Human chromosome 21q22.2-qter carries a gene(s) responsible for downregulation of mlc2a and PEBP in Down syndrome model mice
- 30 April 2004
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 317 (2) , 491-499
- https://doi.org/10.1016/j.bbrc.2004.03.069
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education, Culture, Sports, Science and Technology
- Ministry of Health, Labour and Welfare
This publication has 29 references indexed in Scilit:
- Mice containing a human chromosome 21 model behavioral impairment and cardiac anomalies of Down's syndrome.Human Molecular Genetics, 2001
- Down syndrome congenital heart disease: A narrowed region and a candidate geneGenetics in Medicine, 2001
- Too much of a good thing: mechanisms of gene action in Down syndromeTrends in Genetics, 2001
- Genetic Dissection of Region Associated with Behavioral Abnormalities in Mouse Models for Down SyndromePediatric Research, 2000
- 10 Years ofGenomics,Chromosome 21, and Down SyndromeGenomics, 1998
- Ts1Cje, a partial trisomy 16 mouse model for Down syndrome, exhibits learning and behavioral abnormalitiesProceedings of the National Academy of Sciences, 1998
- A mouse model for Down syndrome exhibits learning and behaviour deficitsNature Genetics, 1995
- Down syndrome phenotypes: the consequences of chromosomal imbalance.Proceedings of the National Academy of Sciences, 1994
- Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.Proceedings of the National Academy of Sciences, 1989
- TRISOMY IN MANAnnual Review of Genetics, 1984