Zobrazeno 1 - 9
of 9
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,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecf228c92b20f8d0556563396b51b214
https://doi.org/10.1021/pr2011582
https://doi.org/10.1021/pr2011582
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2aa9d0d1fdf12510a3c6f34de5e55a4
https://doi.org/10.1007/s00335-011-9321-y
https://doi.org/10.1007/s00335-011-9321-y
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f6876a9b75b8e5f77288827a3a4e5b87
https://pubmed.ncbi.nlm.nih.gov/22541289
https://pubmed.ncbi.nlm.nih.gov/22541289
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
Autor:
Sturgeon, Xiaolu1, Gardiner, Katheleen J.1 katheleen.gardiner@ucdenver.edu
Publikováno v:
Mammalian Genome. Jun2011, Vol. 22 Issue 5/6, p261-271. 11p. 1 Diagram, 5 Charts, 1 Graph.
Publikováno v:
Journal of Bioinformatics & Computational Biology; Jun2018, Vol. 16 Issue 3, pN.PAG-N.PAG, 17p
Autor:
Ahmed, Md. Mahiuddin, Dhanasekaran, A. Ranjitha, Tong, Suhong, Wiseman, Frances K., Fisher, Elizabeth M.C., Tybulewicz, Victor L.J., Gardiner, Katheleen J.
Publikováno v:
Human Molecular Genetics; May2013, Vol. 22 Issue 9, p1709-1724, 16p
Autor:
Remi Kalir, Antero Garcia
An introduction to annotation as a genre--a synthesis of reading, thinking, writing, and communication--and its significance in scholarship and everyday life.Annotation--the addition of a note to a text--is an everyday and social activity that provid
Autor:
Mara Dierssen, Rafa de la Torre
Down syndrome (DS) is the most common example of neurogenetic aneuploid disorder leading to mental retardation. In most cases, DS results from an extra copy of chromosome 21 (HSA21) producing deregulated gene expression in brain that gives raise to s