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Items: 1 to 20 of 43

1.

Clinical and Molecular Characterization of Children with Neonatal Diabetes Mellitus at a Tertiary Care Center in Northern India.

Jain V, Satapathy A, Yadav J, Sharma R, Radha V, Mohan V, De Franco E, Ellard S.

Indian Pediatr. 2017 Jun 15;54(6):467-471.

2.

Methylomic changes in individuals with psychosis, prenatally exposed to endocrine disrupting compounds: Lessons from diethylstilbestrol.

Rivollier F, Chaumette B, Bendjemaa N, Chayet M, Millet B, Jaafari N, Barhdadi A, Lemieux Perreault LP, Provost S, Dubé MP, Gaillard R, Krebs MO, Kebir O.

PLoS One. 2017 Apr 13;12(4):e0174783. doi: 10.1371/journal.pone.0174783. eCollection 2017.

3.

Is famine exposure during developmental life in rural Bangladesh associated with a metabolic and epigenetic signature in young adulthood? A historical cohort study.

Finer S, Iqbal MS, Lowe R, Ogunkolade BW, Pervin S, Mathews C, Smart M, Alam DS, Hitman GA.

BMJ Open. 2016 Nov 23;6(11):e011768. doi: 10.1136/bmjopen-2016-011768.

4.

A Genome-Wide mQTL Analysis in Human Adipose Tissue Identifies Genetic Variants Associated with DNA Methylation, Gene Expression and Metabolic Traits.

Volkov P, Olsson AH, Gillberg L, Jørgensen SW, Brøns C, Eriksson KF, Groop L, Jansson PA, Nilsson E, Rönn T, Vaag A, Ling C.

PLoS One. 2016 Jun 20;11(6):e0157776. doi: 10.1371/journal.pone.0157776. eCollection 2016.

5.

Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans.

Sanchez-Delgado M, Riccio A, Eggermann T, Maher ER, Lapunzina P, Mackay D, Monk D.

Trends Genet. 2016 Jul;32(7):444-55. doi: 10.1016/j.tig.2016.05.001. Epub 2016 May 24. Review.

PMID:
27235113
6.

Mechanisms and Disease Associations of Haplotype-Dependent Allele-Specific DNA Methylation.

Do C, Lang CF, Lin J, Darbary H, Krupska I, Gaba A, Petukhova L, Vonsattel JP, Gallagher MP, Goland RS, Clynes RA, Dwork A, Kral JG, Monk C, Christiano AM, Tycko B.

Am J Hum Genet. 2016 May 5;98(5):934-955. doi: 10.1016/j.ajhg.2016.03.027.

7.

Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type Ib in a patient with multilocus imprinting disturbance: a female-dominant phenomenon?

Sano S, Matsubara K, Nagasaki K, Kikuchi T, Nakabayashi K, Hata K, Fukami M, Kagami M, Ogata T.

J Hum Genet. 2016 Aug;61(8):765-9. doi: 10.1038/jhg.2016.45. Epub 2016 Apr 28.

PMID:
27121328
8.

Genome-wide DNA methylation analysis of transient neonatal diabetes type 1 patients with mutations in ZFP57.

Bak M, Boonen SE, Dahl C, Hahnemann JM, Mackay DJ, Tümer Z, Grønskov K, Temple IK, Guldberg P, Tommerup N.

BMC Med Genet. 2016 Apr 14;17:29. doi: 10.1186/s12881-016-0292-4.

9.

Maintaining memory of silencing at imprinted differentially methylated regions.

Voon HP, Gibbons RJ.

Cell Mol Life Sci. 2016 May;73(9):1871-9. doi: 10.1007/s00018-016-2157-6. Epub 2016 Feb 16. Review.

10.

Intrahaplotypic Variants Differentiate Complex Linkage Disequilibrium within Human MHC Haplotypes.

Lam TH, Tay MZ, Wang B, Xiao Z, Ren EC.

Sci Rep. 2015 Nov 23;5:16972. doi: 10.1038/srep16972.

11.

Identification of Genes Whose Expression Profile Is Associated with Non-Progression towards AIDS Using eQTLs.

