Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Geraldine Meyer"'
Autor:
Audrey Petit Le Manac’h, Yves Roquelaure, Catherine Ha, Julie Bodin, Geraldine Meyer, Frederic Bigot, Martin Veaudor, Alexis Descatha, Marcel Goldberg, Ellen Imbernon
Publikováno v:
Scandinavian Journal of Work, Environment & Health, Vol 37, Iss 5, Pp 394-401 (2011)
OBJECTIVE: De Quervain’s disease (DQD) is a significant cause of musculoskeletal pain among workers. The aim of this study was to assess the relative importance of personal and occupational risk factors for DQD in a working population. METHODS: A t
Externí odkaz:
https://doaj.org/article/0004791cf37f4f6aa68f203ec63ee33f
Autor:
Marine Lanfranchi, Sozerko Yandiev, Géraldine Meyer-Dilhet, Salma Ellouze, Martijn Kerkhofs, Raphael Dos Reis, Audrey Garcia, Camille Blondet, Alizée Amar, Anita Kneppers, Hélène Polvèche, Damien Plassard, Marc Foretz, Benoit Viollet, Kei Sakamoto, Rémi Mounier, Cyril F. Bourgeois, Olivier Raineteau, Evelyne Goillot, Julien Courchet
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-17 (2024)
Abstract The cellular mechanisms underlying axonal morphogenesis are essential to the formation of functional neuronal networks. We previously identified the autism-linked kinase NUAK1 as a central regulator of axon branching through the control of m
Externí odkaz:
https://doaj.org/article/4e8f983c4969417aad556f0a4f0dc423
Publikováno v:
Transgenic Research
11. Transgenic Technology Meeting (TT2013)
11. Transgenic Technology Meeting (TT2013), International Society for Transgenic Technologies (ISTT). INT., Feb 2013, Guangzhou, China. 250 p
HAL
11. Transgenic Technology Meeting (TT2013)
11. Transgenic Technology Meeting (TT2013), International Society for Transgenic Technologies (ISTT). INT., Feb 2013, Guangzhou, China. 250 p
HAL
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::21b90dcd1a83280446ccfc2fbf6d8b61
https://hal.inrae.fr/hal-02746345
https://hal.inrae.fr/hal-02746345
Autor:
Martin Veaudor, Catherine Ha, Marcel Goldberg, Yves Roquelaure, Ellen Imbernon, Geraldine Meyer, Frederic Bigot, Alexis Descatha, Julie Bodin, Audrey Petit Le Manac'h
Publikováno v:
Scandinavian Journal of Work, Environment and Health
Scandinavian Journal of Work, Environment and Health, Nordic Association of Occupational Safety and Health (NOROSH), 2011, 37 (5), pp.394-401. ⟨10.5271/sjweh.3160⟩
Scandinavian Journal of Work, Environment and Health, 2011, 37 (5), pp.394-401. ⟨10.5271/sjweh.3160⟩
Scandinavian Journal of Work, Environment & Health, Vol 37, Iss 5, Pp 394-401 (2011)
Scandinavian Journal of Work, Environment and Health, Nordic Association of Occupational Safety and Health (NOROSH), 2011, 37 (5), pp.394-401. ⟨10.5271/sjweh.3160⟩
Scandinavian Journal of Work, Environment and Health, 2011, 37 (5), pp.394-401. ⟨10.5271/sjweh.3160⟩
Scandinavian Journal of Work, Environment & Health, Vol 37, Iss 5, Pp 394-401 (2011)
International audience; OBJECTIVE: De Quervain's disease (DQD) is a significant cause of musculoskeletal pain among workers. The aim of this study was to assess the relative importance of personal and occupational risk factors for DQD in a working po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b884beaba0c8cd417470960c1a2bab14
https://pubmed.ncbi.nlm.nih.gov/21431276
https://pubmed.ncbi.nlm.nih.gov/21431276
Publikováno v:
STAR Protocols, Vol 1, Iss 1, Pp 100027- (2020)
Summary: The cerebral cortex is composed of an exquisitely complex network of interconnected neurons supporting the higher cognitive functions of the brain. Here, we provide a fully detailed, step-by-step protocol to perform in utero cortical electro
Externí odkaz:
https://doaj.org/article/1c184a1a20db4f77b861f16e8bcf8aeb
Autor:
Virginie Courchet, Amanda J. Roberts, Géraldine Meyer-Dilhet, Peggy Del Carmine, Tommy L. Lewis, Franck Polleux, Julien Courchet
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-14 (2018)
Nuak1 is an autism spectrum disorder candidate gene. Here the authors report behavioral and cortical development in mice heterozygous for Nuak1, suggesting loss of function mutations in one copy of Nuak1 may contribute to neurodevelopmental disorders
Externí odkaz:
https://doaj.org/article/86a0b1965c3547f0820ef0dd3daf13b6
Autor:
Chloé Felgerolle, Betty Hébert, Maryvonne Ardourel, Géraldine Meyer-Dilhet, Arnaud Menuet, Kimberley Pinto-Morais, Jean-Charles Bizot, Jacques Pichon, Sylvain Briault, Olivier Perche
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 13 (2019)
Fragile X Syndrome (FXS), the most common inherited form of human intellectual disability (ID) associated with autistic-like behaviors, is characterized by dys-sensitivity to sensory stimuli, especially vision. In the absence of Fragile Mental Retard
Externí odkaz:
https://doaj.org/article/e55b2e0075e84808ae6537433adec1fd
Autor:
Olivier Perche, Chloé Felgerolle, Maryvonne Ardourel, Audrey Bazinet, Arnaud Pâris, Rafaëlle Rossignol, Géraldine Meyer-Dilhet, Anne-Laure Mausset-Bonnefont, Betty Hébert, David Laurenceau, Céline Montécot-Dubourg, Arnaud Menuet, Jean-Charles Bizot, Jacques Pichon, Isabelle Ranchon-Cole, Sylvain Briault
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 12 (2018)
Fragile X Syndrome (FXS) is caused by a deficiency in Fragile X Mental Retardation Protein (FMRP) leading to global sensorial abnormalities, among which visual defects represent a critical part. These visual defects are associated with cerebral neuro
Externí odkaz:
https://doaj.org/article/111446a59bbf4b50b07bf98d5b7f80f2