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المؤلفون: Wolfgang H. Oertel, Bertrand Friguet, Gesine Respondek, Günter U. Höglinger, Matthias Höllerhage, Agathe Tarze, Stefanie Müssner, Mohamed Salama, Christel Depienne, Agnès Rastetter, Anderson de Andrade, Pierre Champy, Elizabeth Sumi Yamada
المساهمون: Guellaen, Georges, Experimental Neurology, Philipps University, Experimental Neuropathology Laboratory, University Hospital João de Barros Barreto-Federal University of Para - Universidade Federal do Pará - UFPA [Belém, Brazil] (UFPA), German Research Center for Neurodegenerative Diseases - Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE), Department of Neurology, Technische Universität Munchen - Université Technique de Munich [Munich, Allemagne] (TUM), Neurologie et thérapeutique expérimentale, Université Pierre et Marie Curie - Paris 6 (UPMC)-IFR70-Institut National de la Santé et de la Recherche Médicale (INSERM), 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), Laboratoire de Biologie Cellulaire du vieillissement, Université Pierre et Marie Curie - Paris 6 (UPMC)-IFR83, Laboratoire de Pharmacognosie (BioCIS), Université Paris-Sud - Paris 11 (UP11)-Centre National de la Recherche Scientifique (CNRS), This work was supported by the Deutsche Forschungsgemeinschaft (HO2402/6-1, HO2402/8-1), the German Ministry of Education and Research (BMBF EF 10-54), the Centre National de la Recherche Scientifique (CNRS), a Marie Curie Incoming International Fellowship (21996 to E.S.Y.) and the German Academic Exchange Service (DAAD to A.C.F.d.A.)., University Hospital João de Barros Barreto-Federal University of Para - Universidade Federal do Para [Belem - Brésil], Institut National de la Santé et de la Recherche Médicale (INSERM)-IFR70-Université Pierre et Marie Curie - Paris 6 (UPMC), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Biologie Intégrative (IFR-BI), Université Pierre et Marie Curie - Paris 6 (UPMC)-Ecole Superieure de Physique et de Chimie Industrielles de la Ville de Paris (ESPCI Paris), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Ecole Superieure de Physique et de Chimie Industrielles de la Ville de Paris (ESPCI Paris), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
المصدر: Experimental neurology 253, 113-125 (2014). doi:10.1016/j.expneurol.2013.12.017
Experimental Neurology
Experimental Neurology, 2014, 253, pp.113-25. ⟨10.1016/j.expneurol.2013.12.017⟩
Experimental Neurology, Elsevier, 2014, 253, pp.113-25. ⟨10.1016/j.expneurol.2013.12.017⟩
Web of Scienceمصطلحات موضوعية: MESH: Neurons, pharmacology [Enzyme Inhibitors], drug effects [Gene Expression Regulation], genetics [Gene Expression Regulation], drug effects [Microglia], MESH: Dose-Response Relationship, Drug, Mice, Lactones, chemistry.chemical_compound, 0302 clinical medicine, MESH: Animals, Phosphorylation, pharmacology [Furans], Enzyme Inhibitors, genetics [Arginine], Neurons, 0303 health sciences, Kinase, Neurodegeneration, neurodegeneration, MESH: Arginine, Tryptophan, Brain, MESH: Gene Expression Regulation, Mitochondria, MESH: tau Proteins, Cell biology, MESH: Microglia, Neurology, Biochemistry, MESH: Enzyme Inhibitors, drug effects [Brain], Microglia, genetics [Tryptophan], Tauopathy, Microtubule-Associated Proteins, MESH: Lactones, Genetically modified mouse, MESH: Mutation, MESH: Mice, Transgenic, MESH: Mitochondria, Annonacin, Mice, Transgenic, genetics [Mutation], MAPT protein, human, tau Proteins, Biology, Arginine, MESH: Brain, 03 medical and health sciences, drug effects [Phosphorylation], Developmental Neuroscience, MESH: Mice, Inbred C57BL, mental disorders, [SDV.BBM] Life Sciences [q-bio]/Biochemistry, Molecular Biology, medicine, Animals, Humans, drug effects [Neurons], [SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology, ddc:610, Mortality, genetics [Phosphorylation], Furans, MESH: Mice, MESH: Tryptophan, 030304 developmental biology, MESH: Humans, MESH: Mortality, MESH: Phosphorylation, Dose-Response Relationship, Drug, Cyclin-dependent kinase 5, tauopathy, MESH: Furans, metabolism [Microtubule-Associated Proteins], annonacin, metabolism [Mitochondria], medicine.disease, Mice, Inbred C57BL, MESH: Microtubule-Associated Proteins, genetics [tau Proteins], Somatodendritic compartment, Gene Expression Regulation, chemistry, environmental neurotoxin, metabolism [Brain], Mutation, pharmacology [Lactones], genetics [Mitochondria], microtubule-associated protein tau, 030217 neurology & neurosurgery
