| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1014018027 |
| P356 | DOI | 10.1186/1756-8935-4-1 |
| P932 | PMC publication ID | 3038880 |
| P698 | PubMed publication ID | 21281512 |
| P5875 | ResearchGate publication ID | 49798611 |
| P50 | author | Adele Murrell | Q61918646 |
| P2093 | author name string | Kathryn Woodfine | |
| Joanna E Huddleston | |||
| P2860 | cites work | Genomic imprinting in mammals: emerging themes and established theories | Q21145256 |
| CTCF binding at the H19 imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to Igf2 | Q24295238 | ||
| Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57 | Q24312925 | ||
| A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints | Q24322379 | ||
| Genome-wide maps of chromatin state in pluripotent and lineage-committed cells | Q24632506 | ||
| The human colon cancer methylome shows similar hypo- and hypermethylation at conserved tissue-specific CpG island shores | Q24649374 | ||
| The evolution of the DLK1-DIO3 imprinted domain in mammals | Q27333130 | ||
| Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene | Q28145754 | ||
| Using galaxy to perform large-scale interactive data analyses | Q28277397 | ||
| The H19 locus acts in vivo as a tumor suppressor | Q28508794 | ||
| Transgenic RNAi reveals essential function for CTCF in H19 gene imprinting | Q28590627 | ||
| CTCF maintains differential methylation at the Igf2/H19 locus | Q28593901 | ||
| Genomic imprinting: parental influence on the genome | Q29616227 | ||
| Cohesin is required for higher-order chromatin conformation at the imprinted IGF2-H19 locus | Q30946870 | ||
| Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer. | Q33325473 | ||
| The human retinoblastoma gene is imprinted | Q33521315 | ||
| H19 imprinting control region methylation requires an imprinted environment only in the male germ line. | Q33648826 | ||
| Unlocking the secrets of the genome | Q33745487 | ||
| Cytosine methylation and human cancer | Q33845225 | ||
| A novel variant of Inpp5f is imprinted in brain, and its expression is correlated with differential methylation of an internal CpG island | Q33862945 | ||
| The neuronatin gene resides in a "micro-imprinted" domain on human chromosome 20q11.2. | Q34090093 | ||
| Sex-specific parent-of-origin allelic expression in the mouse brain | Q34383242 | ||
| From genome to epigenome | Q34556459 | ||
| Epigenomics: genome-wide study of methylation phenomena. | Q34998071 | ||
| Limited evolutionary conservation of imprinting in the human placenta | Q35025042 | ||
| The nucleotides responsible for the direct physical contact between the chromatin insulator protein CTCF and the H19 imprinting control region manifest parent of origin-specific long-distance insulation and methylation-free domains | Q35964289 | ||
| Origins of extreme sexual dimorphism in genomic imprinting. | Q36436505 | ||
| Mechanisms regulating imprinted genes in clusters. | Q36805477 | ||
| Somatically acquired hypomethylation of IGF2 in breast and colorectal cancer | Q36835706 | ||
| Genome-wide analysis of DNA methylation patterns | Q36967594 | ||
| Epigenetic profiling at mouse imprinted gene clusters reveals novel epigenetic and genetic features at differentially methylated regions | Q37287372 | ||
| Genetics and epigenetics: stability and plasticity during cellular differentiation | Q37382613 | ||
| Comparison of methyl-DNA immunoprecipitation (MeDIP) and methyl-CpG binding domain (MBD) protein capture for genome-wide DNA methylation analysis reveal CpG sequence coverage bias | Q39659346 | ||
| Imprinted DLK1 is a putative tumor suppressor gene and inactivated by epimutation at the region upstream of GTL2 in human renal cell carcinoma. | Q40324607 | ||
| Imprinting of PEG1/MEST isoform 2 in human placenta | Q40366681 | ||
| Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumour | Q40441171 | ||
| Zac1 regulates an imprinted gene network critically involved in the control of embryonic growth | Q42602582 | ||
| Biallelic expression of imprinted genes in the mouse germ line: implications for erasure, establishment, and mechanisms of genomic imprinting | Q46630830 | ||
| Universal primer applications for pyrosequencing. | Q54565752 | ||
