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المؤلفون: Alice Goldenberg, Gaël Nicolas, Maud Blanluet, Sandra Chantot-Bastaraud, Gabriella Vera, Boris Keren, Géraldine Joly-Helas, Thierry Frebourg, Didier Hannequin, Jean-Pierre Siffroi, Kévin Cassinari, Nathalie Le Meur, Bertrand Mace, Pascal Chambon
المساهمون: Couvet, Sandrine, UNIROUEN - UFR Santé (UNIROUEN UFR Santé), Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Normandie Université (NU), Génomique et Médecine Personnalisée du Cancer et des Maladies Neuropsychiatriques (GPMCND), Normandie Université (NU)-Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Maladies génétiques d'expression pédiatrique [CHU Trousseau] (Inserm U933), Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Trousseau [APHP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), UF de Génétique chromosomique [CHU Trousseau], CHU Trousseau [APHP], Service de Génétique médicale [CHU Pitié-Salpêtrière], CHU Pitié-Salpêtrière [AP-HP]
المصدر: American Journal of Medical Genetics Part A
American Journal of Medical Genetics Part A, 2021, 185 (10), pp.3057-3061. ⟨10.1002/ajmg.a.62361⟩مصطلحات موضوعية: MESH: Abnormalities, Multiple, MESH: Chromosome Deletion, [SDV]Life Sciences [q-bio], MESH: Chromosomes, Human, Pair 2, Chromosomal translocation, Chromosomal rearrangement, postzygotic, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, Biology, MESH: Cervical Vertebrae, Germline, MESH: Intellectual Disability, MESH: Uniparental Disomy, Gene duplication, Genetics, medicine, MESH: In Situ Hybridization, Fluorescence, Genetics (clinical), MESH: Humans, medicine.diagnostic_test, MESH: Genetic Predisposition to Disease, MESH: Scoliosis, Chromosome, Karyotype, MESH: Male, MESH: Translocation, Genetic, MESH: Siblings, [SDV] Life Sciences [q-bio], MESH: Karyotyping, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Uniparental Isodisomy, rescue, unbalanced translocation, MESH: Chromosome Banding, MESH: Chromosomes, mosaic, MESH: Mosaicism, MESH: Kyphosis, MESH: Chromosomes, Human, Pair 11, MESH: Female, Fluorescence in situ hybridization
وصف الملف: application/pdf
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المؤلفون: Evgenia, Globa, Natalia, Zelinska, Yulia, Shcherbak, Joelle, Bignon-Topalovic, Anu, Bashamboo, Ken, MсElreavey
المساهمون: Ministry of Health of Ukraine, Génétique du Développement humain - Human developmental genetics, Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), This work is funded in part by a research grant from the European Society of Pediatric Endocrinology, and by the Agence Nationale de la Recherche (ANR), ANR-10-LABX-73 REVIVE, ANR-17-CE14-0038-01, ANR-19-CE14-0022 and ANR-19-CE14-0012 and by the Ministry of Health of Ukraine (0117U003036)., ANR-10-LABX-0073,REVIVE,Stem Cells in Regenerative Biology and Medicine(2010), ANR-17-CE14-0038,MGonDev,Etude des mécanismes du développement des gonades chez l'homme(2017), ANR-19-CE14-0022,SexDiff,Régulation de la détermination du sexe et de la différenciation ovarienne : implications dans les troubles du développement sexuel(2019), ANR-19-CE14-0012,RNA-SEX,Fonction de l'ARN hélicase dans la détermination du sexe chez les vertébrés et les troubles du développement du sexe chez l'homme (DSD)(2019)
المصدر: Frontiers in Endocrinology
