Thrasher AJ - Search Results

1

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans.

Tuijnenburg P, Lango Allen H, Burns SO, Greene D, Jansen MH, Staples E, Stephens J, Carss KJ, Biasci D, Baxendale H, Thomas M, Chandra A, Kiani-Alikhan S, Longhurst HJ, Seneviratne SL, Oksenhendler E, Simeoni I, de Bree GJ, Tool ATJ, van Leeuwen EMM, Ebberink EHTM, Meijer AB, Tuna S, Whitehorn D, Brown M, Turro E, Thrasher AJ, Smith KGC, Thaventhiran JE, Kuijpers TW; NIHR BioResource–Rare Diseases Consortium. Tuijnenburg P, et al. Among authors: thrasher aj. J Allergy Clin Immunol. 2018 Oct;142(4):1285-1296. doi: 10.1016/j.jaci.2018.01.039. Epub 2018 Mar 2. J Allergy Clin Immunol. 2018. PMID: 29477724 Free PMC article.

2

Wiskott-Aldrich syndrome: a disorder of haematopoietic cytoskeletal regulation.

Thrasher AJ, Burns S. Thrasher AJ, et al. Microsc Res Tech. 1999 Oct 15;47(2):107-13. doi: 10.1002/(SICI)1097-0029(19991015)47:2<107::AID-JEMT3>3.0.CO;2-H. Microsc Res Tech. 1999. PMID: 10523789 Review.

3

Diagnosis of X-linked lymphoproliferative disease by analysis of SLAM-associated protein expression.

Gilmour KC, Cranston T, Jones A, Davies EG, Goldblatt D, Thrasher A, Kinnon C, Nichols KE, Gaspar HB. Gilmour KC, et al. Eur J Immunol. 2000 Jun;30(6):1691-7. doi: 10.1002/1521-4141(200006)30:6<1691::AID-IMMU1691>3.0.CO;2-K. Eur J Immunol. 2000. PMID: 10898506 Free article.

4

The Wiskott-Aldrich syndrome: disordered actin dynamics in haematopoietic cells.

Thrasher AJ, Burns S, Lorenzi R, Jones GE. Thrasher AJ, et al. Immunol Rev. 2000 Dec;178:118-28. doi: 10.1034/j.1600-065x.2000.17803.x. Immunol Rev. 2000. PMID: 11213796 Review.

5

Protein assays for diagnosis of Wiskott-Aldrich syndrome and X-linked thrombocytopenia.

Qasim W, Gilmour KC, Heath S, Ashton E, Cranston T, Thomas A, Finn A, Davies EG, Thrasher AJ, Kinnon C, Jones A, Gaspar HB. Qasim W, et al. Among authors: thrasher aj. Br J Haematol. 2001 Jun;113(4):861-5. doi: 10.1046/j.1365-2141.2001.02832.x. Br J Haematol. 2001. PMID: 11442475 Free article.

6

Configuration of human dendritic cell cytoskeleton by Rho GTPases, the WAS protein, and differentiation.

Burns S, Thrasher AJ, Blundell MP, Machesky L, Jones GE. Burns S, et al. Among authors: thrasher aj. Blood. 2001 Aug 15;98(4):1142-9. doi: 10.1182/blood.v98.4.1142. Blood. 2001. PMID: 11493463 Free article.

7

T cell transduction and suicide with an enhanced mutant thymidine kinase.

Qasim W, Thrasher AJ, Buddle J, Kinnon C, Black ME, Gaspar HB. Qasim W, et al. Among authors: thrasher aj. Gene Ther. 2002 Jun;9(12):824-7. doi: 10.1038/sj.gt.3301690. Gene Ther. 2002. PMID: 12040465

8

The impact of retroviral suicide gene transduction procedures on T cells.

Qasim W, King D, Buddle J, Verfuerth S, Kinnon C, Thrasher AJ, Gaspar HB. Qasim W, et al. Among authors: thrasher aj. Br J Haematol. 2003 Nov;123(4):712-9. doi: 10.1046/j.1365-2141.2003.04672.x. Br J Haematol. 2003. PMID: 14616977 Free article.

9

Transfection-free and scalable recombinant AAV vector production using HSV/AAV hybrids.

Booth MJ, Mistry A, Li X, Thrasher A, Coffin RS. Booth MJ, et al. Gene Ther. 2004 May;11(10):829-37. doi: 10.1038/sj.gt.3302226. Gene Ther. 2004. PMID: 14985784

10

Gene therapy for severe combined immune deficiency.

Qasim W, Gaspar HB, Thrasher AJ. Qasim W, et al. Among authors: thrasher aj. Expert Rev Mol Med. 2004 Jul 2;6(13):1-15. doi: 10.1017/S1462399404007884. Expert Rev Mol Med. 2004. PMID: 15236670 Review.

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