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Items: 14


Comparative analysis of the primate X-inactivation center region and reconstruction of the ancestral primate XIST locus.

Horvath JE, Sheedy CB, Merrett SL, Diallo AB, Swofford DL, NISC Comparative Sequencing Program, Green ED, Willard HF.

Genome Res. 2011 Jun;21(6):850-62. doi: 10.1101/gr.111849.110. Epub 2011 Apr 25.


Characterization of Xpr (Xpct) reveals instability but no effects on X-chromosome pairing or Xist expression.

Sun S, Fukue Y, Nolen L, Sadreyev R, Lee JT.

Transcription. 2010 Jul-Aug;1(1):46-56. doi: 10.4161/trns.1.1.12401.


Isolation, X location and activity of the marsupial homologue of SLC16A2, an XIST-flanking gene in eutherian mammals.

Koina E, Wakefield MJ, Walcher C, Disteche CM, Whitehead S, Ross M, Marshall Graves JA.

Chromosome Res. 2005;13(7):687-98. Epub 2005 Oct 24.


Two unrelated patients with inversions of the X chromosome and non-specific mental retardation: physical and transcriptional mapping of their common breakpoint region in Xq13.1.

Villard L, Briault S, Lossi AM, Paringaux C, Belougne J, Colleaux L, Pincus DR, Woollatt E, Lespinasse J, Munnich A, Moraine C, Fontès M, Gecz J.

J Med Genet. 1999 Oct;36(10):754-8.


Human XIST yeast artificial chromosome transgenes show partial X inactivation center function in mouse embryonic stem cells.

Heard E, Mongelard F, Arnaud D, Chureau C, Vourc'h C, Avner P.

Proc Natl Acad Sci U S A. 1999 Jun 8;96(12):6841-6.


Expression of genes from the human active and inactive X chromosomes.

Brown CJ, Carrel L, Willard HF.

Am J Hum Genet. 1997 Jun;60(6):1333-43.


Lack of X inactivation associated with maternal X isodisomy: evidence for a counting mechanism prior to X inactivation during human embryogenesis.

Migeon BR, Jeppesen P, Torchia BS, Fu S, Dunn MA, Axelman J, Schmeckpeper BJ, Fantes J, Zori RT, Driscoll DJ.

Am J Hum Genet. 1996 Jan;58(1):161-70.


Deficient transcription of XIST from tiny ring X chromosomes in females with severe phenotypes.

Migeon BR, Luo S, Stasiowski BA, Jani M, Axelman J, Van Dyke DL, Weiss L, Jacobs PA, Yang-Feng TL, Wiley JE.

Proc Natl Acad Sci U S A. 1993 Dec 15;90(24):12025-9.


Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.

Wolff DJ, Brown CJ, Schwartz S, Duncan AM, Surti U, Willard HF.

Am J Hum Genet. 1994 Jul;55(1):87-95. Review.


Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivation.

Callen DF, Eyre HJ, Dolman G, Garry-Battersby MB, McCreanor JR, Valeba A, McGill JJ.

J Med Genet. 1995 Feb;32(2):113-6.


Assignment of the dystonia-parkinsonism syndrome locus, DYT3, to a small region within a 1.8-Mb YAC contig of Xq13.1.

Haberhausen G, Schmitt I, Köhler A, Peters U, Rider S, Chelly J, Terwilliger JD, Monaco AP, Müller U.

Am J Hum Genet. 1995 Sep;57(3):644-50.

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