Frontiers in Endocrinology, 2022, 13, pp.810782. ⟨10.3389/fendo.2022.810782⟩مصطلحات موضوعية: Male, MESH: Mutation, 46, XX Disorders of Sex Development, MESH: Sexual Development, phenotype, Endocrinology, Diabetes and Metabolism, [SDV]Life Sciences [q-bio], Sex Chromosome Disorders of Sex Development, Disorders of Sex Development, MESH: Sex Chromosome Disorders of Sex Development, XY and 46, MESH: Hypogonadism, XX disorders of sex development, Humans, MESH: In Situ Hybridization, Fluorescence, genes, In Situ Hybridization, Fluorescence, MESH: 46, XX Disorders of Sex Development, MESH: Humans, Hypogonadism, Sexual Development, MESH: Male, karyotype, whole exome sequencing (WES), Mutation, Female, MESH: Disorders of Sex Development, MESH: Female
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21578f481b9d8654fc6a3070541cca4e
https://hal.science/hal-04150382 -
3
المؤلفون: Sylvain Godreuil, Ahmed Loukil, Coralie L'Ollivier, Anselme Millogo, Diakourga Arthur Djibougou, Michel Drancourt
المساهمون: Centre Hospitalier Universitaire Souro Sanou [Bobo-Dioulasso] (CHUSS), Institut Hospitalier Universitaire Méditerranée Infection (IHU Marseille), Institut de Recherche pour le Développement (IRD en Occitanie) (IRD (Occitanie)), Assistance Publique - Hôpitaux de Marseille (APHM), Service de Santé des Armées, Institut de Recherche en Sciences de la Santé Bobo Dioulasso (INSSA), Université Polytechnique Nazi Boni Bobo-Dioulasso (UNB), Centre Muraz [Bobo-Dioulasso, Burkina Faso]
المصدر: Emerging Infectious Diseases, Vol 27, Iss 6, Pp 1758-1760 (2021)
Emerging Infectious Diseases
Emerging Infectious Diseases, Centers for Disease Control and Prevention, 2021, 27 (6), pp.1758-1760. ⟨10.3201/eid2706.200748⟩مصطلحات موضوعية: Letter, Epidemiology, Infectious and parasitic diseases, RC109-216, 0302 clinical medicine, [SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseases, mycobacterial diseases, Stool specimens, MESH: In Situ Hybridization, Fluorescence, 030212 general & internal medicine, bacteria, Mycobacterium leprae, In Situ Hybridization, Fluorescence, health care economics and organizations, [SDV.MHEP.ME]Life Sciences [q-bio]/Human health and pathology/Emerging diseases, biology, Fecal excretion, Entamoeba coli, Infectious Diseases, Tuberculosis and other mycobacteria, Medicine, Leprosy, DDD, Microbiology (medical), Genotype, 030231 tropical medicine, In situ hybridization, Microbiology, Enteritis, Mycobacterium, 03 medical and health sciences, FISH, Burkina Faso, parasitic diseases, Research Letter, medicine, Humans, MESH: Burkina Faso, Letters to the Editor, Feces, MESH: Humans, biology.organism_classification, medicine.disease, [SDV.MP.BAC]Life Sciences [q-bio]/Microbiology and Parasitology/Bacteriology, Fecal Excretion of Mycobacterium leprae, Burkina Faso, MESH: Leprosy, bacterial infections, MESH: Mycobacterium leprae, Bacteria
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المؤلفون: Diane Frankel, Isabelle Nanni, L’Houcine Ouafik, Clara Camilla, Eric Pellegrino, Nathalie Beaufils, Laurent Greillier, Hervé Dutau, Philippe Astoul, Elise Kaspi, Patrice Roll
المساهمون: Ouafik, L'Houcine, 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), Hôpital de la Timone [CHU - APHM] (TIMONE), Hôpital Nord [CHU - APHM], Institut de neurophysiopathologie (INP), Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS), CHU Marseille, Aix Marseille Université (AMU)
المصدر: International Journal of Molecular Sciences; Volume 23; Issue 18; Pages: 10556
International Journal of Molecular Sciences
