Higgs DR - Search Results

1

ATRX Plays a Key Role in Maintaining Silencing at Interstitial Heterochromatic Loci and Imprinted Genes.

Voon HP, Hughes JR, Rode C, De La Rosa-Velázquez IA, Jenuwein T, Feil R, Higgs DR, Gibbons RJ. Voon HP, et al. Among authors: higgs dr. Cell Rep. 2015 Apr 21;11(3):405-18. doi: 10.1016/j.celrep.2015.03.036. Epub 2015 Apr 9. Cell Rep. 2015. PMID: 25865896 Free PMC article.

2

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. Among authors: higgs dr. 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.

3

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS).

Gibbons RJ, Pellagatti A, Garrick D, Wood WG, Malik N, Ayyub H, Langford C, Boultwood J, Wainscoat JS, Higgs DR. Gibbons RJ, et al. Among authors: higgs dr. Nat Genet. 2003 Aug;34(4):446-9. doi: 10.1038/ng1213. Nat Genet. 2003. PMID: 12858175

4

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: higgs dr. 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.

5

Acquired somatic ATRX mutations in myelodysplastic syndrome associated with alpha thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations.

Steensma DP, Higgs DR, Fisher CA, Gibbons RJ. Steensma DP, et al. Among authors: higgs dr. Blood. 2004 Mar 15;103(6):2019-26. doi: 10.1182/blood-2003-09-3360. Epub 2003 Oct 30. Blood. 2004. PMID: 14592816 Free article.

6

A conserved truncated isoform of the ATR-X syndrome protein lacking the SWI/SNF-homology domain.

Garrick D, Samara V, McDowell TL, Smith AJ, Dobbie L, Higgs DR, Gibbons RJ. Garrick D, et al. Among authors: higgs dr. Gene. 2004 Feb 4;326:23-34. doi: 10.1016/j.gene.2003.10.026. Gene. 2004. PMID: 14729260

7

Comparative analysis of the alpha-like globin clusters in mouse, rat, and human chromosomes indicates a mechanism underlying breaks in conserved synteny.

Tufarelli C, Hardison R, Miller W, Hughes J, Clark K, Ventress N, Frischauf AM, Higgs DR. Tufarelli C, et al. Among authors: higgs dr. Genome Res. 2004 Apr;14(4):623-30. doi: 10.1101/gr.2143604. Genome Res. 2004. PMID: 15060003 Free PMC article.

8

Globin gene activation during haemopoiesis is driven by protein complexes nucleated by GATA-1 and GATA-2.

Anguita E, Hughes J, Heyworth C, Blobel GA, Wood WG, Higgs DR. Anguita E, et al. Among authors: higgs dr. EMBO J. 2004 Jul 21;23(14):2841-52. doi: 10.1038/sj.emboj.7600274. Epub 2004 Jun 24. EMBO J. 2004. PMID: 15215894 Free PMC article.

9

Acquired alpha-thalassemia in association with myelodysplastic syndrome and other hematologic malignancies.

Steensma DP, Gibbons RJ, Higgs DR. Steensma DP, et al. Among authors: higgs dr. Blood. 2005 Jan 15;105(2):443-52. doi: 10.1182/blood-2004-07-2792. Epub 2004 Sep 9. Blood. 2005. PMID: 15358626 Free article. Review.

10

Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia.

Steensma DP, Gibbons RJ, Mesa RA, Tefferi A, Higgs DR. Steensma DP, et al. Among authors: higgs dr. Eur J Haematol. 2005 Jan;74(1):47-53. doi: 10.1111/j.1600-0609.2004.00363.x. Eur J Haematol. 2005. PMID: 15613106

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