Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Wiskott-Aldrich Syndrome/pathology"'
Autor:
Marc Descatoire, Remi Fritzen, Samuel Rotman, Genevieve Kuntzelman, Xavier Charles Leber, Stephanie Droz-Georget, Adrian J. Thrasher, Elisabetta Traggiai, Fabio Candotti
Publikováno v:
Cell reports, vol. 38, no. 10, pp. 110474
This project was supported by grant 310030-179251 from the Suisse National Science Foundation (SNF) (to F.C.), funds from the BLACKSWAN Foundation (BSF-005) (to M.D.), and the Wellcome Trust (to A.J.T.). A main feature of Wiskott-Aldrich syndrome (WA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2407bb8879bb1fc7ea248046e8ed071e
https://doi.org/10.1016/j.celrep.2022.110474
https://doi.org/10.1016/j.celrep.2022.110474
Autor:
Ayumi Yoshizaki, Martha Kirby, Tadafumi Yokoyama, Fabio Candotti, Stacie M. Anderson, Karen L. Simon
Publikováno v:
Plos One, vol. 10, no. 10, pp. e0139729
PLoS ONE, Vol 10, Iss 10, p e0139729 (2015)
PLoS ONE
PLoS ONE, Vol 10, Iss 10, p e0139729 (2015)
PLoS ONE
The Wiskott-Aldrich syndrome (WAS) is a rare X-linked primary immunodeficiency characterized by recurrent infections, thrombocytopenia, eczema, and high incidence of malignancy and autoimmunity. The cellular mechanisms underlying autoimmune complicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53f42af01d0e94c1507375de942da127
https://serval.unil.ch/resource/serval:BIB_E2770578213B.P001/REF.pdf
https://serval.unil.ch/resource/serval:BIB_E2770578213B.P001/REF.pdf