International Journal of Molecular Sciences, 2022, 23 (18), pp.10556. ⟨10.3390/ijms231810556⟩مصطلحات موضوعية: MESH: Gene Rearrangement, [SDV.CAN]Life Sciences [q-bio]/Cancer, MESH: Protein-Tyrosine Kinases, Catalysis, Inorganic Chemistry, immunocytochemistry, FISH, [SDV.CAN] Life Sciences [q-bio]/Cancer, MESH: In Situ Hybridization, Fluorescence, Physical and Theoretical Chemistry, MESH: High-Throughput Nucleotide Sequencing, Molecular Biology, Spectroscopy, MESH: Anaplastic Lymphoma Kinase, adenocarcinoma, MESH: Humans, NGS, ALK, ROS1, lung cancer, cytology, Organic Chemistry, MESH: Retrospective Studies, MESH: Immunohistochemistry, General Medicine, MESH: Lung Neoplasms, Computer Science Applications, MESH: Proto-Oncogene Proteins, MESH: Carcinoma, Non-Small-Cell Lung
وصف الملف: application/pdf
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5
المؤلفون: Jean-Pierre Siffroi, Solveig Heide, Alexandra Afenjar, Damien Sternberg, Arnaud Isapof, Mathias Schwartz, Sandra Whalen, Marie-France Portnoï, Boris Keren, Sandra Chantot-Bastaraud, Brigitte Chabrol
المساهمون: Service de génétique et embryologie médicales [CHU Trousseau], CHU Trousseau [APHP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Institut du Cerveau = Paris Brain Institute (ICM), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Service de Biochimie Métabolique et Centre de Génétique moléculaire et chromosomique [CHU Pitié Salpêtrière], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU), Service de Neuropédiatrie [CHU Trousseau], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Trousseau [APHP], Hôpital de la Timone [CHU - APHM] (TIMONE), Service de Génétique médicale [CHU Pitié-Salpêtrière], CHU Pitié-Salpêtrière [AP-HP], Couvet, Sandrine, UF de Génétique chromosomique [CHU Trousseau], Maladies génétiques d'expression pédiatrique [CHU Trousseau] (Inserm U933), Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Trousseau [APHP], UF Neurométabolique Bioclinique et Génétique [CHU Pitié-Salpêtrière]
المصدر: American Journal of Medical Genetics Part A
American Journal of Medical Genetics Part A, 2018, 176 (1), pp.151-155. ⟨10.1002/ajmg.a.38515⟩مصطلحات موضوعية: Male, 0301 basic medicine, choline acetyl-transferase, [SDV]Life Sciences [q-bio], Vesicular Acetylcholine Transport Proteins, MESH: Amino Acid Sequence, single nucleotide polymorphisms array, Congenital myasthenia, 0302 clinical medicine, MESH: In Situ Hybridization, Fluorescence, In Situ Hybridization, Fluorescence, Genetics (clinical), MESH: Genetic Association Studies, Oligonucleotide Array Sequence Analysis, MESH: Choline O-Acetyltransferase, Genetics, MESH: Polymorphism, Single Nucleotide, Congenital myasthenic syndrome, MESH: Infant, Choline acetyltransferase, Phenotype, [SDV] Life Sciences [q-bio], Female, Chromosome Deletion, compound heterozygoty, MESH: Myasthenic Syndromes, Congenital, vesicular acetyl-choline transporter, MESH: Mutation, MESH: Chromosome Deletion, Genes, Recessive, Locus (genetics), Single-nucleotide polymorphism, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, Biology, MESH: Phenotype, Polymorphism, Single Nucleotide, DNA sequencing, Choline O-Acetyltransferase, 03 medical and health sciences, medicine, Humans, Amino Acid Sequence, Gene, MESH: Genes, Recessive, Genetic Association Studies, Myasthenic Syndromes, Congenital, MESH: Humans, MESH: Vesicular Acetylcholine Transport Proteins, Chromosomes, Human, Pair 10, Infant, medicine.disease, MESH: Male, 030104 developmental biology, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, MESH: Chromosomes, Human, Pair 10, MESH: Oligonucleotide Array Sequence Analysis, Mutation, MESH: Female, 030217 neurology & neurosurgery
