| scholarly article | Q13442814 |
| P50 | author | David Kunkel | Q74623782 |
| Karl Pfeifer | Q56876131 | ||
| P2093 | author name string | Claudia Gebert | |
| Alexander Grinberg | |||
| P2860 | cites work | Parental imprinting of the mouse H19 gene | Q22122365 |
| CTCF binding at the H19 imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to Igf2 | Q24295238 | ||
| KDM1B is a histone H3K4 demethylase required to establish maternal genomic imprints | Q24312768 | ||
| Multiple nucleosome positioning sites regulate the CTCF-mediated insulator function of the H19 imprinting control region | Q24537340 | ||
| Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects | Q24632842 | ||
| Chromatin dynamics during epigenetic reprogramming in the mouse germ line | Q24633764 | ||
| Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene | Q28145754 | ||
| CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus | Q28145756 | ||
| Disruption of imprinting caused by deletion of the H19 gene region in mice | Q28287765 | ||
| An enhancer deletion affects both H19 and Igf2 expression | Q28288348 | ||
| Efficient in vivo manipulation of mouse genomic sequences at the zygote stage | Q29547306 | ||
| Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour | Q57976817 | ||
| Mitochondria and the death of oocytes | Q59075483 | ||
| DNA-methylation analysis by the bisulfite-assisted genomic sequencing method | Q60852367 | ||
| Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor | Q61657063 | ||
| Temporal and regional changes in DNA methylation in the embryonic, extraembryonic and germ cell lineages during mouse embryo development | Q69396959 | ||
| Epigenetic mechanisms underlying the imprinting of the mouse H19 gene | Q72094721 | ||
| Functional association of CTCF with the insulator upstream of the H19 gene is parent of origin-specific and methylation-sensitive | Q74014247 | ||
| Loss of imprinting of insulin-like growth factor-II in Wilms' tumor commonly involves altered methylation but not mutations of CTCF or its binding site | Q74114381 | ||
| Alpha-fetoprotein gene regulation: lessons from transgenic mice | Q33592945 | ||
| Characterization of novel parent-specific epigenetic modifications upstream of the imprinted mouse H19 gene. | Q33781581 | ||
| Genomic imprinting recapitulated in the human beta-globin locus | Q33900452 | ||
| Active demethylation of the paternal genome in the mouse zygote | Q33901068 | ||
| Regulatory mechanisms at the mouse Igf2/H19 locus. | Q34012897 | ||
| Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis | Q34056205 | ||
| Genomic imprinting and cancer; new paradigms in the genetics of neoplasia. | Q34232354 | ||
| Completion of mouse embryogenesis requires both the maternal and paternal genomes | Q34267351 | ||
| Analysis of sequence upstream of the endogenous H19 gene reveals elements both essential and dispensable for imprinting | Q34277546 | ||
| Parental-origin-specific epigenetic modification of the mouse H19 gene | Q34363043 | ||
| H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream of H19. | Q35194017 | ||
| A transcriptional insulator at the imprinted H19/Igf2 locus | Q35199693 | ||
| Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. | Q35211749 | ||
| Analysis of the H19ICR insulator | Q35856849 | ||
| CTCF is the master organizer of domain-wide allele-specific chromatin at the H19/Igf2 imprinted region | Q36421340 | ||
| Epigenetic deregulation of imprinting in congenital diseases of aberrant growth | Q36449310 | ||
| Enhancer blocking activity of the insulator at H19-ICR is independent of chromatin barrier establishment | Q36711228 | ||
| CTCF regulates allelic expression of Igf2 by orchestrating a promoter-polycomb repressive complex 2 intrachromosomal loop | Q36959918 | ||
| A randomly integrated transgenic H19 imprinting control region acquires methylation imprinting independently of its establishment in germ cells | Q37302230 | ||
| The H19 differentially methylated region marks the parental origin of a heterologous locus without gametic DNA methylation | Q37424408 | ||
| A 5' 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development | Q40022869 | ||
| Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops | Q42632085 | ||
| The CpG island searcher: a new WWW resource. | Q44689233 | ||
| The H19 methylation imprint is erased and re-established differentially on the parental alleles during male germ cell development | Q47811571 | ||
