DNA methylation in genomic imprinting
Open Access
- 1 April 1997
- journal article
- review article
- Published by Elsevier in Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
- Vol. 386 (2) , 131-140
- https://doi.org/10.1016/s1383-5742(96)00049-x
Abstract
No abstract availableKeywords
This publication has 70 references indexed in Scilit:
- Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequenciesCurrent Biology, 1995
- Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15Nature Genetics, 1995
- Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control regionNature Genetics, 1994
- Epigenetic lesions at the H19 locus in Wilms' tumour patientsNature Genetics, 1994
- Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumourNature Genetics, 1994
- Role for DNA methylation in genomic imprintingNature, 1993
- Modification of 15q11 — q13 DNA methylation imprints in unique Angelman and Prader — Willi patientsHuman Molecular Genetics, 1993
- Targeted mutation of the DNA methyltransferase gene results in embryonic lethalityPublished by Elsevier ,1992
- Monoallelic expression of the human H19 geneNature Genetics, 1992
- Sex difference in methylation of single-copy genes in human meiotic germ cells: Implications for X chromosome inactivation, parental imprinting, and origin of CpG mutationsSomatic Cell and Molecular Genetics, 1990