203 related articles for article (PubMed ID: 21178274)
1. DOCK8 immune deficiency as a model for primary cytoskeletal dysfunction.
McGhee SA; Chatila TA
Dis Markers; 2010; 29(3-4):151-6. PubMed ID: 21178274
[TBL] [Abstract][Full Text] [Related]
2. Wiskott-Aldrich syndrome: a disorder of haematopoietic cytoskeletal regulation.
Thrasher AJ; Burns S
Microsc Res Tech; 1999 Oct; 47(2):107-13. PubMed ID: 10523789
[TBL] [Abstract][Full Text] [Related]
3. The Wiskott-Aldrich syndrome: The actin cytoskeleton and immune cell function.
Blundell MP; Worth A; Bouma G; Thrasher AJ
Dis Markers; 2010; 29(3-4):157-75. PubMed ID: 21178275
[TBL] [Abstract][Full Text] [Related]
4. The Cdc42/Rac interactive binding region motif of the Wiskott Aldrich syndrome protein (WASP) is necessary but not sufficient for tight binding to Cdc42 and structure formation.
Rudolph MG; Bayer P; Abo A; Kuhlmann J; Vetter IR; Wittinghofer A
J Biol Chem; 1998 Jul; 273(29):18067-76. PubMed ID: 9660763
[TBL] [Abstract][Full Text] [Related]
5. [Reorganization of the actin cytoskeleton by WASP family proteins].
Miki H
Seikagaku; 2002 Sep; 74(9):1149-61. PubMed ID: 12402455
[No Abstract] [Full Text] [Related]
6. Activation of compensatory pathways via Rac2 in the absence of the Cdc42 effector Wiskott-Aldrich syndrome protein in Dendritic cells.
Baptista MAP; Westerberg LS
Small GTPases; 2019 Mar; 10(2):81-88. PubMed ID: 28129089
[TBL] [Abstract][Full Text] [Related]
7. Linking cellular activation to cytoskeletal reorganization: Wiskott-Aldrich syndrome as a model.
Stewart DM; Tian L; Nelson DL
Curr Opin Allergy Clin Immunol; 2001 Dec; 1(6):525-33. PubMed ID: 11964736
[TBL] [Abstract][Full Text] [Related]
8. Waltzing with WASP.
Ramesh N; Antón IM; Martínez-Quiles N; Geha RS
Trends Cell Biol; 1999 Jan; 9(1):15-9. PubMed ID: 10087612
[TBL] [Abstract][Full Text] [Related]
9. Dedicator of cytokinesis protein 2 couples with lymphoid enhancer-binding factor 1 to regulate expression of CD21 and B-cell differentiation.
Jing Y; Kang D; Liu L; Huang H; Chen A; Yang L; Jiang P; Li N; Miller H; Liu Z; Zhu X; Yang J; Wang X; Sun J; Liu Z; Liu W; Zhou X; Liu C
J Allergy Clin Immunol; 2019 Nov; 144(5):1377-1390.e4. PubMed ID: 31405607
[TBL] [Abstract][Full Text] [Related]
10. SLP-76 coordinates Nck-dependent Wiskott-Aldrich syndrome protein recruitment with Vav-1/Cdc42-dependent Wiskott-Aldrich syndrome protein activation at the T cell-APC contact site.
Zeng R; Cannon JL; Abraham RT; Way M; Billadeau DD; Bubeck-Wardenberg J; Burkhardt JK
J Immunol; 2003 Aug; 171(3):1360-8. PubMed ID: 12874226
[TBL] [Abstract][Full Text] [Related]
11. Dedicator of cytokinesis 8 interacts with talin and Wiskott-Aldrich syndrome protein to regulate NK cell cytotoxicity.
Ham H; Guerrier S; Kim J; Schoon RA; Anderson EL; Hamann MJ; Lou Z; Billadeau DD
J Immunol; 2013 Apr; 190(7):3661-9. PubMed ID: 23455509
[TBL] [Abstract][Full Text] [Related]
12. A DOCK8-WIP-WASp complex links T cell receptors to the actin cytoskeleton.
Janssen E; Tohme M; Hedayat M; Leick M; Kumari S; Ramesh N; Massaad MJ; Ullas S; Azcutia V; Goodnow CC; Randall KL; Qiao Q; Wu H; Al-Herz W; Cox D; Hartwig J; Irvine DJ; Luscinskas FW; Geha RS
J Clin Invest; 2016 Oct; 126(10):3837-3851. PubMed ID: 27599296
[TBL] [Abstract][Full Text] [Related]
13. FLI1 Induces Megakaryopoiesis Gene Expression Through WAS/WIP-Dependent and Independent Mechanisms; Implications for Wiskott-Aldrich Syndrome.
Wang C; Sample KM; Gajendran B; Kapranov P; Liu W; Hu A; Zacksenhaus E; Li Y; Hao X; Ben-David Y
Front Immunol; 2021; 12():607836. PubMed ID: 33717090
[TBL] [Abstract][Full Text] [Related]
14. Cdc42, Rac1, and the Wiskott-Aldrich syndrome protein are involved in the cytoskeletal regulation of B lymphocytes.
Westerberg L; Greicius G; Snapper SB; Aspenström P; Severinson E
Blood; 2001 Aug; 98(4):1086-94. PubMed ID: 11493455
[TBL] [Abstract][Full Text] [Related]
15. Deficiency of Wiskott-Aldrich syndrome protein has opposing effect on the pro-oncogenic pathway activation in nonmalignant versus malignant lymphocytes.
Han SS; Wen KK; Vyas YM
Oncogene; 2021 Jan; 40(2):345-354. PubMed ID: 33139832
[TBL] [Abstract][Full Text] [Related]
16. Two GTPases, Cdc42 and Rac, bind directly to a protein implicated in the immunodeficiency disorder Wiskott-Aldrich syndrome.
Aspenström P; Lindberg U; Hall A
Curr Biol; 1996 Jan; 6(1):70-5. PubMed ID: 8805223
[TBL] [Abstract][Full Text] [Related]
17. The Wiskott-Aldrich syndrome protein (WASP): roles in signaling and cytoskeletal organization.
Snapper SB; Rosen FS
Annu Rev Immunol; 1999; 17():905-29. PubMed ID: 10358777
[TBL] [Abstract][Full Text] [Related]
18. Antagonistic cross-talk between Rac and Cdc42 GTPases regulates generation of reactive oxygen species.
Diebold BA; Fowler B; Lu J; Dinauer MC; Bokoch GM
J Biol Chem; 2004 Jul; 279(27):28136-42. PubMed ID: 15123662
[TBL] [Abstract][Full Text] [Related]
19. Protein-tyrosine kinase and GTPase signals cooperate to phosphorylate and activate Wiskott-Aldrich syndrome protein (WASP)/neuronal WASP.
Torres E; Rosen MK
J Biol Chem; 2006 Feb; 281(6):3513-20. PubMed ID: 16293614
[TBL] [Abstract][Full Text] [Related]
20. The Wiskott-Aldrich syndrome protein regulates nuclear translocation of NFAT2 and NF-kappa B (RelA) independently of its role in filamentous actin polymerization and actin cytoskeletal rearrangement.
Huang W; Ochs HD; Dupont B; Vyas YM
J Immunol; 2005 Mar; 174(5):2602-11. PubMed ID: 15728466
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]