The role and interaction of imprinted genes in human fetal growth

Differential expression of imprinted genes in normal and IUGR human placentas

(2014) Andreas I. Diplas et al.   Epigenetics

Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment

(2014) F. Court et al.   GENOME RESEARCH

Altered expression of the imprinted transcription factor PLAGL1 deregulates a network of genes in the human IUGR placenta

(2014) Isabel Iglesias-Platas et al.   HUMAN MOLECULAR GENETICS

Paternally Expressed, Imprinted Insulin-Like Growth Factor-2 in Chorionic Villi Correlates Significantly with Birth Weight

(2014) Charalambos Demetriou et al.   PLoS One

CDKN1Cmutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome

(2013) F Brioude et al.   JOURNAL OF MEDICAL GENETICS

Elevated Expression of H19 and Igf2 in the Female Mouse Eye

(2013) Björn Reinius et al.   PLoS One

Maternal Inheritance of a Promoter Variant in the Imprinted PHLDA2 Gene Significantly Increases Birth Weight

(2012) Miho Ishida et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Epigenetic state and expression of imprinted genes in umbilical cord correlates with growth parameters in human pregnancy

(2012) Ai Lin Lim et al.   JOURNAL OF MEDICAL GENETICS

Clinical significance of copy number variations in the 11p15.5 imprinting control regions: new cases and review of the literature

(2012) Matthias Begemann et al.   JOURNAL OF MEDICAL GENETICS

The role of imprinted genes in humans

(2012) Miho Ishida et al.   MOLECULAR ASPECTS OF MEDICINE

Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome

(2012) Valerie A Arboleda et al.   NATURE GENETICS

Imprinted gene expression in fetal growth and development

(2012) L. Lambertini et al.   PLACENTA

IGF1 molecular anomalies demonstrate its critical role in fetal, postnatal growth and brain development

(2011) Irène Netchine et al.   BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM

Fetal overgrowth in the Cdkn1c mouse model of Beckwith-Wiedemann syndrome

(2011) S. J. Tunster et al.   Disease Models & Mechanisms

Distinct physiological and behavioural functions for parental alleles of imprinted Grb10

(2011) Alastair S. Garfield et al.   NATURE

Ontogeny of growth-regulating genes in the placenta

(2011) N. Kumar et al.   PLACENTA

IGF2 Actions on Trophoblast in Human Placenta Are Regulated by the Insulin-Like Growth Factor 2 Receptor, Which Can Function as Both a Signaling and Clearance Receptor1

(2010) Lynda K. Harris et al.   BIOLOGY OF REPRODUCTION

Birthweight and the risk of childhood-onset type 1 diabetes: a meta-analysis of observational studies using individual patient data

(2010) C. R. Cardwell et al.   DIABETOLOGIA

Gene expression pattern ofIGF2,PHLDA2,PEG10andCDKN1Cimprinted genes in spontaneous miscarriages or fetal deaths

(2010) Sofia Dória et al.   Epigenetics

Effect of Maternal Tobacco Smoke Exposure on the Placental Transcriptome

(2010) H. Bruchova et al.   PLACENTA

High-Resolution Analysis of Parent-of-Origin Allelic Expression in the Mouse Brain

(2010) C. Gregg et al.   SCIENCE

Birth Weight, Early Weight Gain, and Subsequent Risk of Type 1 Diabetes: Systematic Review and Meta-Analysis

(2009) T. Harder et al.   AMERICAN JOURNAL OF EPIDEMIOLOGY

Deletion of Gtl2 , imprinted non-coding RNA, with its differentially methylated region induces lethal parent-origin-dependent defects in mice

(2009) Nozomi Takahashi et al.   HUMAN MOLECULAR GENETICS

Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression

(2009) David Monk et al.   HUMAN MOLECULAR GENETICS

Insulin and the IGF system in the human placenta of normal and diabetic pregnancies

(2009) Ursula Hiden et al.   JOURNAL OF ANATOMY

The Imprinted Phlda2 Gene Regulates Extraembryonic Energy Stores

(2009) S. J. Tunster et al.   MOLECULAR AND CELLULAR BIOLOGY

Minireview: Pref-1: Role in Adipogenesis and Mesenchymal Cell Fate

(2009) Hei Sook Sul   MOLECULAR ENDOCRINOLOGY

The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes

(2009) Chris Wallace et al.   NATURE GENETICS

Developmental Origins of Adult Disease

(2009) Rebecca A. Simmons   PEDIATRIC CLINICS OF NORTH AMERICA

Placental Glycogen Stores are Increased in Mice with H19 Null Mutations but not in those with Insulin or IGF Type 1 Receptor Mutations

(2009) Diego R. Esquiliano et al.   PLACENTA

Imprinted tumor suppressor genesARHI andPEG3 are the most frequently down-regulated in human ovarian cancers by loss of heterozygosity and promoter methylation

(2008) Weiwei Feng et al.   CANCER