Towards unravelling the Igf2/H19 imprinted domain

BioEssays

Volumn 17, Issue 10, 1995, Pages 835-838

  Viville, Stéphane ^a   Surani, M Azim ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

H19 RNA; MUSCLE PROTEIN;

ANIMAL; ARTICLE; GENE EXPRESSION REGULATION; GENETICS; GENOME IMPRINTING; MOUSE; PRENATAL DEVELOPMENT;

ANIMAL; EMBRYO AND FETAL DEVELOPMENT; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENOMIC IMPRINTING; MICE; MUSCLE PROTEINS; SUPPORT, NON-U.S. GOV'T;

EID: 0029379777     PISSN: 02659247     EISSN: 15211878     Source Type: Journal    
DOI: 10.1002/bies.950171004     Document Type: Article

References (23)

1. Disruption of imprinting caused by deletion of the H19 gene region in mice
2. Differential imprinting and expression of maternal and paternal genomes
3. Molecular and embryological investigations of parental imprinting on mouse chromosome 7
4. Parental imprinting of the mouse Insulin‐like growth factor II gene
5. Parental imprinting of the mouse H19 gene
6. Tissue‐ and developmental stage‐specific imprinting of the mouse proinsulin gene, Ins2
7. Genomic imprinting of Mash2, a mouse gene required for trophoblast development
8. Physical linkage of two mammalian imprinted genes, H19 and Igf2
9. Paternal origin of 11p15 duplications in the Beckwith‐Wiedemann syndrome
10. Constitutional relaxation of insulin‐like growth factor II gene imprinting associated with Wilms' tumour and gigantism
11. Relaxation of imprinted genes in human cancer
12. Allelic methylation of H19 and IGF2 in the Beckwith‐Wiedemann syndrome
13. Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin‐like growth factor II (Igf2) gene
14. Parental‐origin‐specific modification of the mouse H19 gene
15. Epigenetic mechanisms underlying the imprinting of the mouse H19 gene
16. A paternal‐specific methylation imprint marks the alleles of the mouse H19 gene
17. Comparative analysis of Igf‐2/H19 imprinted domain: identification of a highly conserved intergenic DNasel hypersensitive region
18. Two regulatory domains flank the mouse H19 gene
19. Targeted mutation of the DNA methyltransferase gene results in embryonic lethality
20. Role of DNA methylation in genomic imprinting
21. Inherited microdeletions in the Angelman and Prader‐Willi syndromes define an imprinting centre on human chromosome 15
22. Ectopic expression of the H19 gene in mice causes prenatal lethality