| Structural characterization of Rasgrf1 and a novel linked imprinted locus. | Q48561797 | ||
| Timing of establishment of paternal methylation imprints in the mouse | Q48806810 | ||
| Methylation imprints of the imprint control region of the SNRPN-gene in human gametes and preimplantation embryos | Q48821601 | ||
| Methylation dynamics of imprinted genes in mouse germ cells. | Q48863844 | ||
| A paternal-specific methylation imprint marks the alleles of the mouse H19 gene | Q49057890 | ||
| Maternal methylation imprints on human chromosome 15 are established during or after fertilization. | Q50717827 | ||
| Antagonism between DNA hypermethylation and enhancer-blocking activity at the H19 DMD is uncovered by CpG mutations. | Q52088468 | ||
| Epigenetic modifications in an imprinting cluster are controlled by a hierarchy of DMRs suggesting long-range chromatin interactions. | Q52109754 | ||
| Elucidation of the minimal sequence required to imprint H19 transgenes. | Q52135344 | ||
| Acquisition of the H19 methylation imprint occurs differentially on the parental alleles during spermatogenesis. | Q52177094 | ||
| Imprinting of mouse Kvlqt1 is developmentally regulated. | Q52188959 | ||
| Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes | Q52214150 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Genomic imprinting and cancer: from primordial germ cells to somatic cells. | Q55101929 | ||
| Epigenetic reprogramming in mouse primordial germ cells | Q57086629 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1108-1115 | |
| P577 | publication date | 2009-12-28 | |
| P1433 | published in | Molecular and Cellular Biology | Q3319478 |
| P1476 | title | H19 imprinting control region methylation requires an imprinted environment only in the male germ line | |
| P478 | volume | 30 |
| Q50981168 | Antisense noncoding RNA promoter regulates the timing of de novo methylation of an imprinting control region. |
| Q34442748 | BACs as tools for the study of genomic imprinting |
| Q33691538 | Complete biallelic insulation at the H19/Igf2 imprinting control region position results in fetal growth retardation and perinatal lethality |
| Q37288310 | DNA methylation in spermatogenesis and male infertility |
| Q35909876 | Epigenetic mechanisms of genomic imprinting: common themes in the regulation of imprinted regions in mammals, plants, and insects |
| Q37961857 | Epigenetics and brain evolution |
| Q47961972 | Fate of methylated/unmethylated H19 imprinting control region after paternal and maternal pronuclear injection |
| Q37961799 | Genetic and epigenetic dysregulation of imprinted genes in the brain |
| Q35857104 | Genomic imprinting: recognition and marking of imprinted loci |
| Q42736811 | H19ICR mediated transcriptional silencing does not require target promoter methylation. |
| Q30373538 | Imprinted DNA methylation reconstituted at a non-imprinted locus. |
| Q34846587 | Insertion of an imprinted insulator into the IgH locus reveals developmentally regulated, transcription-dependent control of V(D)J recombination. |
| Q102331721 | Long non-coding RNA H19 - a new player in the pathogenesis of liver diseases |
| Q37394080 | Low paternal dietary folate alters the mouse sperm epigenome and is associated with negative pregnancy outcomes |
| Q36316644 | More than insulator: multiple roles of CTCF at the H19-Igf2 imprinted domain. |
| Q91344812 | Paternal activation of CB2 cannabinoid receptor impairs placental and embryonic growth via an epigenetic mechanism |
| Q36559183 | Promoter cross-talk via a shared enhancer explains paternally biased expression of Nctc1 at the Igf2/H19/Nctc1 imprinted locus. |
| Q42602150 | Quantitative analysis of DNA methylation at all human imprinted regions reveals preservation of epigenetic stability in adult somatic tissue. |
| Q36606998 | The H19 imprinting control region mediates preimplantation imprinted methylation of nearby sequences in yeast artificial chromosome transgenic mice |
| Q34984578 | The chicken HS4 insulator element does not protect the H19 ICR from differential DNA methylation in yeast artificial chromosome transgenic mouse |
| Q35910635 | Transgenic epigenetics: using transgenic organisms to examine epigenetic phenomena |
| Q31164486 | epiG: statistical inference and profiling of DNA methylation from whole-genome bisulfite sequencing data |
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