Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Marie‐Helene Aubriot‐Lorton"'
Autor:
Charlée Nardin, Candice Lesage, Eléonore Goubeau, Marie‐Helene Aubriot‐Lorton, Vanessa Lacheretz‐Szablewski, Nicolas Ortonne, Ines Saizonou, François Aubin, Olivier Dereure, Sophie Dalac‐Rat
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0af2dd063a8de03c453f6bdc7ea32163
https://doi.org/10.1111/jdv.18657
https://doi.org/10.1111/jdv.18657
Autor:
Alexandre Guilhem, Marion Ciudad, Marie-Hélène Aubriot-Lorton, Hélène Greigert, Claudie Cladière, Vanessa Leguy-Seguin, Sylvain Audia, Maxime Samson, Bernard Bonnotte
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Hereditary hemorrhagic telangiectasia (HHT) is a rare inherited disease due to heterozygous loss-of-function mutations on the BMP9/10 pathway (ENG, ACVRL1 or MADH4 mainly). HHT endothelial cells are prone to lose their quiescence, leading to progress
Externí odkaz:
https://doaj.org/article/8fc7267375d643fe8500fdc415098eb6
Autor:
Shai Rosenberg, Iva Simeonova, Franck Bielle, Maite Verreault, Bertille Bance, Isabelle Le Roux, Mailys Daniau, Arun Nadaradjane, Vincent Gleize, Sophie Paris, Yannick Marie, Marine Giry, Marc Polivka, Dominique Figarella-Branger, Marie-Hélène Aubriot-Lorton, Chiara Villa, Alexandre Vasiljevic, Emmanuèle Lechapt-Zalcman, Michel Kalamarides, Ariane Sharif, Karima Mokhtari, Stefano Maria Pagnotta, Antonio Iavarone, Anna Lasorella, Emmanuelle Huillard, Marc Sanson
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-9 (2018)
Chordoid glioma is a slow growing diencephalic tumor whose mutational landscape is poorly characterized. Here, the authors perform whole-exome and RNA-sequencing and find that 15 of 16 chordoid glioma cases studied harbor the same PRKCA mutation whic
Externí odkaz:
https://doaj.org/article/47f7d121d4304c4ca98cb2dbb0a6edde