Spadoni JL, Rucart P, Le Clerc S, van Manen D, Coulonges C, Ulveling D, Laville V, Labib T, Taing L, Delaneau O, Montes M, Schuitemaker H, Noirel J, Zagury JF.

PLoS One. 2015 Sep 14;10(9):e0136989. doi: 10.1371/journal.pone.0136989. eCollection 2015.

12.

Single nucleotide polymorphisms/haplotypes associated with multiple rubella-specific immune response outcomes post-MMR immunization in healthy children.

Ovsyannikova IG, Salk HM, Larrabee BR, Pankratz VS, Poland GA.

Immunogenetics. 2015 Oct;67(10):547-61. doi: 10.1007/s00251-015-0864-z. Epub 2015 Sep 2.

13.

Germline-derived DNA methylation and early embryo epigenetic reprogramming: The selected survival of imprints.

Monk D.

Int J Biochem Cell Biol. 2015 Oct;67:128-38. doi: 10.1016/j.biocel.2015.04.014. Epub 2015 May 9. Review.

PMID:
25966912
14.

Nanog positively regulates Zfp57 expression in mouse embryonic stem cells.

Yamaguchi Y, Takamura H, Tada Y, Akagi T, Oyama K, Miyashita T, Tajima H, Kitagawa H, Fushida S, Yokota T, Ohta T, Koide H.

Biochem Biophys Res Commun. 2014 Oct 31;453(4):817-20. doi: 10.1016/j.bbrc.2014.10.020. Epub 2014 Oct 14.

PMID:
25445595
15.

The specification of imprints in mammals.

Hanna CW, Kelsey G.

Heredity (Edinb). 2014 Aug;113(2):176-83. doi: 10.1038/hdy.2014.54. Epub 2014 Jun 18. Review.

16.

Genome-wide DNA methylation profiling identifies a folate-sensitive region of differential methylation upstream of ZFP57-imprinting regulator in humans.

Amarasekera M, Martino D, Ashley S, Harb H, Kesper D, Strickland D, Saffery R, Prescott SL.

FASEB J. 2014 Sep;28(9):4068-76. doi: 10.1096/fj.13-249029. Epub 2014 Jun 2.

17.

A familial disorder of altered DNA-methylation.

Caliebe A, Richter J, Ammerpohl O, Kanber D, Beygo J, Bens S, Haake A, Jüttner E, Korn B, Mackay DJ, Martin-Subero JI, Nagel I, Sebire NJ, Seidmann L, Vater I, von Kaisenberg CS, Temple IK, Horsthemke B, Buiting K, Siebert R.

J Med Genet. 2014 Jun;51(6):407-12. doi: 10.1136/jmedgenet-2013-102149. Epub 2014 Apr 10.

PMID:
24721835
18.

High grade glioblastoma is associated with aberrant expression of ZFP57, a protein involved in gene imprinting, and of CPT1A and CPT1C that regulate fatty acid metabolism.

Cirillo A, Di Salle A, Petillo O, Melone MA, Grimaldi G, Bellotti A, Torelli G, De' Santi MS, Cantatore G, Marinelli A, Galderisi U, Peluso G.

Cancer Biol Ther. 2014 Jun 1;15(6):735-41. doi: 10.4161/cbt.28408. Epub 2014 Mar 11.

19.

The stem cell transcription factor ZFP57 induces IGF2 expression to promote anchorage-independent growth in cancer cells.

Tada Y, Yamaguchi Y, Kinjo T, Song X, Akagi T, Takamura H, Ohta T, Yokota T, Koide H.

Oncogene. 2015 Feb 5;34(6):752-60. doi: 10.1038/onc.2013.599. Epub 2014 Jan 27.

PMID:
24469060
20.

Fine mapping genetic determinants of the highly variably expressed MHC gene ZFP57.

Plant K, Fairfax BP, Makino S, Vandiedonck C, Radhakrishnan J, Knight JC.

Eur J Hum Genet. 2014 Apr;22(4):568-71. doi: 10.1038/ejhg.2013.244. Epub 2013 Nov 6.

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