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Items: 1 to 20 of 131

1.

Analysis of expressed SNPs identifies variable extents of expression from the human inactive X chromosome.

Cotton AM, Ge B, Light N, Adoue V, Pastinen T, Brown CJ.

Genome Biol. 2013 Nov 1;14(11):R122. doi: 10.1186/gb-2013-14-11-r122.

2.

Variable escape from X-chromosome inactivation: identifying factors that tip the scales towards expression.

Peeters SB, Cotton AM, Brown CJ.

Bioessays. 2014 Aug;36(8):746-56. doi: 10.1002/bies.201400032. Epub 2014 Jun 10. Review.

3.

X-chromosome genetic association test accounting for X-inactivation, skewed X-inactivation, and escape from X-inactivation.

Wang J, Yu R, Shete S.

Genet Epidemiol. 2014 Sep;38(6):483-93. doi: 10.1002/gepi.21814. Epub 2014 Jul 8.

4.

Landscape of DNA methylation on the X chromosome reflects CpG density, functional chromatin state and X-chromosome inactivation.

Cotton AM, Price EM, Jones MJ, Balaton BP, Kobor MS, Brown CJ.

Hum Mol Genet. 2015 Mar 15;24(6):1528-39. doi: 10.1093/hmg/ddu564. Epub 2014 Nov 7.

5.

DNA methylation profiles of human active and inactive X chromosomes.

Sharp AJ, Stathaki E, Migliavacca E, Brahmachary M, Montgomery SB, Dupre Y, Antonarakis SE.

Genome Res. 2011 Oct;21(10):1592-600. doi: 10.1101/gr.112680.110. Epub 2011 Aug 23.

6.

The probability to initiate X chromosome inactivation is determined by the X to autosomal ratio and X chromosome specific allelic properties.

Monkhorst K, de Hoon B, Jonkers I, Mulugeta Achame E, Monkhorst W, Hoogerbrugge J, Rentmeester E, Westerhoff HV, Grosveld F, Grootegoed JA, Gribnau J.

PLoS One. 2009;4(5):e5616. doi: 10.1371/journal.pone.0005616. Epub 2009 May 19.

7.

Dynamics of gene silencing during X inactivation using allele-specific RNA-seq.

Marks H, Kerstens HH, Barakat TS, Splinter E, Dirks RA, van Mierlo G, Joshi O, Wang SY, Babak T, Albers CA, Kalkan T, Smith A, Jouneau A, de Laat W, Gribnau J, Stunnenberg HG.

Genome Biol. 2015 Aug 3;16:149. doi: 10.1186/s13059-015-0698-x.

8.

[X chromosome inactivation patterns in patients with Rett syndrome and their mothers and the parental origin of the priority inactive X chromosome].

Jiang SL, Bao XH, Song FY, Pan H, Li MR, Wu XR.

Zhonghua Er Ke Za Zhi. 2006 Sep;44(9):648-52. Chinese.

PMID:
17217653
9.

Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation.

Cotton AM, Lam L, Affleck JG, Wilson IM, Peñaherrera MS, McFadden DE, Kobor MS, Lam WL, Robinson WP, Brown CJ.

Hum Genet. 2011 Aug;130(2):187-201. doi: 10.1007/s00439-011-1007-8. Epub 2011 May 20.

10.

Female human pluripotent stem cells rapidly lose X chromosome inactivation marks and progress to a skewed methylation pattern during culture.

Geens M, Seriola A, Barbé L, Santalo J, Veiga A, Dée K, Van Haute L, Sermon K, Spits C.

Mol Hum Reprod. 2016 Apr;22(4):285-98. doi: 10.1093/molehr/gaw004. Epub 2016 Jan 19.

PMID:
26786180
11.

DNA methylation profiling in X;autosome translocations supports a role for L1 repeats in the spread of X chromosome inactivation.

Bala Tannan N, Brahmachary M, Garg P, Borel C, Alnefaie R, Watson CT, Thomas NS, Sharp AJ.

Hum Mol Genet. 2014 Mar 1;23(5):1224-36. doi: 10.1093/hmg/ddt553. Epub 2013 Nov 1.

12.

Genetics and epigenetics of the X chromosome.

Morey C, Avner P.

Ann N Y Acad Sci. 2010 Dec;1214:E18-33. doi: 10.1111/j.1749-6632.2010.05943.x. Review.

PMID:
21382199
13.

Characterization of X chromosome inactivation using integrated analysis of whole-exome and mRNA sequencing.

Szelinger S, Malenica I, Corneveaux JJ, Siniard AL, Kurdoglu AA, Ramsey KM, Schrauwen I, Trent JM, Narayanan V, Huentelman MJ, Craig DW.

PLoS One. 2014 Dec 12;9(12):e113036. doi: 10.1371/journal.pone.0113036. eCollection 2014.

14.

Random X inactivation and extensive mosaicism in human placenta revealed by analysis of allele-specific gene expression along the X chromosome.

Moreira de Mello JC, de Araújo ES, Stabellini R, Fraga AM, de Souza JE, Sumita DR, Camargo AA, Pereira LV.

PLoS One. 2010 Jun 4;5(6):e10947. doi: 10.1371/journal.pone.0010947.

15.

Escape from X inactivation varies in mouse tissues.

Berletch JB, Ma W, Yang F, Shendure J, Noble WS, Disteche CM, Deng X.

PLoS Genet. 2015 Mar 18;11(3):e1005079. doi: 10.1371/journal.pgen.1005079. eCollection 2015 Mar.

16.

X-inactivation in female human embryonic stem cells is in a nonrandom pattern and prone to epigenetic alterations.

Shen Y, Matsuno Y, Fouse SD, Rao N, Root S, Xu R, Pellegrini M, Riggs AD, Fan G.

Proc Natl Acad Sci U S A. 2008 Mar 25;105(12):4709-14. doi: 10.1073/pnas.0712018105. Epub 2008 Mar 13.

17.

Strong purifying selection at genes escaping X chromosome inactivation.

Park C, Carrel L, Makova KD.

Mol Biol Evol. 2010 Nov;27(11):2446-50. doi: 10.1093/molbev/msq143. Epub 2010 Jun 9.

18.

Heritable skewed X-chromosome inactivation leads to haemophilia A expression in heterozygous females.

Renault NK, Dyack S, Dobson MJ, Costa T, Lam WL, Greer WL.

Eur J Hum Genet. 2007 Jun;15(6):628-37. Epub 2007 Mar 7.

19.

Familial skewed X-chromosome inactivation linked to a component of the cohesin complex, SA2.

Renault NK, Renault MP, Copeland E, Howell RE, Greer WL.

J Hum Genet. 2011 May;56(5):390-7. doi: 10.1038/jhg.2011.25. Epub 2011 Mar 17.

PMID:
21412246
20.

Eutherian mammals use diverse strategies to initiate X-chromosome inactivation during development.

Okamoto I, Patrat C, Thépot D, Peynot N, Fauque P, Daniel N, Diabangouaya P, Wolf JP, Renard JP, Duranthon V, Heard E.

Nature. 2011 Apr 21;472(7343):370-4. doi: 10.1038/nature09872. Epub 2011 Apr 6. Erratum in: Nature. 2011 Jun 9;474(7350):239-40.

PMID:
21471966
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