| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1159/000090843 |
| P698 | PubMed publication ID | 16575191 |
| P2093 | author name string | F M Smith | |
| A Ward | |||
| A S Garfield | |||
| P2860 | cites work | Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome. | Q41066237 |
| Regulation of embryonic growth and lysosomal targeting by the imprinted Igf2/Mpr gene | Q41415190 | ||
| Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark | Q44406695 | ||
| The imprinted signaling protein XL alpha s is required for postnatal adaptation to feeding. | Q44992718 | ||
| Meg1/Grb10 overexpression causes postnatal growth retardation and insulin resistance via negative modulation of the IGF1R and IR cascades. | Q45308583 | ||
| Mouse mutants lacking the type 2 IGF receptor (IGF2R) are rescued from perinatal lethality in Igf2 and Igf1r null backgrounds | Q47645757 | ||
| Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest | Q48016474 | ||
| Imprinted gene in postnatal growth role | Q48035614 | ||
| Roles of growth hormone and insulin-like growth factor 1 in mouse postnatal growth. | Q52142765 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith–Wiedemann syndrome | Q58236969 | ||
| IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes | Q24317066 | ||
| Placental overgrowth in mice lacking the imprinted gene Ipl | Q24530568 | ||
| Transposable elements: targets for early nutritional effects on epigenetic gene regulation | Q24681243 | ||
| Glypican-3-deficient mice exhibit developmental overgrowth and some of the abnormalities typical of Simpson-Golabi-Behmel syndrome | Q28139404 | ||
| Regulation of skeletal muscle mass in mice by a new TGF-beta superfamily member | Q28237287 | ||
| Genomic imprinting in mammalian development: a parental tug-of-war | Q28278146 | ||
| Mice lacking p27(Kip1) display increased body size, multiple organ hyperplasia, retinal dysplasia, and pituitary tumors | Q29616203 | ||
| IGF-1 receptor regulates lifespan and resistance to oxidative stress in mice | Q29616382 | ||
| Role of insulin-like growth factors in embryonic and postnatal growth | Q29620034 | ||
| Deficiency in p57Kip2 expression induces preeclampsia-like symptoms in mice | Q33345572 | ||
| M6P/IGF2R imprinting evolution in mammals | Q33908331 | ||
| Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor | Q33932429 | ||
| Mice lacking paternally expressed Pref-1/Dlk1 display growth retardation and accelerated adiposity | Q34284044 | ||
| Imprinting-mutation mechanisms in Prader-Willi syndrome | Q34388796 | ||
| Imprinting and disease | Q35043723 | ||
| Early nutrition, epigenetic changes at transposons and imprinted genes, and enhanced susceptibility to adult chronic diseases | Q35617527 | ||
| Variable and tissue-specific hormone resistance in heterotrimeric Gs protein alpha-subunit (Gsalpha) knockout mice is due to tissue-specific imprinting of the gsalpha gene | Q36214949 | ||
| Increased IGF-II protein affects p57kip2 expression in vivo and in vitro: implications for Beckwith-Wiedemann syndrome | Q36969422 | ||
| P433 | issue | 1-4 | |
| P304 | page(s) | 279-291 | |
| P577 | publication date | 2006-01-01 | |
| P1433 | published in | Cytogenetics and Genome Research | Q1524623 |
| P1476 | title | Regulation of growth and metabolism by imprinted genes | |
| P478 | volume | 113 |
| Q24652620 | A mono-allelic bivalent chromatin domain controls tissue-specific imprinting at Grb10 |
| Q28082766 | A review of inter- and intraspecific variation in the eutherian placenta |
| Q64889113 | Abundances of placental imprinted genes CDKN1C, PHLDA2 and IGF-2 are related to low birth weight and early catch-up growth in full-term infants born small for gestational age. |
| Q37251251 | Alterations in methylation and expression levels of imprinted genes H19 and Igf2 in the fetuses of diabetic mice |
| Q36808158 | An imprinted gene network that controls mammalian somatic growth is down-regulated during postnatal growth deceleration in multiple organs |
