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Items: 1 to 20 of 37

1.

Long Non-Coding RNA KCNQ1OT1 Promotes Cataractogenesis via miR-214 and Activation of the Caspase-1 Pathway.

Jin X, Jin H, Shi Y, Guo Y, Zhang H.

Cell Physiol Biochem. 2017;42(1):295-305. doi: 10.1159/000477330. Epub 2017 May 25.

PMID:
28535504
2.

A cross-talk between DNA methylation and H3 lysine 9 dimethylation at the KvDMR1 region controls the induction of Cdkn1c in muscle cells.

Andresini O, Ciotti A, Rossi MN, Battistelli C, Carbone M, Maione R.

Epigenetics. 2016 Nov;11(11):791-803. Epub 2016 Sep 9.

PMID:
27611768
3.

Regulation of functional KCNQ1OT1 lncRNA by β-catenin.

Sunamura N, Ohira T, Kataoka M, Inaoka D, Tanabe H, Nakayama Y, Oshimura M, Kugoh H.

Sci Rep. 2016 Feb 12;6:20690. doi: 10.1038/srep20690.

PMID:
26868975
4.

Long non-coding RNA chromogenic in situ hybridisation signal pattern correlation with breast tumour pathology.

Zhang Z, Weaver DL, Olsen D, deKay J, Peng Z, Ashikaga T, Evans MF.

J Clin Pathol. 2016 Jan;69(1):76-81. doi: 10.1136/jclinpath-2015-203275. Epub 2015 Aug 31.

PMID:
26323944
5.

In Pursuit of New Imprinting Syndromes by Epimutation Screening in Idiopathic Neurodevelopmental Disorder Patients.

Mayo S, Monfort S, Roselló M, Oltra S, Orellana C, Martínez F.

Biomed Res Int. 2015;2015:341986. doi: 10.1155/2015/341986. Epub 2015 May 27.

PMID:
26106604
6.

No evidence for copy number and methylation variation in H19 and KCNQ10T1 imprinting control regions in children born small for gestational age.

Murphy R, Thompson JM, Tost J, Mitchell EA; Auckland Birthweight Collaborative Study Group.

BMC Med Genet. 2014 Jun 17;15:67. doi: 10.1186/1471-2350-15-67.

PMID:
24934635
7.

The heterogeneity of hyperinsulinaemic hypoglycaemia in 19 patients with Beckwith-Wiedemann syndrome due to KvDMR1 hypomethylation.

Senniappan S, Ismail D, Shipster C, Beesley C, Hussain K.

J Pediatr Endocrinol Metab. 2015 Jan;28(1-2):83-6. doi: 10.1515/jpem-2013-0390.

PMID:
24468603
8.

A novel tetranucleotide repeat polymorphism within KCNQ1OT1 confers risk for hepatocellular carcinoma.

Wan J, Huang M, Zhao H, Wang C, Zhao X, Jiang X, Bian S, He Y, Gao Y.

DNA Cell Biol. 2013 Nov;32(11):628-34. doi: 10.1089/dna.2013.2118. Epub 2013 Aug 28.

PMID:
23984860
9.

Expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 and the methylation patterns at the KvDMR1 and H19/IGF2 imprinting control regions is conserved between human and bovine.

Robbins KM, Chen Z, Wells KD, Rivera RM.

J Biomed Sci. 2012 Nov 15;19:95. doi: 10.1186/1423-0127-19-95.

PMID:
23153226
10.

DNA methylation patterns of imprinting centers for H19, SNRPN, and KCNQ1OT1 in single-cell clones of human amniotic fluid mesenchymal stem cell.

Peng HH, Chang SD, Chao AS, Wang CN, Cheng PJ, Hwang SM, Wang TH.

Taiwan J Obstet Gynecol. 2012 Sep;51(3):342-9. doi: 10.1016/j.tjog.2012.07.004.

PMID:
23040914
11.

KCNQ1OT1 hypomethylation: a novel disguised genetic predisposition in sporadic pediatric adrenocortical tumors?