وصف الملف: application/pdf
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المؤلفون: Georg Homuth, Andrea Schulz, Deborah Janowitz, Matthias Rose, Sandra Van der Auwera, Henry Völzke, Hans J. Grabe, Henriette E. Meyer zu Schwabedissen, Matthias Nauck, Harald J. Freyberger
المصدر: European archives of psychiatry and clinical neuroscience 264(S1), 45-54 (2014). doi:10.1007/s00406-014-0536-2
مصطلحات موضوعية: Oncology, Adult, Male, medicine.medical_specialty, Genotype, genetics [Depressive Disorder], Tryptophan Hydroxylase, Serotonergic, Polymorphism, Single Nucleotide, psychology [Depressive Disorder], Young Adult, Internal medicine, Germany, Surveys and Questionnaires, medicine, genetics [Serotonin Plasma Membrane Transport Proteins], Humans, Pharmacology (medical), Genetic Predisposition to Disease, Child Abuse, ddc:610, Child, Biological Psychiatry, Depression (differential diagnoses), Genetic Association Studies, Aged, Retrospective Studies, Aged, 80 and over, Serotonin Plasma Membrane Transport Proteins, Depressive Disorder, TPH2, TPH2 protein, human, Beck Depression Inventory, General Medicine, Tryptophan hydroxylase, psychology [Child Abuse], Middle Aged, Serotonin pathway, Psychiatry and Mental health, 5-HTTLPR, Study of Health in Pomerania, genetics [Polymorphism, Single Nucleotide], Female, Gene-Environment Interaction, Psychology, genetics [Tryptophan Hydroxylase], Clinical psychology, Follow-Up Studies
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::106cdb23d788b2b8004e34b1b49d83b6
https://pub.dzne.de/record/135998 -
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المؤلفون: Markus M. Nöthen, Lutz Priebe, Jan O. Korbel, Sebastian M. Waszak, Elisabeth Mangold, Andreas Schlattl, Franziska Degenhardt, Stefanie Heilmann, Sven Cichon, Christian Hammer, Per Hoffmann, Marcella Rietschel, Beate Niesler, Adrian M. Stütz, Gudrun A. Rappold
المصدر: Bipolar disorders 16(7), 764-768 (2014). doi:10.1111/bdi.12207
مصطلحات موضوعية: Male, pathology [Mood Disorders], Single-nucleotide polymorphism, Tryptophan Hydroxylase, Serotonergic, Hippocampus, Polymorphism, Single Nucleotide, Linkage Disequilibrium, medicine, Humans, Genetic Predisposition to Disease, Copy-number variation, ddc:610, genetics [Mood Disorders], 1000 Genomes Project, genetics [Genetic Predisposition to Disease], Biological Psychiatry, Serotonin transporter, Genetics, biology, TPH2, Mood Disorders, TPH2 protein, human, Tryptophan hydroxylase, medicine.disease, Amygdala, Psychiatry and Mental health, pathology [Hippocampus], pathology [Amygdala], biology.protein, genetics [Polymorphism, Single Nucleotide], Major depressive disorder, Female, Psychology, genetics [Tryptophan Hydroxylase]
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المؤلفون: Peter Zill, Florian Seemüller, Brigitta Bondy, Wolfgang Maier, Richard Musil, Dan Rujescu, Sebastian Meyer, Robert Fisher, Michael Riedel, Isabella Heuser, Hans-Jürgen Möller, Ilja Spellmann, Wolfgang Gaebel, Marcella Rietschel, Rebecca Schennach, Mazda Adli, Wolfram Bender
المساهمون: University of Zurich, Musil, Richard
المصدر: European neuropsychopharmacology 23(7), 663-674 (2013). doi:10.1016/j.euroneuro.2012.08.009
مصطلحات موضوعية: Male, drug therapy [Depressive Disorder, Major], Poison control, genetics [Monoamine Oxidase], Suicide, Attempted, Tryptophan Hydroxylase, Logistic regression, genetics [Brain-Derived Neurotrophic Factor], psychology [Depressive Disorder, Major], 2738 Psychiatry and Mental Health, Risk Factors, statistics & numerical data [Suicide, Attempted], 2736 Pharmacology (medical), Pharmacology (medical), Major depressive episode, Suicidal ideation, Serotonin transporter, Serotonin Plasma Membrane Transport Proteins, biology, Middle Aged, Antidepressive Agents, Psychiatry and Mental health, genetics [European Continental Ancestry Group], monoamine oxidase A, human, 3004 Pharmacology, 2728 Neurology (clinical), Neurology, adverse effects [Antidepressive Agents], Major depressive disorder, Female, medicine.symptom, Monoamine oxidase A, genetics [Tryptophan Hydroxylase], 2803 Biological Psychiatry, Clinical psychology, Cart, Adult, medicine.medical_specialty, Adolescent, Genotype, 610 Medicine & health, White People, Suicidal Ideation, Internal medicine, medicine, genetics [Serotonin Plasma Membrane Transport Proteins], Humans, ddc:610, Monoamine Oxidase, Biological Psychiatry, Genetic Association Studies, Aged, Pharmacology, Depressive Disorder, Major, Models, Statistical, Polymorphism, Genetic, business.industry, Brain-Derived Neurotrophic Factor, TPH2 protein, human, genetics [Depressive Disorder, Major], 10060 Epidemiology, Biostatistics and Prevention Institute (EBPI), medicine.disease, therapeutic use [Antidepressive Agents], Haplotypes, Case-Control Studies, 2808 Neurology, biology.protein, TPH1 protein, human, Neurology (clinical), business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a313a8aa670d19b641d1cf1e0b11f87b
