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1دورية أكاديمية
المؤلفون: Ramón Martínez-Mármol, Ashraf Muhaisen, Tiziana Cotrufo, Cristina Roselló-Busquets, Oriol Ros, Marc Hernaiz-Llorens, Francesc Pérez-Branguli, Rosa Maria Andrés, Antoni Parcerisas, Marta Pascual, Fausto Ulloa, Eduardo Soriano
المصدر: Frontiers in Molecular Neuroscience, Vol 16 (2023)
مصطلحات موضوعية: axon guidance, macropinocytosis, Netrin-1, syntaxin-1, UNC5 receptors, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Jung Park, Matthias Gebhardt, Svitlana Golovchenko, Francesc Perez-Branguli, Takako Hattori, Christine Hartmann, Xin Zhou, Benoit deCrombrugghe, Michael Stock, Holm Schneider, Klaus von der Mark
المصدر: Biology Open, Vol 4, Iss 5, Pp 608-621 (2015)
مصطلحات موضوعية: Hypertrophic chondrocyte, Osteoprogenitor cell, Transdifferentiation, Trabecular osteoblast, Science, Biology (General), QH301-705.5
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Francesc Perez-Branguli, Yvrick Zagar, Daniel K Shanley, Isabella A Graef, Alain Chédotal, Kevin J Mitchell
المصدر: PLoS ONE, Vol 11, Iss 7, p e0158686 (2016)
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Pavitra Purohit, Francesc Perez-Branguli, Iryna Prots, Eva Borger, Frank Gunn-Moore, Oliver Welzel, Kristina Loy, Eva Maria Wenzel, Teja W Grömer, Sebastian Brachs, Max Holzer, Rolf Buslei, Kristin Fritsch, Martin Regensburger, Konrad J Böhm, Beate Winner, Dirk Mielenz
المصدر: PLoS ONE, Vol 9, Iss 8, p e103976 (2014)
وصف الملف: electronic resource
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المؤلفون: Eduardo Soriano, Cristina Roselló-Busquets, Tiziana Cotrufo, Marta Pascual, Oriol Ros, Rosa Andrés, Fausto Ulloa, Marc Hernaiz-Llorens, Francesc Pérez-Brangulí, Ramón Martínez-Mármol, Ashraf Muhaisen
مصطلحات موضوعية: nervous system, Chemorepulsion, Chemistry, media_common.quotation_subject, Netrin, Cell migration, Axon guidance, Syntaxin 1, Endocytosis, Growth cone, Internalization, Cell biology, media_common
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::93752e079abb1d70814eda5892e5d4e9
https://doi.org/10.1101/2021.05.20.444954 -
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المؤلفون: Wenqiang Fan, Francesc Pérez-Brangulí, Isabel Y. Buchsbaum, Silvia Cappello, Daniela Gräf, Annika Schray, Zacharias Kohl, Jürgen Winkler, Tom Börstler, Tatyana Pozner, Benedikt Berninger, Martin Regensburger, Beate Winner, Himanshu K. Mishra
المصدر: Human Molecular Genetics
Perez-Branguli, F, Buchsbaum, I Y, Pozner, T, Regensburger, M, Fan, W, Schray, A, Börstler, T, Mishra, H, Gräf, D, Kohl, Z, Winkler, J, Berninger, B, Cappello, S & Winner, B 2018, ' Human SPG11 cerebral organoids reveal cortical neurogenesis impairment ', Human Molecular Genetics . https://doi.org/10.1093/hmg/ddy397مصطلحات موضوعية: Genotype, Hereditary spastic paraplegia, Neurogenesis, Fluorescent Antibody Technique, Biology, 03 medical and health sciences, Glycogen Synthase Kinase 3, Genetics, Organoid, medicine, Spastic, Humans, Molecular Biology, Genetics (clinical), Alleles, beta Catenin, Cerebral Cortex, 0303 health sciences, 030305 genetics & heredity, Proteins, General Medicine, Human brain, medicine.disease, Neural stem cell, nervous system diseases, Organoids, medicine.anatomical_structure, Phenotype, Mutation, General Article, Disease Susceptibility, Paraplegia, Cognition Disorders, Neuroscience, Neural development, Biomarkers
