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المؤلفون: Chang, Hong, Li, Lingyi, Peng, Tao, Grigoroiu-Serbanescu, Maria, Bergen, Sarah E., Landén, Mikael, Hultman, Christina M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Cichon, Sven, Nöthen, Markus M., Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean Pierre, Henry, Chantal, Rietschel, Marcella, Backlund, Lena, Frisén, Louise, Lavebratt, Catharina, Schalling, Martin, Ösby, Urban, Mühleisen, Thomas W., Leber, Markus, Degenhardt, Franziska, Treutlein, Jens, Mattheisen, Manuel, Hofmann, Andrea, Breuer, René, Meier, Sandra, Herms, Stefan, Hoffmann, Per, Lacour, André, Witt, Stephanie H., Streit, Fabian, Lucae, Susanne, Maier, Wolfgang, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Pfennig, Andrea, Bauer, Michael, Hautzinger, Martin, Wright, Adam, Fullerton, Janice M., Schofield, Peter R., Montgomery, Grant W., Medland, Sarah E., Gordon, Scott D., Becker, Tim, Schumacher, Johannes, Propping, Peter, Xiao, Xiao, Li, Ming
المساهمون: Etain, Bruno, Institut Mondor de Recherche Biomédicale (IMRB), Institut National de la Santé et de la Recherche Médicale (INSERM)-IFR10-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12), Fondation FondaMental [Créteil], Hôpital Lariboisière-Fernand-Widal [APHP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Pôle de Psychiatrie [Hôpital Henri Mondor], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital H. Mondor - A. Chenevier, Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy), Swedish Bipolar Study Group, MooDS Consortium
المصدر: Chang, H, Li, L, Peng, T, Grigoroiu-Serbanescu, M, Bergen, S E, Landén, M, Hultman, C M, Forstner, A J, Strohmaier, J, Hecker, J, Schulze, T G, Müller-Myhsok, B, Reif, A, Mitchell, P B, Martin, N G, Cichon, S, Nöthen, M M, Jamain, S, Leboyer, M, Bellivier, F, Etain, B, Kahn, J P, Henry, C, Rietschel, M, Backlund, L, Frisén, L, Lavebratt, C, Schalling, M, Ösby, U, Mühleisen, T W, Leber, M, Degenhardt, F, Treutlein, J, Mattheisen, M, Hofmann, A, Breuer, R, Meier, S, Herms, S, Hoffmann, P, Lacour, A, Witt, S H, Streit, F, Lucae, S, Maier, W, Schwarz, M, Vedder, H, Kammerer-Ciernioch, J, Pfennig, A, Bauer, M, Hautzinger, M, Wright, A, Fullerton, J M, Schofield, P R, Montgomery, G W, Medland, S E, Gordon, S D, Becker, T, Schumacher, J, Propping, P, Xiao, X & Li, M 2017, ' Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1 ', Molecular Neurobiology, vol. 54, no. 7, pp. 5166-5176 . https://doi.org/10.1007/s12035-016-0041-x
MOLECULAR NEUROBIOLOGY
Molecular Neurobiology
Molecular Neurobiology, Humana Press, 2017, 54 (7), pp.5166-5176. ⟨10.1007/s12035-016-0041-x⟩مصطلحات موضوعية: Male, 0301 basic medicine, Linkage disequilibrium, MESH: Choline Dehydrogenase, CHDH, [SDV.MHEP.PSM] Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health, Genetic evidence, Genome-wide association study, Linkage Disequilibrium, MESH: Genotype, MESH: Bipolar Disorder, Genetics, MESH: Polymorphism, Single Nucleotide, MESH: Genetic Predisposition to Disease, Brain, Cognitive ability, Phenotype, MESH: Linkage Disequilibrium, Neurology, Schizophrenia, Female, Chromosomes, Human, Pair 3, Adult, Genotype, Bipolar disorder, MESH: Chromosomes, Human, Pair 3, Neuroscience (miscellaneous), Biology, MESH: Phenotype, Polymorphism, Single Nucleotide, MESH: Brain, Expression quantitative trait loci (eQTL), 03 medical and health sciences, Cellular and Molecular Neuroscience, medicine, Humans, SNP, Genetic Predisposition to Disease, Choline Dehydrogenase, Gene, Genetic association, MESH: Humans, MESH: Adult, medicine.disease, MESH: Male, 030104 developmental biology, Mood disorders, [SDV.MHEP.PSM]Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health, MESH: Genome-Wide Association Study, Gene expression, MESH: Female, Genome-Wide Association Study
وصف الملف: application/vnd.openxmlformats-officedocument.wordprocessingml.document
