Gene Expression, lcsh:Medicine, Diseases, Pathogenesis, [SDV.BC.BC]Life Sciences [q-bio]/Cellular Biology/Subcellular Processes [q-bio.SC], 0302 clinical medicine, Gene expression, lcsh:Science, In Situ Hybridization, Fluorescence, Genetics, 0303 health sciences, Middle Aged, Cadherins, Subtelomere, Chromatin, Muscular Dystrophy, Facioscapulohumeral, Epigenetics, Female, Chromosomes, Human, Pair 4, Adult, Adolescent, Induced Pluripotent Stem Cells, Locus (genetics), Biology, Chromatin structure, Article, Young Adult, 03 medical and health sciences, Imaging, Three-Dimensional, [SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], Humans, Muscle, Skeletal, Gene, Aged, 030304 developmental biology, lcsh:R, Infant, Dystrophy, [SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology, Fibroblasts, Chromosome 4, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Case-Control Studies, Mutation, lcsh:Q, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bd636a86000d8f6d6952d1613d637c7Test
https://hal.archives-ouvertes.fr/hal-01951503v2/documentTest -
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المؤلفون: Frédérique Magdinier, Rafaëlle Bernard, Stéphane Roche, Emmanuelle Salort-Campana, Natacha Broucqsault, Julia Morere, Marie-Cécile Gaillard, Karine Nguyen, Marc Bartoli, Camille Dion, Nicolas Lévy, Armand Tasmadjian, Francesca Puppo, Catherine Vovan, Gwenaëlle Bouget, Charlene Chaix, Shahram Attarian
المساهمون: 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), Centre de référence des maladies neuromusculaires et de la SLA, Hôpital de la Timone [CHU - APHM] (TIMONE), Département de génétique médicale [Hôpital de la Timone - APHM], 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), ANR-09-GENO-0038,FSHDecrypt,Analyse à grande échelle de la région 4qTer : décodage génétique et épigénétique du locus de la dystrophie musculaire Facio-Scapulo-Humérale(2009), Institut National de la Santé et de la Recherche Médicale (INSERM)-Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone [CHU - APHM] (TIMONE)-Centre National de la Recherche Scientifique (CNRS), Bartoli, Marc, Physiopathologie moléculaire: des maladies rares aux maladies communes - Analyse à grande échelle de la région 4qTer : décodage génétique et épigénétique du locus de la dystrophie musculaire Facio-Scapulo-Humérale - - FSHDecrypt2009 - ANR-09-GENO-0038 - GENO - VALID
المصدر: Neurology
Neurology, 2014, 83 (8), pp.733-742. ⟨10.1212/WNL.0000000000000708⟩
ResearcherID
Neurology, American Academy of Neurology, 2014, 83 (8), pp.733-742. ⟨10.1212/WNL.0000000000000708⟩مصطلحات موضوعية: Male, Oncology, Pathology, Penetrance, Epigenesis, Genetic, 0302 clinical medicine, 0303 health sciences, [SDV.MHEP] Life Sciences [q-bio]/Human health and pathology, DNA methylation, Bisulfite, Methylation, Muscular Dystrophy, Facioscapulohumeral, Pedigree, 3. Good health, Phenotype, Female, Epigenetics, Chromosomes, Human, Pair 4, medicine.symptom, Adult, musculoskeletal diseases, Heterozygote, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, Biology, Asymptomatic, MeDIP, Young Adult, 03 medical and health sciences, Internal medicine, [SDV.BBM] Life Sciences [q-bio]/Biochemistry, Molecular Biology, medicine, Humans, Genetic Predisposition to Disease, [SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology, Genetic Testing, Methylated DNA immunoprecipitation, 030304 developmental biology, FSHD, D4Z4, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Neurology (clinical), Asymptomatic carrier, 030217 neurology & neurosurgery, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology, DNA hypomethylation
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e4412972dca3cbbdd3552b7409a092fTest
https://hal.science/hal-01610019/documentTest -
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المؤلفون: Rafael Fonseca, Stéphanie Poulain, Xavier Leleu, Sylvie Galiègue-Zouitina, Salomon Manier, Rachid Aijjou, Natacha Broucqsault, Olivier Nibourel, Valérie Soenen, Patrick Duthilleul, Esteban Braggio, Christophe Roumier
المصدر: Clinical Lymphoma Myeloma and Leukemia. 11:106-108
مصطلحات موضوعية: Male, Genetics, Comparative Genomic Hybridization, Cancer Research, medicine.diagnostic_test, Genome, Human, Protein Array Analysis, Macroglobulinemia, Hematology, Biology, Polymorphism, Single Nucleotide, TNFAIP3, Oncology, Polymorphism (computer science), Cancer cell, medicine, Humans, SNP, Female, Waldenstrom Macroglobulinemia, Gene, Comparative genomic hybridization, Fluorescence in situ hybridization
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6df39063d8dc8f420ea336c852bff29Test
https://doi.org/10.3816/clml.2011.n.021Test -
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المؤلفون: Salomon Manier, Elisabeth Bertrand, Sylvie Galiègue-Zouitina, Aline Renneville, Catherine Roche-Lestienne, Charles Herbaux, Patrick Duthilleul, Amélie Lainelle, Christophe Roumier, Stéphanie Poulain, Sabine Tricot, Agnès Daudignon, Natacha Broucqsault, Rachid Aiijou, Valérie Soenen, Bruno Quesnel, Claude Preudhomme, Xavier Leleu, Pierre Morel
المصدر: American journal of hematology. 88(11)
مصطلحات موضوعية: Adult, Male, DNA Copy Number Variations, Loss of Heterozygosity, Biology, medicine.disease_cause, Loss of heterozygosity, Cohort Studies, Chromosome Duplication, medicine, Humans, Gene, Chromosome 13, Aged, Genetics, Aged, 80 and over, Chromosome Aberrations, Mutation, Tumor Suppressor Proteins, Hematology, DNA Methylation, Middle Aged, medicine.disease, Uniparental disomy, Neoplasm Proteins, Gene expression profiling, Chromosome 4, Gene Expression Regulation, Female, France, Chromosome Deletion, Waldenstrom Macroglobulinemia, CD79 Antigens, SNP array, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::520a935ab75a36ada1e945227fc36f07Test
https://pubmed.ncbi.nlm.nih.gov/23861223Test