Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Maryvonne Ardourel"'
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:
Maryvonne Ardourel, Arnaud Pâris, Chloé Felgerolle, Fabien Lesne, Isabelle Ranchon-Cole, Sylvain Briault, Olivier Perche
Publikováno v:
Experimental Eye Research. 224:109238
FMRP, the fragile X mental retardation protein coded by the FMR1 gene, is an RNA-binding protein that assists transport, stabilization and translational regulation of specific synaptic mRNAs. Its expression has been found in multiple cell types of ce
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:
Katy Bernard-Hélary, Maryvonne Ardourel, Pierre J. Magistretti, Tobias Hévor, Jean-François Cloix
Publikováno v:
Glia. 37:379-382
In order to assess the participation of astrocytic gluconeogenesis in the synthesis of glycogen, mouse astrocytes were stably transfected with antisense cDNA of fructose-1,6-bisphosphatase (FBPase) and with sense and antisense cDNAs of glycogen synth
Autor:
A. Shevelev, Piotr Kopiński, A. Ly, M. Chatel, Maryvonne Ardourel, Tadeusz Popiela, Jerzy Trojan, Trojan La, Huynh-Thien Duc, Thierry Dufour, Jean Christophe Francois, M. X. Wei, M. Bierwagen, Christian R. Andres, Y. Pan, H. Kasprzak, Donald D. Anthony
Publikováno v:
Biomedicine & Pharmacotherapy. 64:576-578
The treatment of cancer by antisense anti-IGF-I cellular therapy inducing immune response has evoked interest among many promising strategies. Here, we reported some results obtained from patients with cancer, mainly glioblastoma treated by this stra
Publikováno v:
Toxicology. 153:179-187
Methionine sulfoximine is a xenobiotic amino acid derived from methionine. One of its major properties is to display a glycogenic activity in the brain. After studying this property, we investigate here a possible action of this xenobiotic on the exp
Autor:
Michel Doudeau, Séverine Morisset-Lopez, Hélène Bénédetti, Béatrice Vallée, Sandrine Villette, Tobias Hévor, Chantal Pichon, Fabienne Godin, Maryvonne Ardourel
Publikováno v:
Biochemical and Biophysical Research Communications
Biochemical and Biophysical Research Communications, Elsevier, 2012, 418 (4), pp.689-94. ⟨10.1016/j.bbrc.2012.01.079⟩
Biochemical and Biophysical Research Communications, Elsevier, 2012, 418 (4), pp.689-94. ⟨10.1016/j.bbrc.2012.01.079⟩
International audience; Neurofibromatosis type 1 is a common genetic disease that causes nervous system tumors, and cognitive deficits. It is due to mutations within the NF1 gene, which encodes the Nf1 protein. Nf1 has been shown to be involved in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1691c660781adba9d0858f3c2ab59f08
https://hal.archives-ouvertes.fr/hal-00721861
https://hal.archives-ouvertes.fr/hal-00721861