Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Gregory Mougel"'
Autor:
Théo Charnay, Gregory Mougel, Cyril Amouroux, Iva Gueorguieva, Florence Joubert, Morgane Pertuit, Rachel Reynaud, Anne Barlier, Thierry Brue, Alexandru Saveanu
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2023)
Isolated ACTH deficiency (IAD) is a life-threatening condition, particularly in the neonatal period, while a main consequence of undiagnosed isolated ACTH deficiency in survivors is cognitive impairment. TBX19 is involved in the differentiation and p
Externí odkaz:
https://doaj.org/article/405bf89880e44097afccf954195d820f
Autor:
Gregoire Mondielli, Gregory Mougel, Florent Darriet, Catherine Roche, Adeline Querdray, Christophe Lisbonis, Romain Appay, Henry Dufour, Olivier Chinot, Thomas Graillon, Anne Barlier
Publikováno v:
Cancers, Vol 14, Iss 18, p 4448 (2022)
Recurrent or high-grade meningiomas are an unmet medical need. Recently, we demonstrated that targeting mTOR by everolimus was relevant both in vitro and in humans. However, everolimus induces an AKT activation that may impact the anti-proliferative
Externí odkaz:
https://doaj.org/article/d76997f4ba954382ba1ef0864183fc29
Autor:
Rachel Fourneaux, Rachel Reynaud, Gregory Mougel, Sarah Castets, Patricia Bretones, Benjamin Dauriat, Thomas Edouard, Gerald Raverot, Anne Barlier, Thierry Brue, Frederic Castinetti, Alexandru Saveanu
Publikováno v:
European Journal of Endocrinology
European Journal of Endocrinology, 2022, 187 (6), pp.787-795. ⟨10.1530/EJE-22-0520⟩
European Journal of Endocrinology, 2022, 187 (6), pp.787-795. ⟨10.1530/EJE-22-0520⟩
Design Thyroid-stimulating hormone deficiency (TSHD) is a rare disease. It may be isolated, secondary to abnormalities of genes involved in TSH biosynthesis, or associated with other pituitary deficits or abnormalities of genes involved in pituitary
Autor:
Thi Thom Mac, Frederic Castinetti, Céline Bar, Sophie Julia, Marlene Pasquet, Pauline Romanet, Alexandru Saveanu, Gregory Mougel, Teddy Fauquier, Nicolas Jullien, Anne Barlier, Rachel Reynaud, Thierry Brue
Publikováno v:
Journal of Neuroendocrinology.
Autor:
Arnaud Lagarde, Gregory Mougel, Lucie Coppin, Magalie Haissaguerre, Collen Lauriane Le, Marc Klein, Marie-Francoise Odou, Antoine Tabarin, Hedia Brixi, Brigitte Delemer, Anne Barlier, Pauline Romanet
Publikováno v:
Endocrine Abstracts.
Autor:
Arnaud Lagarde, Grégory Mougel, Lucie Coppin, Magalie Haissaguerre, Lauriane Le Collen, Amira Mohamed, Marc Klein, Marie-Françoise Odou, Antoine Tabarin, Hedia Brixi, Thomas Cuny, Brigitte Delemer, Anne Barlier, Pauline Romanet
Publikováno v:
Endocrine Connections, Vol 11, Iss 11, Pp 1-8 (2022)
Purpose: Mosaicism is a feature of several inherited tumor syndromes. Only a few cases of mosaicism have been described in multiple endocrine neoplasia type 1 (MEN1). Next-generation sequencing (NGS) offers new possibilities for detecti ng mosaicism.
Externí odkaz:
https://doaj.org/article/950beb9810fc45259d37eaf1892dd502
Autor:
Pauline Romanet, Justine Galluso, Peter Kamenicky, Mirella Hage, Marily Theodoropoulou, Catherine Roche, Thomas Graillon, Heather C. Etchevers, Daniel De Murat, Grégory Mougel, Dominique Figarella-Branger, Henry Dufour, Thomas Cuny, Guillaume Assié, Anne Barlier
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 14, p 7570 (2021)
Forty percent of somatotroph tumors harbor recurrent activating GNAS mutations, historically called the gsp oncogene. In gsp-negative somatotroph tumors, GNAS expression itself is highly variable; those with GNAS overexpression most resemble phenotyp
Externí odkaz:
https://doaj.org/article/4ba9e9b36cea487b968081e74e713037