المؤلفون: Sara H. Isakson, Anat Stemmer-Rachamimov, Christopher L. Moertel, David A. Largaespada, David H. Gutmann, Ludwine Messiaen, Alexander W. Coutts, G. Elizabeth Pluhar, Jeremie Vitte, Adrienne L. Watson, Scott C. Fahrenkrug, Nancy Ratner, Daniel F. Carlson, Marco Giovannini, Anthony E. Rizzardi, Eva Dombi, Mark N. Kirstein, Kyle B. Williams, James Fisher, Tilat A. Rizvi, Sonika Dahiya, Brigitte C. Widemann

المصدر: Communications Biology, Vol 1, Iss 1, Pp 1-11 (2018)
Communications biology, vol 1, iss 1
Communications Biology

مصطلحات موضوعية: 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, Medicine (miscellaneous), Disease, General Biochemistry, Genetics and Molecular Biology, Article, Neurofibromatosis, Loss of heterozygosity, 03 medical and health sciences, 0302 clinical medicine, Rare Diseases, Medicine, Protein kinase A, neoplasms, lcsh:QH301-705.5, Cancer, biology, business.industry, Genetically engineered, Kinase, Neurosciences, medicine.disease, Neurofibromin 1, eye diseases, 3. Good health, Brain Disorders, nervous system diseases, Brain Cancer, 030104 developmental biology, lcsh:Biology (General), 030220 oncology & carcinogenesis, biology.protein, Cancer research, Cancer development, General Agricultural and Biological Sciences, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9518b2ff866c564aba25172576226edfTest
http://link.springer.com/article/10.1038/s42003-018-0163-yTest

المؤلفون: Tilat A. Rizvi, Brigitte C. Widemann, Eva Dombi, David A. Largaespada, Ludwine Messiaen, Christopher L. Moertel, Adrienne L. Watson, Sonika Dahiya, Sara H. Osum, David H. Gutmann, Anat Stemmer-Rachamimov, Nancy Ratner, Marco Giovannini, Jeremie Vitte

المصدر: Neuro Oncol

مصطلحات موضوعية: Drug, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, business.industry, Genetically engineered, media_common.quotation_subject, medicine.disease, eye diseases, nervous system diseases, Animal model, Oncology, Genome editing, Tumor Models, Animal Disease Models, Cancer research, Medicine, Neurology (clinical), Neurofibromatosis, business, neoplasms, media_common

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c9a93d1b8975e865c13942bec9647d0Test
https://doi.org/10.1093/neuonc/noz175.1122Test

المؤلفون: Gabriele Lorenzo Capone, Marco Giovannini, Anna Laura Putignano, Roberta Sestini, Jeremie Vitte, Laura Papi, Irene Paganini

المصدر: Journal of neuro-oncology. 137(1)

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Cancer Research, Chromosomes, Human, Pair 22, Schwannoma, Biology, medicine.disease_cause, 03 medical and health sciences, Young Adult, otorhinolaryngologic diseases, medicine, Missense mutation, Humans, Genetic Predisposition to Disease, SMARCB1, Neurofibromatosis type 2, Schwannomatosis, Child, neoplasms, Aged, Mutation, Neurofibromin 2, Spinal Neoplasms, Neuroma, Acoustic, SMARCB1 Protein, Middle Aged, medicine.disease, nervous system diseases, 030104 developmental biology, Neurology, Oncology, Cancer research, Female, Neurology (clinical), Carcinogenesis, Chromosome 22, Neurilemmoma

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19bdd2dd63543c91474d30cc4db3d1cdTest
https://pubmed.ncbi.nlm.nih.gov/29230670Test

المؤلفون: Jeremie Vitte, Marco Giovannini

المصدر: Heat Shock Proteins ISBN: 9783319172101

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Chemotherapy, biology, business.industry, medicine.medical_treatment, medicine.disease, medicine.disease_cause, Neurofibromin 1, nervous system diseases, Merlin (protein), Radiation therapy, otorhinolaryngologic diseases, medicine, Cancer research, biology.protein, Neurofibromatosis type 2, Neurofibromatosis, business, Carcinogenesis, PI3K/AKT/mTOR pathway

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::1e09f41cb3efa55096a651035d985026Test
https://doi.org/10.1007/978-3-319-17211-8_13Test

المؤلفون: Jeremie Vitte, Charles Duyckaerts, Alexis Brice, Sabine Traver, André Maues De Paula, Giorgio Rovelli, Olga Corti, Suzanne Lesage

المصدر: Journal of neuropathology and experimental neurology. 69(9)

