| scholarly article | Q13442814 |
| P356 | DOI | 10.1074/JBC.M208437200 |
| P698 | PubMed publication ID | 12270940 |
| P50 | author | Karl Pfeifer | Q56876131 |
| P2093 | author name string | Eric Lee | |
| Paul E Love | |||
| Alexander Grinberg | |||
| Madhulika Srivastava | |||
| Brian Rottinghaus | |||
| Ella Frolova | |||
| Steven P Boe | |||
| P2860 | cites work | Parental imprinting of the mouse H19 gene | Q22122365 |
| A modified and improved method for bisulphite based cytosine methylation analysis | Q24544058 | ||
| Fluorescent dyes for lymphocyte migration and proliferation studies | Q28138476 | ||
| Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse | Q28142099 | ||
| 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 | ||
| Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element | Q28588115 | ||
| Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans | Q28594559 | ||
| Efficient in vivo manipulation of mouse genomic sequences at the zygote stage | Q29547306 | ||
| Genomic imprinting: parental influence on the genome | Q29616227 | ||
| Role for DNA methylation in genomic imprinting | Q29618669 | ||
| An upstream repressor element plays a role in Igf2 imprinting | Q30684867 | ||
| Beckwith-Wiedemann syndrome: imprinting in clusters revisited | Q33838090 | ||
| Regulatory mechanisms at the mouse Igf2/H19 locus. | Q34012897 | ||
| Parental-origin-specific epigenetic modification of the mouse H19 gene | Q34363043 | ||
| Insulators: many functions, many mechanisms. | Q34515901 | ||
| Chromosome methylation patterns during mammalian preimplantation development | Q35205639 | ||
| Igf2 imprinting does not require its own DNA methylation or H19 RNA. | Q35205921 | ||
| Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. | Q35211749 | ||
| The structural H19 gene is required for transgene imprinting | Q35934507 | ||
| Differential effects of zeta and eta transgenes on early alpha/beta T cell development | Q36363091 | ||
| Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome. | Q41066237 | ||
| Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene. | Q41979401 | ||
| Allele-specific expression and total expression levels of imprinted genes during early mouse development: implications for imprinting mechanisms | Q46872744 | ||
| Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5. | Q48000452 | ||
| Bisulfite sequencing in preimplantation embryos: DNA methylation profile of the upstream region of the mouse imprinted H19 gene | Q48933258 | ||
| A paternal-specific methylation imprint marks the alleles of the mouse H19 gene | Q49057890 | ||
| Elucidation of the minimal sequence required to imprint H19 transgenes. | Q52135344 | ||
| Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19. | Q52164786 | ||
| H19 gene expression is up-regulated exclusively by stabilization of the RNA during muscle cell differentiation. | Q53900112 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Monoallelic Expression of Reactivated Imprinted Genes in Embryonal Carcinoma Cell Hybrids | Q57406108 | ||
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 5977-5983 | |
| P577 | publication date | 2002-09-20 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Imprint control element-mediated secondary methylation imprints at the Igf2/H19 locus | |
| P478 | volume | 278 |
| Q27317100 | A Non-Coding RNA Within the Rasgrf1 Locus in Mouse Is Imprinted and Regulated by Its Homologous Chromosome in Trans |
| Q35856849 | Analysis of the H19ICR insulator |
| Q28473208 | Antagonism between DNA and H3K27 methylation at the imprinted Rasgrf1 locus |
| Q37274362 | Applications of the site-specific recombinase Cre to the study of genomic imprinting |
| Q37749881 | Cohesin: a regulator of genome integrity and gene expression |
| Q47114189 | Developmental peculiarities in placentae of ovine uniparental conceptuses. |
| Q34353718 | Developmental profile of H19 differentially methylated domain (DMD) deletion alleles reveals multiple roles of the DMD in regulating allelic expression and DNA methylation at the imprinted H19/Igf2 locus |
| Q52100224 | Diabetic environment in utero and predisposition to type 2 diabetes. |
| Q42736811 | H19ICR mediated transcriptional silencing does not require target promoter methylation. |
| Q54981321 | In Inflamed Intestinal Tissues and Epithelial Cells, Interleukin 22 Signaling Increases Expression of H19 Long Noncoding RNA, Which Promotes Mucosal Regeneration. |
| Q47102226 | Loss of imprinting mutations define both distinct and overlapping roles for misexpression of IGF2 and of H19 lncRNA. |
| Q34189788 | Sequences sufficient for programming imprinted germline DNA methylation defined. |
| Q43123488 | TRIM28 Controls Genomic Imprinting through Distinct Mechanisms during and after Early Genome-wide Reprogramming |
| Q37424408 | The H19 differentially methylated region marks the parental origin of a heterologous locus without gametic DNA methylation |
| Q28505070 | The H19 long noncoding RNA gives rise to microRNAs miR-675-3p and miR-675-5p to promote skeletal muscle differentiation and regeneration |
| Q35221412 | Timing and sequence requirements defined for embryonic maintenance of imprinted DNA methylation at Rasgrf1. |
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