Genomic imprinting in the brain
- 1 August 1997
- journal article
- review article
- Published by Elsevier in Current Opinion in Neurobiology
- Vol. 7 (4), 463-468
- https://doi.org/10.1016/s0959-4388(97)80023-2
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangementsNature Genetics, 1997
- A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndromeNature Genetics, 1997
- 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
- Genomic imprinting and the differential roles of parental genomes in brain developmentDevelopmental Brain Research, 1996
- Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger proteinNature Genetics, 1996
- Distribution of parthenogenetic cells in the mouse brain and their influence on brain development and behavior.Proceedings of the National Academy of Sciences, 1995
- Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader–Willi syndrome regionNature Genetics, 1992
- Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader–Willi syndrome critical regionNature Genetics, 1992
- Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesisNature, 1984