about
ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome.Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57Epigenetics: a molecular link between environmental factors and type 2 diabetesEpigenetic Biomarkers of Preterm Birth and Its Risk FactorsNew insights from monogenic diabetes for "common" type 2 diabetesNutrition, epigenetics, and metabolic syndromeChromatin regulators of genomic imprintingPathogenesis of the metabolic syndrome: insights from monogenic disordersGenetics and pathophysiology of neonatal diabetes mellitus.Insulin pump therapy in transient neonatal diabetes mellitus.Degree of methylation of ZAC1 (PLAGL1) is associated with prenatal and post-natal growth in healthy infants of the EDEN mother child cohort.Investigating parent of origin effects in studies of type 2 diabetes and obesityMammalian genomic imprinting.ncRNAimprint: a comprehensive database of mammalian imprinted noncoding RNAs.Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome.Acquired non-type 1 diabetes in childhood: subtypes, diagnosis, and management.Unlocking the secrets of the pancreatic beta cell: man and mouse provide the key.Mutations in the Kir6.2 subunit of the KATP channel and permanent neonatal diabetes: new insights and new treatment.Frontiers in research on maternal diabetes-induced neural tube defects: Past, present and futureThe effect of early, comprehensive genomic testing on clinical care in neonatal diabetes: an international cohort study.Coincidence of a novel KCNJ11 missense variant R365H with a paternally inherited 6q24 duplication in a patient with transient neonatal diabetes.Epigenetics and obesity.Genomic imprinting: employing and avoiding epigenetic processes.Diabetes mellitus in neonates and infants: genetic heterogeneity, clinical approach to diagnosis, and therapeutic options.Demonstration of all-or-none loss of imprinting in mRNA expression in single cells.Epigenetic discordance at imprinting control regions in twins.Human imprinting syndromes.The role of pancreatic imaging in monogenic diabetes mellitus.Specific changes in the expression of imprinted genes in prostate cancer--implications for cancer progression and epigenetic regulation.Genes, assisted reproductive technology and trans-illumination.Epigenetic deregulation of genomic imprinting in humans: causal mechanisms and clinical implications.Long noncoding RNA: significance and potential in skin biology.Insulin gene mutations and diabetesDNA methylation and its role in the pathogenesis of diabetes.Role of DNA methylation in imprinting disorders: an updated review.Epigenetic consequences of a changing human diet.Prematurity and Genetic Testing for Neonatal Diabetes.Concurrent course of transient neonatal diabetes with cholestasis and paucity of interlobular bile ducts: a case report.Genomic imprinting as a cause of disease.Long Noncoding RNAs in Mammalian Development and Diseases.
P2860
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P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Transient neonatal diabetes, a disorder of imprinting.
@ast
Transient neonatal diabetes, a disorder of imprinting.
@en
type
label
Transient neonatal diabetes, a disorder of imprinting.
@ast
Transient neonatal diabetes, a disorder of imprinting.
@en
prefLabel
Transient neonatal diabetes, a disorder of imprinting.
@ast
Transient neonatal diabetes, a disorder of imprinting.
@en
P2860
P356
P1476
Transient neonatal diabetes, a disorder of imprinting
@en
P2093
J P H Shield
P2860
P304
P356
10.1136/JMG.39.12.872
P407
P577
2002-12-01T00:00:00Z