| scholarly article | Q13442814 |
| P50 | author | Stephen W. Scherer | Q7610775 |
| Philip Stanier | Q50983740 | ||
| Philippe Arnaud | Q58463723 | ||
| Robert Feil | Q30380330 | ||
| Déborah Bourc'his | Q50578765 | ||
| P2093 | author name string | David Monk | |
| Gudrun E Moore | |||
| Alexandre Wagschal | |||
| Layla Parker-Katiraee | |||
| Pari-Sima Müller | |||
| P2860 | cites work | CTCF binding at the H19 imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to Igf2 | Q24295238 |
| The Polycomb group protein EZH2 directly controls DNA methylation | Q24299020 | ||
| Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genes | Q24546155 | ||
| Genome-wide maps of chromatin state in pluripotent and lineage-committed cells | Q24632506 | ||
| DNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNA | Q24645346 | ||
| DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency | Q24677959 | ||
| The Polycomb group protein Eed protects the inactive X-chromosome from differentiation-induced reactivation | Q25257656 | ||
| High-resolution profiling of histone methylations in the human genome | Q27860906 | ||
| CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus | Q28145756 | ||
| Temporal regulation of the expression of syncytin (HERV-W), maternally imprinted PEG10, and SGCE in human placenta | Q28181115 | ||
| A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21 | Q28185233 | ||
| A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids | Q28208083 | ||
| Set domain-containing protein, G9a, is a novel lysine-preferring mammalian histone methyltransferase with hyperactivity and specific selectivity to lysines 9 and 27 of histone H3 | Q28214048 | ||
| Construction and evolution of imprinted loci in mammals | Q28239760 | ||
| Epigenetic dynamics of the Kcnq1 imprinted domain in the early embryo. | Q50644071 | ||
| Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation. | Q52086106 | ||
| The imprinted mouse Igf2r/Air cluster--a model maternal imprinting system. | Q53001244 | ||
| Imprinted X inactivation maintained by a mouse Polycomb group gene | Q63407354 | ||
| Asb4, Ata3, and Dcn are novel imprinted genes identified by high-throughput screening using RIKEN cDNA microarray | Q77577356 | ||
| SUZ12 is required for both the histone methyltransferase activity and the silencing function of the EED-EZH2 complex | Q28269256 | ||
| The non-coding Air RNA is required for silencing autosomal imprinted genes | Q28504980 | ||
| PGC7/Stella protects against DNA demethylation in early embryogenesis | Q28506319 | ||
| Deletion of Peg10, an imprinted gene acquired from a retrotransposon, causes early embryonic lethality | Q28507386 | ||
| Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting | Q28508038 | ||
| Genome imprinting regulated by the mouse Polycomb group protein Eed | Q28510758 | ||
| Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome | Q28592236 | ||
| Retrotransposon silencing by DNA methylation can drive mammalian genomic imprinting | Q28762910 | ||
| Role of histone methyltransferase G9a in CpG methylation of the Prader-Willi syndrome imprinting center | Q30310519 | ||
| Zac1 (Lot1), a potential tumor suppressor gene, and the gene for epsilon-sarcoglycan are maternally imprinted genes: identification by a subtractive screen of novel uniparental fibroblast lines | Q30856368 | ||
| Maximum likelihood inference of imprinting and allele-specific expression from EST data | Q31066335 | ||
| Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6. | Q33680910 | ||
| Genomic imprinting: intricacies of epigenetic regulation in clusters. | Q34271454 | ||
| Epigenetic regulation of mammalian genomic imprinting | Q34326896 | ||
| Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes. | Q34363546 | ||
| Mouse embryos with paternal duplication of an imprinted chromosome 7 region die at midgestation and lack placental spongiotrophoblast. | Q34371975 | ||
| Cloning of the cDNA encoding mouse PP5/TFPI-2 and mapping of the gene to chromosome 6. | Q34409609 | ||
| Co-evolution of X-chromosome inactivation and imprinting in mammals | Q34409829 | ||
| Specific expression of PP5/TFPI2 mRNA by syncytiotrophoblasts in human placenta as revealed by in situ hybridization | Q34464607 | ||
| Limited evolutionary conservation of imprinting in the human placenta | Q35025042 | ||
| Allele-specific histone modifications regulate expression of the Dlk1-Gtl2 imprinted domain | Q35645900 | ||
| CTCF is the master organizer of domain-wide allele-specific chromatin at the H19/Igf2 imprinted region | Q36421340 | ||
| G9a histone methyltransferase contributes to imprinting in the mouse placenta | Q36421353 | ||
| Origins of extreme sexual dimorphism in genomic imprinting. | Q36436505 | ||
| How imprinting centres work | Q36436525 | ||
| Genomic imprinting in the placenta | Q36436530 | ||
| Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops | Q42632085 | ||
| Genomic imprinting of PPP1R9A encoding neurabin I in skeletal muscle and extra-embryonic tissues | Q43073580 | ||
