Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Xiaolu Sturgeon"'
Publikováno v:
Journal of Proteome Research. 11:1251-1263
The Ts65Dn mouse model of Down syndrome (DS) is trisomic for orthologs of 88 of 161 classical protein coding genes present on human chromosome 21 (HSA21). Ts65Dn mice display learning and memory impairments and neuroanatomical, electrophysiological,
Autor:
Xiaolu Sturgeon, Katheleen Gardiner
Publikováno v:
Mammalian Genome. 22:261-271
A comprehensive representation of the gene content of the long arm of human chromosome 21 (Hsa21q) remains of interest for the study of Down syndrome, its associated phenotypic features, and mouse models. Here we compare transcript catalogs for Hsa21
Publikováno v:
Progress in brain research. 197
Major efforts in Down syndrome (DS) research have been directed at the identification and functional characterization of genes encoded by human chromosome 21 (HSA21). In parallel with this, tissue samples and cell lines derived from individuals with
Major efforts in Down syndrome (DS) research have been directed at the identification and functional characterization of genes encoded by human chromosome 21 (HSA21). In parallel with this, tissue samples and cell lines derived from individuals with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7b8faece6ce0487a3cf4467cb60f36f
https://doi.org/10.1016/b978-0-444-54299-1.00005-4
https://doi.org/10.1016/b978-0-444-54299-1.00005-4