المؤلفون: Christophe Charasse, Miguel A. Alonso, Rodrick Montjean, Dominique Pouthier, Leila Balafrej, Pierre Ronco, Jacques Dantal, Georges Deschênes, Jean-Michel Vallat, Eric LeGuern, Guillaume Canaud, Alain Bonnardeaux, Anne Guiochon-Mantel, Marie-Josèphe Tête, Olivier Gribouval, Olivia Boyer, Laurence Richard, Christelle Arrondel, Philippe Petiot, Geneviève Benoit, Odile Dubourg, Alexandre Karras, Evelyne Huynh Cong, Isabelle Broutin, Emmanuelle Plaisier, Corinne Antignac, Géraldine Mollet, Claire Pouteil-Noble, Marie-Claire Gubler, Sophie Saunier, Benoît Funalot, Patrice Deteix, Fabien Nevo

المساهمون: Néphropathies héréditaires et rein en développement (UMR_S 983), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Necker - Enfants Malades [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Service de néphrologie pédiatrique [CHU Necker], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Necker - Enfants Malades [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Université Paris Descartes - Paris 5 (UPD5), CHU Tenon [AP-HP], Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Université Pierre et Marie Curie - Paris 6 (UPMC), Service de Biochimie et Génétique Moléculaire [CHU Limoges], CHU Limoges, Centre de référence national neuropathies périphériques rares [CHU Limoges], Service de Neurologie [CHU Limoges], Service de néphrologie pédiatrique, Université de Montréal (UdeM)-CHU Sainte Justine [Montréal], SARS International Centre for Marine Molecular Biology, Neuropathies héréditaires et rein en développement, Institut National de la Santé et de la Recherche Médicale (INSERM), Equipe Avenir Tour Lavoisier, Université Paris Descartes - Paris 5 (UPD5)-CHU Necker - Enfants Malades [AP-HP], Service de néphrologie et transplantation, Hôpital Edouard Herriot [CHU - HCL], Hospices Civils de Lyon (HCL)-Hospices Civils de Lyon (HCL), Centre de Recherche Guy- Bernier, Hôpital Maisonneuve-Rosemont, Service de transplantation et soins intensifs, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris Descartes - Paris 5 (UPD5)-CHU Necker - Enfants Malades [AP-HP], CH de Saint-Brieuc, Service de Néphrologie et Immunologie Clinique, Hôtel Dieu-Centre hospitalier universitaire de Nantes (CHU Nantes), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Robert Debré, Université Paris Diderot - Paris 7 (UPD7), CHU Gabriel Montpied [Clermont-Ferrand], CHU Clermont-Ferrand, Institut de Myologie, Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Association française contre les myopathies (AFM-Téléthon)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Pierre et Marie Curie - Paris 6 (UPMC), Service de neurologie, Hospices Civils de Lyon (HCL)-Hôpital de la Croix-Rousse [CHU - HCL], Hospices Civils de Lyon (HCL), Service de Néphrologie, Centre Hospitalier de Luxembourg [Luxembourg] (CHL), CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière (CRICM), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Service de génétique moléculaire, pharmacogénétique et hormonologie, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Bicêtre, Laboratoire de cristallographie et RMN biologiques (LCRB - UMR 8015), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université Paris Descartes - Paris 5 (UPD5), Remodelage et Reparation du Tissu Renal, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centro de Biología Molecular Severo Ochoa [Madrid] (CBMSO), Universidad Autonoma de Madrid (UAM)-Consejo Superior de Investigaciones