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Conservation of Repeats at the Mammalian KCNQ1OT1-CDKN1C Region Suggests a Role in Genomic Imprinting.

De Donato M, Hussain T, Rodulfo H, Peters SO, Imumorin IG, Thomas BN.

Evol Bioinform Online. 2017 Jun 16;13:1176934317715238. doi: 10.1177/1176934317715238. eCollection 2017.


Fetal and neonatal programming of postnatal growth and feed efficiency in swine.

Ji Y, Wu Z, Dai Z, Wang X, Li J, Wang B, Wu G.

J Anim Sci Biotechnol. 2017 May 5;8:42. doi: 10.1186/s40104-017-0173-5. eCollection 2017. Review.


PHF13 is a molecular reader and transcriptional co-regulator of H3K4me2/3.

Chung HR, Xu C, Fuchs A, Mund A, Lange M, Staege H, Schubert T, Bian C, Dunkel I, Eberharter A, Regnard C, Klinker H, Meierhofer D, Cozzuto L, Winterpacht A, Di Croce L, Min J, Will H, Kinkley S.

Elife. 2016 May 25;5. pii: e10607. doi: 10.7554/eLife.10607.


Epigenetic landscape of germline specific genes in the sporophyte cells of Arabidopsis thaliana.

Jung CH, O'Brien M, Singh MB, Bhalla PL.

Front Plant Sci. 2015 May 13;6:328. doi: 10.3389/fpls.2015.00328. eCollection 2015.


Defining CD4 T cell memory by the epigenetic landscape of CpG DNA methylation.

Komori HK, Hart T, LaMere SA, Chew PV, Salomon DR.

J Immunol. 2015 Feb 15;194(4):1565-79. doi: 10.4049/jimmunol.1401162. Epub 2015 Jan 9.


The role of maternal-specific H3K9me3 modification in establishing imprinted X-chromosome inactivation and embryogenesis in mice.

Fukuda A, Tomikawa J, Miura T, Hata K, Nakabayashi K, Eggan K, Akutsu H, Umezawa A.

Nat Commun. 2014 Nov 14;5:5464. doi: 10.1038/ncomms6464.


Next-generation sequencing: from understanding biology to personalized medicine.

Frese KS, Katus HA, Meder B.

Biology (Basel). 2013 Mar 1;2(1):378-98. doi: 10.3390/biology2010378.


Genome-wide histone state profiling of fibroblasts from the opossum, Monodelphis domestica, identifies the first marsupial-specific imprinted gene.

Douglas KC, Wang X, Jasti M, Wolff A, VandeBerg JL, Clark AG, Samollow PB.

BMC Genomics. 2014 Jan 31;15:89. doi: 10.1186/1471-2164-15-89.


Truncation of Ube3a-ATS unsilences paternal Ube3a and ameliorates behavioral defects in the Angelman syndrome mouse model.

Meng L, Person RE, Huang W, Zhu PJ, Costa-Mattioli M, Beaudet AL.

PLoS Genet. 2013;9(12):e1004039. doi: 10.1371/journal.pgen.1004039. Epub 2013 Dec 26.


Chromosome-wide profiling of X-chromosome inactivation and epigenetic states in fetal brain and placenta of the opossum, Monodelphis domestica.

Wang X, Douglas KC, Vandeberg JL, Clark AG, Samollow PB.

Genome Res. 2014 Jan;24(1):70-83. doi: 10.1101/gr.161919.113. Epub 2013 Sep 24.


Transgene- and locus-dependent imprinting reveals allele-specific chromosome conformations.

Lonfat N, Montavon T, Jebb D, Tschopp P, Nguyen Huynh TH, Zakany J, Duboule D.

Proc Natl Acad Sci U S A. 2013 Jul 16;110(29):11946-51. doi: 10.1073/pnas.1310704110. Epub 2013 Jul 1.


The human imprintome: regulatory mechanisms, methods of ascertainment, and roles in disease susceptibility.

Skaar DA, Li Y, Bernal AJ, Hoyo C, Murphy SK, Jirtle RL.

ILAR J. 2012;53(3-4):341-58. doi: 10.1093/ilar.53.3-4.341. Review.


Targeted DNA methylation analysis by high throughput sequencing in porcine peri-attachment embryos.

Morrill BH, Cox L, Ward A, Heywood S, Prather RS, Isom SC.

J Reprod Dev. 2013;59(3):314-20. Epub 2013 Feb 22.


Haploinsufficiency of the paternal-effect gene Dnmt3L results in transient DNA hypomethylation in progenitor cells of the male germline.

Niles KM, Yeh JR, Chan D, Landry M, Nagano MC, Trasler JM.

Hum Reprod. 2013 Feb;28(2):519-30. doi: 10.1093/humrep/des395. Epub 2012 Nov 15.


The endoglycosidase heparanase enters the nucleus of T lymphocytes and modulates H3 methylation at actively transcribed genes via the interplay with key chromatin modifying enzymes.

He YQ, Sutcliffe EL, Bunting KL, Li J, Goodall KJ, Poon IK, Hulett MD, Freeman C, Zafar A, McInnes RL, Taya T, Parish CR, Rao S.

Transcription. 2012 May-Jun;3(3):130-45. doi: 10.4161/trns.19998.


A genome-wide screen in human embryonic stem cells reveals novel sites of allele-specific histone modification associated with known disease loci.

Prendergast JG, Tong P, Hay DC, Farrington SM, Semple CA.

Epigenetics Chromatin. 2012 May 19;5(1):6. doi: 10.1186/1756-8935-5-6.


The impact of recent alcohol use on genome wide DNA methylation signatures.

Philibert RA, Plume JM, Gibbons FX, Brody GH, Beach SR.

Front Genet. 2012 Apr 10;3:54. doi: 10.3389/fgene.2012.00054. eCollection 2012.


An unexpected function of the Prader-Willi syndrome imprinting center in maternal imprinting in mice.

Wu MY, Jiang M, Zhai X, Beaudet AL, Wu RC.

PLoS One. 2012;7(4):e34348. doi: 10.1371/journal.pone.0034348. Epub 2012 Apr 4.


Coordinated changes in AHRR methylation in lymphoblasts and pulmonary macrophages from smokers.

Monick MM, Beach SR, Plume J, Sears R, Gerrard M, Brody GH, Philibert RA.

Am J Med Genet B Neuropsychiatr Genet. 2012 Mar;159B(2):141-51. doi: 10.1002/ajmg.b.32021. Epub 2012 Jan 9.


Nutrition, epigenetics, and metabolic syndrome.

Wang J, Wu Z, Li D, Li N, Dindot SV, Satterfield MC, Bazer FW, Wu G.

Antioxid Redox Signal. 2012 Jul 15;17(2):282-301. doi: 10.1089/ars.2011.4381. Epub 2012 Jan 13. Review.

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