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المؤلفون: Francois-Xavier Mahon, Kelly Airiau, Béatrice Turcq, Francis Belloc
المساهمون: Centre National de la Recherche Scientifique (CNRS)
المصدر: Leukemia Research
Leukemia Research, Elsevier, 2017, 61, pp.44-52. ⟨10.1016/j.leukres.2017.08.014⟩مصطلحات موضوعية: 0301 basic medicine, Cancer Research, [SDV]Life Sciences [q-bio], Resistance, Dasatinib, Fusion Proteins, bcr-abl, Apoptosis, Stem cell factor, Proto-Oncogene Proteins c-fyn, Polymerase Chain Reaction, 0302 clinical medicine, hemic and lymphatic diseases, MESH: Protein Kinase Inhibitors, MESH: In Situ Hybridization, Fluorescence, In Situ Hybridization, Fluorescence, ABL, Chemistry, MEK inhibitor, Chronic myeloid leukemia, MESH: Dasatinib, Hematology, MESH: Drug Resistance, Neoplasm, 3. Good health, Oncology, 030220 oncology & carcinogenesis, SRC kinase, Tyrosine kinase, Proto-oncogene tyrosine-protein kinase Src, medicine.drug, MAP Kinase Signaling System, Blotting, Western, Antineoplastic Agents, 03 medical and health sciences, FYN, Leukemia, Myelogenous, Chronic, BCR-ABL Positive, medicine, MESH: Blotting, Western, Humans, Protein Kinase Inhibitors, MESH: K562 Cells, [SDV.GEN]Life Sciences [q-bio]/Genetics, MESH: Humans, MESH: MAP Kinase Signaling System, Cell growth, MESH: Apoptosis, MESH: Fusion Proteins, bcr-abl, MESH: Polymerase Chain Reaction, MESH: Proto-Oncogene Proteins c-fyn, 030104 developmental biology, MESH: Leukemia, Myelogenous, Chronic, BCR-ABL Positive, Drug Resistance, Neoplasm, Immunology, Cancer research, MESH: Antineoplastic Agents, K562 Cells, MEK/ERK
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المؤلفون: Christopher M. Ziegler, Florian Mueller, Emily A. Bruce, Philip Eisenhauer, Daniel Zenklusen, Benjamin R. King, Aubin Samacoits, Christophe Zimmer, Jason Botten
المساهمون: University of Vermont [Burlington], Imagerie et Modélisation - Imaging and Modeling, Centre National de la Recherche Scientifique (CNRS)-Institut Pasteur [Paris], Centre de Bioinformatique, Biostatistique et Biologie Intégrative (C3BI), Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS), Université de Montréal (UdeM), We also gratefully acknowledge funding support from NIH grants T32 HL076122-10 (B.R.K.), T32 AI055402 (C.M.Z.), R21 AI088059 (J.B.), and P20RR021905 and P30GM118228 (Immunobiology and Infectious Disease COBRE awards) (J.B.). D.Z. is supported by the Canadian Institute for Health Research (project grant-366682), the Fond de Recherche du Quebec (Chercheur-boursier Junior 2), and the Canadian Foundation for Innovation. C.Z., F.M., and A.S. were supported by the Institut Pasteur and the Fondation pour la Recherche Médicale (FRM). B.R.K. was supported by a Chateaubriand fellowship from the Office for Science and Technology at the Embassy of France in the United States. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript, We gratefully acknowledge J. Lindsay Whitton for providing us with LCMV strain Arm53b and Samir Rahman, Philippe Clerc, Christian Weber, and Sophie Abélanet for technical assistance. We thank Pablo Navarro and Jason Stumpff for graciously offering the use of their microscopy equipment and for providing their expertise and Jean-Michel Arbona and Wei Ouyang for helpful discussions., Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS)
المصدر: Journal of Virology
Journal of Virology, American Society for Microbiology, 2018, 92 (12), pp.e2241-17. ⟨10.1128/JVI.02241-17⟩
