565 related articles for article (PubMed ID: 25931402)
21. [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]
22. Disruption of hSWI/SNF complexes in T cells by WAS mutations distinguishes X-linked thrombocytopenia from Wiskott-Aldrich syndrome.
Sarkar K; Sadhukhan S; Han SS; Vyas YM
Blood; 2014 Nov; 124(23):3409-19. PubMed ID: 25253772
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Hematopoietic Stem Cell Transplantation for X-Linked Thrombocytopenia With Mutations in the WAS gene.
Oshima K; Imai K; Albert MH; Bittner TC; Strauss G; Filipovich AH; Morio T; Kapoor N; Dalal J; Schultz KR; Casper JT; Notarangelo LD; Ochs HD; Nonoyama S
J Clin Immunol; 2015 Jan; 35(1):15-21. PubMed ID: 25388447
[TBL] [Abstract][Full Text] [Related]
25. Identification of WASP mutations, mutation hotspots and genotype-phenotype disparities in 24 patients with the Wiskott-Aldrich syndrome.
Greer WL; Shehabeldin A; Schulman J; Junker A; Siminovitch KA
Hum Genet; 1996 Dec; 98(6):685-90. PubMed ID: 8931701
[TBL] [Abstract][Full Text] [Related]
26. Clinical, Laboratory Features and Clinical Courses of Patients with Wiskott Aldrich Syndrome and X-linked Thrombocytopenia-A single center study.
Bildik HN; Cagdas D; Ozturk Kura A; Oskay Halacli S; Sanal O; Tezcan I
Immunol Invest; 2022 Jul; 51(5):1272-1283. PubMed ID: 34098853
[TBL] [Abstract][Full Text] [Related]
27. The Wiskott-Aldrich syndrome.
Ochs HD; Thrasher AJ
J Allergy Clin Immunol; 2006 Apr; 117(4):725-38; quiz 739. PubMed ID: 16630926
[TBL] [Abstract][Full Text] [Related]
28. Genetic characteristics of eighty-seven patients with the Wiskott-Aldrich syndrome.
Gulácsy V; Freiberger T; Shcherbina A; Pac M; Chernyshova L; Avcin T; Kondratenko I; Kostyuchenko L; Prokofjeva T; Pasic S; Bernatowska E; Kutukculer N; Rascon J; Iagaru N; Mazza C; Tóth B; Erdos M; van der Burg M; Maródi L;
Mol Immunol; 2011 Feb; 48(5):788-92. PubMed ID: 21185603
[TBL] [Abstract][Full Text] [Related]
29. [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]
30. 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]
31. Clinical and genetic analysis of 2 rare cases of Wiskott-Aldrich syndrome from Chinese minorities: Two case reports.
Liu H; Wang Y; Li Y; Tao L; Zhang Y; He X; Zhou Y; Liu X; Wang Y; Li L
Medicine (Baltimore); 2021 Apr; 100(16):e25527. PubMed ID: 33879693
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Intermittent low platelet counts hampering diagnosis of X-linked thrombocytopenia in children: report of two unrelated cases and a novel mutation in the gene coding for the Wiskott-Aldrich syndrome protein.
Medina SS; Siqueira LH; Colella MP; Yamaguti-Hayakawa GG; Duarte BKL; Dos Santos Vilela MM; Ozelo MC
BMC Pediatr; 2017 Jun; 17(1):151. PubMed ID: 28641574
[TBL] [Abstract][Full Text] [Related]
34. Wiskott-Aldrich syndrome in a girl caused by heterozygous WASP mutation and extremely skewed X-chromosome inactivation: a novel association with maternal uniparental isodisomy 6.
Takimoto T; Takada H; Ishimura M; Kirino M; Hata K; Ohara O; Morio T; Hara T
Neonatology; 2015; 107(3):185-90. PubMed ID: 25633059
[TBL] [Abstract][Full Text] [Related]
35. The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutations of the same gene.
Zhu Q; Zhang M; Blaese RM; Derry JM; Junker A; Francke U; Chen SH; Ochs HD
Blood; 1995 Nov; 86(10):3797-804. PubMed ID: 7579347
[TBL] [Abstract][Full Text] [Related]
36. Report of clinical presentations and two novel mutations in patients with Wiskott-Aldrich syndrome/X-linked Thrombocytopenia.
Udomkittivorakul N; Wattanasirichaigoon D; Manuyakorn W; Pongphitcha P; Khongkraparn A; Tunlayadechanont P; Sirachainan N
Platelets; 2022 Jul; 33(5):792-796. PubMed ID: 34705590
[TBL] [Abstract][Full Text] [Related]
37. Wiskott-Aldrich syndrome protein and platelets.
Oda A; Ochs HD
Immunol Rev; 2000 Dec; 178():111-7. PubMed ID: 11213795
[TBL] [Abstract][Full Text] [Related]
38. X-linked thrombocytopenia in a female with a complex familial pattern of X-chromosome inactivation.
Daza-Cajigal V; Martínez-Pomar N; Garcia-Alonso A; Heine-Suñer D; Torres S; Vega AK; Molina IJ; Matamoros N
Blood Cells Mol Dis; 2013 Aug; 51(2):125-9. PubMed ID: 23689198
[TBL] [Abstract][Full Text] [Related]
39. Identification of a Novel Gene Mutation in a Chinese Pedigree with X-linked Thrombocytopenia.
Zhang JW; Luo YX; Yang YL; Long B; Lu Y; Zhang XZ
Clin Lab; 2018 Oct; 64(11):. PubMed ID: 30549999
[TBL] [Abstract][Full Text] [Related]
40. New insights into the biology of Wiskott-Aldrich syndrome (WAS).
Thrasher AJ
Hematology Am Soc Hematol Educ Program; 2009; ():132-8. PubMed ID: 20008191
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]