| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/DVG.1020170309 |
| P698 | PubMed publication ID | 8565330 |
| P50 | author | Wolf Reik | Q15994704 |
| Robert Feil | Q30380330 | ||
| Nicholas Allen | Q58887759 | ||
| P2093 | author name string | Handel MA | |
| P2860 | cites work | Parental imprinting of the mouse H19 gene | Q22122365 |
| Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region | Q28242397 | ||
| Disruption of imprinting caused by deletion of the H19 gene region in mice | Q28287765 | ||
| Cloning and sequencing of a cDNA encoding DNA methyltransferase of mouse cells | Q29399636 | ||
| Role for DNA methylation in genomic imprinting | Q29618669 | ||
| The ontogeny of allele-specific methylation associated with imprinted genes in the mouse. | Q34059933 | ||
| Nuclease hypersensitive sites in chromatin | Q34164152 | ||
| Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. | Q34314269 | ||
| Parental-origin-specific epigenetic modification of the mouse H19 gene | Q34363043 | ||
| Chromatin as an essential part of the transcriptional mechanim | Q36740976 | ||
| Genomic imprinting of Mash2, a mouse gene required for trophoblast development | Q38298288 | ||
| The bulk chromatin structure of a murine transgene does not vary with its transcriptional or DNA methylation status | Q40021738 | ||
| Allele-specific replication timing of imprinted gene regions | Q41541045 | ||
| Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene. | Q41979401 | ||
| Evolution of Insulin-Like Growth Factor II: Characterization of the Mouse IGF-II Gene and Identification of Two Pseudo-Exons | Q42615815 | ||
| Promoter-specific imprinting of the human insulin-like growth factor-II gene | Q46095293 | ||
| Parental imprinting of the Mas protooncogene in mouse | Q46725382 | ||
| Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting | Q48084682 | ||
| Mosaic and polymorphic imprinting of the WT1 gene in humans | Q48084685 | ||
| Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method | Q48086267 | ||
| Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal. | Q48125063 | ||
| A paternal-specific methylation imprint marks the alleles of the mouse H19 gene | Q49057890 | ||
| Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line | Q50792932 | ||
| Tissue- and developmental stage-specific imprinting of the mouse proinsulin gene, Ins2. | Q52209136 | ||
| Comparative analysis of Igf-2/H19 imprinted domain: identification of a highly conserved intergenic DNase I hypersensitive region. | Q52213159 | ||
| Discriminating translation of insulin-like growth factor-II (IGF-II) during mouse embryogenesis. | Q52213178 | ||
| Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome. | Q52215312 | ||
| Identification of an antisense transcript from the IGF-II locus in mouse. | Q52223595 | ||
| The 5' ends of Drosophila heat shock genes in chromatin are hypersensitive to DNase I. | Q52526056 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Embryological and molecular investigations of parental imprinting on mouse chromosome 7. | Q55052972 | ||
| Epigenetic control of transgene expression and imprinting by genotype-specific modifiers | Q57086711 | ||
| Functional Polymorphism in the Parental Imprinting of the Human IGF2R Gene | Q57500167 | ||
| The insulin–like growth factor type–2 receptor gene is imprinted in the mouse but not in humans | Q58061470 | ||
| A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes | Q68019576 | ||
| Genome imprinting phenomena on mouse chromosome 7 | Q68650344 | ||
| Cellular mosaicism in the methylation and expression of hemizygous loci in the mouse | Q69417100 | ||
| Analysis of hypersensitive sites in chromatin | Q69705456 | ||
| The presence and active transcription of three independent leader exons in the mouse insulin-like growth factor II gene | Q70146295 | ||
| A strain-specific modifier on mouse chromosome 4 controls the methylation of independent transgene loci | Q70176882 | ||
| Parental imprinting of an Igf-2 transgene | Q70478296 | ||
| Epigenetic mechanisms underlying the imprinting of the mouse H19 gene | Q72094721 | ||
| Tissue-specific and allele-specific replication timing control in the imprinted human Prader-Willi syndrome region | Q72130899 | ||
| Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia | Q72686253 | ||
| Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour | Q72703028 | ||
| Epigenetic lesions at the H19 locus in Wilms' tumour patients | Q72703033 | ||
| The inactive X chromosome in female mammals is distinguished by a lack of histone H4 acetylation, a cytogenetic marker for gene expression | Q72863039 | ||
| P433 | issue | 3 | |
| P304 | page(s) | 240-252 | |
| P577 | publication date | 1995-01-01 | |
| P1433 | published in | Genesis | Q5532784 |
| P1476 | title | Chromatin structure and imprinting: developmental control of DNase-I sensitivity in the mouse insulin-like growth factor 2 gene | |
| P478 | volume | 17 |
| Q30684867 | An upstream repressor element plays a role in Igf2 imprinting |
| Q36421340 | CTCF is the master organizer of domain-wide allele-specific chromatin at the H19/Igf2 imprinted region |
| Q36238491 | Chromosome loops, insulators, and histone methylation: new insights into regulation of imprinting in clusters. |
| Q52164786 | Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19. |
| Q53608718 | Epigenetic regulation of the imprinted U2af1-rs1 gene during retinoic acid-induced differentiation of embryonic stem cells. |
| Q95817510 | Focus on genome imprinting |
| Q35250186 | Genomic imprinting: a chromatin connection |
| Q39733758 | Imprinting regulation of the murine Meg1/Grb10 and human GRB10 genes; roles of brain-specific promoters and mouse-specific CTCF-binding sites. |
| Q33957648 | Parental allele-specific chromatin configuration in a boundary-imprinting-control element upstream of the mouse H19 gene |
| Q48637146 | Parental chromosome-specific chromatin conformation in the imprinted U2af1-rs1 gene in the mouse. |
| Q31864191 | Relationship between DNA methylation, histone H4 acetylation and gene expression in the mouse imprinted Igf2-H19 domain. |
| Q73077079 | Role of histone acetylation and DNA methylation in the maintenance of the imprinted expression of the H19 and Igf2 genes |
| Q53658423 | Transcription cooperation by NFAT.C/EBP composite enhancer complex. |
| Q52180058 | Transcriptional regulation and biological significance of the insulin like growth factor II gene. |
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