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المؤلفون: Frank Bellivier, Andrej Marusic, Hugh Gurling, R Abou Jamra, Johannes Schumacher, Margot Albus, D Bacq, Céline Charon, Walter J. Muir, François Ferrero, Douglas Blackwood, Thomas G. Schulze, Margitta Borrmann-Hassenbach, S. Roche, A. Malafosse, Bruno Giros, Patrick McKeon, M. Rietschel, Sven Cichon, Bruno Etain, Carmel Kealey, Markus M. Nöthen, Flavie Mathieu, Christian Dina, Arnaud Lemainque, Mark Lathrop, Stephanie Ohlraun, Sophie Gallina, Wolfgang Maier, C. Henry, Thomas Bourgeron, Z M Dernovsek, C Betard, Martin Preisig, Marion Leboyer, Peter Propping
المساهمون: Neurobiologie et Psychiatrie, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Service de psychiatrie, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Henri Mondor-Hôpital Albert Chenevier, Division Genetic Epidemiology in Psychiatry, Central Institute of Mental Health [Mannheim], University Hospital Mannheim | Universitätsmedizin Mannheim-University Hospital Mannheim | Universitätsmedizin Mannheim, Department of Psychiatry, Rheinische Friedrich-Wilhelms-Universität Bonn, Department of Psychiatry and Psychotherapy, District Hospital Haar, Smurfit Institute of Genetics, Trinity College Dublin, Department of Pharmacology, University of Pennsylvania, Département de psychiatrie, Centre hospitalier Charles Perrens [Bordeaux], Génétique des maladies multifactorielles (GMM), Université de Lille, Droit et Santé-Centre National de la Recherche Scientifique (CNRS), Molecular Psychiatry Laboratory - Department of Psychiatry and Behavioural Sciences, Windeyer Institute for Medical Sciences-Royal Free Hospital [London, UK], Pôle de Psychiatrie, Faculté de Médecine-IFR10-Groupe hospitalier Henri Mondor-Albert Chenevier, Department of psychiatry, Lausanne University Hospital, Geneva University Hospital (HUG), Life & Brain Center - Department of Genomics, Institute of Human Genetics, Institute of Public Health of the Republic of Slovenia, University Psychiatric Hospital, Génomique fonctionnelle et développement, Institut Pasteur [Paris] (IP)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre National de Génotypage (CNG), Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Guellaen, Georges, Medical Faculty [Mannheim]-Medical Faculty [Mannheim], Windeyer Institute for Medical Sciences-Royal Free and University College London Medical School, University of Pennsylvania [Philadelphia], Hôpital Charles Perrens, University Hospital - Lausanne, Institut Pasteur [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM)
المصدر: Molecular Psychiatry
Molecular Psychiatry, 2006, 11 (7), pp.685-94. ⟨10.1038/sj.mp.4001815⟩
Molecular Psychiatry, no. 11, pp. 685-694
Molecular Psychiatry, Nature Publishing Group, 2006, 11 (7), pp.685-94. ⟨10.1038/sj.mp.4001815⟩مصطلحات موضوعية: Male, Proband, Bipolar Disorder, [SDV.MHEP.PSM] Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health, 0302 clinical medicine, MESH: Bipolar Disorder, MESH: Child, Chromosomes, Human, Age of Onset, Child, Genetics, Chromosome Mapping, 3. Good health, Europe, Psychiatry and Mental health, Phenotype, Schizophrenia, Microsatellite, Female, Chromosomes, Human, Pair 3, Psychology, Adult, Adolescent, MESH: Age of Onset, MESH: Chromosomes, Human, Pair 3, MESH: Phenotype, MESH: Chromosomes, Human, Statistics, Nonparametric, Article, Genetic determinism, Genomic Imprinting, 03 medical and health sciences, Cellular and Molecular Neuroscience, Genetic linkage, medicine, Humans, Bipolar disorder, Molecular Biology, MESH: Genome, Human, MESH: Adolescent, Linkage (software), MESH: Humans, Genome, Human, MESH: Adult, medicine.disease, MESH: Male, MESH: Genomic Imprinting, 030227 psychiatry, MESH: Lod Score, [SDV.MHEP.PSM]Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health, MESH: Statistics, Nonpar, MESH: Microsatellite Repeats, MESH: Europe, Lod Score, Age of onset, MESH: Chromosome Mapping, MESH: Female, 030217 neurology & neurosurgery, Microsatellite Repeats
وصف الملف: application/pdf
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المؤلفون: Philippe Froguel, Kazuo Hara, Kazuki Yasuda, Shuichi Otabe, Cécile Lecoeur, Takashi Kadowaki, Kazuyuki Tobe, Céline Populaire, Philippe Boutin, Emmanuelle Durand, Terumasa Okada, Christian Dina, Yasumichi Mori, Vincent Vatin
