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Items: 1 to 20 of 110

1.

Methylation profile of genes on the human X chromosome.

Kelkar A, Deobagkar D.

Epigenetics. 2010 Oct 1;5(7):612-8. doi: 10.4161/epi.5.7.12797. Epub 2010 Oct 1.

PMID:
20657171
2.

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.

3.

DNA methylation analysis of a de novo balanced X;13 translocation in a girl with abnormal phenotype: evidence for functional duplication of the whole short arm of the X chromosome.

Myszka A, Karpinski P, Makowska I, Lassota M, Przelozna B, Slezak R, Sasiadek MM.

J Appl Genet. 2010;51(3):331-5. doi: 10.1007/BF03208863.

PMID:
20720308
4.

Genotyping by morphology...

Wondergem MJ, Ossenkoppele GJ.

Blood. 2011 Mar 3;117(9):2566. No abstract available.

5.

Gene body-specific methylation on the active X chromosome.

Hellman A, Chess A.

Science. 2007 Feb 23;315(5815):1141-3.

6.

Human active X-specific DNA methylation events showing stability across time and tissues.

Joo JE, Novakovic B, Cruickshank M, Doyle LW, Craig JM, Saffery R.

Eur J Hum Genet. 2014 Dec;22(12):1376-81. doi: 10.1038/ejhg.2014.34. Epub 2014 Apr 9.

7.

The inactive X chromosome is epigenetically unstable and transcriptionally labile in breast cancer.

Chaligné R, Popova T, Mendoza-Parra MA, Saleem MA, Gentien D, Ban K, Piolot T, Leroy O, Mariani O, Gronemeyer H, Vincent-Salomon A, Stern MH, Heard E.

Genome Res. 2015 Apr;25(4):488-503. doi: 10.1101/gr.185926.114. Epub 2015 Feb 4.

8.

Spread of X inactivation on chromosome 15 is associated with a more severe phenotype in a girl with an unbalanced t(X; 15) translocation.

Yeung KS, Chee YY, Luk HM, Kan AS, Tang MH, Lau ET, Shuen AY, Lo IF, Chan KY, Chung BH.

Am J Med Genet A. 2014 Oct;164A(10):2521-8. doi: 10.1002/ajmg.a.36670. Epub 2014 Jul 16.

PMID:
25044945
10.

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.

11.

[Chromatin modifications during X-chromosome inactivation in female mammals].

Shevchenko AI, Pavlova SV, Dement'eva EV, Golubeva DV, Zakiian SM.

Genetika. 2006 Sep;42(9):1225-34. Russian.

PMID:
17100090
12.

5meCpG epigenetic marks neighboring a primate-conserved core promoter short tandem repeat indicate X-chromosome inactivation.

Machado FB, Machado FB, Faria MA, Lovatel VL, Alves da Silva AF, Radic CP, De Brasi CD, Rios ÁF, de Sousa Lopes SM, da Silveira LS, Ruiz-Miranda CR, Ramos ES, Medina-Acosta E.

PLoS One. 2014 Jul 31;9(7):e103714. doi: 10.1371/journal.pone.0103714. eCollection 2014.

13.

The lncRNA Firre anchors the inactive X chromosome to the nucleolus by binding CTCF and maintains H3K27me3 methylation.

Yang F, Deng X, Ma W, Berletch JB, Rabaia N, Wei G, Moore JM, Filippova GN, Xu J, Liu Y, Noble WS, Shendure J, Disteche CM.

Genome Biol. 2015 Mar 12;16:52. doi: 10.1186/s13059-015-0618-0.

14.

Genetic and epigenetic X-chromosome variations in a parthenogenetic human embryonic stem cell line.

Liu W, Yin Y, Jiang Y, Kou C, Luo Y, Huang S, Zheng Y, Li S, Li Q, Guo L, Gao S, Sun X.

J Assist Reprod Genet. 2011 Apr;28(4):303-13. doi: 10.1007/s10815-010-9517-1. Epub 2010 Dec 15.

15.

FMR1 gene expansion, large deletion of Xp, and skewed X-inactivation in a girl with mental retardation and autism.

Vazna A, Musova Z, Vlckova M, Novotna D, Dvorakova L, Hrdlicka M, Havlovicova M, Sedlacek Z.

Am J Med Genet A. 2010 May;152A(5):1273-7. doi: 10.1002/ajmg.a.33352.

PMID:
20425835
16.

Repressive but not activating epigenetic modifications are aberrant on the inactive X chromosome in live cloned cattle.

Geng-Sheng C, Yu G, Kun W, Fang-Rong D, Ning L.

Dev Growth Differ. 2009 Aug;51(6):585-94. doi: 10.1111/j.1440-169X.2009.01120.x.

PMID:
21314675
17.

Spread of X-chromosome inactivation into chromosome 15 is associated with Prader-Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation.

Sakazume S, Ohashi H, Sasaki Y, Harada N, Nakanishi K, Sato H, Emi M, Endoh K, Sohma R, Kido Y, Nagai T, Kubota T.

Hum Genet. 2012 Jan;131(1):121-30. doi: 10.1007/s00439-011-1051-4. Epub 2011 Jul 7.

PMID:
21735174
18.

Molecular and cytogenetic analysis of the spreading of X inactivation in a girl with microcephaly, mild dysmorphic features and t(X;5)(q22.1;q31.1).

Giorda R, Bonaglia MC, Milani G, Baroncini A, Spada F, Beri S, Menozzi G, Rusconi M, Zuffardi O.

Eur J Hum Genet. 2008 Aug;16(8):897-905. doi: 10.1038/ejhg.2008.28. Epub 2008 Feb 27.

19.

Human Naive Pluripotent Stem Cells Model X Chromosome Dampening and X Inactivation.

Sahakyan A, Kim R, Chronis C, Sabri S, Bonora G, Theunissen TW, Kuoy E, Langerman J, Clark AT, Jaenisch R, Plath K.

Cell Stem Cell. 2017 Jan 5;20(1):87-101. doi: 10.1016/j.stem.2016.10.006. Epub 2016 Dec 15.

PMID:
27989770
20.

Evidence of influence of genomic DNA sequence on human X chromosome inactivation.

Wang Z, Willard HF, Mukherjee S, Furey TS.

PLoS Comput Biol. 2006 Sep 1;2(9):e113. Epub 2006 Jul 17.

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