Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Betty Hébert"'
Autor:
Danijela Bataveljic, Helena Pivonkova, Vidian de Concini, Betty Hébert, Pascal Ezan, Sylvain Briault, Alexis-Pierre Bemelmans, Jacques Pichon, Arnaud Menuet, Nathalie Rouach
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-16 (2024)
Abstract Fragile X syndrome (FXS) is an inherited form of intellectual disability caused by the loss of the mRNA-binding fragile X mental retardation protein (FMRP). FXS is characterized by neuronal hyperexcitability and behavioral defects, however t
Externí odkaz:
https://doaj.org/article/40827fccee0c456e9d2c8a8770f2efbe
Autor:
Maryvonne Ardourel, Chloé Felgerolle, Arnaud Pâris, Niyazi Acar, Khaoula Ramchani Ben Othman, Natsuko Ueda, Rafaelle Rossignol, Audrey Bazinet, Betty Hébert, Sylvain Briault, Isabelle Ranchon-Cole, Olivier Perche
Publikováno v:
Nutrients, Vol 13, Iss 9, p 3216 (2021)
To prevent ocular pathologies, new generation of dietary supplements have been commercially available. They consist of nutritional supplement mixing components known to provide antioxidative properties, such as unsaturated fatty acid, resveratrol or
Externí odkaz:
https://doaj.org/article/6b447c2048834d0c80f878308948b1e7
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
Autor:
Khaoula Ramchani Ben Othman, Arnaud Pâris, Rafaëlle Rossignol, Sylvain Briault, Chloé Felgerolle, Maryvonne Ardourel, Olivier Perche, Isabelle Ranchon-Cole, Natsuko Ueda, Niyazi Acar, Betty Hébert, Audrey Bazinet
Publikováno v:
Nutrients, Vol 13, Iss 3216, p 3216 (2021)
Nutrients
Nutrients, MDPI, 2021, 13 (9), pp.3216. ⟨10.3390/nu13093216⟩
Nutrients; Volume 13; Issue 9; Pages: 3216
Nutrients
Nutrients, MDPI, 2021, 13 (9), pp.3216. ⟨10.3390/nu13093216⟩
Nutrients; Volume 13; Issue 9; Pages: 3216
International audience; To prevent ocular pathologies, new generation of dietary supplements have been commercially available. They consist of nutritional supplement mixing components known to provide antioxidative properties, such as unsaturated fat
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
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
Autor:
Jacques Pichon, Laurianne Lesné, Betty Hébert, Anthony Laugeray, Olivier Richard, Stéphane Mortaud, Ameziane Herzine, Arnaud Menuet, Séverine Mazaud-Guittot, Bernard Jégou, Olivier Perche, Sylvain Briault, Céline Montécot-Dubourg, Marine Aguillon-Naury
Publikováno v:
Frontiers in Behavioral Neuroscience
Frontiers in Behavioral Neuroscience, Frontiers, 2014, 8, pp.390. ⟨10.3389/fnbeh.2014.00390⟩
Frontiers in Behavioral Neuroscience, Frontiers, 2014, 8, ⟨10.3389/fnbeh.2014.00390⟩
Frontiers in Behavioral Neuroscience, 2014, 8, pp.390. ⟨10.3389/fnbeh.2014.00390⟩
Frontiers in Behavioral Neuroscience, Frontiers, 2014, 8, pp.390. ⟨10.3389/fnbeh.2014.00390⟩
Frontiers in Behavioral Neuroscience, Frontiers, 2014, 8, ⟨10.3389/fnbeh.2014.00390⟩
Frontiers in Behavioral Neuroscience, 2014, 8, pp.390. ⟨10.3389/fnbeh.2014.00390⟩
International audience; Glufosinate ammonium (GLA) is one of the most widely used herbicides in agriculture. As is the case for most pesticides, potential adverse effects of GLA have not been studied from the perspective of developmental neurotoxicit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c21ea59d523d78775bf2ec97b34fe33e
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01121829/file/fnbeh-08-00390.pdf
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01121829/file/fnbeh-08-00390.pdf
Autor:
Dominique Cahard, Béatrice Laudier, Jacques Pichon, Betty Hébert, Olivier Perche, Anthony Laugeray, Angélique Quartier, Frédéric Laumonnier, Susanna Pietropaolo, Sylvain Briault, Wim E. Crusio, Laurence Got, Sandra Même, Arnaud Menuet, Sandrine Lefeuvre, Nicolas Doisne
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, BioMed Central, 2014, 9, pp.124. ⟨10.1186/s13023-014-0124-6⟩
Orphanet Journal of Rare Diseases, 2014, 9, pp.124. ⟨10.1186/s13023-014-0124-6⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2014, 9, pp.124. ⟨10.1186/s13023-014-0124-6⟩
Orphanet Journal of Rare Diseases, 2014, 9, pp.124. ⟨10.1186/s13023-014-0124-6⟩
Background Fragile X Syndrome (FXS) is the most common form of inherited intellectual disability and is also associated with autism spectrum disorders. Previous studies implicated BKCa channels in the neuropathogenesis of FXS, but the main question w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94f8c953934da5add575cbcaf9370247
https://www.hal.inserm.fr/inserm-01089760
https://www.hal.inserm.fr/inserm-01089760