| Mechanisms of imprinting of the Prader-Willi/Angelman region. | Q55050189 | ||
| Genomic imprinting and cancer: from primordial germ cells to somatic cells. | Q55101929 | ||
| Loss of IGF2 imprinting: a potential marker of colorectal cancer risk | Q73128690 | ||
| Multiple imprinted and stemness genes provide a link between normal and tumor progenitor cells of the developing human kidney | Q79734415 | ||
| Identification and quantification of differentially methylated loci by the pyrosequencing technology | Q79800237 | ||
| Pyrosequencing protocol using a universal biotinylated primer for mutation detection and SNP genotyping | Q80643394 | ||
| P433 | issue | 1 | |
| P921 | main subject | DNA methylation | Q874745 |
| P304 | page(s) | 1 | |
| P577 | publication date | 2011-01-31 | |
| P1433 | published in | Epigenetics & Chromatin | Q15765513 |
| P1476 | title | Quantitative analysis of DNA methylation at all human imprinted regions reveals preservation of epigenetic stability in adult somatic tissue | |
| P478 | volume | 4 |
| Q42796148 | 5-Hydroxymethylation marks a class of neuronal gene regulated by intragenic methylcytosine levels |
| Q63352564 | A randomized controlled trial of folic acid intervention in pregnancy highlights a putative methylation-regulated control element at ZFP57 |
| Q34426327 | A systematic review and meta-analysis of DNA methylation levels and imprinting disorders in children conceived by IVF/ICSI compared with children conceived spontaneously |
| Q35624942 | Aberrant methylation of imprinted genes is associated with negative hormone receptor status in invasive breast cancer |
| Q35956263 | Abnormal Hypermethylation at Imprinting Control Regions in Patients with S-Adenosylhomocysteine Hydrolase (AHCY) Deficiency |
| Q64088724 | Alteration of Genomic Imprinting Status of Human Parthenogenetic Induced Pluripotent Stem Cells during Neural Lineage Differentiation |
| Q33712659 | Analysis of DNA methylation acquisition at the imprinted Dlk1 locus reveals asymmetry at CpG dyads |
| Q35854896 | Association of cord blood methylation fractions at imprinted insulin-like growth factor 2 (IGF2), plasma IGF2, and birth weight |
| Q37478200 | Association of maternal and nutrient supply line factors with DNA methylation at the imprinted IGF2/H19 locus in multiple tissues of newborn twins. |
| Q33823348 | Asymmetric DNA methylation of CpG dyads is a feature of secondary DMRs associated with the Dlk1/Gtl2 imprinting cluster in mouse |
| Q33859274 | BNDF methylation in mothers and newborns is associated with maternal exposure to war trauma. |
| Q36027913 | Breast cancer risk and imprinting methylation in blood |
| Q90137081 | Cadmium exposure and MEG3 methylation differences between Whites and African Americans in the NEST Cohort |
| Q90722510 | Comparison of DNA methylation patterns of parentally imprinted genes in placenta derived from IVF conceptions in two different culture media |
| Q35076810 | Comprehensive analyses of imprinted differentially methylated regions reveal epigenetic and genetic characteristics in hepatoblastoma. |
| Q34675182 | Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutations |
| Q34786014 | DNA methylation analysis reveals distinct methylation signatures in pediatric germ cell tumors |
| Q36312121 | DNA methylation at differentially methylated regions of imprinted genes is resistant to developmental programming by maternal nutrition |
| Q34262644 | DNA methylation dynamics of the human preimplantation embryo |
| Q34901834 | DNA methyltransferase candidate polymorphisms, imprinting methylation, and birth outcome |
| Q35666171 | Deoxyribonucleic acid methylation profiling of single human blastocysts by methylated CpG-island amplification coupled with CpG-island microarray |
| Q34342504 | Differentially methylated regions of imprinted genes in prenatal, perinatal and postnatal human tissues. |
| Q52660446 | Effects of Cadmium Exposure on DNA Methylation at Imprinting Control Regions and Genome-Wide in Mothers and Newborn Children. |
| Q28730353 | Epigenetic and genetic variation at the IGF2/H19 imprinting control region on 11p15.5 is associated with cerebellum weight |
| Q39351600 | Epigenetic consequences of a changing human diet |