Científicas [Madrid] (CSIC), Service de Génétique Médicale [CHU Necker], Néphropathies héréditaires et rein en développement ( UMR_S 983 ), Assistance publique - Hôpitaux de Paris (AP-HP)-Institut National de la Santé et de la Recherche Médicale ( INSERM ) -CHU Necker - Enfants Malades [AP-HP], CHU Necker - Enfants Malades [AP-HP]-Assistance publique - Hôpitaux de Paris (AP-HP), Université Paris Descartes - Paris 5 ( UPD5 ), Service de néphrologie et dialyses, Assistance publique - Hôpitaux de Paris (AP-HP)-CHU Tenon [APHP], Université Pierre et Marie Curie - Paris 6 ( UPMC ), Université de Montréal-CHU Sainte Justine [Montréal], Institut National de la Santé et de la Recherche Médicale ( INSERM ), Université Paris Descartes - Paris 5 ( UPD5 ) -CHU Necker - Enfants Malades [AP-HP], Université Claude Bernard Lyon 1 ( UCBL ), Université de Lyon-Université de Lyon-Hospices Civils de Lyon ( HCL ) -Centre Hospitalier Lyon Sud [CHU - HCL] ( CHLS ), Hospices Civils de Lyon ( HCL ), Assistance publique - Hôpitaux de Paris (AP-HP)-Université Paris Descartes - Paris 5 ( UPD5 ) -CHU Necker - Enfants Malades [AP-HP], Hôtel Dieu-Centre hospitalier universitaire de Nantes ( CHU Nantes ), Assistance publique - Hôpitaux de Paris (AP-HP)-Hôpital Robert Debré, Université Paris Diderot - Paris 7 ( UPD7 ), CHU Gabriel Montpied ( CHU ), Université Pierre et Marie Curie - Paris 6 ( UPMC ) -Commissariat à l'énergie atomique et aux énergies alternatives ( CEA ) -Assistance publique - Hôpitaux de Paris (AP-HP)-Association française contre les myopathies ( AFM-Téléthon ) -Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Centre National de la Recherche Scientifique ( CNRS ), Hospices Civils de Lyon ( HCL ) -Hôpital de la Croix-Rousse [CHU - HCL], Centre Hospitalier de Luxembourg, Centre de Référence pour les Epilepsies Rares, Assistance publique - Hôpitaux de Paris (AP-HP)-CHU Pitié-Salpêtrière [APHP]-Centre de Référence pour les Epilepsies Rares, Service de Génétique [Pitié-Salpêtrière], Université Pierre et Marie Curie - Paris 6 ( UPMC ) -Assistance publique - Hôpitaux de Paris (AP-HP)-CHU Pitié-Salpêtrière [APHP], Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière ( CRICM ), 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 ), Université Paris-Sud - Paris 11 ( UP11 ) -Assistance publique - Hôpitaux de Paris (AP-HP)-Hôpital Bicêtre, Laboratoire de cristallographie et RMN biologiques ( LCRB - UMR 8015 ), Université Paris Descartes - Paris 5 ( UPD5 ) -Centre National de la Recherche Scientifique ( CNRS ), Université Pierre et Marie Curie - Paris 6 ( UPMC ) -Institut National de la Santé et de la Recherche Médicale ( INSERM ), Centro de Biología Molecular Severo Ochoa ( CBMSO ), Universidad Autonoma de Madrid ( UAM ) -Consejo Superior de Investigaciones Científicas [Spain] ( CSIC ), RONCO, Pierre, Université Pierre et Marie Curie - Paris 6 (UPMC)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Association française contre les myopathies (AFM-Téléthon)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Université Paris Descartes - Paris 5 (UPD5)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Universidad Autónoma de Madrid (UAM)-Consejo Superior de Investigaciones Científicas [Madrid] (CSIC), CHU de Saint-Brieuc, Agence Nationale de la Recherche (France), Association Française contre les Myopathies, Fondation pour la Recherche Médicale, Fonds de la Recherche en Sante du Québec, Ministerio de Ciencia e Innovación (España)

