المؤلفون: Valerie Matagne, Emilie Borloz, Yann Ehinger, Lydia Saidi, Laurent Villard, Jean-Christophe Roux

المصدر: Neurobiology of Disease, Vol 149, Iss , Pp 105235- (2021)

مصطلحات موضوعية: Rett syndrome, Mecp2, AAV9, Gene therapy, Animal models, Side effects, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S0969996120305118; https://doaj.org/toc/1095-953X

URL الوصول: https://doaj.org/article/39d10c44a9204322bf33bfa08c307bad

المؤلفون: Yann Ehinger, Julie Bruyère, Nicolas Panayotis, Yah‐Se Abada, Emilie Borloz, Valérie Matagne, Chiara Scaramuzzino, Hélène Vitet, Benoit Delatour, Lydia Saidi, Laurent Villard, Frédéric Saudou, Jean‐Christophe Roux

المصدر: EMBO Molecular Medicine, Vol 12, Iss 2, Pp n/a-n/a (2020)

مصطلحات موضوعية: Mecp2, Rett, BDNF, huntingtin, axonal transport, Medicine (General), R5-920, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1757-4676; https://doaj.org/toc/1757-4684

URL الوصول: https://doaj.org/article/094d5708255640e8bd9f8ac0e89b5fea

المؤلفون: Marie-Solenne Felix, Emilie Borloz, Khaled Metwally, Ambre Dauba, Benoit Larrat, Valerie Matagne, Yann Ehinger, Laurent Villard, Anthony Novell, Serge Mensah, Jean-Christophe Roux

المصدر: Pharmaceutics, Vol 13, Iss 8, p 1245 (2021)

مصطلحات موضوعية: gene therapy, AAV9, focused ultrasound, blood-brain barrier, microbubbles, Pharmacy and materia medica, RS1-441

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1999-4923/13/8/1245; https://doaj.org/toc/1999-4923

URL الوصول: https://doaj.org/article/9ae232de04cf41178cf94772dee6a02c

المؤلفون: Yann Ehinger, Valerie Matagne, Valérie Cunin, Emilie Borloz, Michel Seve, Sandrine Bourgoin-Voillard, Ana Borges-Correia, Laurent Villard, Jean-Christophe Roux

المصدر: International Journal of Molecular Sciences, Vol 22, Iss 9, p 4316 (2021)

مصطلحات موضوعية: astrocytes, iTRAQ quantitative proteomic approach, Mecp2, neuronal arborization, Rett syndrome, secretome, Biology (General), QH301-705.5, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1422-0067/22/9/4316; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067

URL الوصول: https://doaj.org/article/57012a67b5d74695b923eb55bfecc99d

المؤلفون: Lucile Brun, Emilie Borloz, Marie-Solenne Felix, Jordane Louis Durand, Laurent Villard

المصدر: Epilepsy Research. 193:107160

مصطلحات موضوعية: Neurology, Neurology (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::24c889afa2b5f019800f237fb6bd194a
https://doi.org/10.1016/j.eplepsyres.2023.107160

المؤلفون: Emilie Borloz, Laurent Villard, Jean-Christophe Roux

المساهمون: Marseille medical genetics - Centre de génétique médicale de Marseille (MMG), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Département de génétique médicale [Hôpital de la Timone - APHM], Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone [CHU - APHM] (TIMONE)-Institut National de la Santé et de la Recherche Médicale (INSERM), Gall, Valérie

المصدر: Faculty Reviews
Faculty Reviews, 2021, 10, ⟨10.12703/r/10-59⟩

مصطلحات موضوعية: Nervous system, Down syndrome, congenital, hereditary, and neonatal diseases and abnormalities, Urinary system, [SDV]Life Sciences [q-bio], Rett syndrome, peripheral systems, Review Article, [SDV.GEN] Life Sciences [q-bio]/Genetics, Bioinformatics, comorbidities, MECP2, Neurodevelopmental disorder, Intellectual disability, medicine, Endocrine system, Mecp2, ComputingMilieux_MISCELLANEOUS, [SDV.GEN]Life Sciences [q-bio]/Genetics, [SDV.MHEP] Life Sciences [q-bio]/Human health and pathology, business.industry, medicine.disease, [SDV] Life Sciences [q-bio], medicine.anatomical_structure, business, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8e87f84539492aaeab01690660bc6e7
https://hal-amu.archives-ouvertes.fr/hal-03664868

المؤلفون: Frédéric Saudou, Julie Bruyère, Lydia Saidi, Yann Ehinger, Chiara Scaramuzzino, Emilie Borloz, Hélène Vitet, Benoît Delatour, Laurent Villard, Yah-Se Abada, Jean-Christophe Roux, Valerie Matagne, Nicolas Panayotis

المساهمون: CHU Pitié-Salpêtrière [AP-HP], Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Marseille medical genetics - Centre de génétique médicale de Marseille (MMG), Institut National de la Santé et de la Recherche Médicale (INSERM)-Aix Marseille Université (AMU), [GIN] Grenoble Institut des Neurosciences (GIN), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Grenoble Alpes (UGA), Institut du Cerveau et de la Moëlle Epinière = Brain and Spine Institute (ICM), Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière [AP-HP], Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Institut du Cerveau = Paris Brain Institute (ICM), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)

المصدر: EMBO Molecular Medicine
EMBO Molecular Medicine, Wiley Open Access, 2020, 12 (2), ⟨10.15252/emmm.201910889⟩
EMBO Molecular Medicine, Wiley Open Access, 2020, 12 (2), pp.e10889. ⟨10.15252/emmm.201910889⟩
EMBO Molecular Medicine, Vol 12, Iss 2, Pp n/a-n/a (2020)
Web of Science
EMBO Molecular Medicine, 2020, 12 (2), pp.e10889. ⟨10.15252/emmm.201910889⟩

مصطلحات موضوعية: Male, Medicine (General), Huntingtin, Methyl-CpG-Binding Protein 2, [SDV]Life Sciences [q-bio], QH426-470, medicine.disease_cause, Mice, 0302 clinical medicine, Neurotrophic factors, Homeostasis, Phosphorylation, Mice, Knockout, Huntingtin Protein, 0303 health sciences, Mutation, Phenotype, 3. Good health, Cell biology, Knockout mouse, Female, [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], axonal transport, congenital, hereditary, and neonatal diseases and abnormalities, huntingtin, Rett syndrome, Biology, Gene Therapy & Genetic Disease, MECP2, 03 medical and health sciences, R5-920, Report, Chemical Biology, mental disorders, Rett Syndrome, Genetics, medicine, Animals, Pharmacology & Drug Discovery, Mecp2, 030304 developmental biology, [SDV.GEN]Life Sciences [q-bio]/Genetics, Rett, Brain-Derived Neurotrophic Factor, medicine.disease, nervous system diseases, Mice, Inbred C57BL, Disease Models, Animal, BDNF, nervous system, [SDV.SP.PHARMA]Life Sciences [q-bio]/Pharmaceutical sciences/Pharmacology, Genetics, Gene Therapy & Genetic Disease, 030217 neurology & neurosurgery, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology, Reports, Neuroscience

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f3fb438750db968abd6786b5e3b342b
https://hal.archives-ouvertes.fr/hal-03035540