| Q34793925 | Antagonistic roles in fetal development and adult physiology for the oppositely imprinted Grb10 and Dlk1 genes |
| Q33402663 | Brain-derived neurotrophic factor modulation of Kv1.3 channel is disregulated by adaptor proteins Grb10 and nShc |
| Q38131371 | Brain-expressed imprinted genes and adult behaviour: the example of Nesp and Grb10. |
| Q36079417 | Causes and consequences of obesity: epigenetics or hypokinesis? |
| Q33285306 | Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7. |
| Q37598629 | Chromatin mechanisms in genomic imprinting |
| Q24632903 | Coevolution of retroelements and tandem zinc finger genes |
| Q34305206 | Culture of oocytes and risk of imprinting defects. |
| Q35186705 | DNA methylation dynamics at imprinted genes during bovine pre-implantation embryo development. |
| Q61455991 | DNA methylation in development and disease: an overview for prostate researchers |
| Q51609015 | DNA methylation variability at growth-related imprints does not contribute to overweight in monozygotic twins discordant for BMI. |
| Q36149236 | Depression in pregnancy, infant birth weight and DNA methylation of imprint regulatory elements |
| Q24632557 | Distinct physiological and behavioural functions for parental alleles of imprinted Grb10 |
| Q38600504 | Dopaminergic and behavioral changes in a loss-of-imprinting model of Cdkn1c |
| Q38108660 | Dosage-sensitivity of imprinted genes expressed in the brain: 15q11-q13 and neuropsychiatric illness |
| Q92639002 | Early-life exposure to severe famine is associated with higher methylation level in the IGF2 gene and higher total cholesterol in late adulthood: the Genomic Research of the Chinese Famine (GRECF) study |
| Q27339409 | Elevated paternal glucocorticoid exposure alters the small noncoding RNA profile in sperm and modifies anxiety and depressive phenotypes in the offspring. |
| Q28757092 | Environmental exposures and gene regulation in disease etiology |
| Q26781132 | Epigenetic marks: regulators of livestock phenotypes and conceivable sources of missing variation in livestock improvement programs |
| Q34302493 | Epigenetic mechanisms of depression and antidepressant action |
| Q38205048 | Epigenetic regulation of the Igf2/H19 gene cluster |
| Q34323245 | Epigenetics in sports. |
| Q34995527 | Epigenetics lessons from twins: prospects for autoimmune disease. |
| Q36156376 | Expressed alleles of imprinted IGF2, DLK1 and MEG3 colocalize in 3D-preserved nuclei of porcine fetal cells |
| Q43887658 | Expression of insulin-like growth factor 2 in mesenchymal neoplasms |
| Q36730925 | Gene-environment interactions and epigenetic basis of human diseases |
| Q35541780 | Genetics and epigenetics of obesity |
| Q35711242 | Genome Scan for Parent-of-Origin QTL Effects on Bovine Growth and Carcass Traits |
| Q91596236 | Genomic imprinting and its effects on postnatal growth and adult metabolism |
| Q35105543 | Genomic imprinting of Grb10: coadaptation or conflict? |
| Q38172016 | Genomic imprinting--the struggle of the genders at the molecular level |
| Q37172147 | Genomic organization and control of the grb7 gene family |
| Q36024859 | Global gene expression profiling reveals similarities and differences among mouse pluripotent stem cells of different origins and strains. |
| Q35649390 | Hematopoietic reconstitution with androgenetic and gynogenetic stem cells |
| Q48599505 | Human in vitro oocyte maturation is not associated with increased imprinting error rates at LIT1, SNRPN, PEG3 and GTL2. |
| Q24633385 | Imprint switch mutations at Rasgrf1 support conflict hypothesis of imprinting and define a growth control mechanism upstream of IGF1 |
| Q42623438 | Imprinting detection by extending a regression-based QTL analysis method |
| Q37080106 | In vivo and in vitro differentiation of uniparental embryonic stem cells into hematopoietic and neural cell types |
| Q57659859 | Influence of maternal nutrition on the metabolic syndrome and cardiovascular risk in the offspring |
| Q52657456 | Intergenerational response to the endocrine disruptor vinclozolin is influenced by maternal genotype and crossing scheme. |