المصدر: New England Journal of Medicine
New England Journal of Medicine, Massachusetts Medical Society, 2011, 365 (25), pp.2377-88. ⟨10.1056/NEJMoa1109122⟩
ResearcherID
New England Journal of Medicine, Massachusetts Medical Society, 2011, 365 (25), pp.2377-88. 〈10.1056/NEJMoa1109122〉
New England Journal of Medicine, 2011, 365 (25), pp.2377-88. ⟨10.1056/NEJMoa1109122⟩
Digital.CSIC. Repositorio Institucional del CSIC
instname

مصطلحات موضوعية: Male, Charcot–Marie–Tooth neuropathy, Pathology, MESH : Actins, MESH : Charcot-Marie-Tooth Disease, urologic and male genital diseases, Mice, Myelin, 0302 clinical medicine, MESH : Child, Charcot-Marie-Tooth Disease, MESH: Child, MESH: Charcot-Marie-Tooth Disease, Medicine, MESH: Animals, Age of Onset, Child, 0303 health sciences, MESH: Middle Aged, Glomerulosclerosis, Focal Segmental, General Medicine, female genital diseases and pregnancy complications, MESH : Age of Onset, 3. Good health, MESH : Phenotype, [ SDV.BBM.GTP ] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], Myelin maintenance, MESH: Young Adult, [SDV.BBM.GTP] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], MESH: Myelin and Lymphocyte-Associated Proteolipid Proteins, MESH: Proteolipids, MESH : Heterozygote, medicine.medical_specialty, Proteolipids, MESH: Age of Onset, MESH : Young Adult, Formins, MESH: Phenotype, MESH: Actins, 03 medical and health sciences, MESH : Adolescent, [SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], Humans, MESH: Myelin Proteins, MESH : Middle Aged, MESH: Adolescent, MESH: Humans, MESH : Humans, Membrane Transport Proteins, Kidney metabolism, MESH: Adult, medicine.disease, MESH : Glomerulosclerosis, Focal Segmental, INF2, Endocrinology, Mutation, MESH: Schwann Cells, MESH: Female, 030217 neurology & neurosurgery, Kidney, MESH: Membrane Transport Proteins, Glomerulosclerosis, Focal segmental glomerulosclerosis, MESH : Membrane Transport Proteins, Peripheral myelin protein 22, MESH : Myelin and Lymphocyte-Associated Proteolipid Proteins, MESH : Female, MESH: Heterozygote, Myelin and Lymphocyte-Associated Proteolipid Proteins, Microfilament Proteins, Middle Aged, MESH : Adult, MESH : Kidney, Phenotype, medicine.anatomical_structure, Female, MESH : Mutation, Myelin Proteins, Adult, Heterozygote, MESH: Mutation, Adolescent, MESH : Microfilament Proteins, MESH: Glomerulosclerosis, Focal Segmental, MESH : Male, MESH : Schwann Cells, MESH : Myelin Proteins, Young Adult, MESH: Microfilament Proteins, Glomerulopathy, Internal medicine, MESH : Mice, Animals, MESH: Mice, 030304 developmental biology, urogenital system, business.industry, Myelin protein zero, MESH: Kidney, Actins, MESH: Male, MESH : Proteolipids, Schwann Cells, MESH : Animals, business

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0457b8025e982b6d35601f1dc4de4b88
https://www.hal.inserm.fr/inserm-00919173

المؤلفون: Lee A. Witters, Jérôme Salles, Françoise Sargueil, Bertrand Garbay, Claude Cassagne, Anja Knoll-Gellida

المساهمون: Unité de Nutrition Humaine (UNH), Institut National de la Recherche Agronomique (INRA)-Université d'Auvergne - Clermont-Ferrand I (UdA)-Clermont Université, Laboratoire de biogenèse membranaire (LBM), Université de Bordeaux (UB)-Centre National de la Recherche Scientifique (CNRS), Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)

المصدر: Biochimica et Biophysica Acta Molecular and Cell Biology of Lipids
Biochimica et Biophysica Acta Molecular and Cell Biology of Lipids, 2003, 1631 (3), pp.229-238. ⟨10.1016/s1388-1981(03)00041-6⟩
Biochimica et Biophysica Acta Molecular and Cell Biology of Lipids, Elsevier, 2003, 1631 (3), pp.229-238. ⟨10.1016/s1388-1981(03)00041-6⟩