المساهمون: Génétique des maladies multifactorielles (GMM), Université de Lille, Droit et Santé - Centre National de la Recherche Scientifique (CNRS), Science et Ingénierie des Matériaux et Procédés (SIMaP), Université Joseph Fourier - Grenoble 1 (UJF) - Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP) - Institut National Polytechnique de Grenoble (INPG) - Centre National de la Recherche Scientifique (CNRS) - Université Grenoble Alpes (UGA), Physique, Aucune, Institut de Chimie de la Matière Condensée de Bordeaux (ICMCB), Université de Bordeaux (UB) - Centre National de la Recherche Scientifique (CNRS), Développement artériel, Université Paris Descartes - Paris 5 (UPD5) - Institut National de la Santé et de la Recherche Médicale (INSERM), Mercator Océan, Société Civile CNRS Ifremer IRD Météo-France SHOM, Itoh laboratory, Division of Materials Physics, Osaka University [Osaka] - School of Engineering Science, Section of Genomic Medicine, Imperial College London, Genome Centre, Imperial College London - Hammersmith campus, Université de Lille, Droit et Santé-Centre National de la Recherche Scientifique (CNRS), Université Joseph Fourier - Grenoble 1 (UJF)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-Institut National Polytechnique de Grenoble (INPG)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut Polytechnique de Bordeaux-Université de Bordeaux (UB), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Osaka University [Osaka]-School of Engineering Science, Imperial College London-Hammersmith campus, Université Joseph Fourier - Grenoble 1 (UJF)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP)-Institut National Polytechnique de Grenoble (INPG)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes (UGA), Centre National de la Recherche Scientifique (CNRS)-Université de Bordeaux (UB)
المصدر: Diabetes
Diabetes, American Diabetes Association, 2002, 51 (4), pp.1247-55مصطلحات موضوعية: MESH : Chromosomes, Human, Pair 20, MESH : Transcription Factors, Genetic Linkage, MESH: Basic Helix-Loop-Helix Leucine Zipper Transcription Factors, Endocrinology, Diabetes and Metabolism, Chromosomes, Human, Pair 20, MESH : Japan, Type 2 diabetes, MESH: Genetic Markers, MESH : Chromosomes, Human, Pair 3, Genome, MESH : Chromosomes, Human, Pair 1, MESH : Chromosomes, Human, Pair 7, 0302 clinical medicine, Japan, MESH : Diabetes Mellitus, Type 2, MESH: Chromosomes, Human, Pair 20, MESH : Genetic Markers, Age of Onset, MESH: Japan, Genetics, 0303 health sciences, education.field_of_study, MESH: Middle Aged, MESH: Nuclear Family, Basic Helix-Loop-Helix Leucine Zipper Transcription Factors, MESH: Genetic Predisposition to Disease, Chromosome Mapping, MESH: Transcription Factors, Middle Aged, MESH : Adult, MESH : Chromosomes, Human, Pair 15, 3. Good health, MESH : Age of Onset, DNA-Binding Proteins, Hepatocyte Nuclear Factor 4, Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 3, MESH: Hepatocyte Nuclear Factor 4, MESH : DNA-Binding Proteins, MESH : Basic Helix-Loop-Helix Leucine Zipper Transcription Factors, Chromosomes, Human, Pair 7, MESH: Diabetes Mellitus, Type 2, Adult, Genetic Markers, MESH : Genome, Human, MESH: Chromosomes, Human, Pair 7, MESH: Chromosomes, Human, Pair 1, MESH: Age of Onset, Population, MESH: Chromosomes, Human, Pair 3, 030209 endocrinology & metabolism, Susceptibility gene, Biology, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, MESH: Phosphoproteins, Nuclear Family, 03 medical and health sciences, MESH : Hepatocyte Nuclear Factor 4, Internal Medicine, medicine, Humans, Genetic Predisposition to Disease, MESH : Middle Aged, education, Gene, MESH: Genome, Human, 030304 developmental biology, Linkage (software), Chromosomes, Human, Pair 15, MESH: Humans, Genome, Human, MESH : Humans, Chromosome, MESH: Adult, medicine.disease, Phosphoproteins, Sib pairs, Diabetes Mellitus, Type 2, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, MESH : Genetic Predisposition to Disease, MESH : Nuclear Family, MESH : Phosphoproteins, MESH: Chromosome Mapping, MESH: Linkage (Genetics), MESH: DNA-Binding Proteins, MESH : Linkage (Genetics), MESH : Chromosome Mapping, Transcription Factors, MESH: Chromosomes, Human, Pair 15
