155 related articles for article (PubMed ID: 25082437)
1. A novel large deletion and single nucleotide insertion in the Wiskott-Aldrich syndrome protein gene.
Gulácsy V; Soltész B; Petrescu C; Bataneant M; Gyimesi E; Serban M; Maródi L; Tóth B
Eur J Haematol; 2015 Jul; 95(1):93-8. PubMed ID: 25082437
[TBL] [Abstract][Full Text] [Related]
2. Characterization of a deletion mutation involving exons 3-7 of the WASP gene detected in a patient with Wiskott-Aldrich syndrome.
Ariga T; Yamada M; Ito S; Iwamura M; Iseki M; Sakiyama Y
Hum Mutat; 1997; 10(4):310-6. PubMed ID: 9338585
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. An Alu-mediated deletion at Xp11.23 leading to Wiskott-Aldrich syndrome.
Lutskiy MI; Jones LN; Rosen FS; Remold-O'Donnell E
Hum Genet; 2002 May; 110(5):515-9. PubMed ID: 12073025
[TBL] [Abstract][Full Text] [Related]
5. A familial case of Wiskott-Aldrich Syndrome with a hotspot mutation in exon 2 of the WAS Gene.
Park SK; Kim CS; Song DK; Kim JY; Choi IJ; Kim DK
J Korean Med Sci; 2007 Dec; 22(6):998-1001. PubMed ID: 18162713
[TBL] [Abstract][Full Text] [Related]
6. A novel Wiskott-Aldrich syndrome protein (WASP) complex mutation identified in a WAS patient results in an aberrant product at the C-terminus from two transcripts with unusual polyA signals.
Andreu N; García-Rodríguez M; Volpini V; Frecha C; Molina IJ; Fontan G; Fillat C
J Hum Genet; 2006; 51(2):92-97. PubMed ID: 16372137
[TBL] [Abstract][Full Text] [Related]
7. [Analysis of clinical features and gene mutations in 6 patients with Wiskott-Aldrich syndrome].
Jiang MH; Wang ZY; Su J; Cao LJ; Li JQ; Sun XH; Bai X; Wang GF; Ruan CG
Zhonghua Xue Ye Xue Za Zhi; 2011 Sep; 32(9):577-82. PubMed ID: 22338148
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Novel WASP mutation in a patient with Wiskott-Aldrich syndrome: Case report and review of the literature.
Eghbali M; Sadeghi-Shabestari M; Najmi Varzaneh F; Zare Bidoki A; Rezaei N
Allergol Immunopathol (Madr); 2016; 44(5):450-4. PubMed ID: 26993433
[TBL] [Abstract][Full Text] [Related]
11. Analysis of clinical and molecular characteristics of Wiskott-Aldrich syndrome in 24 patients from 23 unrelated Chinese families.
Zhang ZY; Xiao HQ; Jiang LP; Zhou Y; Zhao Q; Yu J; Liu W; Yang XQ; Zhao XD
Pediatr Allergy Immunol; 2010 May; 21(3):522-32. PubMed ID: 20546529
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. A novel protocol to identify mutations in patients with wiskott-Aldrich syndrome.
Jones LN; Lutskiy MI; Cooley J; Kenney DM; Rosen FS; Remold-O'Donnell E
Blood Cells Mol Dis; 2002; 28(3):392-8. PubMed ID: 12367583
[TBL] [Abstract][Full Text] [Related]
14. Molecular diagnosis of Wiskott-Aldrich syndrome in Taiwan.
Chien YH; Hwu WL; Ariga T; Chang KW; Yang YH; Lin KH; Chiang BL
J Microbiol Immunol Infect; 2004 Oct; 37(5):276-81. PubMed ID: 15497008
[TBL] [Abstract][Full Text] [Related]
15. Wiskott-Aldrich syndrome caused by a new mutation associated with multifocal dermal juvenile xanthogranulomas.
Jesenak M; Plamenova I; Plank L; Banovcin P
Pediatr Dermatol; 2013; 30(5):e91-3. PubMed ID: 23157619
[TBL] [Abstract][Full Text] [Related]
16. [Mutation analysis of WASP gene and prenatal diagnosis of Wiskott-Aldrich syndrome].
Liu N; Shi H; Kong X; Wu Q; Xu X; Bai Q; Feng Y; Zhao Z
Zhonghua Er Ke Za Zhi; 2014 Sep; 52(9):662-6. PubMed ID: 25476427
[TBL] [Abstract][Full Text] [Related]
17. 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]
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. 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]
20. Two cases of Wiskott-Aldrich syndrome in neonates due to gene mutations.
Zhang S; Zhang R; Chen C; Sun J
Fetal Pediatr Pathol; 2013 Jul; 32(4):312-5. PubMed ID: 23301916
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
