Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Aurelie Charlet"'
Autor:
Ana Sofia Rocha, Valerie Vidal, Marjolijn Mertz, Timothy J. Kendall, Aurelie Charlet, Hitoshi Okamoto, Andreas Schedl
Publikováno v:
Cell Reports, Vol 13, Iss 9, Pp 1757-1764 (2015)
Liver zonation, the spatial separation of different metabolic pathways along the liver sinusoids, is fundamental for proper functioning of this organ, and its disruption can lead to the development of metabolic disorders such as hyperammonemia. Metab
Externí odkaz:
https://doaj.org/article/3e027cb5dce345af9dea4f0ceda8821c
Autor:
Martine Cohen-Solal, Robert Brommage, Filippo Massa, Wolfgang Hans, Martin Hrabé de Angelis, Aurelie Charlet, Agnès Boutet, Ana-Sofia Rocha, Thomas Funck-Brentano, Fariba Jian Motamedi, Clara Panzolini, Glenda Comai, Kristina Tanneberger, Christine Hartmann, Jürgen Behrens, Andreas Schedl
Publikováno v:
Journal of Bone and Mineral Research. 33:875-887
The X-linked WTX/AMER1 protein constitutes an important component of the β-catenin destruction complex that can both enhance and suppress canonical β-catenin signaling. Somatic mutations in WTX/AMER1 have been found in a proportion of the pediatric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a635409efb57c43d2624193eb01a13ad
https://doi.org/10.1002/jbmr.3387
https://doi.org/10.1002/jbmr.3387
Autor:
Glenda, Comai, Agnès, Boutet, Kristina, Tanneberger, Filippo, Massa, Ana-Sofia, Rocha, Aurelie, Charlet, Clara, Panzolini, Fariba, Jian Motamedi, Robert, Brommage, Wolfgang, Hans, Thomas, Funck-Brentano, Martin, Hrabe de Angelis, Christine, Hartmann, Martine, Cohen-Solal, Jürgen, Behrens, Andreas, Schedl
Publikováno v:
J. Bone Min. Res. 33, 875-887 (2018)
The X-linked WTX/AMER1 protein constitutes an important component of the β-catenin destruction complex that can both enhance and suppress canonical β-catenin signaling. Somatic mutations in WTX/AMER1 have been found in a proportion of the pediatric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::23acbabf529c4152c9cff66331866e87
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=52717
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=52717
Autor:
Jonathan Lefebvre, Stephen T Bradford, Fabian A. Buske, Sandra Lacas-Gervais, Aurelie Charlet, Andreas Schedl, Charlotte Gimpel, Franz Schaefer, Michael Clarkson, Herbert Schulz, Yutaka Hata, Filippo Massa
Publikováno v:
Kidney International
Kidney International, Nature Publishing Group, 2015, 88 (2), pp.321-31
Kidney International, Nature Publishing Group, 2015, 88 (2), pp.321-31
International audience; The Wilms' tumor suppressor WT1 is a key regulator of podocyte function that is mutated in Denys-Drash and Frasier syndromes. Here we have used an integrative approach employing ChIP, exon array, and genetic analyses in mice t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bda45d261f545c0a5a6d79beb7337074
https://doi.org/10.1038/ki.2015.140
https://doi.org/10.1038/ki.2015.140
Autor:
Aurelie Charlet, Fariba Jian Motamedi, Glenda Comai, Haroun Dhib, Andreas Schedl, Roberto Bandiera, Agnès Boutet
Publikováno v:
Genesis
Genesis, Wiley-Blackwell, 2017, 55 (11), pp.e23074. ⟨10.1002/dvg.23074⟩
Genesis, Wiley-Blackwell, 2017, 55 (11), pp.e23074. ⟨10.1002/dvg.23074⟩
International audience; WTX/AMER1 is an important developmental regulator, mutations in which have been identified in a proportion of patients suffering from the renal neoplasm Wilms' tumor and in the bone malformation syndrome Osteopathia Striata wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bada8196a0518b3ba07a3a52b49cbc67
https://pubmed.ncbi.nlm.nih.gov/28960679
https://pubmed.ncbi.nlm.nih.gov/28960679