These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
458 related articles for article (PubMed ID: 15203732)
1. Identification of WASP mutations in 10 Australian families with Wiskott-Aldrich syndrome and X-linked thrombocytopenia. Bourne HC; Weston S; Prasad M; Edkins E; Benson EM Pathology; 2004 Jun; 36(3):262-4. PubMed ID: 15203732 [TBL] [Abstract][Full Text] [Related]
2. Mutations of the WASP gene in 10 Japanese patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia. Itoh S; Nonoyama S; Morio T; Imai K; Okawa H; Ochs HD; Shimadzu M; Yata J Int J Hematol; 2000 Jan; 71(1):79-83. PubMed ID: 10729999 [TBL] [Abstract][Full Text] [Related]
3. Two novel mutations identified in the Wiskott-Aldrich syndrome protein gene cause Wiskott-Aldrich syndrome and thrombocytopenia. Andreu N; Matamoros N; Escudero A; Fillat C Int J Mol Med; 2007 May; 19(5):777-82. PubMed ID: 17390083 [TBL] [Abstract][Full Text] [Related]
4. Novel mutations in the Wiskott-Aldrich syndrome protein gene and their effects on transcriptional, translational, and clinical phenotypes. Lemahieu V; Gastier JM; Francke U Hum Mutat; 1999; 14(1):54-66. PubMed ID: 10447259 [TBL] [Abstract][Full Text] [Related]
5. Identification of six novel WASP gene mutations in patients suffering from Wiskott-Aldrich syndrome. Brooimans RA; van den Berg AJ; Tamminga RY; Revesz T; Wulffraat NM; Zegers BJ Hum Mutat; 2000 Apr; 15(4):386-7. PubMed ID: 10737997 [TBL] [Abstract][Full Text] [Related]
6. Wiskott-Aldrich syndrome in Argentina: 17 unique, including nine novel, mutations. El-Hakeh J; Rosenzweig S; Oleastro M; Basack N; Berozdnik L; Molina F; Rivas EM; Zelazko M; Danielian S Hum Mutat; 2002 Feb; 19(2):186-7. PubMed ID: 11793485 [TBL] [Abstract][Full Text] [Related]
7. Mutation spectrum in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia: identification of twelve different mutations in the WASP gene. Schwartz M; Békássy A; Donnér M; Hertel T; Hreidarson S; Kerndrup G; Stormorken H; Stokland T; Tranebjaerg L; Orstavik KH; Skovby F Thromb Haemost; 1996 Apr; 75(4):546-50. PubMed ID: 8743175 [TBL] [Abstract][Full Text] [Related]
8. Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCR. Proust A; Guillet B; Picard C; de Saint Basile G; Pondarré C; Tamary H; Dreyfus M; Tchernia G; Fischer A; Delaunay J Blood Cells Mol Dis; 2007; 39(1):102-6. PubMed ID: 17400488 [TBL] [Abstract][Full Text] [Related]
9. Wiskott-Aldrich syndrome/X-linked thrombocytopenia in China: Clinical characteristic and genotype-phenotype correlation. Liu DW; Zhang ZY; Zhao Q; Jiang LP; Liu W; Tu WW; Song WX; Zhao XD Pediatr Blood Cancer; 2015 Sep; 62(9):1601-8. PubMed ID: 25931402 [TBL] [Abstract][Full Text] [Related]
10. Molecular biology of the Wiskott-Aldrich syndrome. Rengan R; Ochs HD Rev Immunogenet; 2000; 2(2):243-55. PubMed ID: 11258421 [TBL] [Abstract][Full Text] [Related]
11. Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus. Kolluri R; Shehabeldin A; Peacocke M; Lamhonwah AM; Teichert-Kuliszewska K; Weissman SM; Siminovitch KA Hum Mol Genet; 1995 Jul; 4(7):1119-26. PubMed ID: 8528198 [TBL] [Abstract][Full Text] [Related]
12. A novel termination codon mutation of the WAS gene in a Thai family with Wiskott-Aldrich syndrome. Chatchatee P; Srichomthong C; Chewatavorn A; Shotelersuk V Int J Mol Med; 2003 Dec; 12(6):939-41. PubMed ID: 14612970 [TBL] [Abstract][Full Text] [Related]
13. Detection of six novel mutations in WASP gene in fifteen Iranian Wiskott-Aldrich patients. Safaei S; Fazlollahi MR; Houshmand M; Hamidieh AA; Bemanian MH; Alavi S; Mousavi F; Pourpak Z; Moin M Iran J Allergy Asthma Immunol; 2012 Dec; 11(4):345-8. PubMed ID: 23264413 [TBL] [Abstract][Full Text] [Related]
14. Mutations that cause the Wiskott-Aldrich syndrome impair the interaction of Wiskott-Aldrich syndrome protein (WASP) with WASP interacting protein. Stewart DM; Tian L; Nelson DL J Immunol; 1999 Apr; 162(8):5019-24. PubMed ID: 10202051 [TBL] [Abstract][Full Text] [Related]
15. 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. PubMed ID: 9713366 [TBL] [Abstract][Full Text] [Related]
16. Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia. Devriendt K; Kim AS; Mathijs G; Frints SG; Schwartz M; Van Den Oord JJ; Verhoef GE; Boogaerts MA; Fryns JP; You D; Rosen MK; Vandenberghe P Nat Genet; 2001 Mar; 27(3):313-7. PubMed ID: 11242115 [TBL] [Abstract][Full Text] [Related]
17. [Identification of two novel WASP gene mutations in 3 boys with Wiskott-Aldrich syndrome]. Jiang LP; Xu YH; Yang XQ; Liu EM; Wang LJ; Lau YL; Chan KW Zhonghua Er Ke Za Zhi; 2003 Aug; 41(8):590-3. PubMed ID: 14744380 [TBL] [Abstract][Full Text] [Related]
18. WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia. Derry JM; Kerns JA; Weinberg KI; Ochs HD; Volpini V; Estivill X; Walker AP; Francke U Hum Mol Genet; 1995 Jul; 4(7):1127-35. PubMed ID: 8528199 [TBL] [Abstract][Full Text] [Related]
19. [WASP gene mutation analysis of a family of X-linked thrombocytopenia]. Shi RM; Liu ZG; Yang YH Zhongguo Dang Dai Er Ke Za Zhi; 2010 Oct; 12(10):784-7. PubMed ID: 20959042 [TBL] [Abstract][Full Text] [Related]