Journal of Virology, 2018, 92 (12), pp.e2241-17. ⟨10.1128/JVI.02241-17⟩مصطلحات موضوعية: 0301 basic medicine, viruses, genome replication and transcription, Immunology, cyclical, Microbiology, smFISH, 03 medical and health sciences, Transcription (biology), Viral entry, Virology, gene probes, MESH: In Situ Hybridization, Fluorescence, LCMV, arenavirus, Polymerase, Messenger RNA, Arenavirus, MESH: Humans, 030102 biochemistry & molecular biology, biology, MESH: Virus Replication, RNA, RNA virus, persistence, biology.organism_classification, 3. Good health, MESH: Cell Line, MESH: Staining and Labeling, 030104 developmental biology, Viral replication, kinetics, Insect Science, MESH: RNA, Viral, biology.protein, MESH: Lymphocytic choriomeningitis virus, MESH: RNA Probes, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, MESH: A549 Cells, MESH: Genome, Viral
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cc772f98ceaf453b6b3d9dc5f080187
https://hal-pasteur.archives-ouvertes.fr/pasteur-02075021 -
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المؤلفون: Teresa Garnatje, Oriane Hidalgo, Sonja Siljak-Yakovlev, Joan Vallès, Bernard Godelle, Vlatka Zoldoš
المساهمون: Ecologie Systématique et Evolution (ESE), Université Paris-Sud - Paris 11 (UP11)-AgroParisTech-Centre National de la Recherche Scientifique (CNRS), Institut des Sciences de l'Evolution de Montpellier (UMR ISEM), Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-École Pratique des Hautes Études (EPHE), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Université de Montpellier (UM)-Institut de recherche pour le développement [IRD] : UR226-Centre National de la Recherche Scientifique (CNRS), University of Zagreb, Universitat de Barcelona (UB), Institut Botànic de Barcelona (IBB), Consejo Superior de Investigaciones Científicas [Spain] (CSIC), Comparative Plant and Fungal Biology, Royal Botanic Gardens, École pratique des hautes études (EPHE), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Université de Montpellier (UM)-Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Centre National de la Recherche Scientifique (CNRS)-Institut de recherche pour le développement [IRD] : UR226, Universitat de Barcelona, Centre National de la Recherche Scientifique (France), Generalitat de Catalunya, Ministerio de Economía, Industria y Competitividad (España)
المصدر: PLoS ONE
PLoS ONE, 2017, 12 (8), pp.e0182318. ⟨10.1371/journal.pone.0182318⟩
PLoS ONE, Public Library of Science, 2017, 12 (8), pp.e0182318. ⟨10.1371/journal.pone.0182318⟩
Recercat. Dipósit de la Recerca de Catalunya
instname
Digital.CSIC. Repositorio Institucional del CSIC
PLoS ONE, Vol 12, Iss 8, p e0182318 (2017)
Dipòsit Digital de la UB
Universidad de Barcelonaمصطلحات موضوعية: 0301 basic medicine, MESH: Genome, Plant, Gene Expression, lcsh:Medicine, Plant Science, Asteraceae, MESH: Genome Size, Genome Size, MESH: Asteraceae, Heterochromatin, MESH: In Situ Hybridization, Fluorescence, lcsh:Science, MESH: Phylogeny, Genome Evolution, In Situ Hybridization, Fluorescence, Phylogeny, MESH: Evolution, Molecular, Data Management, Genetics, Multidisciplinary, MESH: DNA, Ribosomal, biology, Chromosome Biology, Plant Anatomy, [SDV.BID.EVO]Life Sciences [q-bio]/Biodiversity/Populations and Evolution [q-bio.PE], Chromosome Mapping, Karyotype, Genomics, Chromatin, Phylogenetics, MESH: Heterochromatin, Molecular phylogenetics, Pol·len, Pollen, Epigenetics, Karyotypes, Genome, Plant, Research Article, Computer and Information Sciences, Genome