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86b56d195217ca4d97f86a937b29b0a4
http://europepmc.org/articles/PMC6400051 -
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المؤلفون: Beate Winner, Tom Boerstler, Holger Wend, Himanshu K. Mishra, Zacharias Kohl, Marina Leone, Steven Havlicek, Jürgen Winkler, Martina Brückner, Iryna Prots, Fred H. Gage, Francesc Pérez-Brangulí, Felix B. Engel, Georgia Minakaki, Lukas Anneser, Leah Boyer, Jürgen Behrens, André Reis, Angelika Lampert, Martin Hampl, Gerhard Schuierer, Jochen Klucken
المصدر: Annals of Neurology
Annals of neurology 79(5), 826-840 (2016). doi:10.1002/ana.24633مصطلحات موضوعية: 0301 basic medicine, Hereditary spastic paraplegia, Autophagy, Neurogenesis, Biology, medicine.disease, Phenotype, Neural stem cell, Gene expression profiling, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Neurology, medicine, Neurology (clinical), ddc:610, Amyotrophic lateral sclerosis, Induced pluripotent stem cell, Neuroscience, 030217 neurology & neurosurgery, Research Articles, Research Article
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المؤلفون: Georg Schett, Gerhard Krönke, Tobias Rothe, Beate Winner, Daniel Metzger, Francesc Pérez-Brangulí, Hiroshi Ichinose, Maria Faas, Natacha Ipseiz, Stefanie C. Lang
المساهمون: University Hospital Erlangen = Uniklinikum Erlangen, Friedrich-Alexander Universität Erlangen-Nürnberg (FAU), Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Tokyo Institute of Technology [Tokyo] (TITECH), univOAK, Archive ouverte
المصدر: The Journal of Immunology
Journal of Immunology
Journal of Immunology, 2017, 198 (10), pp.3878-3885. ⟨10.4049/jimmunol.1600638⟩مصطلحات موضوعية: Central Nervous System, 0301 basic medicine, Encephalomyelitis, Autoimmune, Experimental, Multiple Sclerosis, [SDV.IMM] Life Sciences [q-bio]/Immunology, medicine.medical_treatment, Immunology, Central nervous system, Regulator, Inflammation, Biology, Nitric Oxide, Article, Mice, 03 medical and health sciences, Adenosine Triphosphate, 0302 clinical medicine, Central Nervous System Diseases, Nuclear Receptor Subfamily 4, Group A, Member 1, medicine, Animals, Humans, Immunology and Allergy, Cells, Cultured, Microglia, Multiple sclerosis, Experimental autoimmune encephalomyelitis, Neurodegenerative Diseases, Macrophage Activation, medicine.disease, Mice, Inbred C57BL, 030104 developmental biology, Cytokine, medicine.anatomical_structure, Gene Expression Regulation, nervous system, Nuclear receptor, [SDV.IMM]Life Sciences [q-bio]/Immunology, Cytokines, medicine.symptom, Neuroscience, 030217 neurology & neurosurgery
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8313c6ff487af18beedb8f0a0aaa0668
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المؤلفون: Juan Blasi, Domenica Saul, Teja W. Groemer, Francesc Pérez-Brangulí, Jürgen Winkler, Christine Rummel, Steven Havlicek, Beate Winner, Himanshu K. Mishra, Daniela Graef, Martin Regensburger, Zacharias Kohl, Elisabeth Sock, Iryna Prots, Jonatan Dorca-Arévalo, Ursula Schlötzer-Schrehardt
