189 related articles for article (PubMed ID: 10653325)
21. Detection of a novel splice-site mutation that results in skipping exon 3 of the WASP gene in a patient with Wiskott-Aldrich syndrome.
Ariga T; Yamada M; Pudua FR; Sakiyama Y
Biochim Biophys Acta; 1996 Dec; 1317(3):158-60. PubMed ID: 8988230
[TBL] [Abstract][Full Text] [Related]
22. Mutational analysis of the WASP gene in 2 Korean families with Wiskott-Aldrich syndrome.
Jo EK; Futatani T; Kanegane H; Kubota T; Lee YH; Jung JA; Song CH; Park JK; Nonoyama S; Miyawaki T
Int J Hematol; 2003 Jul; 78(1):40-4. PubMed ID: 12894849
[TBL] [Abstract][Full Text] [Related]
23. Genotype-proteotype linkage in the Wiskott-Aldrich syndrome.
Lutskiy MI; Rosen FS; Remold-O'Donnell E
J Immunol; 2005 Jul; 175(2):1329-36. PubMed ID: 16002738
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. 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]
27. Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysis.
Giliani S; Fiorini M; Mella P; Candotti F; Schumacher RF; Wengler GS; Lalatta F; Fasth A; Badolato R; Ugazio AG; Albertini A; Notarangelo LD
Prenat Diagn; 1999 Jan; 19(1):36-40. PubMed ID: 10073904
[TBL] [Abstract][Full Text] [Related]
28. The genotype of the original Wiskott phenotype.
Binder V; Albert MH; Kabus M; Bertone M; Meindl A; Belohradsky BH
N Engl J Med; 2006 Oct; 355(17):1790-3. PubMed ID: 17065640
[TBL] [Abstract][Full Text] [Related]
29. Two novel mutations of Wiskott-Aldrich syndrome: the molecular prediction of interaction between the mutated WASP L101P with WASP-interacting protein by molecular modeling.
Kim MK; Kim ES; Kim DS; Choi IH; Moon T; Yoon CN; Shin JS
Biochim Biophys Acta; 2004 Oct; 1690(2):134-40. PubMed ID: 15469902
[TBL] [Abstract][Full Text] [Related]
30. Molecular characterization of two Malaysian patients with Wiskott-Aldrich syndrome.
Baharin MF; Kader Ibrahim SB; Yap SH; Abdul Manaf AM; Mat Ripen A; Dhaliwal JS
Malays J Pathol; 2015 Aug; 37(2):153-8. PubMed ID: 26277674
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. High prevalence of nonsense, frame shift, and splice-site mutations in 16 patients with full-blown Wiskott-Aldrich syndrome.
Wengler GS; Notarangelo LD; Berardelli S; Pollonni G; Mella P; Fasth A; Ugazio AG; Parolini O
Blood; 1995 Nov; 86(10):3648-54. PubMed ID: 7579329
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. 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]
35. Detection of lymphocytes and granulocytes expressing the mutant WASP message in carriers of Wiskott-Aldrich syndrome.
Ariga T; Yamada M; Wada T; Saitoh S; Sakiyama Y
Br J Haematol; 1999 Mar; 104(4):893-900. PubMed ID: 10192456
[TBL] [Abstract][Full Text] [Related]
36. Clinical course of patients with WASP gene mutations.
Imai K; Morio T; Zhu Y; Jin Y; Itoh S; Kajiwara M; Yata J; Mizutani S; Ochs HD; Nonoyama S
Blood; 2004 Jan; 103(2):456-64. PubMed ID: 12969986
[TBL] [Abstract][Full Text] [Related]
37. Expression of human Wiskott-Aldrich syndrome protein in patients' cells leads to partial correction of a phenotypic abnormality of cell surface glycoproteins.
Huang MM; Tsuboi S; Wong A; Yu XJ; Oh-Eda M; Derry JM; Francke U; Fukuda M; Weinberg KI; Kohn DB
Gene Ther; 2000 Feb; 7(4):314-20. PubMed ID: 10694812
[TBL] [Abstract][Full Text] [Related]
38. Haploidentical bone marrow transplantation in a pediatric patient with Wiskott-Aldrich syndrome. A case report.
Pury S; López Orozco M; Pichichero G; Sasia LV; Morell D; Álvarez MS; Basquiera AL; Mas ME; Salvucci K
Arch Argent Pediatr; 2024 Feb; 122(1):e202310061. PubMed ID: 37471507
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. [Analysis of prenatal diagnosis for seven high-risk fetuses with Wiskott-Aldrich syndrome].
Zhao Q; Zhang ZY; Zhao XD; Jiang LP; Zhao Y; Yang XQ
Zhonghua Er Ke Za Zhi; 2012 Jan; 50(1):15-9. PubMed ID: 22456069
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