| Q38215131 | Is metabolic rate a universal 'pacemaker' for biological processes? |
| Q37061240 | Linking prenatal maternal adversity to developmental outcomes in infants: the role of epigenetic pathways |
| Q33649809 | Long noncoding RNAs in imprinting and X chromosome inactivation |
| Q42646815 | Low protein diet fed exclusively during mouse oocyte maturation leads to behavioural and cardiovascular abnormalities in offspring. |
| Q36742624 | Maternal Diet during Pregnancy Induces Gene Expression and DNA Methylation Changes in Fetal Tissues in Sheep |
| Q37497577 | Maternal imprinting at the H19-Igf2 locus maintains adult haematopoietic stem cell quiescence. |
| Q28592629 | Maternal inheritance of the Gnas cluster mutation Ex1A-T affects size, implicating NESP55 in growth |
| Q43175364 | Maternal low-protein diet during mouse pre-implantation development induces vascular dysfunction and altered renin-angiotensin-system homeostasis in the offspring |
| Q37367108 | Maternal prenatal depression is associated with decreased placental expression of the imprinted gene PEG3 |
| Q34607086 | Maternal stress, preterm birth, and DNA methylation at imprint regulatory sequences in humans |
| Q36854306 | Mechanisms of disease: the developmental origins of disease and the role of the epigenotype. |
| Q33790395 | Metabolic syndrome components in murine models |
| Q50640391 | Methylation analysis of the intergenic differentially methylated region of DLK1-GTL2 in human. |
| Q34297140 | Methylation defect in imprinted genes detected in patients with an Albright's hereditary osteodystrophy like phenotype and platelet Gs hypofunction |
| Q35950176 | Mice with a disruption of the imprinted Grb10 gene exhibit altered body composition, glucose homeostasis, and insulin signaling during postnatal life |
| Q30581898 | Myod and H19-Igf2 locus interactions are required for diaphragm formation in the mouse. |
| Q37690666 | Natural breaking of the maternal silence at the mouse and human imprinted Prader-Willi locus: A whisper with functional consequences. |
| Q34749691 | Non-coding RNAs in imprinted gene clusters |
| Q34967058 | Non-coding RNAs, epigenetic memory and the passage of information to progeny |
| Q34716902 | Paternal and maternal influences on differences in birth weight between Europeans and Indians born in the UK |
| Q37701759 | Perinatal high methyl donor alters gene expression in IGF system in male offspring without altering DNA methylation |
| Q28298905 | Persistent epigenetic differences associated with prenatal exposure to famine in humans |
| Q37242244 | Physiological dysfunctions associated with mutations of the imprinted Gnas locus. |
| Q57252792 | Positive darwinian selection at the imprinted MEDEA locus in plants |
| Q28285118 | Psychosis and autism as diametrical disorders of the social brain |
| Q34022943 | Retrotransposition and genomic imprinting |
| Q92380905 | Searching for parent-of-origin effects on cardiometabolic traits in imprinted genomic regions |
| Q36578863 | Severe obesity and insulin resistance due to deletion of the maternal Gsalpha allele is reversed by paternal deletion of the Gsalpha imprint control region |
| Q48764255 | Superovulation alters the expression of imprinted genes in the midgestation mouse placenta |
| Q51922783 | Temporal and spatial expression of a growth-regulated network of imprinted genes in growth plate. |
| Q55053919 | The evolutionary biology of child health. |
| Q37733830 | The role of imprinted genes in mediating susceptibility to neuropsychiatric disorders. |
| Q37634610 | The role of scaffold proteins in JNK signalling |
| Q47553897 | Two approaches reveal a new paradigm of 'switchable or genetics-influenced allele-specific DNA methylation' with potential in human disease. |
| Q89965058 | Why and How Imprinted Genes Drive Fetal Programming |
| Q61442992 | Wnt/β-catenin signaling pathway safeguards epigenetic stability and homeostasis of mouse embryonic stem cells |
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