Higgs DR - Search Results

1

Reactivation of a developmentally silenced embryonic globin gene.

King AJ, Songdej D, Downes DJ, Beagrie RA, Liu S, Buckley M, Hua P, Suciu MC, Marieke Oudelaar A, Hanssen LLP, Jeziorska D, Roberts N, Carpenter SJ, Francis H, Telenius J, Olijnik AA, Sharpe JA, Sloane-Stanley J, Eglinton J, Kassouf MT, Orkin SH, Pennacchio LA, Davies JOJ, Hughes JR, Higgs DR, Babbs C. King AJ, et al. Among authors: higgs dr. Nat Commun. 2021 Jul 21;12(1):4439. doi: 10.1038/s41467-021-24402-3. Nat Commun. 2021. PMID: 34290235 Free PMC article.

2

Deletion of the mouse alpha-globin regulatory element (HS -26) has an unexpectedly mild phenotype.

Anguita E, Sharpe JA, Sloane-Stanley JA, Tufarelli C, Higgs DR, Wood WG. Anguita E, et al. Among authors: higgs dr. Blood. 2002 Nov 15;100(10):3450-6. doi: 10.1182/blood-2002-05-1409. Epub 2002 Jul 5. Blood. 2002. PMID: 12393394 Free article.

3

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.

4

Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease.

Tufarelli C, Stanley JA, Garrick D, Sharpe JA, Ayyub H, Wood WG, Higgs DR. Tufarelli C, et al. Among authors: higgs dr. Nat Genet. 2003 Jun;34(2):157-65. doi: 10.1038/ng1157. Nat Genet. 2003. PMID: 12730694

5

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

6

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.

7

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.

8

Annotation of cis-regulatory elements by identification, subclassification, and functional assessment of multispecies conserved sequences.

Hughes JR, Cheng JF, Ventress N, Prabhakar S, Clark K, Anguita E, De Gobbi M, de Jong P, Rubin E, Higgs DR. Hughes JR, et al. Among authors: higgs dr. Proc Natl Acad Sci U S A. 2005 Jul 12;102(28):9830-5. doi: 10.1073/pnas.0503401102. Epub 2005 Jul 5. Proc Natl Acad Sci U S A. 2005. PMID: 15998734 Free PMC article.

9

How transcriptional and epigenetic programmes are played out on an individual mammalian gene cluster during lineage commitment and differentiation.

Higgs DR, Vernimmen D, De Gobbi M, Anguita E, Hughes J, Buckle V, Iborra F, Garrick D, Wood WG. Higgs DR, et al. Biochem Soc Symp. 2006;(73):11-22. doi: 10.1042/bss0730011. Biochem Soc Symp. 2006. PMID: 16626283 Free article.

10

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: higgs dr. Science. 2006 May 26;312(5777):1215-7. doi: 10.1126/science.1126431. Science. 2006. PMID: 16728641

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