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Items: 1 to 20 of 33

1.

WASP: a key immunological multitasker.

Thrasher AJ, Burns SO.

Nat Rev Immunol. 2010 Mar;10(3):182-92. doi: 10.1038/nri2724. Review.

PMID:
20182458
2.

Activating mutations of N-WASP alter Shigella pathogenesis.

Adamovich DA, Nakamura F, Worth A, Burns S, Thrasher AJ, Hartwig JH, Snapper SB.

Biochem Biophys Res Commun. 2009 Jul 3;384(3):284-9. doi: 10.1016/j.bbrc.2009.04.050. Epub 2009 Apr 18.

3.

The cellular context of T cell signaling.

Dustin ML.

Immunity. 2009 Apr 17;30(4):482-92. doi: 10.1016/j.immuni.2009.03.010. Review.

4.

Recent advances in understanding the pathophysiology of Wiskott-Aldrich syndrome.

Bosticardo M, Marangoni F, Aiuti A, Villa A, Grazia Roncarolo M.

Blood. 2009 Jun 18;113(25):6288-95. doi: 10.1182/blood-2008-12-115253. Epub 2009 Apr 7. Review.

5.

A syndrome with congenital neutropenia and mutations in G6PC3.

Boztug K, Appaswamy G, Ashikov A, Schäffer AA, Salzer U, Diestelhorst J, Germeshausen M, Brandes G, Lee-Gossler J, Noyan F, Gatzke AK, Minkov M, Greil J, Kratz C, Petropoulou T, Pellier I, Bellanné-Chantelot C, Rezaei N, Mönkemöller K, Irani-Hakimeh N, Bakker H, Gerardy-Schahn R, Zeidler C, Grimbacher B, Welte K, Klein C.

N Engl J Med. 2009 Jan 1;360(1):32-43. doi: 10.1056/NEJMoa0805051. Erratum in: N Engl J Med. 2011 Apr 28;364(17):1682.

6.

The many causes of severe congenital neutropenia.

Dale DC, Link DC.

N Engl J Med. 2009 Jan 1;360(1):3-5. doi: 10.1056/NEJMp0806821. No abstract available.

7.

The who, how and where of antigen presentation to B cells.

Batista FD, Harwood NE.

Nat Rev Immunol. 2009 Jan;9(1):15-27. doi: 10.1038/nri2454. Review.

PMID:
19079135
8.

A large kindred with X-linked neutropenia with an I294T mutation of the Wiskott-Aldrich syndrome gene.

Beel K, Cotter MM, Blatny J, Bond J, Lucas G, Green F, Vanduppen V, Leung DW, Rooney S, Smith OP, Rosen MK, Vandenberghe P.

Br J Haematol. 2009 Jan;144(1):120-6. doi: 10.1111/j.1365-2141.2008.07416.x. Epub 2008 Nov 1.

9.

The actin regulator coronin 1A is mutant in a thymic egress-deficient mouse strain and in a patient with severe combined immunodeficiency.

Shiow LR, Roadcap DW, Paris K, Watson SR, Grigorova IL, Lebet T, An J, Xu Y, Jenne CN, Föger N, Sorensen RU, Goodnow CC, Bear JE, Puck JM, Cyster JG.

Nat Immunol. 2008 Nov;9(11):1307-15. doi: 10.1038/ni.1662. Epub 2008 Oct 5.

10.

WASP confers selective advantage for specific hematopoietic cell populations and serves a unique role in marginal zone B-cell homeostasis and function.

Westerberg LS, de la Fuente MA, Wermeling F, Ochs HD, Karlsson MC, Snapper SB, Notarangelo LD.

Blood. 2008 Nov 15;112(10):4139-47. doi: 10.1182/blood-2008-02-140715. Epub 2008 Sep 4.

11.

Wiskott-Aldrich syndrome.

Notarangelo LD, Miao CH, Ochs HD.

Curr Opin Hematol. 2008 Jan;15(1):30-6. Review.

PMID:
18043243
12.

Limiting the proliferation of polyploid cells.

Ganem NJ, Pellman D.

Cell. 2007 Nov 2;131(3):437-40. Review.

13.

Wiskott Aldrich syndrome protein (WASP) and N-WASP are critical for T cell development.

Cotta-de-Almeida V, Westerberg L, Maillard MH, Onaldi D, Wachtel H, Meelu P, Chung UI, Xavier R, Alt FW, Snapper SB.

Proc Natl Acad Sci U S A. 2007 Sep 25;104(39):15424-9. Epub 2007 Sep 18.

14.

Unregulated actin polymerization by WASp causes defects of mitosis and cytokinesis in X-linked neutropenia.

Moulding DA, Blundell MP, Spiller DG, White MR, Cory GO, Calle Y, Kempski H, Sinclair J, Ancliff PJ, Kinnon C, Jones GE, Thrasher AJ.

J Exp Med. 2007 Sep 3;204(9):2213-24. Epub 2007 Aug 27.

15.

Defective DNA repair and increased genomic instability in Cernunnos-XLF-deficient murine ES cells.

Zha S, Alt FW, Cheng HL, Brush JW, Li G.

Proc Natl Acad Sci U S A. 2007 Mar 13;104(11):4518-23. Epub 2007 Mar 7.

16.

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).

Klein C, Grudzien M, Appaswamy G, Germeshausen M, Sandrock I, Schäffer AA, Rathinam C, Boztug K, Schwinzer B, Rezaei N, Bohn G, Melin M, Carlsson G, Fadeel B, Dahl N, Palmblad J, Henter JI, Zeidler C, Grimbacher B, Welte K.

Nat Genet. 2007 Jan;39(1):86-92. Epub 2006 Dec 24.

PMID:
17187068
17.

Requirement for coronin 1 in T lymphocyte trafficking and cellular homeostasis.

Föger N, Rangell L, Danilenko DM, Chan AC.

Science. 2006 Aug 11;313(5788):839-42.

18.

Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia.

Ancliff PJ, Blundell MP, Cory GO, Calle Y, Worth A, Kempski H, Burns S, Jones GE, Sinclair J, Kinnon C, Hann IM, Gale RE, Linch DC, Thrasher AJ.

Blood. 2006 Oct 1;108(7):2182-9. Epub 2006 Jun 27.

19.

WASP deficiency leads to global defects of directed leukocyte migration in vitro and in vivo.

Snapper SB, Meelu P, Nguyen D, Stockton BM, Bozza P, Alt FW, Rosen FS, von Andrian UH, Klein C.

J Leukoc Biol. 2005 Jun;77(6):993-8. Epub 2005 Mar 17.

20.

Wiskott-Aldrich syndrome protein deficiency leads to reduced B-cell adhesion, migration, and homing, and a delayed humoral immune response.

Westerberg L, Larsson M, Hardy SJ, Fernández C, Thrasher AJ, Severinson E.

Blood. 2005 Feb 1;105(3):1144-52. Epub 2004 Sep 21.

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