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المؤلفون: Laurent Abel, Patricia Tortevoye, Anne Boland, Vincent Pedergnana, Minji Byun, Sabine Plancoulaine, Delphine Bacq-Daian, Antoine Gessain, Jean-Laurent Casanova
المساهمون: Génétique Humaine des Maladies Infectieuses (Inserm U980), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Epidémiologie et Physiopathologie des Virus Oncogènes / Oncogenic Virus Epidemiology and Pathophysiology (EPVO (UMR_3569 / U-Pasteur_3)), Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller University [New York], Centre National de Génotypage (CNG), Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Herrada, Anthony
المصدر: European Journal of Human Genetics
European Journal of Human Genetics, 2012, 20 (6), pp.690-695. ⟨10.1038/ejhg.2011.260⟩مصطلحات موضوعية: Male, viruses, [SDV]Life Sciences [q-bio], MESH: Herpesviridae Infections, Antibodies, Viral, Genetic analysis, MESH: Aged, 80 and over, Seroepidemiologic Studies, MESH: Child, Cameroon, Child, Genetics (clinical), Genetics, Aged, 80 and over, MESH: Aged, education.field_of_study, MESH: Middle Aged, MESH: Genetic Predisposition to Disease, Family aggregation, virus diseases, Herpesviridae Infections, Middle Aged, Major gene, MESH: Infant, [SDV] Life Sciences [q-bio], Child, Preschool, Herpesvirus 8, Human, Female, Chromosomes, Human, Pair 3, Adult, Adolescent, Population, MESH: Chromosomes, Human, Pair 3, Locus (genetics), Genes, Recessive, Biology, Article, Genetic linkage, Seroprevalence, Humans, Family, Genetic Predisposition to Disease, education, Gene, MESH: Family, MESH: Genes, Recessive, Aged, MESH: Adolescent, MESH: Herpesvirus 8, Human, MESH: Humans, MESH: Seroepidemiologic Studies, MESH: Child, Preschool, Infant, MESH: Adult, MESH: Cameroon, Virology, MESH: Male, MESH: Female, MESH: Antibodies, Viral
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المؤلفون: Sylvia Quemener, M. Collet, Marc De Braekeleer, Huyen Anh Nguyen, Frédéric Morel, Caroline Benech, Claude Férec, Anne-Hélène Saliou, Audrey Basinko, Marie-Josée Le Bris, Philippe Parent, Aurore Perrin, Nathalie Douet-Guilbert
المساهمون: Génétique moléculaire et génétique épidémiologique, Université de Brest (UBO)-Institut National de la Santé et de la Recherche Médicale (INSERM), Laboratoire de cytogénétique [Brest], Centre Hospitalier Régional Universitaire de Brest (CHRU Brest)-Hôpital Morvan [Brest], Laboratoire d'histologie, d'embryologie et de cytogénétique, Université de Bretagne Occidentale - UFR Médecine et Sciences de la Santé (UBO UFR MSS), Université de Brest (UBO)-Université de Brest (UBO), Groupe d'Etude de la Thrombose de Bretagne Occidentale (GETBO), Université de Brest (UBO)-Institut Brestois Santé Agro Matière (IBSAM), Service de Gynécologie-Obstétrique (BREST - Gynéco-Obs), Centre Hospitalier Régional Universitaire de Brest (CHRU Brest), Service de Pédiatrie et de Génétique Médicale, Génétique, génomique fonctionnelle et biotechnologies (UMR 1078) (GGB), Institut Brestois Santé Agro Matière (IBSAM), Université de Brest (UBO)-Université de Brest (UBO)-EFS-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre de Recherche en Cancérologie Nantes-Angers (CRCNA), Centre Hospitalier Universitaire d'Angers (CHU Angers), PRES Université Nantes Angers Le Mans (UNAM)-PRES Université Nantes Angers Le Mans (UNAM)-Hôtel-Dieu de Nantes-Institut National de la Santé et de la Recherche Médicale (INSERM)-Hôpital Laennec-Centre National de la Recherche Scientifique (CNRS)-Faculté de Médecine d'Angers-Centre hospitalier universitaire de Nantes (CHU Nantes)
المصدر: American Journal of Medical Genetics Part A