| Q35738521 | Epigenetic regulation of Newborns' imprinted genes related to gestational growth: patterning by parental race/ethnicity and maternal socioeconomic status. |
| Q39195595 | Epigenetic status in the offspring of spontaneous and assisted conception |
| Q34183395 | Erythrocyte folate concentrations, CpG methylation at genomically imprinted domains, and birth weight in a multiethnic newborn cohort |
| Q35711242 | Genome Scan for Parent-of-Origin QTL Effects on Bovine Growth and Carcass Traits |
| Q36056485 | Genome-wide methylation analysis in Silver-Russell syndrome patients |
| Q37083431 | Imprinted chromatin around DIRAS3 regulates alternative splicing of GNG12-AS1, a long noncoding RNA. |
| Q37342817 | Imprinted genes and imprinting control regions show predominant intermediate methylation in adult somatic tissues |
| Q61804540 | Imprinting methylation in SNRPN and MEST1 in adult blood predicts cognitive ability |
| Q35226250 | In vitro lead exposure changes DNA methylation and expression of IGF2 and PEG1/MEST. |
| Q35987798 | Insulin-like growth factor 2/H19 methylation at birth and risk of overweight and obesity in children |
| Q34473768 | Intronic parent-of-origin dependent differential methylation at the Actn1 gene is conserved in rodents but is not associated with imprinted expression |
| Q36874343 | Lead Exposure during Early Human Development and DNA Methylation of Imprinted Gene Regulatory Elements in Adulthood. |
| Q34586415 | Leukocyte DNA as surrogate for the evaluation of imprinted Loci methylation in mammary tissue DNA. |
| Q35809876 | Loss of DNA methylation at imprinted loci is a frequent event in hepatocellular carcinoma and identifies patients with shortened survival. |
| Q28383380 | Maternal cadmium, iron and zinc levels, DNA methylation and birth weight |
| Q38692978 | Maternal inflammatory diet and adverse pregnancy outcomes: Circulating cytokines and genomic imprinting as potential regulators? |
| Q33920719 | Methylation variation at IGF2 differentially methylated regions and maternal folic acid use before and during pregnancy |
| Q42339448 | Modeling DNA methylation by analyzing the individual configurations of single molecules |
| Q52682306 | New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome. |
| Q35857389 | No Evidence for a Parent-of-Origin Specific Differentially Methylated Region Linked to RASGRF1. |
| Q37618677 | Ontogeny, conservation and functional significance of maternally inherited DNA methylation at two classes of non-imprinted genes. |
| Q34351507 | PEG1/MEST and IGF2 DNA methylation in CIN and in cervical cancer. |
| Q64996792 | Placental CpG methylation of HPA-axis genes is associated with cognitive impairment at age 10 among children born extremely preterm |
| Q50420528 | Placental CpG methylation of infants born extremely preterm predicts cognitive impairment later in life. |
| Q37658004 | Potential mechanisms of aberrant DNA hypomethylation on the x chromosome in uterine leiomyomas |
| Q34251884 | Quantitative cross-validation and content analysis of the 450k DNA methylation array from Illumina, Inc. |
| Q35161545 | Reduced DNA methylation at the PEG3 DMR and KvDMR1 loci in children exposed to alcohol in utero: a South African Fetal Alcohol Syndrome cohort study |
| Q91049292 | Reduced MEK inhibition preserves genomic stability in naive human embryonic stem cells |
| Q37936455 | Setting up and maintaining differential insulators and boundaries for genomic imprinting. |
| Q36209154 | Space/population and time/age in DNA methylation variability in humans: a study on IGF2/H19 locus in different Italian populations and in mono- and di-zygotic twins of different age. |
| Q35554558 | Targeted disruption of DNMT1, DNMT3A and DNMT3B in human embryonic stem cells |
| Q21144904 | The Kcnq1ot1 long non-coding RNA affects chromatin conformation and expression of Kcnq1, but does not regulate its imprinting in the developing heart |
| Q36931989 | The human imprintome: regulatory mechanisms, methods of ascertainment, and roles in disease susceptibility |
| Q91910501 | The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype |
| Q37428393 | Widespread recovery of methylation at gametic imprints in hypomethylated mouse stem cells following rescue with DNMT3A2. |
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