Wijnen M, Alders M, Zwaan CM, Wagner A, van den Heuvel-Eibrink MM.

Pediatr Blood Cancer. 2012 Sep;59(3):565-6. doi: 10.1002/pbc.23398.

PMID:
22610651
12.

Abnormal methylation of KCNQ1OT1 and differential methylation of H19 imprinting control regions in human ICSI embryos.

Khoueiry R, Ibala-Romdhane S, Al-Khtib M, Blachère T, Lornage J, Guérin JF, Lefèvre A.

Zygote. 2013 May;21(2):129-38. doi: 10.1017/S0967199411000694. Epub 2012 Feb 2.

PMID:
22300968
13.

The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases.

Chiesa N, De Crescenzo A, Mishra K, Perone L, Carella M, Palumbo O, Mussa A, Sparago A, Cerrato F, Russo S, Lapi E, Cubellis MV, Kanduri C, Cirillo Silengo M, Riccio A, Ferrero GB.

Hum Mol Genet. 2012 Jan 1;21(1):10-25. doi: 10.1093/hmg/ddr419. Epub 2011 Sep 14.

PMID:
21920939
14.

Vitrification at the germinal vesicle stage does not affect the methylation profile of H19 and KCNQ1OT1 imprinting centers in human oocytes subsequently matured in vitro.

Al-Khtib M, Perret A, Khoueiry R, Ibala-Romdhane S, Blachère T, Greze C, Lornage J, Lefèvre A.

Fertil Steril. 2011 May;95(6):1955-60. doi: 10.1016/j.fertnstert.2011.02.029. Epub 2011 Mar 21.

PMID:
21420679
15.

DNA methylation studies on imprinted loci in a male monozygotic twin pair discordant for Beckwith-Wiedemann syndrome.

Tierling S, Souren NY, Reither S, Zang KD, Meng-Hentschel J, Leitner D, Oehl-Jaschkowitz B, Walter J.

Clin Genet. 2011 Jun;79(6):546-53. doi: 10.1111/j.1399-0004.2010.01482.x.

PMID:
20618351
16.

Clone- and gene-specific aberrations of parental imprinting in human induced pluripotent stem cells.

Pick M, Stelzer Y, Bar-Nur O, Mayshar Y, Eden A, Benvenisty N.

Stem Cells. 2009 Nov;27(11):2686-90. doi: 10.1002/stem.205.

PMID:
19711451
17.

Abnormal methylation at the KvDMR1 imprinting control region in clinically normal children conceived by assisted reproductive technologies.

Gomes MV, Huber J, Ferriani RA, Amaral Neto AM, Ramos ES.

Mol Hum Reprod. 2009 Aug;15(8):471-7. doi: 10.1093/molehr/gap038. Epub 2009 Jun 3.

PMID:
19494037
18.

[Epimutations of the KCNQ1OT1 imprinting center of chromosome 11 in early human embryo lethality].

Sazhenova EA, Lebedev IN.

Genetika. 2008 Dec;44(12):1609-16. Russian.

PMID:
19178079
19.

Dynamic CpG methylation of the KCNQ1OT1 gene during maturation of human oocytes.

Khoueiry R, Ibala-Rhomdane S, Méry L, Blachère T, Guérin JF, Lornage J, Lefèvre A.

J Med Genet. 2008 Sep;45(9):583-8. doi: 10.1136/jmg.2008.057943. Erratum in: J Med Genet. 2008 Dec;45(12):832.. Khoureiry, R [corrected to Khoueiry, R].

PMID:
18762571
20.

Kcnq1ot1/Lit1 noncoding RNA mediates transcriptional silencing by targeting to the perinucleolar region.

Mohammad F, Pandey RR, Nagano T, Chakalova L, Mondal T, Fraser P, Kanduri C.

Mol Cell Biol. 2008 Jun;28(11):3713-28. doi: 10.1128/MCB.02263-07. Epub 2008 Feb 25.

PMID:
18299392

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