evolution, DNA, Plant, Reichardia, DNA, Ribosomal, Chromosomes, Molecular Evolution, Evolutionary genetics, Evolution, Molecular, [SDV.GEN.GPL]Life Sciences [q-bio]/Genetics/Plants genetics, Cytogenetics, 03 medical and health sciences, Constitutive heterochromatin, Evolutionary Systematics, MESH: DNA, Plant, Genome size, Taxonomy, Evolutionary Biology, Heterocromatina, lcsh:R, Biology and Life Sciences, Computational Biology, Chromosome, Cell Biology, Genètica evolutiva, Chromosome Pairs, biology.organism_classification, 030104 developmental biology, Genetic Loci, lcsh:Q, MESH: Chromosome Mapping
وصف الملف: application/pdf
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9Extensive Amplification of Telomeric Repeats in the Karyotypically Highly Diverse African Pygmy Mice
المساهمون: Institut des Sciences de l'Evolution de Montpellier (UMR ISEM), École pratique des hautes études (EPHE), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Université de Montpellier (UM)-Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Centre National de la Recherche Scientifique (CNRS)-Institut de recherche pour le développement [IRD] : UR226
المصدر: Cytogenetic and Genome Research
Cytogenetic and Genome Research, Karger, 2017, 152 (2), pp.55-64. ⟨10.1159/000478297⟩مصطلحات موضوعية: 0301 basic medicine, Male, Karyotype, Nannomys, MESH: Base Sequence, Genome, MESH: Gene Amplification, X-inactivation, 03 medical and health sciences, Sex-autosome fusion, Mice, African pygmy mouse, Gene duplication, Genetics, Animals, MESH: Animals, MESH: In Situ Hybridization, Fluorescence, MESH: Metaphase, MESH: Phylogeny, Molecular Biology, MESH: Mice, Genetics (clinical), In Situ Hybridization, Fluorescence, Metaphase, Phylogeny, Repetitive Sequences, Nucleic Acid, Replication timing, MESH: Repetitive Sequences, Nucleic Acid, biology, Base Sequence, Chromosomal evolution, Gene Amplification, MESH: Karyotype, Telomere, biology.organism_classification, MESH: Male, [SDV.GEN.GA]Life Sciences [q-bio]/Genetics/Animal genetics, 030104 developmental biology, Eukaryotic chromosome fine structure, Female, Robertsonian fusion, MESH: Telomere, MESH: Female
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3ab5451be9ab1981fd7fe801cf67c4a
https://pubmed.ncbi.nlm.nih.gov/28738367 -
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المؤلفون: Judith W. M. Jeuken, Pim J. French, Catherine Carpentier, Khê Hoang-Xuan, Jean-Yves Delattre, Ahmed Idbaih, Olivier Delattre, Johannes L. Teepen, Johan M. Kros, Thierry Gorlia, Mathilde C.M. Kouwenhoven, Martin J. van den Bent
المساهمون: Biologie des Interactions Neurones / Glie, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Service de Neurologie [CHU Pitié-Salpêtrière], IFR70-CHU Pitié-Salpêtrière [AP-HP], Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Department of Neurology, Erasmus University Medical Center [Rotterdam] (Erasmus MC), Department of Pathology, Radboud University Medical Center [Nijmegen], EORTC, European Organization for Research and Treatment of Cancer DataCenter, St. Elisabeth Hospital, Unité de génétique et biologie des cancers (U830), Université Paris Descartes - Paris 5 (UPD5)-Institut Curie [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM), UPMC - Département de neurologie 2 - Mazarin, Université Pierre et Marie Curie - Paris 6 (UPMC)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Pitié-Salpêtrière [AP-HP], Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Service de neurologie 1 [CHU