American Journal of Medical Genetics Part A, Wiley, 2010, 152A (10), pp.2646-50. ⟨10.1002/ajmg.a.32982⟩مصطلحات موضوعية: Adult, Male, MESH: Gene Rearrangement, [SDV]Life Sciences [q-bio], MESH: Chromosomes, Human, Pair 3, MESH: Chromosomes, Human, Pair 2, Chromosomal translocation, MESH: Amniotic Fluid, Chromosomal rearrangement, Biology, Translocation, Genetic, law.invention, 03 medical and health sciences, MESH: Pregnancy, law, Pregnancy, Genetics, Humans, Crossing Over, Genetic, Lymphocytes, Genetics (clinical), ComputingMilieux_MISCELLANEOUS, 030304 developmental biology, MESH: Crossing Over, Genetic, Gene Rearrangement, Recombination, Genetic, 0303 health sciences, MESH: Humans, 030305 genetics & heredity, MESH: Adult, Amniotic Fluid, MESH: Male, MESH: Translocation, Genetic, Transmission (mechanics), MESH: Karyotyping, Chromosomes, Human, Pair 2, Karyotyping, MESH: Lymphocytes, MESH: Recombination, Genetic, Female, Chromosomes, Human, Pair 3, MESH: Chromosomes, Human, Pair 18, Chromosomes, Human, Pair 18, MESH: Female
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المؤلفون: Suzanna Bota, Sophie Moreno-Swirc, Jeannette Bourguignon, Mathieu Salaün, Luc Thiberville, Richard Sesboüé, Josette Métayer
المساهمون: Laboratoire d'Informatique, de Traitement de l'Information et des Systèmes (LITIS), Institut national des sciences appliquées Rouen Normandie (INSA Rouen Normandie), Institut National des Sciences Appliquées (INSA)-Normandie Université (NU)-Institut National des Sciences Appliquées (INSA)-Normandie Université (NU)-Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Université Le Havre Normandie (ULH), Normandie Université (NU), Génétique médicale et fonctionnelle du cancer et des maladies neuropsychiatriques, Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Service d'Anatomie et Cytologie Pathologique [CHU Rouen], CHU Rouen, Normandie Université (NU)-Normandie Université (NU)-Université de Rouen Normandie (UNIROUEN), Service de pneumologie, oncologie thoracique et soins intensifs respiratoires [Rouen], Normandie Université (NU)-Normandie Université (NU)-Hôpital Charles Nicolle [Rouen]-CHU Rouen, Supported by a research grant from the Comités Départementaux de la Ligue contre le Cancer (Eure et Seine Maritime), and the French Cancéropole Nord Ouest., Breton, Céline, Université Le Havre Normandie (ULH), Normandie Université (NU)-Institut national des sciences appliquées Rouen Normandie (INSA Rouen Normandie), Institut National des Sciences Appliquées (INSA)-Normandie Université (NU)-Institut National des Sciences Appliquées (INSA), Hôpital Charles Nicolle [Rouen], Normandie Université (NU)-Normandie Université (NU)-CHU Rouen
المصدر: American Journal of Respiratory and Critical Care Medicine
American Journal of Respiratory and Critical Care Medicine, American Thoracic Society, 2008, 177 (8), pp.880-6. ⟨10.1164/rccm.200704-598OC⟩
American Journal of Respiratory and Critical Care Medicine, 2008, 177 (8), pp.880-6. ⟨10.1164/rccm.200704-598OC⟩مصطلحات موضوعية: Male, Pathology, bronchoscopy, Biopsy, Loss of Heterozygosity, Critical Care and Intensive Care Medicine, [SDV.MHEP.PSR]Life Sciences [q-bio]/Human health and pathology/Pulmonology and respiratory tract, Loss of heterozygosity, MESH: Biopsy, 0302 clinical medicine, Bronchoscopy, Longitudinal Studies, MESH: Longitudinal Studies, Microdissection, MESH: Bronchial Neoplasms, MESH: Aged, MESH: Middle Aged, medicine.diagnostic_test, Bronchial Neoplasms, Middle Aged, follow-up studies, 3. Good health, MESH: Precancerous Conditions, 030220 oncology & carcinogenesis, MESH: Survival Analysis, Female, Microsatellite Instability, MESH: Disease Progression, Chromosomes, Human, Pair 3, Carcinoma in Situ, Pulmonary and Respiratory Medicine, Adult, medicine.medical_specialty, MESH: Chromosomes, Human, Pair 3, 03 medical and health sciences, disease progression, Intensive care, medicine, Humans, precancerous conditions, Aged, MESH: Loss of Heterozygosity, MESH: Carcinoma in Situ, MESH: Humans, business.industry, gene deletion, Carcinoma in situ, Microsatellite instability, Histology, MESH: Adult, medicine.disease, Survival Analysis, MESH: Male, 030228 respiratory system, MESH: Gene Deletion, [SDV.MHEP.PSR] Life Sciences [q-bio]/Human health and pathology/Pulmonology and respiratory tract, business, MESH: Female, MESH: Microsatellite Instability