| Peg1/Mest locates distal to the currently defined imprinting region on mouse proximal chromosome 6 and identifies a new imprinting region affecting growth | Q47622270 | ||
| Calcr, a brain-specific imprinted mouse calcitonin receptor gene in the imprinted cluster of the proximal region of chromosome 6 | Q48318024 | ||
| Dnmt3L and the establishment of maternal genomic imprints | Q48874297 | ||
| P433 | issue | 8 | |
| P921 | main subject | gene silencing | Q1431332 |
| P304 | page(s) | 1270-1281 | |
| P577 | publication date | 2008-05-14 | |
| P1433 | published in | Genome Research | Q5533485 |
| P1476 | title | Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing | |
| P478 | volume | 18 |
| Q37271182 | A sensitive functional assay reveals frequent loss of genomic imprinting in human placenta |
| Q38028387 | A survey of tissue-specific genomic imprinting in mammals |
| Q33876968 | Allele-specific H3K79 Di- versus trimethylation distinguishes opposite parental alleles at imprinted regions |
| Q35821083 | Allelic Imbalance Is a Prevalent and Tissue-Specific Feature of the Mouse Transcriptome. |
| Q38647931 | Assessment of imprinting- and genetic variation-dependent monoallelic expression using reciprocal allele descendants between human family trios |
| Q24647126 | Characterization of conserved and nonconserved imprinted genes in swine |
| Q30466805 | Child health, developmental plasticity, and epigenetic programming |
| Q37598629 | Chromatin mechanisms in genomic imprinting |
| Q35077074 | Chromosome-wide analysis of parental allele-specific chromatin and DNA methylation. |
| Q28485279 | Comprehensive analysis of DNA methylation in head and neck squamous cell carcinoma indicates differences by survival and clinicopathologic characteristics |
| Q34401348 | Coordinated allele-specific histone acetylation at the differentially methylated regions of imprinted genes. |
| Q21563370 | Critical evaluation of imprinted gene expression by RNA-Seq: a new perspective |
| Q35008254 | DNMT1 and AIM1 Imprinting in human placenta revealed through a genome-wide screen for allele-specific DNA methylation. |
| Q39025282 | Deregulation of an imprinted gene network in prostate cancer |
| Q33740660 | Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7. |
| Q39697159 | Distinguishing epigenetic marks of developmental and imprinting regulation. |
| Q92021260 | EHMT2 and SETDB1 protect the maternal pronucleus from 5mC oxidation |
| Q58702354 | Effects of maternal nutrition on the expression of genomic imprinted genes in ovine fetuses |
| Q37591200 | Epigenetic modifications at DMRs of placental genes are subjected to variations in normal gestation, pathological conditions and folate supplementation. |
| Q34851403 | Extra-embryonic-specific imprinted expression is restricted to defined lineages in the post-implantation embryo. |
| Q36870334 | Gene silencing and Polycomb group proteins: an overview of their structure, mechanisms and phylogenetics |
| Q39573980 | Genome-wide assessment of imprinted expression in human cells |
| Q37710386 | Genomic imprinting mechanisms in embryonic and extraembryonic mouse tissues |
| Q35040903 | Human imprinted retrogenes exhibit non-canonical imprint chromatin signatures and reside in non-imprinted host genes |
| Q42078835 | Implications of a Chr7q21.11 Microdeletion and the Role of the PCLO Gene in Developmental Delay |
| Q37543706 | Imprinting and extraembryonic tissues-mom takes control |
| Q34864517 | Influence of environmental exposure on human epigenetic regulation |
| Q35562665 | Loss of non-coding RNA expression from the DLK1-DIO3 imprinted locus correlates with reduced neural differentiation potential in human embryonic stem cell lines |
| Q28661720 | Marsupial genome sequences: providing insight into evolution and disease |
| Q55033793 | Maternal Choline Supplementation during Normal Murine Pregnancy Alters the Placental Epigenome: Results of an Exploratory Study. |
| Q48516898 | Maternal H3K27me3 controls DNA methylation-independent imprinting. |
| Q34507316 | Quantitative allele-specific expression and DNA methylation analysis of H19, IGF2 and IGF2R in the human placenta across gestation reveals H19 imprinting plasticity |
| Q53234088 | Regulation of tissue factor pathway inhibitor-2 (TFPI-2) expression by lysine-specific demethylase 1 and 2 (LSD1 and LSD2). |
| Q37988364 | Specific changes in the expression of imprinted genes in prostate cancer--implications for cancer progression and epigenetic regulation |
| Q34696537 | Stability of genomic imprinting in human induced pluripotent stem cells. |
| Q35295496 | The role of imprinted genes in fetal growth abnormalities |
| Q41827984 | The role of imprinted genes in humans |
| Q37324934 | Variants within MECP2, a key transcription regulator, are associated with increased susceptibility to lupus and differential gene expression in patients with systemic lupus erythematosus |
| Q38246516 | What does genetics tell us about imprinting and the placenta connection? |
| Q33886657 | Whole-transcriptome analysis delineates the human placenta gene network and its associations with fetal growth. |
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