Similar articles for PMID: 19307326

Year	Number of Results
1998	3
1999	3
2001	2
2002	3
2003	3
2004	3
2005	6
2006	2
2007	5
2008	2
2009	6
2010	9
2011	6
2012	4
2013	8
2014	7
2015	8
2016	2
2017	1
2018	4
2019	5
2020	4
2021	3
2022	1
2023	1
2024	0

1

The Wiskott-Aldrich syndrome protein is required for iNKT cell maturation and function.

Locci M, Draghici E, Marangoni F, Bosticardo M, Catucci M, Aiuti A, Cancrini C, Marodi L, Espanol T, Bredius RG, Thrasher AJ, Schulz A, Litzman J, Roncarolo MG, Casorati G, Dellabona P, Villa A. Locci M, et al. J Exp Med. 2009 Apr 13;206(4):735-42. doi: 10.1084/jem.20081773. Epub 2009 Mar 23. J Exp Med. 2009. PMID: 19307326 Free PMC article.

2

Wiskott-Aldrich syndrome protein is required for homeostasis and function of invariant NKT cells.

Astrakhan A, Ochs HD, Rawlings DJ. Astrakhan A, et al. J Immunol. 2009 Jun 15;182(12):7370-80. doi: 10.4049/jimmunol.0804256. J Immunol. 2009. PMID: 19494259 Free PMC article.

3

Antigen receptor-induced activation and cytoskeletal rearrangement are impaired in Wiskott-Aldrich syndrome protein-deficient lymphocytes.

Zhang J, Shehabeldin A, da Cruz LA, Butler J, Somani AK, McGavin M, Kozieradzki I, dos Santos AO, Nagy A, Grinstein S, Penninger JM, Siminovitch KA. Zhang J, et al. J Exp Med. 1999 Nov 1;190(9):1329-42. doi: 10.1084/jem.190.9.1329. J Exp Med. 1999. PMID: 10544204 Free PMC article.

4

Effects of Wiskott-Aldrich Syndrome Protein Deficiency on IL-10-Producing Regulatory B Cells in Humans and Mice.

Du HQ, Zhang X, An YF, Ding Y, Zhao XD. Du HQ, et al. Scand J Immunol. 2015 Jun;81(6):483-93. doi: 10.1111/sji.12282. Scand J Immunol. 2015. PMID: 25728049 Free article.

5

Impaired in vitro regulatory T cell function associated with Wiskott-Aldrich syndrome.

Adriani M, Aoki J, Horai R, Thornton AM, Konno A, Kirby M, Anderson SM, Siegel RM, Candotti F, Schwartzberg PL. Adriani M, et al. Clin Immunol. 2007 Jul;124(1):41-8. doi: 10.1016/j.clim.2007.02.001. Epub 2007 May 18. Clin Immunol. 2007. PMID: 17512803 Free PMC article.

6

Wiskott-Aldrich Syndrome causing mutation, Pro373Ser restricts conformational changes essential for WASP activity in T-cells.

Jain N, George B, Thanabalu T. Jain N, et al. Biochim Biophys Acta. 2014 Apr;1842(4):623-34. doi: 10.1016/j.bbadis.2014.01.006. Epub 2014 Jan 15. Biochim Biophys Acta. 2014. PMID: 24440360 Free article.

7

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. Huang W, et al. J Immunol. 2005 Mar 1;174(5):2602-11. doi: 10.4049/jimmunol.174.5.2602. J Immunol. 2005. PMID: 15728466

8

Evolution of highly polymorphic T cell populations in siblings with the Wiskott-Aldrich Syndrome.

Lutskiy MI, Park JY, Remold SK, Remold-O'Donnell E. Lutskiy MI, et al. PLoS One. 2008;3(10):e3444. doi: 10.1371/journal.pone.0003444. Epub 2008 Oct 20. PLoS One. 2008. PMID: 18941616 Free PMC article.

9

The Wiskott-Aldrich syndrome protein (WASP): roles in signaling and cytoskeletal organization.

Snapper SB, Rosen FS. Snapper SB, et al. Annu Rev Immunol. 1999;17:905-29. doi: 10.1146/annurev.immunol.17.1.905. Annu Rev Immunol. 1999. PMID: 10358777 Review.

10

The role of WASp in T cells and B cells.

Sun X, Wei Y, Lee PP, Ren B, Liu C. Sun X, et al. Cell Immunol. 2019 Jul;341:103919. doi: 10.1016/j.cellimm.2019.04.007. Epub 2019 Apr 17. Cell Immunol. 2019. PMID: 31047647 Review.

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