相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Dominant activating RAC2 mutation with lymphopenia, immunodeficiency, and cytoskeletal defects
Amy P. Hsu et al.
BLOOD (2019)
Heterozygous activating mutation in RAC2 causes infantile-onset combined immunodeficiency with susceptibility to viral infections
Svetlana O. Sharapova et al.
CLINICAL IMMUNOLOGY (2019)
A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency
Vassilios Lougaris et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2019)
The Structural Basis of Oncogenic Mutations G12, G13 and Q61 in Small GTPase K-Ras4B
Shaoyong Lu et al.
SCIENTIFIC REPORTS (2016)
RAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency
Omar K. Alkhairy et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2015)
REGULATION OF SMALL GTPases BY GEFs, GAPs, AND GDIs
Jacqueline Cherfils et al.
PHYSIOLOGICAL REVIEWS (2013)
Human phagocyte defect caused by a Rac2 mutation detected by means of neonatal screening for T-cell lymphopenia
Deborah Accetta et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2011)
Human neutrophil immunodeficiency syndrome is associated with an inhibitory Rac2 mutation
DR Ambruso et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)