Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Claire Bardet"'
Autor:
Elis J. Lira dos Santos, Kenta Nakajima, Julien Po, Ayako Hanai, Volha Zhukouskaya, Martin Biosse Duplan, Agnès Linglart, Takashi Shimada, Catherine Chaussain, Claire Bardet
Publikováno v:
International Journal of Oral Science, Vol 15, Iss 1, Pp 1-10 (2023)
Abstract Elevated fibroblast growth factor 23 (FGF23) in X-linked hypophosphatemia (XLH) results in rickets and phosphate wasting, manifesting by severe bone and dental abnormalities. Burosumab, a FGF23-neutralizing antibody, an alternative to conven
Externí odkaz:
https://doaj.org/article/7315cc6e2b4443c8abd78d6f5c752a46
Autor:
Julia André, Volha V. Zhukouskaya, Anne-Sophie Lambert, Jean-Pierre Salles, Brigitte Mignot, Claire Bardet, Catherine Chaussain, Anya Rothenbuhler, Agnès Linglart
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-8 (2022)
Abstract Background/aim Despite optimal conventional treatment (oral phosphate supplements and active vitamin D analogs), about 40–50% of children with well-controlled X-linked hypophosphatemia (XLH) show linear growth failure, making them less lik
Externí odkaz:
https://doaj.org/article/f6c19042ac8f44099d6965eb56139ed8
Autor:
Volha V. Zhukouskaya, Claire Bardet
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/fb9b46e390b148448a05c2481d72e8b2
Autor:
Axelle Cauliez, Volha V. Zhukouskaya, Stéphane Hilliquin, Jérémy Sadoine, Lotfi Slimani, Corinne Miceli-Richard, Karine Briot, Agnès Linglart, Catherine Chaussain, Claire Bardet
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2021)
X-linked hypophosphatemia (XLH) is the most common form of genetic rickets. Mainly diagnosed during childhood because of growth retardation and deformities of the lower limbs, the disease affects adults with early enthesopathies and joint structural
Externí odkaz:
https://doaj.org/article/e06d9f86dbaf4dde95382cdadce2fce0
Autor:
Carole-Anne Faraji-Bellée, Axelle Cauliez, Benjamin Salmon, Olivier Fogel, Volha Zhukouskaya, Aurélie Benoit, Thorsten Schinke, Christian Roux, Agnès Linglart, Corinne Miceli-Richard, Catherine Chaussain, Karine Briot, Claire Bardet
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
X-linked hypophosphatemia (XLH) is characterized by rickets and osteomalacia, caused by inactivating mutations in the Phosphate-regulating endopeptidase homolog X-linked (PHEX) gene. With aging, adult patients develop paradoxical heterotopic calcific
Externí odkaz:
https://doaj.org/article/9c9b4e95b4994f3ba7f2144dbb94b22e
Publikováno v:
Biomedicines, Vol 9, Iss 11, p 1538 (2021)
Biomedical research seeks to generate experimental results for translation to clinical settings. In order to improve the transition from bench to bedside, researchers must draw justifiable conclusions based on data from an appropriate model. Animal t
Externí odkaz:
https://doaj.org/article/4a84c330c1c24ff9925a39102df696b3
Autor:
Claire Bardet, Sandy Ribes, Yong Wu, Mamadou Tidiane Diallo, Benjamin Salmon, Tilman Breiderhoff, Pascal Houillier, Dominik Müller, Catherine Chaussain
Publikováno v:
Frontiers in Physiology, Vol 8 (2017)
Claudins are a family of proteins that forms paracellular barriers and pores determining tight junctions (TJ) permeability. Claudin-16 and -19 are pore forming TJ proteins allowing calcium and magnesium reabsorption in the thick ascending limb of Hen
Externí odkaz:
