Zobrazeno 1 - 10
of 172
pro vyhledávání: '"Eric Clauser"'
Autor:
Ilektra Kouranti, Waed Abdel Khalek, Stephani Mazurkiewicz, Irmine Loisel-Ferreira, Alexis M. Gautreau, Lionel Pintard, Xavier Jeunemaitre, Eric Clauser
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 9, p 5151 (2022)
Cullin 3 (CUL3) is the scaffold of Cullin3 Ring E3-ligases (CRL3s), which use various BTB-adaptor proteins to ubiquitinate numerous substrates targeting their proteasomal degradation. CUL3 mutations, responsible for a severe form of familial hyperkal
Externí odkaz:
https://doaj.org/article/df16924b81fd48c9b4988f7b209e66ad
Autor:
Marine Guillaud-Bataille, Bruno Ragazzon, Aurélien de Reyniès, Claire Chevalier, Isabelle Francillard, Olivia Barreau, Virginie Steunou, Johann Guillemot, Frédérique Tissier, Marthe Rizk-Rabin, Fernande René-Corail, Abir Al Ghuzlan, Guillaume Assié, Xavier Bertagna, Eric Baudin, Yves Le Bouc, Jérôme Bertherat, Eric Clauser
Publikováno v:
PLoS ONE, Vol 9, Iss 8, p e103744 (2014)
Insulin-like growth factor 2 (IGF2) overexpression is an important molecular marker of adrenocortical carcinoma (ACC), which is a rare but devastating endocrine cancer. It is not clear whether IGF2 overexpression modifies the biology and growth of th
Externí odkaz:
https://doaj.org/article/d93b7d6056db476b9f50e1676676fe75
Autor:
Jérôme Bertherat, Aurélien de Reyniès, Frédérique Tissier, Xavier Bertagna, Eric Clauser, Pierre Launay, Amato Fratticci, Guillaume Assié, Sébastien Gaujoux, Rossella Libé, Bruno Ragazzon
Supplementary Table 3 from Transcriptome Analysis Reveals that p53 and β-Catenin Alterations Occur in a Group of Aggressive Adrenocortical Cancers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f51475e2471099590759280f6187949
https://doi.org/10.1158/0008-5472.22387242
https://doi.org/10.1158/0008-5472.22387242
Autor:
Jérôme Bertherat, Aurélien de Reyniès, Frédérique Tissier, Xavier Bertagna, Eric Clauser, Pierre Launay, Amato Fratticci, Guillaume Assié, Sébastien Gaujoux, Rossella Libé, Bruno Ragazzon
Supplementary Table 2 from Transcriptome Analysis Reveals that p53 and β-Catenin Alterations Occur in a Group of Aggressive Adrenocortical Cancers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34d3bb07c9c702ed21362d6185eabccf
https://doi.org/10.1158/0008-5472.22387245
https://doi.org/10.1158/0008-5472.22387245
Autor:
Jérôme Bertherat, Aurélien de Reyniès, Frédérique Tissier, Xavier Bertagna, Eric Clauser, Pierre Launay, Amato Fratticci, Guillaume Assié, Sébastien Gaujoux, Rossella Libé, Bruno Ragazzon
Supplementary Table 1 from Transcriptome Analysis Reveals that p53 and β-Catenin Alterations Occur in a Group of Aggressive Adrenocortical Cancers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bff0d3afcae040e889e6fb46ed080fc
https://doi.org/10.1158/0008-5472.22387248
https://doi.org/10.1158/0008-5472.22387248
Autor:
Anna Vaczlavik, Eric Clauser, Isadora Pontes Cavalcante, Maria Candida Barisson Villares Fragoso, Jérôme Bertherat, Ludivine Drougat, Marthe Rizk-Rabin, Claudimara Ferini Pacicco Lotfi, Christopher Ribes, Bruno Ragazzon, Karine Perlemoine
Publikováno v:
Endocrine-Related Cancer
Endocrine-Related Cancer, BioScientifica, 2020, 27 (4), pp.221-230. ⟨10.1530/ERC-19-0502⟩
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Endocrine-Related Cancer, BioScientifica, 2020, 27 (4), pp.221-230. ⟨10.1530/ERC-19-0502⟩
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
ARMC5 (Armadillo repeat containing 5 gene) was identified as a new tumor suppressor gene responsible for hereditary adrenocortical tumors and meningiomas. ARMC5 is ubiquitously expressed and encodes a protein which contains a N-terminal Armadillo rep
Autor:
Chloé Rafael, Ilektra Kouranti, Irmine Loisel-Ferreira, Xavier Jeunemaitre, Juliette Hadchouel, Waed Abdel Khalek, Eric Clauser
Publikováno v:
Journal of the American Society of Nephrology
Journal of the American Society of Nephrology, American Society of Nephrology, 2019, 30 (5), pp.811-823. ⟨10.1681/ASN.2017121307⟩
J Am Soc Nephrol
Journal of the American Society of Nephrology, American Society of Nephrology, 2019, 30 (5), pp.811-823. ⟨10.1681/ASN.2017121307⟩
J Am Soc Nephrol
Background Mutations in four genes, WNK lysine deficient protein kinase 1 and 4 ( WNK1 and WNK4 ), kelch like family member 3 ( KLHL3 ), or Cullin 3 ( CUL3 ), can result in familial hyperkalemic hypertension (FHHt), a rare Mendelian form of human art
Autor:
Laurie Soulat-Dufour, Alexandre Boissonnas, Giulia Chinetti, Florence Pinet, Ludivine Laurans, Fabien Lareyre, Andreas Giraud, Léa Guyonnet, Soraya Taleb, Bruno Esposito, Coralie L. Guerin, Marc Derive, Sylvie Lang, Juliette Raffort, José Vilar, Alain Tedgui, Marie Vandestienne, Jean-Sébastien Silvestre, Amir Boufenzer, Hafid Ait-Oufella, Ziad Mallat, Icía Santos-Zas, Rida Al-Rifai, Yujiao Zhang, Patrick Bruneval, Jérémie Joffre, Eric Clauser
Publikováno v:
Journal of Clinical Investigation
Journal of Clinical Investigation, 2021, 131 (2), pp.e142468. ⟨10.1172/JCI142468⟩
J Clin Invest
Journal of Clinical Investigation, 2021, 131 (2), pp.e142468. ⟨10.1172/JCI142468⟩
J Clin Invest
International audience; The triggering receptor expressed on myeloid cells 1 (TREM-1) drives inflammatory responses in several cardiovascular diseases but its role in abdominal aortic aneurysm (AAA) remains unknown. Our objective was to explore the r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1eec9b922594c68eee085f5d8a294f04
https://www.hal.inserm.fr/inserm-03833065
https://www.hal.inserm.fr/inserm-03833065
Autor:
Isadora Cavalcante, Anna Vaczlavik, Ludivine Drougat, Claudimara Lotfi, Maria Fragoso, Eric Clauser, Marthe Rizk-Rabin, Jerome Bertherat, Bruno Ragazzon
Publikováno v:
Endocrine Abstracts.
Autor:
Eric Clauser, Pierre Bougnères, Emmanuelle Motte, Françoise Tilotta, Dominique Le Denmat, Catherine Le Stunff, Catherine Chaussain, Jérémy Sadoine, Claire Briet, Caroline Silve
Publikováno v:
Journal of Bone and Mineral Research. 32:333-346
In humans, activating mutations in the PRKAR1A gene cause acrodysostosis 1 (ACRDYS1). These mutations result in a reduction in PKA activation caused by an impaired ability of cAMP to dissociate mutant PRKAR1A from catalytic PKA subunits. Two striking