Imprinting in Prader–Willi and Angelman syndromes
- 1 May 1998
- journal article
- review article
- Published by Elsevier BV in Trends in Genetics
- Vol. 14 (5), 194-200
- https://doi.org/10.1016/s0168-9525(98)01432-2
Abstract
No abstract availableKeywords
This publication has 55 references indexed in Scilit:
- De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndromeNature Genetics, 1997
- UBE3A/E6-AP mutations cause Angelman syndromeNature Genetics, 1997
- Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN geneNature Genetics, 1996
- Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15Nature Genetics, 1995
- A family of proteins structurally and functionally related to the E6-AP ubiquitin-protein ligase.Proceedings of the National Academy of Sciences of the United States of America, 1995
- Protein ubiquitination involving an E1–E2–E3 enzyme ubiquitin thioester cascadeNature, 1995
- Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control regionNature Genetics, 1994
- Angelman syndrome due to paternal uniparental disomy of chromosome 15: A milder phenotype?American Journal of Medical 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