GABAA receptor β3 subunit gene-deficient heterozygous mice show parent-of-origin and gender-related differences in β3 subunit levels, EEG, and behavior
- 30 June 2005
- journal article
- Published by Elsevier BV in Developmental Brain Research
- Vol. 157 (2), 150-161
- https://doi.org/10.1016/j.devbrainres.2005.03.014
Abstract
No abstract availableKeywords
This publication has 60 references indexed in Scilit:
- Analysis of imprinting in mice with uniparental duplication of proximal chromosomes 7 and 15 by use of a custom oligonucleotide microarrayMammalian Genome, 2004
- Exceptionally mild Angelman syndrome phenotype associated with an incomplete imprinting defectJournal of Medical Genetics, 2002
- Functional characterization of the new human GABAA receptor mutation β3(R192H)Human Genetics, 2002
- Learning about the context in genetically-defined miceBehavioural Brain Research, 2001
- Single gene defects in mice: the role of voltage-dependent calcium channels in absence modelsEpilepsy Research, 1999
- Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neuronsNature Genetics, 1997
- Different Mechanisms and Recurrence Risks of Imprinting Defects in Angelman SyndromeAmerican Journal of Human Genetics, 1997
- Angelman syndrome due to paternal uniparental disomy of chromosome 15: A milder phenotype?American Journal of Medical Genetics, 1994
- Protein kinase C and cAMP-dependent protein kinase phosphorylate the beta subunit of the purified gamma-aminobutyric acid A receptor.Proceedings of the National Academy of Sciences of the United States of America, 1990
- ‘Puppet’ Children A Report on Three CasesDevelopmental Medicine and Child Neurology, 1965