وصف الملف: application/pdf
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المؤلفون: Claudine Junien, Guillaume Jondeau, R Timpl, Jean Weissenbach, Mon-Li Chu, Jean-Pierre Bourdarias, Catherine Boileau, Monique Coulon, Takako Sasaki, Gwenaëlle Collod, Loretta Renkart
المساهمون: Génétique, chromosome et cancer, Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), International Center for Young Scientits National Institute for Materials Science, International Center for Young Scientists, Structure et évolution des génomes (SEG), CNS-Université d'Évry-Val-d'Essonne (UEVE)-Centre National de la Recherche Scientifique (CNRS), Consultation Marfan, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Bichat, Université Paris Descartes - Paris 5 ( UPD5 ) -Institut National de la Santé et de la Recherche Médicale ( INSERM ), Department of Biochemistry & Molecular Biology, Thomas Jefferson University, Max-Planck-Institut für Biochemie ( MPIB ), Max-Planck-Gesellschaft, GENETHON, Genethon, Service de cardiologie et maladies vasculaires, Université de Versailles Saint-Quentin-en-Yvelines ( UVSQ ) -Assistance publique - Hôpitaux de Paris (AP-HP)-Hôpital Ambroise Paré, Service de biochimie, d'hormonologie et de génétique moléculaire, Max-Planck-Institut für Biochemie (MPIB), Généthon, Service de cardiologie et maladies vasculaires [CHU Ambroise Paré], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Ambroise Paré [AP-HP], Service de biochimie, d'hormonologie et de génétique moléculaire [CHU Amrboise Paré], COLLOD-BEROUD, Gwenaëlle, Max-Planck-Institut für Biochemie = Max Planck Institute of Biochemistry (MPIB)
المصدر: European Journal of Human Genetics
European Journal of Human Genetics, 1996, pp.292-5
European Journal of Human Genetics, Nature Publishing Group, 1996, pp.292-5
Eur J Hum Genet
Eur J Hum Genet, 1996, 4 (5), pp.292-5
Europe PubMed Central
European Journal of Human Genetics, Nature Publishing Group, 1996, 4 (5), pp.292-5مصطلحات موضوعية: MESH: Extracellular Matrix Proteins, Male, Candidate gene, MESH: Pedigree, MESH : Male, MESH: Chromosomes, Human, Pair 3, Locus (genetics), [SDV.GEN] Life Sciences [q-bio]/Genetics, MESH: Calcium-Binding Proteins, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, Biology, [SDV.BBM.BM] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology, MESH : Chromosomes, Human, Pair 3, MESH : Fluorescent Antibody Technique, Indirect, Marfan Syndrome, MESH: Marfan Syndrome, Extracellular matrix, MESH : Extracellular Matrix Proteins, Gene mapping, MESH : Calcium-Binding Proteins, Genetics, MESH: Fluorescent Antibody Technique, Indirect, Humans, MESH : Female, Marfan Syndrome type 2, Fluorescent Antibody Technique, Indirect, Gene, Genetics (clinical), [SDV.GEN]Life Sciences [q-bio]/Genetics, Extracellular Matrix Proteins, MESH: Humans, MESH : Marfan Syndrome, Calcium-Binding Proteins, MESH : Humans, Chromosome Mapping, [SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology, MESH: Male, Pedigree, Fibulin, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Genetic marker, MESH : Pedigree, Female, Chromosomes, Human, Pair 3, MESH: Chromosome Mapping, [ SDV.GEN ] Life Sciences [q-bio]/Genetics, MESH: Female, MESH : Chromosome Mapping
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33d0bef435628dba859d29495f22b6f5
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المؤلفون: Christine Kretz, Nicolas Dondaine, Jean-Louis Mandel, Bernard Payrastre, Valérie Tosch, Jocelyn Laporte, Nancy Monroy, Edmar Zanoteli, Holger Maria Rohde, Hélène Tronchère
المساهمون: Institut de génétique et biologie moléculaire et cellulaire (IGBMC), Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Louis Pasteur - Strasbourg I, Chaire Génétique Humaine, Collège de France (CdF (institution)), Université Louis Pasteur - Strasbourg I-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
