Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 90

1.

Methylation of L1Hs promoters is lower on the inactive X, has a tendency of being higher on autosomes in smaller genomes and shows inter-individual variability at some loci.

Singer H, Walier M, Nüsgen N, Meesters C, Schreiner F, Woelfle J, Fimmers R, Wienker T, Kalscheuer VM, Becker T, Schwaab R, Oldenburg J, El-Maarri O.

Hum Mol Genet. 2012 Jan 1;21(1):219-35. doi: 10.1093/hmg/ddr456. Epub 2011 Oct 4.

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.

Inactive X chromosome-specific reduction in placental DNA methylation.

Cotton AM, Avila L, Penaherrera MS, Affleck JG, Robinson WP, Brown CJ.

Hum Mol Genet. 2009 Oct 1;18(19):3544-52. doi: 10.1093/hmg/ddp299. Epub 2009 Jul 7.

4.

Severe XIST hypomethylation clearly distinguishes (SRY+) 46,XX-maleness from Klinefelter syndrome.

Poplinski A, Wieacker P, Kliesch S, Gromoll J.

Eur J Endocrinol. 2010 Jan;162(1):169-75. doi: 10.1530/EJE-09-0768. Epub 2009 Oct 7.

5.

Gender specific differences in levels of DNA methylation at selected loci from human total blood: a tendency toward higher methylation levels in males.

El-Maarri O, Becker T, Junen J, Manzoor SS, Diaz-Lacava A, Schwaab R, Wienker T, Oldenburg J.

Hum Genet. 2007 Dec;122(5):505-14. Epub 2007 Sep 13.

PMID:
17851693
6.

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.

7.

X inactivation-specific methylation of LINE-1 elements by DNMT3B: implications for the Lyon repeat hypothesis.

Hansen RS.

Hum Mol Genet. 2003 Oct 1;12(19):2559-67. Epub 2003 Aug 12.

PMID:
12925568
8.

Tissue-Specific Methylation of Long Interspersed Nucleotide Element-1 of Homo Sapiens (L1Hs) During Human Embryogenesis and Roles in Neural Tube Defects.

Wang L, Chang S, Guan J, Shangguan S, Lu X, Wang Z, Wu L, Zou J, Zhao H, Bao Y, Qiu Z, Niu B, Zhang T.

Curr Mol Med. 2015;15(5):497-507.

PMID:
26122653
9.

Differential methylation of human LINE-1 retrotransposons in malignant cells.

Alves G, Tatro A, Fanning T.

Gene. 1996 Oct 17;176(1-2):39-44.

PMID:
8918229
10.

Methylation-specific PCR allows for fast diagnosis of X chromosome disomy and reveals skewed inactivation of the X chromosome in men with Klinefelter syndrome.

Mehta A, Malek-Jones M, Bolyakov A, Mielnik A, Schlegel PN, Paduch DA.

J Androl. 2012 Sep-Oct;33(5):955-62. Epub 2012 Mar 22.

PMID:
22441764
11.

DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations.

Sharma A, Jamil MA, Nuesgen N, Schreiner F, Priebe L, Hoffmann P, Herns S, Nöthen MM, Fröhlich H, Oldenburg J, Woelfle J, El-Maarri O.

Clin Epigenetics. 2015 Jul 28;7:76. doi: 10.1186/s13148-015-0112-2. eCollection 2015.

12.

Epigenomic and transcriptomic signatures of a Klinefelter syndrome (47,XXY) karyotype in the brain.

Viana J, Pidsley R, Troakes C, Spiers H, Wong CC, Al-Sarraj S, Craig I, Schalkwyk L, Mill J.

Epigenetics. 2014 Apr;9(4):587-99. doi: 10.4161/epi.27806. Epub 2014 Jan 29.

13.

Gene body-specific methylation on the active X chromosome.

Hellman A, Chess A.

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

14.

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.

15.

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
16.

X chromosome-wide analyses of genomic DNA methylation states and gene expression in male and female neutrophils.

Yasukochi Y, Maruyama O, Mahajan MC, Padden C, Euskirchen GM, Schulz V, Hirakawa H, Kuhara S, Pan XH, Newburger PE, Snyder M, Weissman SM.

Proc Natl Acad Sci U S A. 2010 Feb 23;107(8):3704-9. doi: 10.1073/pnas.0914812107. Epub 2010 Feb 2.

17.

Phenotype in X chromosome rearrangements: pitfalls of X inactivation study.

Schluth C, Cossée M, Girard-Lemaire F, Carelle N, Dollfus H, Jeandidier E, Flori E.

Pathol Biol (Paris). 2007 Feb;55(1):29-36. Epub 2006 May 11.

PMID:
16690229
18.

Epigenetic investigation of variably X chromosome inactivated genes in monozygotic female twins discordant for primary biliary cirrhosis.

Mitchell MM, Lleo A, Zammataro L, Mayo MJ, Invernizzi P, Bach N, Shimoda S, Gordon S, Podda M, Gershwin ME, Selmi C, LaSalle JM.

Epigenetics. 2011 Jan;6(1):95-102. doi: 10.4161/epi.6.1.13405. Epub 2011 Jan 1.

19.

A small and active ring X chromosome in a female with features of Kabuki syndrome.

Rodríguez L, Diego-Alvarez D, Lorda-Sanchez I, Gallardo FL, Martínez-Fernández ML, Arroyo-Muñoz ME, Martínez-Frías ML.

Am J Med Genet A. 2008 Nov 1;146A(21):2816-21. doi: 10.1002/ajmg.a.32521.

PMID:
18925662
20.

Steroid sulphatase in man: a non inactivated X-locus with partial gene dosage compensation.

Lykkesfeldt G, Lykkesfeldt AE, Skakkebaek NE.

Hum Genet. 1984;65(4):355-7.

PMID:
6582028

Supplemental Content

Support Center