مصطلحات موضوعية: Adult, medicine.medical_specialty, KDEL, Dopamine, Substantia nigra, Biology, Protein Serine-Threonine Kinases, Endoplasmic Reticulum, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Pathology and Forensic Medicine, Cell Line, Cellular and Molecular Neuroscience, Internal medicine, medicine, Animals, Humans, Point Mutation, Tissue Distribution, Neurons, Lewy body, Endoplasmic reticulum, Dopaminergic, Brain, Parkinson Disease, General Medicine, medicine.disease, Subcellular localization, LRRK2, nervous system diseases, Cell biology, Endocrinology, Neurology, Locus coeruleus, Lewy Bodies, Neurology (clinical)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::461c0bd7b5a5212d48f3c703ebe536cfTest
https://pubmed.ncbi.nlm.nih.gov/20720502Test

المؤلفون: Nasim Warwar, Ruben Attali, Irena Gurt, Judith Melki, Jeremie Vitte

المصدر: Advances in Experimental Medicine and Biology ISBN: 9789048128129

مصطلحات موضوعية: Spliceosome, animal diseases, Survival of motor neuron, Spinal muscular atrophy, SMN1, Biology, medicine.disease, SMA, Spinal muscular atrophies, Phenotype, nervous system diseases, nervous system, RNA splicing, medicine, Neuroscience

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::d737249d861a534c57cee741eeca4d59Test
https://doi.org/10.1007/978-90-481-2813-6_16Test

المؤلفون: Michel Hamon, Jeremie Vitte, Charles Cohen-Salmon, Philipp J. Kahle, Fabien Cornilleau, Margot Fournier, Hilal A. Lashuel, Naïma Hanoun, René Duchateau, Sabine Traver, Katerina E. Paleologou, Cécile Goujet-Zalc, Fernando Perez-Diaz, Chantal Joubert, Françoise Saurini, Olga Corti, Alexis Brice, Christian Haass, Jérôme Garrigue, Hector Ardila-Osorio, Charles Duyckaerts, Jean-Philippe Dullin, Dominique Langui

المساهمون: Neurogenetique Moleculaire, Université d'Évry-Val-d'Essonne (UEVE)-Institut National de la Santé et de la Recherche Médicale (INSERM), Mécanismes adaptatifs : des organismes aux communautés (MAOAC), Muséum national d'Histoire naturelle (MNHN)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS), Institut de médecine moléculaire de Rangueil (I2MR), Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)- Institut Fédératif de Recherche Bio-médicale Institution (IFR150)-Institut National de la Santé et de la Recherche Médicale (INSERM), Vulnérabilité Adaptation et Psychopathologie (VAP), Université Pierre et Marie Curie - Paris 6 (UPMC)-Université Paris Diderot - Paris 7 (UPD7)-Centre National de la Recherche Scientifique (CNRS), 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), Neurologie et thérapeutique expérimentale, Université Pierre et Marie Curie - Paris 6 (UPMC)-IFR70-Institut National de la Santé et de la Recherche Médicale (INSERM), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-IFR150-Institut National de la Santé et de la Recherche Médicale (INSERM), Neuropsychopharmacologie, Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC), Service de Génétique Cytogénétique et Embryologie [CHU Pitié-Salpêtrière], 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 National de la Santé et de la Recherche Médicale (INSERM)-IFR70-Université Pierre et Marie Curie - Paris 6 (UPMC)

المصدر: PLoS ONE
PLoS ONE, 2009, 4 (8), pp.e6629. ⟨10.1371/journal.pone.0006629⟩
PLoS ONE, Public Library of Science, 2009, 4 (8), pp.e6629. ⟨10.1371/journal.pone.0006629⟩
PLoS ONE, Vol 4, Iss 8, p e6629 (2009)

مصطلحات موضوعية: Pathology, lcsh:Medicine, Rat Model, Polymerase Chain Reaction, Parkin, Biochemistry/Protein Folding, Mice, 0302 clinical medicine, Ubiquitin, Phosphorylation, lcsh:Science, Neurological Disorders/Movement Disorders, 0303 health sciences, Multidisciplinary, biology, Parkinsonism, Parkinson Disease, Immunohistochemistry, [SCCO.PSYC]Cognitive science/Psychology, Research Article, Genetically modified mouse, medicine.medical_specialty, Programmed cell death, Neurite, Ubiquitin-Protein Ligases, Transgene, Synucleins, Mice, Transgenic, Motor Activity, Transgenic Mice, Drosophila Model, 03 medical and health sciences, Human Alpha-Synuclein, Internal medicine, medicine, Animals, Cell-Death, DNA Primers, 030304 developmental biology, Synucleinopathies, Base Sequence, Protein, lcsh:R, Ubiquitination, medicine.disease, nervous system diseases, Disease Models, Animal, Endocrinology, Genetics and Genomics/Disease Models, nervous system, biology.protein, lcsh:Q, Lewy Bodies, Inclusion-Body Formation, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62d67272c0e87e69a8e181e414014388Test
https://hal.science/hal-00541956Test