ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome.
about
Silver-Russell syndrome: genetic basis and molecular genetic testingImprinted Zac1 in neural stem cellsDNA methylation patterns in tissues from mid-gestation bovine foetuses produced by somatic cell nuclear transfer show subtle abnormalities in nuclear reprogramming.The Missing lnc(RNA) between the pancreatic β-cell and diabetesGenomic imprinting in diabetes.Epigenetic and genetic diagnosis of Silver-Russell syndrome.Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome.Beckwith Wiedemann imprinting defect found in leucocyte but not buccal DNA in a child born small for gestational ageMolecular and clinical studies in 138 Japanese patients with Silver-Russell syndromeAltered expression of the imprinted transcription factor PLAGL1 deregulates a network of genes in the human IUGR placentaRoles of imprinted genes in neural stem cells.Characterization of global loss of imprinting in fetal overgrowth syndrome induced by assisted reproduction.A novel variation of PLAGL1 in Chinese patients with isolated ventricular septal defectExpression 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.Insights into the molecular mechanism for type 2 diabetes susceptibility at the KCNQ1 locus from temporal changes in imprinting status in human islets.Growth regulation, imprinted genes, and chromosome 11p15.5.Lead Exposure during Early Human Development and DNA Methylation of Imprinted Gene Regulatory Elements in Adulthood.The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region.The human imprintome: regulatory mechanisms, methods of ascertainment, and roles in disease susceptibilityGenetic and epigenetic defects at the 6q24 imprinted locus in a cohort of 13 patients with transient neonatal diabetes: new hypothesis raised by the finding of a unique case with hemizygotic deletion in the critical region.Long Non-Coding RNAs Embedded in the Rb and p53 PathwaysAssociation between long non-coding RNA and human rare diseases (Review).Genomic imprinting in development, growth, behavior and stem cellsDisturbed methylation at multiple imprinted loci: an increasing observation in imprinting disorders.Chromatin structure, epigenetic mechanisms and long-range interactions in the human insulin locus.Cell cycle regulation by long non-coding RNAsEpigenetic deregulation of genomic imprinting in humans: causal mechanisms and clinical implications.Multilocus methylation defects in imprinting disorders.Multitasking C2H2 zinc fingers link Zac DNA binding to coordinated regulation of p300-histone acetyltransferase activity.Deregulation of an imprinted gene network in prostate cancer.Role of DNA methylation in imprinting disorders: an updated review.46,XX ovotesticular disorder in a Mexican patient with Beckwith-Wiedemann syndrome: a case report.A new coactivator function for Zac1's C2H2 zinc finger DNA-binding domain in selectively controlling PCAF activity.Lot1 is a key element of the pituitary adenylate cyclase-activating polypeptide (PACAP)/cyclic AMP pathway that negatively regulates neuronal precursor proliferation.LOT1 (ZAC1/PLAGL1) as member of an imprinted gene network does not harbor Silver-Russell specific variants.A type 2 diabetes-associated SNP in KCNQ1 (rs163184) modulates the binding activity of the locus for Sp3 and Lsd1/Kdm1a, potentially affecting CDKN1C expression.Clinical characterisation of the multiple maternal hypomethylation syndrome in siblings.Aberrant DNA methylation of imprinted loci in superovulated oocytes.Differential expression pattern of ZAC in developing mouse and human pancreas.PLAGL1 epimutation and bladder exstrophy: Coincidence or concurrent etiology?
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ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome.
description
2005 nî lūn-bûn
@nan
2005 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
ZAC, LIT1 (KCNQ1OT1) and p57KI ...... in Beckwith-Wiedemann syndrome
@nl
ZAC, LIT1 (KCNQ1OT1) and p57KI ...... n Beckwith-Wiedemann syndrome.
@ast
ZAC, LIT1 (KCNQ1OT1) and p57KI ...... n Beckwith-Wiedemann syndrome.
@en
ZAC, LIT1 (KCNQ1OT1) and p57KI ...... n Beckwith-Wiedemann syndrome.
@en-gb
type
label
ZAC, LIT1 (KCNQ1OT1) and p57KI ...... in Beckwith-Wiedemann syndrome
@nl
ZAC, LIT1 (KCNQ1OT1) and p57KI ...... n Beckwith-Wiedemann syndrome.
@ast
ZAC, LIT1 (KCNQ1OT1) and p57KI ...... n Beckwith-Wiedemann syndrome.
@en
ZAC, LIT1 (KCNQ1OT1) and p57KI ...... n Beckwith-Wiedemann syndrome.
@en-gb
prefLabel
ZAC, LIT1 (KCNQ1OT1) and p57KI ...... in Beckwith-Wiedemann syndrome
@nl
ZAC, LIT1 (KCNQ1OT1) and p57KI ...... n Beckwith-Wiedemann syndrome.
@ast
ZAC, LIT1 (KCNQ1OT1) and p57KI ...... n Beckwith-Wiedemann syndrome.
@en
ZAC, LIT1 (KCNQ1OT1) and p57KI ...... n Beckwith-Wiedemann syndrome.
@en-gb
P2093
P2860
P356
P1476
ZAC, LIT1 (KCNQ1OT1) and p57KI ...... n Beckwith-Wiedemann syndrome.
@en
P2093
Hidenobu Soejima
Kiyoko Kato
Mitsuo Oshimura
Norio Wake
Takahiro Arima
Tetsuya Kamikihara
Toshiaki Inoue
Toshirou Hayashida
Tunehiro Mukai
Yasuaki Shirayoshi
P2860
P304
P356
10.1093/NAR/GKI555
P407
P577
2005-05-11T00:00:00Z