Pitié-Salpétrière], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Pitié-Salpêtrière [AP-HP], Université Pierre et Marie Curie - Paris 6 ( UPMC ) -Institut National de la Santé et de la Recherche Médicale ( INSERM ), Assistance publique - Hôpitaux de Paris (AP-HP)-CHU Pitié-Salpêtrière [APHP], Erasmus University Medical Center [Rotterdam], Unité de génétique et biologie des cancers ( U830 ), Université Paris Descartes - Paris 5 ( UPD5 ) -Institut Curie-Institut National de la Santé et de la Recherche Médicale ( INSERM ), Département de neurologie 2 - Mazarin, CHU Pitié-Salpêtrière [APHP]-Assistance publique - Hôpitaux de Paris (AP-HP)-Université Pierre et Marie Curie - Paris 6 ( UPMC ), Neurology, CCA - Cancer biology and immunology, CCA - Imaging and biomarkers, CCA - Cancer Treatment and quality of life, Idbaih, Ahmed, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU), Pathology, Neurosurgery
المصدر: Neuropathology
Neuropathology, Wiley, 2008, 28 (4), pp.440-3. ⟨10.1111/j.1440-1789.2008.00863.x⟩
Neuropathology, 2008, 28 (4), pp.440-3. ⟨10.1111/j.1440-1789.2008.00863.x⟩
Idbaih, A, Kouwenhoven, M, Jeuken, J, Carpentier, C, Gorlia, T, Kros, J M, French, P, Teepen, J L, Delattre, O, Delattre, J-Y, van den Bent, M & Hoang-Xuan, K 2008, ' Chromosome 1p loss evaluation in anaplastic oligodendrogliomas ', Neuropathology, vol. 28, no. 4, pp. 440-3 . https://doi.org/10.1111/j.1440-1789.2008.00863.x
Neuropathology, Wiley, 2008, 28 (4), pp.440-3. 〈10.1111/j.1440-1789.2008.00863.x〉
Neuropathology, 28, 440-3
Neuropathology, 28(4), 440-3. Wiley-Blackwell
Neuropathology, 28, 4, pp. 440-3
Neuropathology, 28(4), 440-443. Wiley-Blackwell Publishing Ltdمصطلحات موضوعية: Chromosomes, Artificial, Bacterial, MESH : Oligodendroglioma, [SDV.GEN] Life Sciences [q-bio]/Genetics, MESH : Chromosomes, Human, Pair 1, [ SDV.CAN ] Life Sciences [q-bio]/Cancer, MESH: Nucleic Acid Hybridization, 0302 clinical medicine, MESH : Tumor Markers, Biological, Oligodendroglial Tumor, MESH: In Situ Hybridization, Fluorescence, In Situ Hybridization, Fluorescence, Molecular diagnosis, prognosis and monitoring [UMCN 1.2], Genetics, MESH: Middle Aged, Brain Neoplasms, Nucleic Acid Hybridization, General Medicine, Middle Aged, MESH : Nucleic Acid Hybridization, MESH : In Situ Hybridization, Fluorescence, Chromosomes, Human, Pair 1, 030220 oncology & carcinogenesis, MESH: Brain Neoplasms, Biomarker (medicine), [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], Chromosome Deletion, MESH : Chromosomes, Artificial, Bacterial, MESH: Chromosomes, Artificial, Bacterial, MESH: Chromosomes, Human, Pair 1, MESH: Chromosome Deletion, Oligodendroglioma, Anaplastic oligodendroglioma, [SDV.CAN]Life Sciences [q-bio]/Cancer, In situ hybridization, Biology, Pathology and Forensic Medicine, 03 medical and health sciences, [SDV.CAN] Life Sciences [q-bio]/Cancer, Translational research [ONCOL 3], medicine, Biomarkers, Tumor, Humans, MESH : Middle Aged, [SDV.NEU] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], MESH : Brain Neoplasms, MESH: Oligodendroglioma, Bacterial artificial chromosome, [SDV.GEN]Life Sciences [q-bio]/Genetics, MESH: Humans, MESH : Humans, Chromosome, medicine.disease, MESH : Chromosome Deletion, [ SDV.NEU ] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], MESH: Tumor Markers, Biological, Neurology (clinical), [ SDV.GEN ] Life Sciences [q-bio]/Genetics, 030217 neurology & neurosurgery, Comparative genomic hybridization
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