Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Laurence Dumeige"'
Autor:
Laurence Dumeige, Mélanie Nehlich, Say Viengchareun, Julie Perrot, Eric Pussard, Marc Lombès, Laetitia Martinerie
Publikováno v:
Experimental and Molecular Medicine, Vol 52, Iss 1, Pp 152-165 (2020)
High blood pressure: Exploring inheritance A propensity towards high blood pressure may be passed down through several generations from adults who were born preterm. People who are born prematurely often suffer from kidney (renal) problems, high bloo
Externí odkaz:
https://doaj.org/article/365e4d27f9cd4d4e98be952ee278defc
Autor:
Margaux Laulhé, Laurence Dumeige, Thi An Vu, Imene Hani, Eric Pussard, Marc Lombès, Say Viengchareun, Laetitia Martinerie
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 10, p 5275 (2021)
Sexual dimorphism involves differences between biological sexes that go beyond sexual characteristics. In mammals, differences between sexes have been demonstrated regarding various biological processes, including blood pressure and predisposition to
Externí odkaz:
https://doaj.org/article/d382e1af4ee44f638eaf3db507d7843d
Autor:
Laurence Dumeige, Caroline Storey, Lyvianne Decourtye, Melanie Nehlich, Christophe Lhadj, Say Viengchareun, Laurent Kappeler, Marc Lombès, Laetitia Martinerie
Publikováno v:
International Journal of Molecular Sciences, Vol 18, Iss 2, p 457 (2017)
Sex differences have been identified in various biological processes, including hypertension. The mineralocorticoid signaling pathway is an important contributor to early arterial hypertension, however its sex-specific expression has been scarcely st
Externí odkaz:
https://doaj.org/article/7fe981aa1e3949c3890180b3d973d1dd
Autor:
Mélanie Nehlich, Laurence Dumeige, Say Viengchareun, Julie Perrot, Eric Pussard, Laetitia Martinerie, Marc Lombès
Publikováno v:
Experimental and Molecular Medicine
Experimental and Molecular Medicine, Nature Publishing Group, 2020, ⟨10.1038/s12276-020-0373-5⟩
Experimental and Molecular Medicine, Vol 52, Iss 1, Pp 152-165 (2020)
Experimental & Molecular Medicine
Experimental and Molecular Medicine, 2020, ⟨10.1038/s12276-020-0373-5⟩
Experimental and Molecular Medicine, Nature Publishing Group, 2020, ⟨10.1038/s12276-020-0373-5⟩
Experimental and Molecular Medicine, Vol 52, Iss 1, Pp 152-165 (2020)
Experimental & Molecular Medicine
Experimental and Molecular Medicine, 2020, ⟨10.1038/s12276-020-0373-5⟩
Renal and cardiovascular complications of prematurity are well established, notably the development of hypertension in adulthood. However, the underlying molecular mechanisms remain poorly understood. Our objective was to investigate the impact of pr
Autor:
Imene Hani, Marc Lombès, Laurence Dumeige, Thi An Vu, Laetitia Martinerie, Eric Pussard, Say Viengchareun, Margaux Laulhé
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 5275, p 5275 (2021)
International Journal of Molecular Sciences, Vol 22, Iss 5275, p 5275 (2021)
Sexual dimorphism involves differences between biological sexes that go beyond sexual characteristics. In mammals, differences between sexes have been demonstrated regarding various biological processes, including blood pressure and predisposition to
Autor:
Cécile Brachet, Michel Peuchmaur, Juliane Léger, Capucine Hyon, Jean-Claude Carel, Claire Bouvattier, Alaa El Ghoneimi, Matthieu Peycelon, Dominique Simon, Ken McElreavey, Jérôme Bouligand, Jean-Pierre Siffroi, Dinane Samara-Boustani, Annabel Paye-Jaouen, Laurence Dumeige, Sophie Lambert, Laetitia Martinerie, Elodie Fiot
Publikováno v:
Clinical Endocrinology
Clinical Endocrinology, 2021, 94 (4), pp.667-676. ⟨10.1111/cen.14389⟩
Clinical Endocrinology, 2021, 94 (4), pp.667-676. ⟨10.1111/cen.14389⟩
International audience; Objective: SRY-negative 46,XX testicular and ovotesticular disorders/differences of sex development (T/OTDSD) represent a very rare and unique DSD condition where testicular tissue develops in the absence of a Y chromosome. To
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20d00f8992f2fc8ab9ef8375d9f06125
https://www.hal.inserm.fr/inserm-03790574
https://www.hal.inserm.fr/inserm-03790574
Publikováno v:
Annales d'Endocrinologie. 78:S21-S30
Congenital adrenal hyperplasia is an autosomal recessive disease due to functional abnormalities of adrenal steroid enzymes. The most common form of the disease is due to a 21-hydroxylase deficiency. The classical forms (most severe) are characterize
Autor:
Melanie Nehlich, Laetitia Martinerie, Eric Pussard, Say Viengchareun, Laurence Dumeige, Marc Lombès
Publikováno v:
Endocrine Abstracts.
Autor:
Qiong-Yao Xu, Alexandra Bourdin-Pintueles, Thi-An Vu, Julie Perrot, Ségolène Hescot, Laurence Dumeige, Eric Pussard, Laurent M. Sachs, Géraldine Vitellius, Laura Bessiene, Laetitia Martinerie, Marc Lombès, Say Viengchareun
Publikováno v:
Endocrine Abstracts.
Autor:
Thi An Vu, Laetitia Martinerie, Say Viengchareun, Julie Perrot, Marc Lombès, Alexandra Bourdin-Pintueles, Qing-Yao Xu, Laurent M. Sachs, Eric Pussard, Ségolène Hescot, Laurence Dumeige, Laura Bessiene, Géraldine Vitellius
Publikováno v:
Journal of the Endocrine Society
Glucocorticoid hormone metabolism and action are regulated by the 11-beta hydroxysteroid dehydrogenase (11βHSD) isozymes: the 11βHSD2, mostly expressed in the distal nephron, converts cortisol [F] into cortisone [E] in humans or corticosterone [B]