Ayyub H - Search Results

1

Identification of the transcription factor MAZ as a regulator of erythropoiesis.

Deen D, Butter F, Daniels DE, Ferrer-Vicens I, Ferguson DCJ, Holland ML, Samara V, Sloane-Stanley JA, Ayyub H, Mann M, Frayne J, Garrick D, Vernimmen D. Deen D, et al. Among authors: ayyub h. Blood Adv. 2021 Aug 10;5(15):3002-3015. doi: 10.1182/bloodadvances.2021004609. Blood Adv. 2021. PMID: 34351390 Free PMC article.

2

Alpha-thalassemia caused by a large (62 kb) deletion upstream of the human alpha globin gene cluster.

Hatton CS, Wilkie AO, Drysdale HC, Wood WG, Vickers MA, Sharpe J, Ayyub H, Pretorius IM, Buckle VJ, Higgs DR. Hatton CS, et al. Among authors: ayyub h. Blood. 1990 Jul 1;76(1):221-7. Blood. 1990. PMID: 2364173 Free article.

3

Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation.

Gibbons RJ, McDowell TL, Raman S, O'Rourke DM, Garrick D, Ayyub H, Higgs DR. Gibbons RJ, et al. Among authors: ayyub h. Nat Genet. 2000 Apr;24(4):368-71. doi: 10.1038/74191. Nat Genet. 2000. PMID: 10742099

4

alpha-thalassemia resulting from a negative chromosomal position effect.

Barbour VM, Tufarelli C, Sharpe JA, Smith ZE, Ayyub H, Heinlein CA, Sloane-Stanley J, Indrak K, Wood WG, Higgs DR. Barbour VM, et al. Among authors: ayyub h. Blood. 2000 Aug 1;96(3):800-7. Blood. 2000. PMID: 10910890 Free article.

5

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: ayyub h. Nat Genet. 2003 Jun;34(2):157-65. doi: 10.1038/ng1157. Nat Genet. 2003. PMID: 12730694

6

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: ayyub h. Nat Genet. 2003 Aug;34(4):446-9. doi: 10.1038/ng1213. Nat Genet. 2003. PMID: 12858175

7

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

8

A large deletion in the human alpha-globin cluster caused by a replication error is associated with an unexpectedly mild phenotype.

Rugless MJ, Fisher CA, Old JM, Sloane-Stanley J, Ayyub H, Higgs DR, Garrick D. Rugless MJ, et al. Among authors: ayyub h. Hum Mol Genet. 2008 Oct 1;17(19):3084-93. doi: 10.1093/hmg/ddn205. Epub 2008 Jul 15. Hum Mol Genet. 2008. PMID: 18632685

9

The role of the polycomb complex in silencing alpha-globin gene expression in nonerythroid cells.

Garrick D, De Gobbi M, Samara V, Rugless M, Holland M, Ayyub H, Lower K, Sloane-Stanley J, Gray N, Koch C, Dunham I, Higgs DR. Garrick D, et al. Among authors: ayyub h. Blood. 2008 Nov 1;112(9):3889-99. doi: 10.1182/blood-2008-06-161901. Epub 2008 Aug 8. Blood. 2008. PMID: 18689541 Free PMC article.

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: ayyub h. 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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