[cite web | title = Entrez Gene: KCNQ1OT1 KCNQ1 overlapping transcript 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10984| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Adams MD, Kerlavage AR, Fleischmann RD, "et al." |title=Initial assessment of human gene diversity and expression patterns based upon 83 million nucleotides of cDNA sequence. |journal=Nature |volume=377 |issue= 6547 Suppl |pages= 3–174 |year= 1995 |pmid= 7566098 |doi=
*cite journal | author=Hillier LD, Lennon G, Becker M, "et al." |title=Generation and analysis of 280,000 human expressed sequence tags. |journal=Genome Res. |volume=6 |issue= 9 |pages= 807–28 |year= 1997 |pmid= 8889549 |doi=
*cite journal | author=Lee MP, DeBaun MR, Mitsuya K, "et al." |title=Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=96 |issue= 9 |pages= 5203–8 |year= 1999 |pmid= 10220444 |doi=
*cite journal | author=Mitsuya K, Meguro M, Lee MP, "et al." |title=LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids. |journal=Hum. Mol. Genet. |volume=8 |issue= 7 |pages= 1209–17 |year= 1999 |pmid= 10369866 |doi=
*cite journal | author=Smilinich NJ, Day CD, Fitzpatrick GV, "et al." |title=A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=96 |issue= 14 |pages= 8064–9 |year= 1999 |pmid= 10393948 |doi=
*cite journal | author=DeBaun MR, Niemitz EL, McNeil DE, "et al." |title=Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects. |journal=Am. J. Hum. Genet. |volume=70 |issue= 3 |pages= 604–11 |year= 2002 |pmid= 11813134 |doi=
*cite journal | author=Cerrato F, Vernucci M, Pedone PV, "et al." |title=The 5' end of the KCNQ1OT1 gene is hypomethylated in the Beckwith-Wiedemann syndrome. |journal=Hum. Genet. |volume=111 |issue= 1 |pages= 105–7 |year= 2002 |pmid= 12136243 |doi= 10.1007/s00439-002-0751-1
*cite journal | author=DeBaun MR, Niemitz EL, Feinberg AP |title=Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19. |journal=Am. J. Hum. Genet. |volume=72 |issue= 1 |pages= 156–60 |year= 2003 |pmid= 12439823 |doi=
*cite journal | author=Gicquel C, Gaston V, Mandelbaum J, "et al." |title=In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene. |journal=Am. J. Hum. Genet. |volume=72 |issue= 5 |pages= 1338–41 |year= 2003 |pmid= 12772698 |doi=
*cite journal | author=Diaz-Meyer N, Day CD, Khatod K, "et al." |title=Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome. |journal=J. Med. Genet. |volume=40 |issue= 11 |pages= 797–801 |year= 2004 |pmid= 14627666 |doi=
*cite journal | author=Soejima H, Nakagawachi T, Zhao W, "et al." |title=Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer. |journal=Oncogene |volume=23 |issue= 25 |pages= 4380–8 |year= 2004 |pmid= 15007390 |doi= 10.1038/sj.onc.1207576
*cite journal | author=Du M, Zhou W, Beatty LG, "et al." |title=The KCNQ1OT1 promoter, a key regulator of genomic imprinting in human chromosome 11p15.5. |journal=Genomics |volume=84 |issue= 2 |pages= 288–300 |year= 2005 |pmid= 15233993 |doi= 10.1016/j.ygeno.2004.03.008
*cite journal | author=Thakur N, Tiwari VK, Thomassin H, "et al." |title=An antisense RNA regulates the bidirectional silencing property of the Kcnq1 imprinting control region. |journal=Mol. Cell. Biol. |volume=24 |issue= 18 |pages= 7855–62 |year= 2004 |pmid= 15340049 |doi= 10.1128/MCB.24.18.7855-7862.2004
*cite journal | author=Arima T, Kamikihara T, Hayashida T, "et al." |title=ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome. |journal=Nucleic Acids Res. |volume=33 |issue= 8 |pages= 2650–60 |year= 2005 |pmid= 15888726 |doi= 10.1093/nar/gki555
*cite journal | author=Higashimoto K, Soejima H, Saito T, "et al." |title=Imprinting disruption of the CDKN1C/KCNQ1OT1 domain: the molecular mechanisms causing Beckwith-Wiedemann syndrome and cancer. |journal=Cytogenet. Genome Res. |volume=113 |issue= 1-4 |pages= 306–12 |year= 2006 |pmid= 16575194 |doi= 10.1159/000090846
*cite journal | author=Geuns E, Hilven P, Van Steirteghem A, "et al." |title=Methylation analysis of KvDMR1 in human oocytes. |journal=J. Med. Genet. |volume=44 |issue= 2 |pages= 144–7 |year= 2007 |pmid= 16950814 |doi= 10.1136/jmg.2006.044149
*cite journal | author=Nakano S, Murakami K, Meguro M, "et al." |title=Expression profile of LIT1/KCNQ1OT1 and epigenetic status at the KvDMR1 in colorectal cancers. |journal=Cancer Sci. |volume=97 |issue= 11 |pages= 1147–54 |year= 2006 |pmid= 16965397 |doi= 10.1111/j.1349-7006.2006.00305.x
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