المصدر: Human Molecular Genetics
مصطلحات موضوعية: Pluripotent Stem Cells, Neurite, Hereditary spastic paraplegia, Biology, Synaptic vesicle, Mice, Prosencephalon, Medizinische Fakultät, Tubulin, Genetics, medicine, Animals, Humans, ddc:610, Spasticity, Induced pluripotent stem cell, Molecular Biology, Cells, Cultured, Genetics (clinical), Neurons, Spastic Paraplegia, Hereditary, Proteins, Articles, General Medicine, Motor neuron, medicine.disease, Axons, Mice, Inbred C57BL, medicine.anatomical_structure, nervous system, Gene Knockdown Techniques, Forebrain, Axoplasmic transport, medicine.symptom, Neuroscience
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8596a2cd99cb4785843be463dbcbe28
https://doi.org/10.1093/hmg/ddu200 -
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المؤلفون: Tomáš Paus, Christian P. Müller, Andreas Hess, Marc Praetner, Christian Alzheimer, Erin Burke Quinlan, Joachim Spranger, Dirk Mielenz, Christian Büttner, Herve Lemaitre, Christian Büchel, Vincent Frouin, Beate Winner, P Schönberger, Arif B. Ekici, Gunter Schumann, D Zilske, Sebastian Brachs, Elif Kirmizi-Alsan, Anbarasu Lourdusamy, Sylvane Desrivières, Tianye Jia, Hugh Garavan, Arun L.W. Bokde, Frauke Nees, J.L. Martinot, Volker Eulenburg, Martin Reichel, Juergen Gallinat, Sabine E. Huber, Davide Amato, Pavitra Purohit, MN Smolka, Herta Flor, Penny A. Gowland, M Mettang, Tobias Bäuerle, Patricia J. Conrod, Marc Schwarz, Tobias Banaschewski, Francesc Pérez-Brangulí, T Stöckl, Verena Rauschenberger, Alexandra Schambony, Andreas Heinz
المصدر: Molecular Psychiatry
Mielenz, D, Reichel, M, Jia, T, Quinlan, E B, Stöckl, T, Mettang, M, Zilske, D, Kirmizi-Alsan, E, Schönberger, P, Praetner, M, E. Huber, S, Amato, D, Schwarz, M, Purohit, P, Brachs, S, Spranger, J, Hessenthaler, A, Büttner, C, Ekici, A B, Perez-Branguli, F, Winner, B, Rauschenberger, V, Banaschewski, T, Bokde, A L W, Buechel, C, Conrod, P J, Desrivieres, S, Flor, H, Frouin, V, Gallinat, J, Garavan, H, Gowland, P, Heinz, A, Martinot, J-L, Lemaitre, H, Nees, F, Paus, T, Smolka, M N, Consortium, T IMAGEN, Schambony, A, Bäuerle, T, Eulenburg, V, Alzheimer, C, Lourdusamy, A, Schumann, G & Mueller, C P 2017, ' EFhd2/Swiprosin-1 is a common genetic determinator for sensation-seeking/low anxiety and alcohol addiction ', Molecular Psychiatry . https://doi.org/10.1038/mp.2017.63مصطلحات موضوعية: 0301 basic medicine, Adult, Male, medicine.medical_specialty, Adolescent, Alcohol Drinking, medicine.drug_class, Anxiety, Polymorphism, Single Nucleotide, 03 medical and health sciences, Cellular and Molecular Neuroscience, Mice, Xenopus laevis, Risk-Taking, Internal medicine, medicine, Sensation seeking, Animals, Humans, ddc:610, Molecular Biology, Mice, Knockout, Benzodiazepine, Calcium-Binding Proteins, medicine.disease, Anxiety Disorders, Mice, Inbred C57BL, Psychiatry and Mental health, Alcoholism, 030104 developmental biology, Endocrinology, Superior frontal gyrus, Anxiogenic, Schizophrenia, Behavioral medicine, Female, Original Article, Psychopharmacology, medicine.symptom, Psychology, Clinical psychology
وصف الملف: application/pdf