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Items: 1 to 20 of 112


Genomic environment predicts expression patterns on the human inactive X chromosome.

Carrel L, Park C, Tyekucheva S, Dunn J, Chiaromonte F, Makova KD.

PLoS Genet. 2006 Sep 29;2(9):e151.


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.


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.


Spread of X-chromosome inactivation into autosomal sequences: role for DNA elements, chromatin features and chromosomal domains.

Cotton AM, Chen CY, Lam LL, Wasserman WW, Kobor MS, Brown CJ.

Hum Mol Genet. 2014 Mar 1;23(5):1211-23. doi: 10.1093/hmg/ddt513.


Targeting of >1.5 Mb of human DNA into the mouse X chromosome reveals presence of cis-acting regulators of epigenetic silencing.

Yang C, McLeod AJ, Cotton AM, de Leeuw CN, Laprise S, Banks KG, Simpson EM, Brown CJ.

Genetics. 2012 Dec;192(4):1281-93. doi: 10.1534/genetics.112.143743.


Comparative sequence and x-inactivation analyses of a domain of escape in human xp11.2 and the conserved segment in mouse.

Tsuchiya KD, Greally JM, Yi Y, Noel KP, Truong JP, Disteche CM.

Genome Res. 2004 Jul;14(7):1275-84.


The role of LINEs and CpG islands in dosage compensation on the chicken Z chromosome.

Melamed E, Arnold AP.

Chromosome Res. 2009;17(6):727-36. doi: 10.1007/s10577-009-9068-4.


XIST RNA and architecture of the inactive X chromosome: implications for the repeat genome.

Hall LL, Lawrence JB.

Cold Spring Harb Symp Quant Biol. 2010;75:345-56. doi: 10.1101/sqb.2010.75.030. Review.


Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: the Lyon repeat hypothesis.

Bailey JA, Carrel L, Chakravarti A, Eichler EE.

Proc Natl Acad Sci U S A. 2000 Jun 6;97(12):6634-9.


Characterisation of inactivation domains and evolutionary strata in human X chromosome through Markov segmentation.

Kelkar A, Thakur V, Ramaswamy R, Deobagkar D.

PLoS One. 2009 Nov 25;4(11):e7885. doi: 10.1371/journal.pone.0007885.


X chromosome inactivation: heterogeneity of heterochromatin.

Sidhu SK, Minks J, Chang SC, Cotton AM, Brown CJ.

Biochem Cell Biol. 2008 Oct;86(5):370-9. doi: 10.1139/o08-100. Review. Erratum in: Biochem Cell Biol. 2009 Feb;87(1):387.


X inactivation in triploidy and trisomy: the search for autosomal transfactors that choose the active X.

Migeon BR, Pappas K, Stetten G, Trunca C, Jacobs PA.

Eur J Hum Genet. 2008 Feb;16(2):153-62.


Random replication of the inactive X chromosome.

Koren A, McCarroll SA.

Genome Res. 2014 Jan;24(1):64-9. doi: 10.1101/gr.161828.113.


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.


The utilization of the human phosphoglycerate kinase gene in the investigation of X-chromosome inactivation.

Goldman MA, Gartler SM, Keitges EA, Riley DE.

Horiz Biochem Biophys. 1986;8:169-205.


Escape from X chromosome inactivation is an intrinsic property of the Jarid1c locus.

Li N, Carrel L.

Proc Natl Acad Sci U S A. 2008 Nov 4;105(44):17055-60. doi: 10.1073/pnas.0807765105.

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