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Similar articles for PubMed (Select 16817970)


Abnormal X: autosome ratio, but normal X chromosome inactivation in human triploid cultures.

Gartler SM, Varadarajan KR, Luo P, Norwood TH, Canfield TK, Hansen RS.

BMC Genet. 2006 Jul 3;7:41.


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.


Skewed X chromosome inactivation in diploid and triploid female human embryonic stem cells.

Liu W, Sun X.

Hum Reprod. 2009 Aug;24(8):1834-43. doi: 10.1093/humrep/dep126. Epub 2009 May 8.


Dosage regulation of the active X chromosome in human triploid cells.

Deng X, Nguyen DK, Hansen RS, Van Dyke DL, Gartler SM, Disteche CM.

PLoS Genet. 2009 Dec;5(12):e1000751. doi: 10.1371/journal.pgen.1000751. Epub 2009 Dec 4.


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. Epub 2007 Oct 31.


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.


Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells.

Sirchia SM, Ramoscelli L, Grati FR, Barbera F, Coradini D, Rossella F, Porta G, Lesma E, Ruggeri A, Radice P, Simoni G, Miozzo M.

Cancer Res. 2005 Mar 15;65(6):2139-46.


X inactivation counting and choice is a stochastic process: evidence for involvement of an X-linked activator.

Monkhorst K, Jonkers I, Rentmeester E, Grosveld F, Gribnau J.

Cell. 2008 Feb 8;132(3):410-21. doi: 10.1016/j.cell.2007.12.036.


X chromosome inactivation is initiated in human preimplantation embryos.

van den Berg IM, Laven JS, Stevens M, Jonkers I, Galjaard RJ, Gribnau J, van Doorninck JH.

Am J Hum Genet. 2009 Jun;84(6):771-9. doi: 10.1016/j.ajhg.2009.05.003. Epub 2009 May 28.


Aberrant patterns of X chromosome inactivation in bovine clones.

Xue F, Tian XC, Du F, Kubota C, Taneja M, Dinnyes A, Dai Y, Levine H, Pereira LV, Yang X.

Nat Genet. 2002 Jun;31(2):216-20. Epub 2002 May 28.


Self-assembly and DNA binding of the blocking factor in x chromosome inactivation.

Nicodemi M, Prisco A.

PLoS Comput Biol. 2007 Nov;3(11):e210. Epub 2007 Sep 18.


X-chromosome inactivation (XCI) patterns in placental tissues of a paternally derived bal t(X;20) case.

Peñaherrera MS, Ma S, Ho Yuen B, Brown CJ, Robinson WP.

Am J Med Genet A. 2003 Apr 1;118A(1):29-34.


X-chromosome inactivation and skin disease.

Sun BK, Tsao H.

J Invest Dermatol. 2008 Dec;128(12):2753-9. doi: 10.1038/jid.2008.145. Epub 2008 May 29. Review.


Epigenetic regulation of X-inactivation in human embryonic stem cells.

Dvash T, Fan G.

Epigenetics. 2009 Jan;4(1):19-22. Epub 2009 Jan 17.


Global analysis of chromosome X gene expression in primary cultures of normal ovarian surface epithelial cells and epithelial ovarian cancer cell lines.

Benoît MH, Hudson TJ, Maire G, Squire JA, Arcand SL, Provencher D, Mes-Masson AM, Tonin PN.

Int J Oncol. 2007 Jan;30(1):5-17.


Meta-analysis of the heterogeneity of X chromosome inactivation in human pluripotent stem cells.

Bruck T, Benvenisty N.

Stem Cell Res. 2011 Mar;6(2):187-93. doi: 10.1016/j.scr.2010.12.001. Epub 2010 Dec 13.


XIST repression in the absence of DNMT1 and DNMT3B.

Vasques LR, Stabellini R, Xue F, Tian XC, Soukoyan M, Pereira LV.

DNA Res. 2005;12(5):373-8. Epub 2006 Jan 11.


Variations of X chromosome inactivation occur in early passages of female human embryonic stem cells.

Dvash T, Lavon N, Fan G.

PLoS One. 2010 Jun 25;5(6):e11330. doi: 10.1371/journal.pone.0011330.

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