Garrick D - Search Results

1

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.

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

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

4

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

5

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.

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

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.

8

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. Among authors: garrick d. Biochem Soc Symp. 2006;(73):11-22. doi: 10.1042/bss0730011. Biochem Soc Symp. 2006. PMID: 16626283 Free article.

9

ATR-X syndrome protein targets tandem repeats and influences allele-specific expression in a size-dependent manner.

Law MJ, Lower KM, Voon HP, Hughes JR, Garrick D, Viprakasit V, Mitson M, De Gobbi M, Marra M, Morris A, Abbott A, Wilder SP, Taylor S, Santos GM, Cross J, Ayyub H, Jones S, Ragoussis J, Rhodes D, Dunham I, Higgs DR, Gibbons RJ. Law MJ, et al. Among authors: garrick d. Cell. 2010 Oct 29;143(3):367-78. doi: 10.1016/j.cell.2010.09.023. Cell. 2010. PMID: 21029860 Free article.

10

Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatin.

Eustermann S, Yang JC, Law MJ, Amos R, Chapman LM, Jelinska C, Garrick D, Clynes D, Gibbons RJ, Rhodes D, Higgs DR, Neuhaus D. Eustermann S, et al. Among authors: garrick d. Nat Struct Mol Biol. 2011 Jun 12;18(7):777-82. doi: 10.1038/nsmb.2070. Nat Struct Mol Biol. 2011. PMID: 21666677

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