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pro vyhledávání: '"Candide Alioli"'
Autor:
Marie-Noëlle Méaux, Maitena Regnier, Aurélie Portefaix, Olivier Borel, Candide Alioli, Olivier Peyruchaud, Mélanie Legrand, Justine Bacchetta
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Autotaxin (ATX) is a secreted enzyme with a lysophospholipase D activity, mainly secreted by adipocytes and widely expressed. Its major function is to convert lysophosphatidylcholine (LPC) into lysophosphatidic acid (LPA), an essential bioactive lipi
Externí odkaz:
https://doaj.org/article/be9e8787e61d4100a3c7887ddae210a3
Publikováno v:
Cells, Vol 11, Iss 1, p 170 (2022)
Cystinosis Metabolic Bone Disease (CMBD) has emerged during the last decade as a well-recognized, long-term complication in patients suffering from infantile nephropathic cystinosis (INC), resulting in significant morbidity and impaired quality of li
Externí odkaz:
https://doaj.org/article/1fedb6585f804cf4bffcef51b579ffef
Autor:
Thomas Quinaux, Aurélia Bertholet-Thomas, Aude Servais, Olivia Boyer, Isabelle Vrillon, Julien Hogan, Sandrine Lemoine, Ségolène Gaillard, Candide Alioli, Sophie Vasseur, Cécile Acquaviva, Olivier Peyruchaud, Irma Machuca-Gayet, Justine Bacchetta
Publikováno v:
Cells, Vol 10, Iss 9, p 2498 (2021)
Bone complications of cystinosis have been recently described. The main objectives of this paper were to determine in vitro the impact of CTNS mutations and cysteamine therapy on human osteoclasts and to carry out a genotype-phenotype analysis relate
Externí odkaz:
https://doaj.org/article/6be2e1f48db7439d86dd22f90459c6fe
Autor:
Adebayo Candide Alioli, Léa Demesmay, Sara Laurencin, Nicolas Beton, Delphine Farlay, Helene Follet, Jerold Chun, Richard Rivera, Daniel Bouvard, Irma Machuca-Gayet, Jean-Pierre Salles, Isabelle Gennero, Olivier Peyruchaud
Publikováno v:
Bone Reports, Vol 13, Iss , Pp 100432- (2020)
Externí odkaz:
https://doaj.org/article/7126ce322d924a1f94babb6264e32888
Autor:
Marie-Noëlle Méaux, Candide Alioli, Agnès Linglart, Sandrine Lemoine, Emmanuelle Vignot, Aurélia Bertholet-Thomas, Olivier Peyruchaud, Sacha Flammier, Irma Machuca-Gayet, Justine Bacchetta
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 107:3275-3286
Context X-linked hypophosphatemia (XLH) is a rare genetic disease caused by a primary excess of fibroblast growth factor 23 (FGF23). FGF23 has been associated with inflammation and impaired osteoclastogenesis, but these pathways have not been investi
Autor:
Candide Alioli, Marie-Noelle Meaux, Julie Bernardor, Irma Machuca-Gayet, Justine Bacchetta, Olivier Peyruchaud
Publikováno v:
Current Osteoporosis Reports
Current Osteoporosis Reports, 2021, 19 (6), pp.553-562. ⟨10.1007/s11914-021-00707-6⟩
Current Osteoporosis Reports, 2021, 19 (6), pp.553-562. ⟨10.1007/s11914-021-00707-6⟩
International audience; Purpose of review: To describe the methods that can be used to obtain functional and mature osteoclasts from peripheral blood mononuclear cells (PBMCs) and report the data obtained with this model in two peculiar diseases, nam
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, MDPI, 2022, 23 (7), pp.3427. ⟨10.3390/ijms23073427⟩
International Journal of Molecular Sciences, MDPI, 2022, 23 (7), pp.3427. ⟨10.3390/ijms23073427⟩
International audience; Lysophosphatidic acid (LPA) is a natural bioactive phospholipid with pleiotropic activities affecting multiple tissues, including bone. LPA exerts its biological functions by binding to G-protein coupled LPA receptors (LPA1-6)
Autor:
Olivier Peyruchaud, Jerold Chun, Delphine Farlay, Léa Demesmay, Jean-Pierre Salles, Isabelle Gennero, Irma Machuca-Gayet, Sara Laurencin, Daniel Bouvard, Nicolas Beton, Hélène Follet, Adebayo Candide Alioli, Richard Rivera
Publikováno v:
Bone Reports, Vol 13, Iss, Pp 100432-(2020)
Akademický článek
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Autor:
Adebayo Candide Alioli, Julie Briot, Carole Pons, Hang Yang, Marie Gairin, Dominique Goudounèche, Laura Cau, Michel Simon, Marie-Claire Méchin
Publikováno v:
Cell Death Discovery, Vol 9, Iss 1, Pp 1-8 (2023)
Abstract Deimination is a post-translational modification catalyzed by a family of enzymes named peptidylarginine deiminases (PADs). PADs transform arginine residues of protein substrates into citrulline. Deimination has been associated with numerous
Externí odkaz:
https://doaj.org/article/84eb5ef9f10c40c28e9b078713a87ddf