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Items: 1 to 20 of 140

1.

Use of zinc-finger nucleases to knock out the WAS gene in K562 cells: a human cellular model for Wiskott-Aldrich syndrome.

Toscano MG, Anderson P, Muñoz P, Lucena G, Cobo M, Benabdellah K, Gregory PD, Holmes MC, Martin F.

Dis Model Mech. 2013 Mar;6(2):544-54. doi: 10.1242/dmm.010652. Epub 2013 Jan 11.

2.

Wiskott-Aldrich syndrome iPS cells produce megakaryocytes with defects in cytoskeletal rearrangement and proplatelet formation.

Ingrungruanglert P, Amarinthnukrowh P, Rungsiwiwut R, Maneesri-le Grand S, Sosothikul D, Suphapeetiporn K, Israsena N, Shotelersuk V.

Thromb Haemost. 2015 Apr;113(4):792-805. doi: 10.1160/TH14-06-0503. Epub 2014 Dec 18.

PMID:
25518736
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.

J Exp Med. 1999 Nov 1;190(9):1329-42.

4.

The open conformation of WASP regulates its nuclear localization and gene transcription in myeloid cells.

Looi CY, Sasahara Y, Watanabe Y, Satoh M, Hakozaki I, Uchiyama M, Wong WF, Du W, Uchiyama T, Kumaki S, Tsuchiya S, Kure S.

Int Immunol. 2014 Jun;26(6):341-52. doi: 10.1093/intimm/dxt072. Epub 2014 Jan 8.

PMID:
24402308
5.

The Wiskott-Aldrich syndrome.

Ochs HD, Thrasher AJ.

J Allergy Clin Immunol. 2006 Apr;117(4):725-38; quiz 739. Review.

PMID:
16630926
6.

Absence of WASp Enhances Hematopoietic and Megakaryocytic Differentiation in a Human Embryonic Stem Cell Model.

Toscano MG, Muñoz P, Sánchez-Gilabert A, Cobo M, Benabdellah K, Anderson P, Ramos-Mejía V, Real PJ, Neth O, Molinos-Quintana A, Gregory PD, Holmes MC, Martin F.

Mol Ther. 2016 Feb;24(2):342-353. doi: 10.1038/mt.2015.196. Epub 2015 Oct 27.

7.

Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndrome.

Facchetti F, Blanzuoli L, Vermi W, Notarangelo LD, Giliani S, Fiorini M, Fasth A, Stewart DM, Nelson DL.

J Pathol. 1998 May;185(1):99-107.

PMID:
9713366
8.

Novel membrane cell projection defects in Wiskott-Aldrich syndrome B cells.

Andreu N, Aran JM, Fillat C.

Int J Mol Med. 2007 Oct;20(4):445-50.

PMID:
17786274
9.

WASP and the phenotypic range associated with deficiency.

Notarangelo LD, Notarangelo LD, Ochs HD.

Curr Opin Allergy Clin Immunol. 2005 Dec;5(6):485-90. Review.

PMID:
16264326
10.

Wiskott-Aldrich syndrome protein-mediated actin dynamics control type-I interferon production in plasmacytoid dendritic cells.

Prete F, Catucci M, Labrada M, Gobessi S, Castiello MC, Bonomi E, Aiuti A, Vermi W, Cancrini C, Metin A, Hambleton S, Bredius R, Notarangelo LD, van der Burg M, Kalinke U, Villa A, Benvenuti F.

J Exp Med. 2013 Feb 11;210(2):355-74. doi: 10.1084/jem.20120363. Epub 2013 Jan 21.

11.

A lentiviral vector encoding the human Wiskott-Aldrich syndrome protein corrects immune and cytoskeletal defects in WASP knockout mice.

Charrier S, Stockholm D, Seye K, Opolon P, Taveau M, Gross DA, Bucher-Laurent S, Delenda C, Vainchenker W, Danos O, Galy A.

Gene Ther. 2005 Apr;12(7):597-606.

PMID:
15616597
12.

Development of hematopoietic stem cell gene therapy for Wiskott-Aldrich syndrome.

Boztug K, Dewey RA, Klein C.

Curr Opin Mol Ther. 2006 Oct;8(5):390-5. Review.

PMID:
17078381
13.

WIP and WASP play complementary roles in T cell homing and chemotaxis to SDF-1alpha.

Gallego MD, de la Fuente MA, Anton IM, Snapper S, Fuhlbrigge R, Geha RS.

Int Immunol. 2006 Feb;18(2):221-32. Epub 2005 Sep 1.

PMID:
16141245
14.

Expression of Wiskott-Aldrich syndrome protein (WASP) gene during hematopoietic differentiation.

Parolini O, Berardelli S, Riedl E, Bello-Fernandez C, Strobl H, Majdic O, Knapp W.

Blood. 1997 Jul 1;90(1):70-5.

15.

WASP (Wiskott-Aldrich syndrome protein) gene mutations and phenotype.

Imai K, Nonoyama S, Ochs HD.

Curr Opin Allergy Clin Immunol. 2003 Dec;3(6):427-36. Review.

PMID:
14612666
16.

Megakaryocyte-specific Profilin1-deficiency alters microtubule stability and causes a Wiskott-Aldrich syndrome-like platelet defect.

Bender M, Stritt S, Nurden P, van Eeuwijk JM, Zieger B, Kentouche K, Schulze H, Morbach H, Stegner D, Heinze KG, Dütting S, Gupta S, Witke W, Falet H, Fischer A, Hartwig JH, Nieswandt B.

Nat Commun. 2014 Sep 4;5:4746. doi: 10.1038/ncomms5746. Erratum in: Nat Commun. 2015;6:6507. Heinze, Katrin [corrected to Heinze, Katrin G].

PMID:
25187265
17.

Retroviral WASP gene transfer into human hematopoietic stem cells reconstitutes the actin cytoskeleton in myeloid progeny cells differentiated in vitro.

Dewey RA, Avedillo Díez I, Ballmaier M, Filipovich A, Greil J, Güngör T, Happel C, Maschan A, Noyan F, Pannicke U, Schwarz K, Snapper S, Welte K, Klein C.

Exp Hematol. 2006 Sep;34(9):1161-9.

PMID:
16939809
18.

Wiskott-Aldrich syndrome.

Notarangelo LD, Miao CH, Ochs HD.

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

PMID:
18043243
19.

The thrombocytopenia of Wiskott Aldrich syndrome is not related to a defect in proplatelet formation.

Haddad E, Cramer E, Rivière C, Rameau P, Louache F, Guichard J, Nelson DL, Fischer A, Vainchenker W, Debili N.

Blood. 1999 Jul 15;94(2):509-18.

20.

The chemotactic defect in wiskott-Aldrich syndrome macrophages is due to the reduced persistence of directional protrusions.

Ishihara D, Dovas A, Park H, Isaac BM, Cox D.

PLoS One. 2012;7(1):e30033. doi: 10.1371/journal.pone.0030033. Epub 2012 Jan 18.

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