Articles frequently viewed together for PMID: 11449489

Year	Number of Results
1995	1
1996	1
2000	1
2006	2
2008	1
2010	1
2011	4
2012	1
2013	2
2015	1
2017	1
2021	1
2024	0

1

Molecular-clinical spectrum of the ATR-X syndrome.

Gibbons RJ, Higgs DR. Gibbons RJ, et al. Am J Med Genet. 2000 Fall;97(3):204-12. doi: 10.1002/1096-8628(200023)97:3<204::AID-AJMG1038>3.0.CO;2-X. Am J Med Genet. 2000. PMID: 11449489 Review.

2

Alpha thalassaemia-mental retardation, X linked.

Gibbons R. Gibbons R. Orphanet J Rare Dis. 2006 May 4;1:15. doi: 10.1186/1750-1172-1-15. Orphanet J Rare Dis. 2006. PMID: 16722615 Free PMC article. Review.

3

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome).

Gibbons RJ, Picketts DJ, Villard L, Higgs DR. Gibbons RJ, et al. Cell. 1995 Mar 24;80(6):837-45. doi: 10.1016/0092-8674(95)90287-2. Cell. 1995. PMID: 7697714 Free article.

4

ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome.

Picketts DJ, Higgs DR, Bachoo S, Blake DJ, Quarrell OW, Gibbons RJ. Picketts DJ, et al. Hum Mol Genet. 1996 Dec;5(12):1899-907. doi: 10.1093/hmg/5.12.1899. Hum Mol Genet. 1996. PMID: 8968741

5

Mutations in the chromatin-associated protein ATRX.

Gibbons RJ, Wada T, Fisher CA, Malik N, Mitson MJ, Steensma DP, Fryer A, Goudie DR, Krantz ID, Traeger-Synodinos J. Gibbons RJ, et al. Hum Mutat. 2008 Jun;29(6):796-802. doi: 10.1002/humu.20734. Hum Mutat. 2008. PMID: 18409179

6

Mutations in PHD-like domain of the ATRX gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndrome.

Badens C, Lacoste C, Philip N, Martini N, Courrier S, Giuliano F, Verloes A, Munnich A, Leheup B, Burglen L, Odent S, Van Esch H, Levy N. Badens C, et al. Clin Genet. 2006 Jul;70(1):57-62. doi: 10.1111/j.1399-0004.2006.00641.x. Clin Genet. 2006. PMID: 16813605

7

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. Cell. 2010 Oct 29;143(3):367-78. doi: 10.1016/j.cell.2010.09.023. Cell. 2010. PMID: 21029860 Free article.

8

Atypical pyridoxine-dependent epilepsy due to a pseudoexon in ALDH7A1.

Milh M, Pop A, Kanhai W, Villeneuve N, Cano A, Struys EA, Salomons GS, Chabrol B, Jakobs C. Milh M, et al. Mol Genet Metab. 2012 Apr;105(4):684-6. doi: 10.1016/j.ymgme.2012.01.011. Epub 2012 Jan 20. Mol Genet Metab. 2012. PMID: 22305855

9

Nuclear-receptor-mediated telomere insertion leads to genome instability in ALT cancers.

Marzec P, Armenise C, Pérot G, Roumelioti FM, Basyuk E, Gagos S, Chibon F, Déjardin J. Marzec P, et al. Cell. 2015 Feb 26;160(5):913-927. doi: 10.1016/j.cell.2015.01.044. Cell. 2015. PMID: 25723166 Free article.

10

The chromatin remodeller ATRX: a repeat offender in human disease.

Clynes D, Higgs DR, Gibbons RJ. Clynes D, et al. Trends Biochem Sci. 2013 Sep;38(9):461-6. doi: 10.1016/j.tibs.2013.06.011. Epub 2013 Aug 1. Trends Biochem Sci. 2013. PMID: 23916100 Review.

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