المصدر: Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2006, 15 (21), pp.3098-106. ⟨10.1093/hmg/ddl250⟩مصطلحات موضوعية: Male, Myotubularin, MESH: Catalytic Domain, Protein tyrosine phosphatase, MESH: Amino Acid Sequence, MESH: Variation (Genetics), MESH: Protein Structure, Tertiary, 0302 clinical medicine, Phosphatidylinositol Phosphates, Catalytic Domain, Chlorocebus aethiops, MESH: Animals, Genetics (clinical), Genetics, 0303 health sciences, MESH: Muscle, Skeletal, MESH: Protein-Tyrosine-Phosphatase, MESH: Arginine, General Medicine, Protein Tyrosine Phosphatases, Non-Receptor, MESH: Phosphatidylinositol Phosphates, Pedigree, Cell biology, MESH: COS Cells, COS Cells, MESH: Phosphoric Monoester Hydrolases, Female, Chromosomes, Human, Pair 3, medicine.symptom, Myopathies, Structural, Congenital, MESH: Myopathies, Structural, Congenital, MESH: Pedigree, Molecular Sequence Data, Phosphatase, MESH: Chromosomes, Human, Pair 3, Mutation, Missense, MESH: Sequence Alignment, Biology, Arginine, Transfection, Cell Line, 03 medical and health sciences, medicine, Animals, Humans, Amino Acid Sequence, Centronuclear myopathy, Muscle, Skeletal, Myopathy, Molecular Biology, 030304 developmental biology, Dynamin, MESH: Mutation, Missense, MESH: Humans, MESH: Molecular Sequence Data, MESH: Transfection, Genetic Variation, [SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology, medicine.disease, Congenital myopathy, MESH: Cercopithecus aethiops, Phosphoric Monoester Hydrolases, MESH: Male, Protein Structure, Tertiary, MESH: Cell Line, DNM2, Protein Tyrosine Phosphatases, Sequence Alignment, MESH: Female, 030217 neurology & neurosurgery
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https://hal.archives-ouvertes.fr/hal-00188169 -
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المؤلفون: Richard Redon, Bernard Jost, Stanislas du Manoir, Thomas Hussenet, Alain Aurias, Nedjoua Mallem
المساهمون: Institut de génétique et biologie moléculaire et cellulaire (IGBMC), Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Louis Pasteur - Strasbourg I, Université Louis Pasteur - Strasbourg I-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
المصدر: Cancer Genetics and Cytogenetics
Cancer Genetics and Cytogenetics, Elsevier, 2006, 169 (2), pp.102-13. ⟨10.1016/j.cancergencyto.2006.03.009⟩مصطلحات موضوعية: Male, Cancer Research, MESH: Oncogenes, medicine.disease_cause, Polymerase Chain Reaction, 0302 clinical medicine, MESH: Aged, 80 and over, Tumor Cells, Cultured, MESH: In Situ Hybridization, Fluorescence, In Situ Hybridization, Fluorescence, Oligonucleotide Array Sequence Analysis, Genetics, Aged, 80 and over, MESH: Aged, 0303 health sciences, Expressed sequence tag, MESH: Middle Aged, medicine.diagnostic_test, Chromosome Mapping, Sarcoma, Amplicon, Middle Aged, 030220 oncology & carcinogenesis, Female, Chromosomes, Human, Pair 3, Adult, MESH: Chromosomes, Human, Pair 3, Biology, Gene dosage, 03 medical and health sciences, MESH: Gene Expression Profiling, medicine, Humans, MESH: Chromosome Aberrations, MESH: Tumor Cells, Cultured, Molecular Biology, 030304 developmental biology, Aged, Chromosome Aberrations, MESH: Humans, Gene Expression Profiling, Chromosome, MESH: Adult, MESH: Polymerase Chain Reaction, [SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology, Oncogenes, Molecular biology, MESH: Male, Chromosome 3, MESH: Oligonucleotide Array Sequence Analysis, MESH: Sarcoma, Carcinogenesis, MESH: Chromosome Mapping, MESH: Female, Fluorescence in situ hybridization, Comparative genomic hybridization
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المؤلفون: André Calas, Alexis Lebon, Hubert Vaudry, Hervé Tostivint, Isabelle Lihrmann, Mireille Morisson, Lucille Joly, Caroline Parmentier, Marc Ekker
