145 related articles for article (PubMed ID: 9616151)
1. A 5' regulatory sequence containing two Ets motifs controls the expression of the Wiskott-Aldrich syndrome protein (WASP) gene in human hematopoietic cells.
Petrella A; Doti I; Agosti V; Giarrusso PC; Vitale D; Bond HM; Cuomo C; Tassone P; Franco B; Ballabio A; Venuta S; Morrone G
Blood; 1998 Jun; 91(12):4554-60. PubMed ID: 9616151
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. The identification and characterization of two promoters and the complete genomic sequence for the Wiskott-Aldrich syndrome gene.
Hagemann TL; Kwan SP
Biochem Biophys Res Commun; 1999 Mar; 256(1):104-9. PubMed ID: 10066431
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Mutations of the Wiskott-Aldrich Syndrome Protein (WASP): hotspots, effect on transcription, and translation and phenotype/genotype correlation.
Jin Y; Mazza C; Christie JR; Giliani S; Fiorini M; Mella P; Gandellini F; Stewart DM; Zhu Q; Nelson DL; Notarangelo LD; Ochs HD
Blood; 2004 Dec; 104(13):4010-9. PubMed ID: 15284122
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Expression of Wiskott-Aldrich syndrome protein (WASP) gene during hematopoietic differentiation.
Parolini O; Berardelli S; Riedl E; Bello-Fernandez C; Strobl H; Majdic O; Knapp W
Blood; 1997 Jul; 90(1):70-5. PubMed ID: 9207440
[TBL] [Abstract][Full Text] [Related]
9. X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP gene.
Villa A; Notarangelo L; Macchi P; Mantuano E; Cavagni G; Brugnoni D; Strina D; Patrosso MC; Ramenghi U; Sacco MG
Nat Genet; 1995 Apr; 9(4):414-7. PubMed ID: 7795648
[TBL] [Abstract][Full Text] [Related]
10. WASP-WIP complex in the molecular pathogenesis of Wiskott-Aldrich syndrome.
Sasahara Y
Pediatr Int; 2016 Jan; 58(1):4-7. PubMed ID: 26331277
[TBL] [Abstract][Full Text] [Related]
11. The mouse homolog of the Wiskott-Aldrich syndrome protein (WASP) gene is highly conserved and maps near the scurfy (sf) mutation on the X chromosome.
Derry JM; Wiedemann P; Blair P; Wang Y; Kerns JA; Lemahieu V; Godfrey VL; Wilkinson JE; Francke U
Genomics; 1995 Sep; 29(2):471-7. PubMed ID: 8666397
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. A role for Wiskott-Aldrich syndrome protein in T-cell receptor-mediated transcriptional activation independent of actin polymerization.
Silvin C; Belisle B; Abo A
J Biol Chem; 2001 Jun; 276(24):21450-7. PubMed ID: 11283014
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. The Wiskott-Aldrich syndrome.
Ochs HD
Semin Hematol; 1998 Oct; 35(4):332-45. PubMed ID: 9801262
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. Mutations of the Wiskott-Aldrich Syndrome Protein affect protein expression and dictate the clinical phenotypes.
Ochs HD
Immunol Res; 2009; 44(1-3):84-8. PubMed ID: 19082760
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