https://www.zora.uzh.ch/id/eprint/89095/ -
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المؤلفون: Leonhard Lennertz, Michael Wagner, Heinz Häfner, Anna Schuhmacher, Dan Rujescu, Rainald Mössner, Boris B. Quednow, Wolfgang Maier, Petra Franke, Marcella Rietschel, Wolfgang Wölwer, Tim Becker, Jens Benninghoff, Wolfgang Gaebel
المساهمون: University of Zurich, Schuhmacher, Anna
المصدر: Journal of psychiatric research 46(8), 1073-1080 (2012). doi:10.1016/j.jpsychires.2012.04.021
Journal of Psychiatric Research; Vol 46
Journal of psychiatric researchمصطلحات موضوعية: Male, medicine.medical_treatment, drug therapy [Schizophrenia], Medizin, Pharmacology, genetics [Cognition Disorders], Neuropsychological Tests, Tryptophan Hydroxylase, Linkage Disequilibrium, 2738 Psychiatry and Mental Health, 0302 clinical medicine, Gene Frequency, genetics [Schizophrenia], International HapMap Project, drug therapy [Gait Disorders, Neurologic], TPH1, Positive and Negative Syndrome Scale, TPH2, Middle Aged, 3. Good health, Psychiatry and Mental health, Schizophrenia, therapeutic use [Antipsychotic Agents], 10076 Center for Integrative Human Physiology, genetics [Polymorphism, Single Nucleotide], Female, Schizophrenic Psychology, Psychology, 2803 Biological Psychiatry, genetics [Tryptophan Hydroxylase], Antipsychotic Agents, Adult, medicine.medical_specialty, Genotype, genetics [Gait Disorders, Neurologic], 610 Medicine & health, Polymorphism, Single Nucleotide, 03 medical and health sciences, etiology [Gait Disorders, Neurologic], Young Adult, Internal medicine, complications [Schizophrenia], medicine, Humans, ddc:610, Antipsychotic, Gait Disorders, Neurologic, Biological Psychiatry, Genetic Association Studies, Aged, Psychiatric Status Rating Scales, Analysis of Variance, TPH2 protein, human, Haplotype, etiology [Cognition Disorders], drug therapy [Cognition Disorders], Tryptophan hydroxylase, medicine.disease, 030227 psychiatry, Endocrinology, Pharmacogenetics, 10054 Clinic for Psychiatry, Psychotherapy, and Psychosomatics, Case-Control Studies, 570 Life sciences, biology, Cognition Disorders, 030217 neurology & neurosurgery
وصف الملف: Investigation.pdf - application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::794ae0b703ad9890e0efcc11a72840ea
https://pub.dzne.de/record/136586 -
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المؤلفون: L Panariello, Domenico Salvatore, Loredana Quadro, Francesca Carlomagno, Alfredo Fusco, V de Franciscis, Massimo Santoro, Vittorio Colantuoni
المساهمون: Carlomagno, F., Salvatore, Domenico, Santoro, M., DE FRANCISCIS, V., Quadro, L., Panariello, L., Colantuoni, V., Fusco, Alfredo, Carlomagno, Francesca, Santoro, Massimo, V. d., Francisci, L., Quadro, L., Panariello, V., Colantuoni
المصدر: Biochemical and biophysical research communications. 207(3)
مصطلحات موضوعية: endocrine system, Base Sequence, Carcinoma, endocrine system diseases, Molecular Sequence Data, Biophysics, RET proto-oncogene, Biology, Medullary, medicine.disease_cause, Biochemistry, Polymerase Chain Reaction, Proto-Oncogene Mas, Thyroid carcinoma, Exon, Proto-Oncogene Proteins, medicine, Carcinoma, Tumor Cells, Cultured, Drosophila Proteins, Humans, Point Mutation, Cysteine, Thyroid Neoplasms, Codon, Molecular Biology, Mutation, genetics, Tryptophan, Tumor Cell, Cultured, genetics, Receptor Protein-Tyrosine Kinase, Base Sequence, Point mutation, Proto-Oncogene Proteins c-ret, Tryptophan, Receptor Protein-Tyrosine Kinases, genetics, Codon, Cysteine, Drosophila Proteins, Exons, Humans, Molecular Sequence Data, Point Mutation, Polymerase Chain Reaction, Proto-Oncogene Proteins c-ret, Proto-Oncogene Protein, Cell Biology, Exons, medicine.disease, Cell culture, Carcinoma, Medullary, Cancer research, genetics, Thyroid Neoplasm
وصف الملف: ELETTRONICO; STAMPA
