Absence of Expression of the Wiskott–Aldrich Syndrome Protein in Peripheral Blood Cells of Wiskott–Aldrich Syndrome Patients
- 1 July 1998
- journal article
- Published by Elsevier in Clinical Immunology and Immunopathology
- Vol. 88 (1) , 22-27
- https://doi.org/10.1006/clin.1998.4557
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- WASPbase: a database of WAS- and XLT-causing mutationsImmunology Today, 1996
- Identification of Regions of the Wiskott-Aldrich Syndrome Protein Responsible for Association with Selected Src Homology 3 DomainsPublished by Elsevier ,1996
- Identification of Itk/Tsk Src Homology 3 Domain LigandsJournal of Biological Chemistry, 1996
- Wiskott–Aldrich syndrome protein (WASp) is a binding partner for c-Src family protein-tyrosine kinasesCurrent Biology, 1996
- Studies of the expression of the Wiskott-Aldrich syndrome protein.Journal of Clinical Investigation, 1996
- Wiskott–Aldrich Syndrome Protein, a Novel Effector for the GTPase CDC42Hs, Is Implicated in Actin PolymerizationCell, 1996
- Two GTPases, Cdc42 and Rac, bind directly to a protein implicated in the immunodeficiency disorder Wiskott–Aldrich syndromeCurrent Biology, 1996
- The protein product of the c-cbl protooncogene is phosphorylated after B cell receptor stimulation and binds the SH3 domain of Bruton's tyrosine kinase.The Journal of Experimental Medicine, 1995
- Rho, Rac, and Cdc42 GTPases regulate the assembly of multimolecular focal complexes associated with actin stress fibers, lamellipodia, and filopodiaCell, 1995
- Isolation of a novel gene mutated in Wiskott-Aldrich syndromeCell, 1994