Genomic imprinting, uniparental disomy and foetal growth

Trends in Endocrinology and Metabolism

Volumn 11, Issue 7, 2000, Pages 270-275

  Preece, Michael A ^a   Moore, Gudrun E ^b  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b QUEEN CHARLOTTE S AND CHELSEA HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

FETUS GROWTH; GENE EXPRESSION; GENOME IMPRINTING; GROWTH DISORDER; HUMAN; METHYLATION; MOLECULAR EVOLUTION; NONHUMAN; PATHOGENESIS; PRENATAL DEVELOPMENT; PRIORITY JOURNAL; REVIEW; UNIPARENTAL DISOMY;

ANIMALS; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; EMBRYONIC AND FETAL DEVELOPMENT; GENOMIC IMPRINTING; HUMANS;

EID: 0033838266     PISSN: 10432760     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1043-2760(00)00277-0     Document Type: Review

References (43)

1. Nuclear transplantation in the mouse embryo by microsurgery and cell fusion
2. Development of mouse embryogenesis requires both the maternal and paternal genomes
3. Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis
4. Genetic studies on hydatidiform moles
5. Two different phenotypes of fetuses with chromosomal triploidy: Correlation with parental origin of the extra haploid set
6. Role of DNA methylation in genomic imprinting
7. Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern
8. Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster
9. A paternal-specific methylation imprint marks the alleles of the mouse H19 gene
10. Maternal-specific methylation of the imprinted mouse specific Igf2r locus identifies the expressed locus as carrying the imprinting signal
11. Imprinted expression of the Igf2r gene depends on an intronic CpG island
12. A mouse model for Prader-Willi syndrome imprinting-centre mutations
13. Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2
14. Characteristics of imprinted genes
15. DNA demethylation in vitro: Involvement of RNA
16. Sex-specific exons control DNA methyltransferase in mammalian germ cells
17. Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex
18. An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript (letter)
19. LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids
20. Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2
21. Genomic imprinting: A chromatin connection
22. Allele-specific replication timing of imprinted gene regions
23. Sex-specific meiotic recombination in the Prader-Willi/Angelman syndrome imprinted region
24. Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies
25. Methylation and imprinting: From host defense to gene regulation?
26. Genomic imprinting: Defusing the ovarian time bomb
27. Genomic imprinting in mammalian development: A parental tug-of-war
28. Growth effects of uniparental disomies and the conflict theory of genomic imprinting
29. Uniparental disomy, isodisomy, and imprinting: Probable effects in man and strategies for their detection
30. Variation in the frequency and type of sperm chromosomal abnormalities among normal men
31. Chromosomal analysis of human oocytes recovered from preovulatory follicles in stimulated cycles
32. Autosomal and X-chromosome imprinting
33. Chromosome 15 uniparental disomy is not frequent in Angelman syndrome
34. The frequency of uniparental disomy in Prader-Willi syndrome
35. New insights reveal complex mechanisms involved in genomic imprinting
36. A clinical overview of overgrowth syndromes
37. Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation
38. Maternal uniparental disomy 7 in the Silver-Russell syndrome
39. An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands
40. Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndrome
41. Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome
42. Gametic imprinting in mammals
43. A catalogue of imprinted genes and parent-of-origin effects in humans and animals