مصطلحات موضوعية: [SDV]Life Sciences [q-bio], MESH: CCAAT-Enhancer-Binding Proteins, Mice, Cytosol, 0302 clinical medicine, MESH: Cytosol, MESH: Reverse Transcriptase Polymerase Chain Reaction, Gene expression, MESH: Animals, MESH: Mice, Neurologic Mutants, MESH: Peripheral Nervous System, 0303 health sciences, Reverse Transcriptase Polymerase Chain Reaction, MESH: Gene Expression Regulation, Enzymologic, myelination, MESH: Transcription Factors, Trembler, Sciatic Nerve, Cell biology, DNA-Binding Proteins, Isoenzymes, acetyl-CoA carboxylase, MESH: Sciatic Nerve, medicine.anatomical_structure, Peripheral nervous system, MESH: Isoenzymes, MESH: DNA Probes, DNA Probes, Sterol Regulatory Element Binding Protein 1, Myelin Proteins, Gene isoform, medicine.medical_specialty, Blotting, Western, Biology, Gene Expression Regulation, Enzymologic, Mice, Neurologic Mutants, MESH: Sterol Regulatory Element Binding Protein 1, 03 medical and health sciences, Internal medicine, Peripheral Nervous System, medicine, Animals, MESH: Myelin Proteins, MESH: Blotting, Northern, MESH: Blotting, Western, RNA, Messenger, MESH: Mice, Molecular Biology, MESH: RNA, Messenger, 030304 developmental biology, Messenger RNA, Acetyl-CoA carboxylase, Promoter, Cell Biology, Blotting, Northern, biology.organism_classification, Sterol regulatory element-binding protein, Endocrinology, nervous system, sterol regulatory element binding protein, CCAAT-Enhancer-Binding Proteins, gene expression, MESH: Acetyl-CoA Carboxylase, MESH: DNA-Binding Proteins, 030217 neurology & neurosurgery, Transcription Factors

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66c1a3ff73e6fa45da75bc6b425453e0
https://doi.org/10.1016/s1388-1981(03)00041-6

المؤلفون: Uggenti, Carolina, De Stefano, M Egle, Costantino, Michele, Loreti, Simona, Pisano, Annalinda, Avallone, Bice, Talora, Claudio, Magnaghi, Valerio, Tata, Ada Maria

المساهمون: Carolina, Uggenti, M., Egle De Stefano, Michele, Costantino, Simona, Loreti, Annalinda, Pisano, Avallone, Bice, Claudio, Talora, Valerio, Magnaghi, Ada Maria, Tata, Department of Biology and Biotechnology 'Charles Darwin', Institut Pasteur, Fondation Cenci Bolognetti - Istituto Pasteur Italia, Fondazione Cenci Bolognetti, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Università degli Studi di Roma 'La Sapienza' = Sapienza University [Rome], Center for Research in Neurobiology 'Daniel Bovet', Università degli Studi di Roma 'La Sapienza' = Sapienza University [Rome], Réseau International des Instituts Pasteur (RIIP), Department of Biology, Università degli studi di Napoli Federico II, Department of Farmaceutical and Biomolecular Sciences, University of Milan, Contract grant sponsor: Progetti di Ricerca 'Sapienza,' Universiy of Roma, contract grant number: C26A122HYC to (A.M.T.). Contract grant sponsor: Association Francaise Contre les Myopathies, contract grant number: 14163/2012 (to V.M.). Contract grant sponsor: ASI (Italian Space Agency) (toM.E.D.S.)

المصدر: Developmental Neurobiology
Developmental Neurobiology, Wiley, 2014, 74 (7), pp.676-91. ⟨10.1002/dneu.22161⟩

مصطلحات موضوعية: MESH: Signal Transduction, MESH: Axons, MESH: Myelin Sheath, Neurogenesis, Arecoline, acetylcholine, MESH: Peripheral Nervous System Agents, MESH: Mice, Knockout, muscarinic receptors, MESH: Nerve Degeneration, MESH: Arecoline, MESH: Myelin Proteins, Animals, MESH: Animals, RNA, Messenger, Rats, Wistar, MESH: Receptor, Muscarinic M4, Cells, Cultured, Myelin Sheath, MESH: RNA, Messenger, MESH: Receptor, Muscarinic M2, Mice, Knockout, Receptor, Muscarinic M2, Receptor, Muscarinic M4, electron microscopy, myelin protein, MESH: Rats, Wistar, MESH: Transcription Factors, Peripheral Nervous System Agents, muscarinic receptors, Schwann cells, acetylcholine, myelin proteins, transcription factors, Sciatic Nerve, Axons, MESH: Neurogenesis, MESH: Sciatic Nerve, nervous system, myelin proteins, schwann cells, transcription factors, Schwann cells, Nerve Degeneration, [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], Schwann Cells, MESH: Schwann Cells, Myelin Proteins, MESH: Cells, Cultured, Signal Transduction, Transcription Factors

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f9a865e4b3fec537788fd72c666e88be
http://hdl.handle.net/11588/572067

