Viprakasit V - Search Results

1

A novel deletion causing alpha thalassemia clarifies the importance of the major human alpha globin regulatory element.

Viprakasit V, Harteveld CL, Ayyub H, Stanley JS, Giordano PC, Wood WG, Higgs DR. Viprakasit V, et al. Blood. 2006 May 1;107(9):3811-2. doi: 10.1182/blood-2005-12-4834. Blood. 2006. PMID: 16627766 Free article. No abstract available.

2

Clinical phenotypes and molecular characterization of Hb H-Paksé disease.

Viprakasit V, Tanphaichitr VS, Pung-Amritt P, Petrarat S, Suwantol L, Fisher C, Higgs DR. Viprakasit V, et al. Haematologica. 2002 Feb;87(2):117-25. Haematologica. 2002. PMID: 11836160

3

Hb H hydrops fetalis syndrome associated with the interaction of two common determinants of alpha thalassaemia (--MED/(alpha)TSaudi(alpha)).

Viprakasit V, Green S, Height S, Ayyub H, Higgs DR. Viprakasit V, et al. Br J Haematol. 2002 Jun;117(3):759-62. doi: 10.1046/j.1365-2141.2002.03427.x. Br J Haematol. 2002. PMID: 12028055 Free article.

4

De novo deletion within the telomeric region flanking the human alpha globin locus as a cause of alpha thalassaemia.

Viprakasit V, Kidd AM, Ayyub H, Horsley S, Hughes J, Higgs DR. Viprakasit V, et al. Br J Haematol. 2003 Mar;120(5):867-75. doi: 10.1046/j.1365-2141.2003.04197.x. Br J Haematol. 2003. PMID: 12614224 Free article.

5

Dinucleotide deletion in -alpha3.7 allele causes a severe form of alpha+ thalassaemia.

Viprakasit V, Ayyub H, May A. Viprakasit V, et al. Eur J Haematol. 2003 Aug;71(2):133-6. doi: 10.1034/j.1600-0609.2003.00106.x. Eur J Haematol. 2003. PMID: 12890155

6

Deletion of the alpha-globin gene cluster as a cause of acquired alpha-thalassemia in myelodysplastic syndrome.

Steensma DP, Viprakasit V, Hendrick A, Goff DK, Leach J, Gibbons RJ, Higgs DR. Steensma DP, et al. Among authors: viprakasit v. Blood. 2004 Feb 15;103(4):1518-20. doi: 10.1182/blood-2003-09-3222. Epub 2003 Oct 23. Blood. 2004. PMID: 14576055 Free article.

7

Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with beta thalassemia.

Viprakasit V, Tanphaichitr VS, Chinchang W, Sangkla P, Weiss MJ, Higgs DR. Viprakasit V, et al. Blood. 2004 May 1;103(9):3296-9. doi: 10.1182/blood-2003-11-3957. Epub 2004 Jan 8. Blood. 2004. PMID: 14715623 Free article.

8

Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease.

Viprakasit V, Tanphaichitr VS, Veerakul G, Chinchang W, Petrarat S, Pung-Amritt P, Higgs DR. Viprakasit V, et al. Am J Hematol. 2004 Mar;75(3):157-63. doi: 10.1002/ajh.10479. Am J Hematol. 2004. PMID: 14978697 Free article.

9

A regulatory SNP causes a human genetic disease by creating a new transcriptional promoter.

De Gobbi M, Viprakasit V, Hughes JR, Fisher C, Buckle VJ, Ayyub H, Gibbons RJ, Vernimmen D, Yoshinaga Y, de Jong P, Cheng JF, Rubin EM, Wood WG, Bowden D, Higgs DR. De Gobbi M, et al. Among authors: viprakasit v. Science. 2006 May 26;312(5777):1215-7. doi: 10.1126/science.1126431. Science. 2006. PMID: 16728641

10

Adventitious changes in long-range gene expression caused by polymorphic structural variation and promoter competition.

Lower KM, Hughes JR, De Gobbi M, Henderson S, Viprakasit V, Fisher C, Goriely A, Ayyub H, Sloane-Stanley J, Vernimmen D, Langford C, Garrick D, Gibbons RJ, Higgs DR. Lower KM, et al. Among authors: viprakasit v. Proc Natl Acad Sci U S A. 2009 Dec 22;106(51):21771-6. doi: 10.1073/pnas.0909331106. Epub 2009 Dec 3. Proc Natl Acad Sci U S A. 2009. PMID: 19959666 Free PMC article.

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