https://doaj.org/article/5bbd6980b7e344d1be7cb7b00bb0bddf
Autor:
Benjamin Salmon, Claire Bardet, Mayssam Khaddam, Jiar Naji, Benjamin R Coyac, Brigitte Baroukh, Franck Letourneur, Julie Lesieur, Franck Decup, Dominique Le Denmat, Antonino Nicoletti, Anne Poliard, Peter S Rowe, Eric Huet, Sibylle Opsahl Vital, Agnès Linglart, Marc D McKee, Catherine Chaussain
Publikováno v:
PLoS ONE, Vol 8, Iss 2, p e56749 (2013)
Mutations in PHEX (phosphate-regulating gene with homologies to endopeptidases on the X-chromosome) cause X-linked familial hypophosphatemic rickets (XLH), a disorder having severe bone and tooth dentin mineralization defects. The absence of function
Externí odkaz:
https://doaj.org/article/820187aed9344615a2c61876bf69651a
Autor:
Nicolas Obtel, Adeline Le Cabec, Thè Nghia Nguyen, Eloise Giabicani, Stijn J. M. Van Malderen, Jan Garrevoet, Aline Percot, Céline Paris, Christopher Dean, Smail Hadj‐Rabia, Pascal Houillier, Tilman Breiderhoff, Claire Bardet, Thibaud Coradin, Fernando Ramirez Rozzi, Catherine Chaussain
Publikováno v:
Annals of the New York Academy of Sciences 1516(1), 197-211 (2022). doi:10.1111/nyas.14865
Annals of the New York Academy of Sciences
Annals of the New York Academy of Sciences, 2022, ⟨10.1111/nyas.14865⟩
Annals of the New York Academy of Sciences, Wiley, 2022, Virtual Special Issue-Tight Junction, 1516 (1), pp.197-211. ⟨10.1111/nyas.14865⟩
Annals of the New York Academy of Sciences
Annals of the New York Academy of Sciences, 2022, ⟨10.1111/nyas.14865⟩
Annals of the New York Academy of Sciences, Wiley, 2022, Virtual Special Issue-Tight Junction, 1516 (1), pp.197-211. ⟨10.1111/nyas.14865⟩
Annals of the New York Academy of Sciences 1516(1), 197-211 (2022). doi:10.1111/nyas.14865
In epithelia, claudin proteins are important components of the tight junctions as they determine the permeability and specificity to ions of the paracellu
In epithelia, claudin proteins are important components of the tight junctions as they determine the permeability and specificity to ions of the paracellu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e1c66356f09c7544ee5746aa998b7ad
https://bib-pubdb1.desy.de/record/482215
https://bib-pubdb1.desy.de/record/482215
Autor:
Stéphane Hilliquin, N. Danièle, B. Baroukh, Severine Charles, Louisa Jauze, Fabienne Rajas, Lotfi Slimani, Agnès Linglart, Jérémy Sadoine, Claire Bardet, Giuseppe Ronzitti, Catherine Chaussain, Volha V. Zhukouskaya, Laetitia van Wittenberghe, Federico Mingozzi, Christian Leborgne
Publikováno v:
Science Advances
Science Advances, 2021, 7 (44), pp.eabj5018. ⟨10.1126/sciadv.abj5018⟩
Science Advances, American Association for the Advancement of Science (AAAS), 2021, 7 (44), pp.eabj5018. ⟨10.1126/sciadv.abj5018⟩
Science Advances, 2021, 7 (44), pp.eabj5018. ⟨10.1126/sciadv.abj5018⟩
Science Advances, American Association for the Advancement of Science (AAAS), 2021, 7 (44), pp.eabj5018. ⟨10.1126/sciadv.abj5018⟩
Description
A new therapeutic approach for the treatment of a skeletal disorder with AAVs bypasses bone resistance to gene transfer.
Adeno-associated virus (AAV) vectors are a well-established gene transfer approach for rare genetic disease
A new therapeutic approach for the treatment of a skeletal disorder with AAVs bypasses bone resistance to gene transfer.
Adeno-associated virus (AAV) vectors are a well-established gene transfer approach for rare genetic disease