Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Charlène Thiebaut"'
Publikováno v:
Life, Vol 11, Iss 11, p 1147 (2021)
PRMT1, the major protein arginine methyltransferase in mammals, catalyzes monomethylation and asymmetric dimethylation of arginine side chains in proteins. Initially described as a regulator of chromatin dynamics through the methylation of histone H4
Externí odkaz:
https://doaj.org/article/89fd1e5237a942578239676696c2e1c5
Autor:
Clémence Chamard-Jovenin, Charlène Thiebaut, Amand Chesnel, Emmanuel Bresso, Chloé Morel, Malika Smail-Tabbone, Marie-Dominique Devignes, Taha Boukhobza, Hélène Dumond
Publikováno v:
Frontiers in Endocrinology, Vol 8 (2017)
Fetal and neonatal exposure to long-chain alkylphenols has been suspected to promote breast developmental disorders and consequently to increase breast cancer risk. However, disease predisposition from developmental exposures remains unclear. In this
Externí odkaz:
https://doaj.org/article/aa6ed05746ef4d8bb74e87c459657491
Autor:
Charlène Thiebaut, Clémence Chamard-Jovenin, Amand Chesnel, Chloé Morel, El-Hadi Djermoune, Taha Boukhobza, Hélène Dumond
Publikováno v:
PLoS ONE, Vol 12, Iss 3, p e0173931 (2017)
Estrogen receptor alpha 36 (ERα36) is a variant of the canonical estrogen receptor alpha (ERα66), widely expressed in hormone sensitive cancer cells and whose high expression level correlates with a poor survival prognosis for breast cancer patient
Externí odkaz:
https://doaj.org/article/65f23304133b4a6395e064879c482459
Autor:
Martin Lehr, Ahmed Dahmani, Léa Huguet, Rania El-Botty, Charlène Thiebaut, Muriel Romancer, Paul Cottu, Elisabetta Marangoni
Publikováno v:
Cancer Research. 82:649-649
Background: Onapristone (ONA) is a progesterone receptor (PR) antagonist that prevents PR-mediated DNA transcription. ONA is currently being evaluated in metastatic breast cancers (MBC), as well as other hormone-dependent cancers. Recently, therapeut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53cf2fcdeca5f8e446a4f5977fa87f25
https://doi.org/10.1158/1538-7445.am2022-649
https://doi.org/10.1158/1538-7445.am2022-649
Autor:
Virginie Vlaeminck-Guillem, Muriel Le Romancer, Olivier Tredan, Coralie Poulard, Charlène Thiebaut
Publikováno v:
Molecular and Cellular Endocrinology
Molecular and Cellular Endocrinology, 2021, 538, pp.111453. ⟨10.1016/j.mce.2021.111453⟩
Molecular and Cellular Endocrinology, 2021, 538, pp.111453. ⟨10.1016/j.mce.2021.111453⟩
International audience; Steroid receptors (SRs) are members of the nuclear receptor family, which are ligand-activated transcription factors. SRs regulate many physiological functions including development and reproduction, though they can also be in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce16e4918cf591fef7105a0a549f0739
https://doi.org/10.1016/j.mce.2021.111453
https://doi.org/10.1016/j.mce.2021.111453