المؤلفون: Christophe Côme, Jérôme Salles, Claude Cassagne, Anja Knoll-Gellida, Patricia Costaglioli, Bertrand Garbay

المساهمون: Unité de Nutrition Humaine (UNH), Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Université de Bordeaux Ségalen [Bordeaux 2], Laboratoire de biogenèse membranaire (LBM), Université de Bordeaux (UB)-Centre National de la Recherche Scientifique (CNRS), Institut National de la Recherche Agronomique (INRA)-Université d'Auvergne - Clermont-Ferrand I (UdA)-Clermont Université

المصدر: FEBS Letters
FEBS Letters, Wiley, 2001, 509 (3), pp.413-416. ⟨10.1016/s0014-5793(01)03205-7⟩
FEBS Letters, 2001, 509 (3), pp.413-416. ⟨10.1016/s0014-5793(01)03205-7⟩

مصطلحات موضوعية: Nervous system, [SDV]Life Sciences [q-bio], Biochemistry, Mice, Myelin, 0302 clinical medicine, Structural Biology, delta-like protein, MESH: Gene Expression Regulation, Developmental, Gene expression, Schwann cells, MESH: Animals, DNA array, Oligonucleotide Array Sequence Analysis, MESH: Mice, Neurologic Mutants, 0303 health sciences, biology, nervous system, Intracellular Signaling Peptides and Proteins, Gene Expression Regulation, Developmental, myelination, Cell Differentiation, differentiation, Trembler, Sciatic Nerve, Phenotype, MESH: Sciatic Nerve, medicine.anatomical_structure, Peripheral nervous system, MESH: Membrane Proteins, Homeotic gene, Myelin Proteins, MESH: Cell Differentiation, MESH: Mutation, Biophysics, Schwann cell, MESH: Phenotype, Schwann cellsc, Mice, Neurologic Mutants, MESH: Gene Expression Profiling, 03 medical and health sciences, MESH: Mice, Inbred C57BL, MESH: Intracellular Signaling Peptides and Proteins, MESH: Homeodomain Proteins, Genetics, medicine, Animals, MESH: Blotting, Northern, MESH: Myelin Proteins, RNA, Messenger, MESH: Mice, Molecular Biology, MESH: RNA, Messenger, 030304 developmental biology, Homeodomain Proteins, Gene Expression Profiling, Membrane Proteins, Cell Biology, Blotting, Northern, biology.organism_classification, Molecular biology, Mice, Inbred C57BL, Mutation, MESH: Oligonucleotide Array Sequence Analysis, MESH: Schwann Cells, cDNA array, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::236d73f83e38e739f1a2d0ab049cb3f9
https://doi.org/10.1016/s0014-5793(01)03205-7

المؤلفون: Anja Knoll, Claude Cassagne, Jacques Bonnet, Jérôme Salles, Françoise Boiron-Sargueil, Bertrand Garbay, Anthony M. Heape

المساهمون: Unité de Nutrition Humaine (UNH), Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Institut National de la Recherche Agronomique (INRA)-Université d'Auvergne - Clermont-Ferrand I (UdA)-Clermont Université

المصدر: Annals of the New York Academy of Sciences
Annals of the New York Academy of Sciences, Wiley, 1999, 883, pp.262-72

مصطلحات موضوعية: Heterozygote, MESH: Myelin Sheath, [SDV]Life Sciences [q-bio], Mutant, Biology, medicine.disease_cause, General Biochemistry, Genetics and Molecular Biology, Mice, Mice, Neurologic Mutants, 03 medical and health sciences, Myelin, 0302 clinical medicine, History and Philosophy of Science, Charcot-Marie-Tooth Disease, MESH: Charcot-Marie-Tooth Disease, medicine, Animals, Humans, MESH: Myelin Proteins, MESH: Animals, MESH: Mice, Gene, Myelin Sheath, MESH: Heterozygote, MESH: Mice, Neurologic Mutants, 030304 developmental biology, Regulation of gene expression, Genetics, 0303 health sciences, Mutation, MESH: Humans, General Neuroscience, Homozygote, Heterozygote advantage, Trembler, biology.organism_classification, MESH: Gene Expression Regulation, Cell biology, Disease Models, Animal, medicine.anatomical_structure, Gene Expression Regulation, Peripheral nervous system, MESH: Disease Models, Animal, Myelin Proteins, 030217 neurology & neurosurgery, MESH: Homozygote

