Wiskott-Aldrich syndrome protein and platelets

Immunological Reviews

Volumn 178, Issue , 2000, Pages 111-117

  Oda, Atsushi ^a   Ochs, Hans D ^b  

^a JAPANESE RED CROSS SOCIETY   (Japan)

^b UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

WISKOTT ALDRICH SYNDROME PROTEIN;

HUMAN; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION; REVIEW; THROMBOCYTE; THROMBOCYTOPENIA; WISKOTT ALDRICH SYNDROME; X CHROMOSOME LINKED DISORDER;

EID: 0034501036     PISSN: 01052896     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1600-065X.2000.17808.x     Document Type: Review

References (57)

1. Isolation of a novel gene mutated in Wiskott-Aldrich syndrome
2. X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP gene
3. The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutations of the same gene
4. The Wiskott-Aldrich syndrome protein (WASP): Roles in signaling and cytoskeletal organization
5. Is Wiskott-Aldrich syndrome a cell trafficking disorder?
6. Waltzing with WASP
7. Scar I and the related Wiskott-Aldrich syndrome protein, WASP, regulate the actin cytoskeleton through the Arp2/3 complex
8. Influence of the C terminus of Wiskott-Aldrich syndrome protein (WASp) and the Arp2/3 complex on actin polymerization
9. Two GTPases, Cdc42 and Rac, bind directly to a protein implicated in the immunodeficiency disorder Wiskott-Aldrich syndrome
10. Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization
11. Identification of N-WASP homologs in human and rat brain
12. The interaction between N-WASP and the Arp2/3 complex links Cdc42-dependent signals to actin assembly
13. Autoinhibition and activation mechanisms of the Wiskott-Aldrich syndrome protein
14. Wiskott-Aldrich syndrome protein induces actin clustering without direct binding to Cdc42
15. Actin polymerization: Where the WASP stings
16. Wiskott-Aldrich syndrome protein regulates podosomes in primary human macrophages
17. Collagen induces tyrosine phosphorylation of Wiskott-Aldrich syndrome protein in human platelets
18. Regulation and function of WASp in platelets by the collagen receptor glycoprotein VI
19. Rapid tyrosine phosphorylation and activation of Btk/Tec kinases in platelets induced by collagen binding or CD32 crosslinking
20. Tyrosine phosphorylation of the Wiskott-Aldrich syndrome protein by Lyn and Btk is regulated by CDC42
21. Involvement of Wiskott-Aldrich syndrome protein in B-cell cytoplasmic tyrosine kinase pathway
22. PH domains in WASP - A bug in the system? Wiskott-Aldrich syndrome protein
23. WlP, a protein associated with Wiskott-Aldrich syndrome protein, induces actin polymerization and redistribution in lymphoid cells
24. Mutations that cause the Wiskott-Aldrich syndrome impair the interaction of Wiskott-Aldrich syndrome protein (WASP) with WASP interacting protein
25. WIP, a binding partner for Wiskott-Aldrich syndrome protein, cooperates with Vav in the regulation of T cell activation
26. Wiskott-Aldrich syndrome/X-linked thrombocytopenia: WASP gene mutations, protein expression, and phenotype
27. WASP levels in platelets and lymphocytes of Wiskott-Aldrich syndrome patients correlate with cell dysfunction
28. A multi-institutional survey of the Wiskott-Aldrich syndrome
29. The Wiskott-Aldrich syndrome: Studies of lymphocytes, granulocytes, and platelets
30. Wiskott-Aldrich syndrome and related X-linked thrombocytopenia
31. Intravenous immunoglobulin, splenectomy, and antibiotic prophylaxis in Wiskott-Aldrich syndrome
32. Pathological events in platelets of Wiskott-Aldrich syndrome patients
33. 2+-dependent neutral protease) in the destructive thrombocytopenia of the Wiskott-Aldrich syndrome
34. The cytoskeletal linker protein moesin: Decreased levels in Wiskott-Aldrich syndrome platelets and identification of a cleavage pathway in normal platelets
35. Heterogeneity in filamentous actin content among individual human blood platelets
36. Actin cytoskeletal function is spared, but apoptosis is increased, in WAS patient hematopoietic cells
37. The thrombocytopenia of Wiskott Aldrich syndrome is not related to a defect in proplatelet formation
38. X-linked syndrome of platelet dysfunction, thrombocytopenia, and imbalanced globin chain synthesis with hemolysis
39. Mapping of a syndrome of X-linked thrombocytopenia with thalassemia to band Xp11-12: Further evidence of genetic heterogeneity of X-linked thrombocytopenia
40. The locus for a novel syndromic form of neuronal intestinal pseudoobstruction maps to Xq28
41. Neurogenic chronic idiopathic intestinal pseudo-obstruction, patent ductus arteriosus, and thombocytopenia segregating as an X linked recessive disorder
42. Dyskeratosis congenita
43. Dyskeratosis congenita associated with elevated fetal hemoglobin, X-linked ocular albinism, and juvenile-onset diabetes mellitus
44. X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions
45. Wiskott-Aldrich syndrome protein-deficient mice reveal a role for WASP in T but not B cell activation
46. Antigen receptor induced activation and cytoskeletal rearrangement are impaired in Wiskott-Aldrich syndrome protein-deficient lymphocytes
47. WASP is involved in proliferation and differentiation of human haemopoietic progenitors in vitro
48. Spontaneous apoptosis in lymphocytes from patients with Wiskott-Aldrich syndrome: Correlation of accelerated cell death and attenuated bcl-2 expression
49. Nonrandom inactivation of the X chromosome in early lineage hematopoietic cells in carriers of Wiskott-Aldrich syndrome
50. Blood platelets are assembled principally at the ends of proplatelet processes produced by differentiated megakaryocytes
51. The platelet collagen receptor glycoprotein VI is a member of the immunoglobulin superfamily closely related to FcαR and the natural killer receptors
52. Collagen receptor signaling in platelets and megakaryocytes
53. Cross linking of CD32 (FcgIIA) and collagen induce tyrosine phosphorylation of Wiskott-Aldrich syndrome protein (WASP) in human platelets
54. Essential roles of Lyn in fibronectin-mediated filamentous actin assembly and cell motility in mast cells
55. Cytoskeletal and adhesive structural polarizations accompany IL-13-induced human macrophage fusion
56. CRKL links p210BCR/ABL with paxillin in chronic myelogenous leukemia cells
57. Fyn-binding protein (Fyb)/SLP-76-associated protein (SLAP), Ena/vasodilator-stimulated phosphoprotein (VASP) proteins and the Arp2/3 complex link T cell receptor (TCR) signaling to the actin cytoskeleton