Garrick D - Search Results

1

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

2

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

3

Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues.

Garrick D, Sharpe JA, Arkell R, Dobbie L, Smith AJ, Wood WG, Higgs DR, Gibbons RJ. Garrick D, et al. PLoS Genet. 2006 Apr;2(4):e58. doi: 10.1371/journal.pgen.0020058. Epub 2006 Apr 21. PLoS Genet. 2006. PMID: 16628246 Free PMC article.

4

Defining the cause of skewed X-chromosome inactivation in X-linked mental retardation by use of a mouse model.

Muers MR, Sharpe JA, Garrick D, Sloane-Stanley J, Nolan PM, Hacker T, Wood WG, Higgs DR, Gibbons RJ. Muers MR, et al. Among authors: garrick d. Am J Hum Genet. 2007 Jun;80(6):1138-49. doi: 10.1086/518369. Epub 2007 Apr 25. Am J Hum Genet. 2007. PMID: 17503331 Free PMC article.

5

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: garrick d. 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

6

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: garrick d. Nat Genet. 2000 Apr;24(4):368-71. doi: 10.1038/74191. Nat Genet. 2000. PMID: 10742099

7

Understanding alpha-globin gene regulation: Aiming to improve the management of thalassemia.

Higgs DR, Garrick D, Anguita E, De Gobbi M, Hughes J, Muers M, Vernimmen D, Lower K, Law M, Argentaro A, Deville MA, Gibbons R. Higgs DR, et al. Among authors: garrick d. Ann N Y Acad Sci. 2005;1054:92-102. doi: 10.1196/annals.1345.012. Ann N Y Acad Sci. 2005. PMID: 16339655 Review.

8

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. Gene. 2004 Feb 4;326:23-34. doi: 10.1016/j.gene.2003.10.026. Gene. 2004. PMID: 14729260

9

The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis.

Bérubé NG, Mangelsdorf M, Jagla M, Vanderluit J, Garrick D, Gibbons RJ, Higgs DR, Slack RS, Picketts DJ. Bérubé NG, et al. Among authors: garrick d. J Clin Invest. 2005 Feb;115(2):258-67. doi: 10.1172/JCI22329. J Clin Invest. 2005. PMID: 15668733 Free PMC article.

10

Switching genes on and off in haemopoiesis.

Garrick D, De Gobbi M, Lynch M, Higgs DR. Garrick D, et al. Biochem Soc Trans. 2008 Aug;36(Pt 4):613-8. doi: 10.1042/BST0360613. Biochem Soc Trans. 2008. PMID: 18631127

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