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3311343506b07e9686d987956e22b2d
https://doi.org/10.1111/j.1749-6632.1999.tb08588.x

المؤلفون: Lucette Pelletier, Jean-Charles Guéry, Karine Lélu, Virginie Robert, Britta Engelhardt, Sophie Laffont, Laurent Delpy, Eliane Foulon

المساهمون: Contrôle de la Réponse Immune B et des Lymphoproliférations (CRIBL), Université de Limoges (UNILIM)-Génomique, Environnement, Immunité, Santé, Thérapeutique (GEIST FR CNRS 3503)-Centre National de la Recherche Scientifique (CNRS), Interactions hôtes-agents pathogènes [Toulouse] (IHAP), Institut National de la Recherche Agronomique (INRA)-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, Centre National de la Recherche Scientifique (CNRS)-Université de Limoges (UNILIM)-Génomique, Environnement, Immunité, Santé, Thérapeutique (GEIST FR CNRS 3503)

المصدر: European Journal of Immunology
European Journal of Immunology, Wiley-VCH Verlag, 2010, 40 (12), pp.3489-98. ⟨10.1002/eji.201040678⟩

مصطلحات موضوعية: CD4-Positive T-Lymphocytes, Adoptive cell transfer, Estrogen receptor, Inbred C57BL, MESH: Estrogens, MESH: Mice, Knockout, Mice, 0302 clinical medicine, Cell Movement, Immunology and Allergy, MESH: Animals, Encephalomyelitis, MESH: Cell Movement, MESH: Estrogen Receptor alpha, Cells, Cultured, Mice, Knockout, Cultured, biology, Brain, MESH: CD4-Positive T-Lymphocytes, Adoptive Transfer, Myelin-Associated Glycoprotein, medicine.anatomical_structure, [SDV.IMM]Life Sciences [q-bio]/Immunology, Female, medicine.symptom, Inflammation Mediators, Myelin Proteins, MESH: Cells, Cultured, medicine.medical_specialty, Encephalomyelitis, Autoimmune, Experimental, Multiple Sclerosis, medicine.drug_class, Knockout, Ovariectomy, Cells, Immunology, MESH: Inflammation Mediators, MESH: Ovariectomy, Inflammation, Myelin oligodendrocyte glycoprotein, 03 medical and health sciences, Experimental, MESH: Brain, Immune system, MESH: Mice, Inbred C57BL, Internal medicine, medicine, Animals, Humans, MESH: Myelin Proteins, MESH: Myelin-Associated Glycoprotein, MESH: Encephalomyelitis, Autoimmune, Experimental, MESH: Mice, MESH: Humans, Animal, Estrogen Receptor alpha, Estrogens, MESH: Multiple Sclerosis, Oligodendrocyte, Mice, Inbred C57BL, Disease Models, Animal, MESH: Adoptive Transfer, MESH: Cytoprotection, Endocrinology, Estrogen, Cytoprotection, Disease Models, biology.protein, Myelin-Oligodendrocyte Glycoprotein, MESH: Disease Models, Animal, MESH: Female, 030217 neurology & neurosurgery, 030215 immunology, Hormone, Autoimmune

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc0b34f0a49a590252844230d3fdcb10
https://hal.archives-ouvertes.fr/hal-00697795

المؤلفون: Giovanni Levi, Luana Benedetti, Marina Grandis, Tiziana Vigo, Stefano Mantero, Angelo Schenone, Gianluigi Mancardi, Michele Abbruzzese, Lucilla Nobbio, Claudio Brancolini

المساهمون: Evolution des régulations endocriniennes (ERE), Muséum national d'Histoire naturelle (MNHN)-Centre National de la Recherche Scientifique (CNRS), Interfaces, Traitements, Organisation et Dynamique des Systèmes (ITODYS (UMR_7086)), Université Paris Diderot - Paris 7 (UPD7)-Centre National de la Recherche Scientifique (CNRS), Institut Jacques Monod (IJM (UMR_7592)), Istituto Clinico Humanitas [Milan] (IRCCS Milan), Humanitas University [Milan] (Hunimed), Department of Neuroscience, Ophtalmology and Genetics, Genova, Centre National de la Recherche Scientifique (CNRS)-Université Paris Diderot - Paris 7 (UPD7)

