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Autor:
Amy E O'Connell, Stefano eVolpi, Kerry eDobbs, Claudia eFiorini, Erdyni eTsitsikov, Helen ede Boer, Isil B Barlan, Jenny M Despotovic, Francisco J Espinosa-Rosales, Celine eHanson, Maria G Kanariou, Roxana eMartinez-Beckerat, Alvaro eMayorga-Sirera, Carmen eMeija-Carvajal, Nesrine eRadwan, Aaron R Weiss, Yu Nee eLee, Sung-Yun ePai, Luigi Daniele Notarangelo
Publikováno v:
Frontiers in Immunology, Vol 5 (2014)
The Wiskott Aldrich syndrome (WAS) is due to mutations of the WAS gene encoding for the cytoskeletal WAS protein (WASp), leading to abnormal downstream signaling from the T cell and B cell antigen receptors (TCR, BCR). We hypothesized that the impair
Externí odkaz:
https://doaj.org/article/f8b96d5993654915a40dd38504003158