المساهمون: Neuroendocrinologie cellulaire et moléculaire, Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Différenciation et communication neuronale et neuroendocrine (DC2N), Neuroscience Paris Seine (NPS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Biologie Paris Seine (IBPS), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Plate-Forme de Recherche en Imagerie Cellulaire de Haute-Normandie (PRIMACEN), Normandie Université (NU)-Normandie Université (NU)-Institute for Research and Innovation in Biomedicine (IRIB), Normandie Université (NU)-Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Laboratoire de Génétique Cellulaire (LGC), Ecole Nationale Vétérinaire de Toulouse (ENVT), Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Recherche Agronomique (INRA), UA 339 Laboratoire de Physiologie des Interactions Cellulaires, Centre National de la Recherche Scientifique (CNRS), University of Ottawa [Ottawa] (uOttawa), Institut Fédératif de Recherches Multidisciplinaires sur les Peptides (IFRMP 23), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre de Lutte Contre le Cancer Henri Becquerel Normandie Rouen (CLCC Henri Becquerel)-Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Normandie Université (NU)-Université Le Havre Normandie (ULH), Normandie Université (NU)-CHU Rouen, Normandie Université (NU)-Centre National de la Recherche Scientifique (CNRS), University of Ottawa [Ottawa], Neurobiologie des signaux intercellulaires (NSI), Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS), Institut National de la Recherche Agronomique (INRA)-Ecole Nationale Vétérinaire de Toulouse (ENVT), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées, CHU Rouen, Normandie Université (NU)-Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre de Lutte Contre le Cancer Henri Becquerel Normandie Rouen (CLCC Henri Becquerel)-Centre National de la Recherche Scientifique (CNRS), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Université de Toulouse (UT), ProdInra, Migration, Lihrmann, Isabelle, Centre National de la Recherche Scientifique (CNRS)-Institut de Biologie Paris Seine (IBPS), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)
المصدر: Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2006, 103 (7), pp.2237-2242. ⟨10.1073/pnas.0510700103⟩
Proceedings of the National Academy of Sciences of the United States of America, 2006, 103 (7), pp.2237-2242. ⟨10.1073/pnas.0510700103⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2006, 103, pp.2237-2242مصطلحات موضوعية: MESH: Somatostatin, [SDV]Life Sciences [q-bio], MESH: Amino Acid Sequence, [SDV.BC.BC]Life Sciences [q-bio]/Cellular Biology/Subcellular Processes [q-bio.SC], chemistry.chemical_compound, Mice, 0302 clinical medicine, Gene Duplication, Gene duplication, radiation hybrid mapping, MESH: Animals, MESH: Phylogeny, Phylogeny, Zebrafish, ComputingMilieux_MISCELLANEOUS, MESH: Evolution, Molecular, Segmental duplication, Genetics, 0303 health sciences, Multidisciplinary, MESH: Peptides, UROTENSIN, MESH: Genomics, MESH: Gene Duplication, MESH: Chickens, Chromosome Mapping, Genomics, Biological Sciences, MESH: Genes, [SDV] Life Sciences [q-bio], duplication, Chromosomes, Human, Pair 1, Tandem exon duplication, Chromosomes, Human, Pair 3, MESH: Rats, Sequence analysis, MESH: Chromosomes, Human, Pair 1, Urotensins, Molecular Sequence Data, MESH: Chromosomes, Human, Pair 3, Locus (genetics), Biology, Evolution, Molecular, 03 medical and health sciences, [SDV.BBM] Life Sciences [q-bio]/Biochemistry, Molecular Biology, [SDV.BC.BC] Life Sciences [q-bio]/Cellular Biology/Subcellular Processes [q-bio.SC], Animals, Humans, [SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology, Amino Acid Sequence, MESH: Zebrafish, Gene, MESH: Mice, 030304 developmental biology, Comparative genomics, MESH: Humans, MESH: Molecular Sequence Data, MESH: Urotensins, neuropeptides, SOMATOSTATIN, multigenic family, MOLECULAR EVOLUTION, Rats, chemistry, Genes, Urotensin-II, Peptides, MESH: Chromosome Mapping, Chickens, 030217 neurology & neurosurgery
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4babcadb3148f5c05075ed1c8e1582d
https://hal-normandie-univ.archives-ouvertes.fr/hal-02427123
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