المصدر: Neurobiology of Disease
Neurobiology of Disease, Elsevier, 2004, 16 (1), pp.263-73. ⟨10.1016/j.nbd.2004.02.007⟩
Neurobiology of Disease, Elsevier, 2004, 16 (1), pp.263-273. ⟨10.1016/j.nbd.2004.02.007⟩
Neurobiology of Disease, Vol 16, Iss 1, Pp 263-273 (2004)

مصطلحات موضوعية: [SDV.NEU.NB]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology, Cell, Stimulation, Animals, Genetically Modified, Myelin, 0302 clinical medicine, Charcot-Marie-Tooth Disease, Peripheral myelin protein 22, MESH: Charcot-Marie-Tooth Disease, MESH: Animals, Axon, [SDV.BDD]Life Sciences [q-bio]/Development Biology, Cells, Cultured, ComputingMilieux_MISCELLANEOUS, 0303 health sciences, Cell Differentiation, Motility, Schwann cell, Cell biology, medicine.anatomical_structure, Neurology, CMT1A, [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], Hereditary neuropathy, Myelin Proteins, MESH: Cells, Cultured, MESH: Cell Differentiation, MESH: Rats, Transgene, Biology, lcsh:RC321-571, [SDV.BDLR.RS]Life Sciences [q-bio]/Reproductive Biology/Sexual reproduction, MESH: Animals, Genetically Modified, 03 medical and health sciences, medicine, Animals, MESH: Myelin Proteins, lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry, 030304 developmental biology, [SDV.BDLR]Life Sciences [q-bio]/Reproductive Biology, [SDV.BDD.MOR]Life Sciences [q-bio]/Development Biology/Morphogenesis, Rats, [SDV.BDD.EO]Life Sciences [q-bio]/Development Biology/Embryology and Organogenesis, PMP22, nervous system, Immunology, Schwann Cells, MESH: Schwann Cells, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0400e1108ee80c03aaa0d470c2014ef9
https://hal.archives-ouvertes.fr/hal-00181102

المؤلفون: p sindou, Anani, T., Garbay, B., Couratier, P., Lagrange, E., Vallat, J.

المساهمون: Service de Neurologie [CHU Limoges], CHU Limoges, Lab. de Biogenèse Membranaire, UMR-CNRS, 5544, Univ. Victor Segalen Bordeaux II, Bordeaux, France, Neuroépidémiologie Tropicale (NET), Institut Génomique, Environnement, Immunité, Santé, Thérapeutique (GEIST), Université de Limoges (UNILIM)-Université de Limoges (UNILIM)-CHU Limoges-Institut d'Epidémiologie Neurologique et de Neurologie Tropicale-Institut National de la Santé et de la Recherche Médicale (INSERM), Sindou, Philippe

المصدر: Revue Neurologique
Revue Neurologique, Elsevier Masson, 1999, 155 (2), pp.97-110
HAL

مصطلحات موضوعية: Male, DNA, Complementary, MESH: Gene Expression, Genotype, MESH: Chromosomes, Human, Pair 1, DNA Mutational Analysis, MESH: Membrane Glycoproteins, MESH: Gap Junctions, Gene Expression, Chromosome Disorders, [SDV.BC]Life Sciences [q-bio]/Cellular Biology, MESH: Phenotype, Severity of Illness Index, Connexins, MESH: Genotype, Charcot-Marie-Tooth Disease, MESH: Severity of Illness Index, MESH: Charcot-Marie-Tooth Disease, Humans, Point Mutation, MESH: Myelin Proteins, MESH: Chromosome Aberrations, MESH: DNA Mutational Analysis, [SDV.BC] Life Sciences [q-bio]/Cellular Biology, Alleles, MESH: Point Mutation, Chromosome Aberrations, MESH: Chromosome Disorders, Membrane Glycoproteins, MESH: Humans, MESH: Alleles, Gap Junctions, MESH: DNA, Complementary, MESH: Male, MESH: Connexins, Phenotype, Chromosomes, Human, Pair 1, Female, MESH: Female, Myelin Proteins

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0b0ae5b0b72a54baf9a9d89c82b11b01
https://hal.archives-ouvertes.fr/hal-02504156