189 related articles for article (PubMed ID: 10653325)
1. Novel mutations, no detectable mRNA and familial genetic analysis of the Wiskott-Aldrich syndrome protein gene in six Japanese patients with Wiskott-Aldrich syndrome.
Sasahara Y; Kawai S; Kumaki S; Ohashi Y; Minegishi M; Tsuchiya S
Eur J Pediatr; 2000; 159(1-2):23-30. PubMed ID: 10653325
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. 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]
4. 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]
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/X-linked thrombocytopenia: WASP gene mutations, protein expression, and phenotype.
Zhu Q; Watanabe C; Liu T; Hollenbaugh D; Blaese RM; Kanner SB; Aruffo A; Ochs HD
Blood; 1997 Oct; 90(7):2680-9. PubMed ID: 9326235
[TBL] [Abstract][Full Text] [Related]
7. Absence of expression of the Wiskott-Aldrich syndrome protein in peripheral blood cells of Wiskott-Aldrich syndrome patients.
MacCarthy-Morrogh L; Gaspar HB; Wang YC; Katz F; Thompson L; Layton M; Jones AM; Kinnon C
Clin Immunol Immunopathol; 1998 Jul; 88(1):22-7. PubMed ID: 9683546
[TBL] [Abstract][Full Text] [Related]
8. Wiskott-Aldrich syndrome: no strict genotype-phenotype correlations but clustering of missense mutations in the amino-terminal part of the WASP gene product.
Schindelhauer D; Weiss M; Hellebrand H; Golla A; Hergersberg M; Seger R; Belohradsky BH; Meindl A
Hum Genet; 1996 Jul; 98(1):68-76. PubMed ID: 8682510
[TBL] [Abstract][Full Text] [Related]
9. Identification of WASP mutations in 14 Spanish families with Wiskott-Aldrich syndrome.
Fillat C; EspaƱol T; Oset M; Ferrando M; Estivill X; Volpini V
Am J Med Genet; 2001 Apr; 100(2):116-21. PubMed ID: 11298372
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
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. 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. 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]
15. Identification of five novel WASP mutations in Chinese families with Wiskott-Aldrich syndrome.
Chan KW; Lee TL; Chung BH; Yang X; Lau YL
Hum Mutat; 2002 Aug; 20(2):151-2. PubMed ID: 12124997
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. 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]
20. [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]
[Next] [New Search]