Transcriptome analysis of genetically matched human induced pluripotent stem cells disomic or trisomic for chromosome 21.
Trisomy of chromosome 21, the genetic cause of Down syndrome, has the potential to alter expression of genes on chromosome 21, as well as other locations throughout the genome. These transcriptome changes are likely to underlie the Down syndrome clinical phenotypes. We have employed RNA-seq to under...
Main Authors: | Patrick K Gonzales, Christine M Roberts, Virginia Fonte, Connor Jacobsen, Gretchen H Stein, Christopher D Link |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2018-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC5870938?pdf=render |
Similar Items
-
Trisomy 21-associated increases in chromosomal instability are unmasked by comparing isogenic trisomic/disomic leukocytes from people with mosaic Down syndrome.
by: Kelly Rafferty, et al.
Published: (2021-01-01) -
Chromosome mis-segregation and cytokinesis failure in trisomic human cells
by: Joshua M Nicholson, et al.
Published: (2015-05-01) -
Chromosome-pairing in trisomic spermatocytes of males with normal or altered karyotypes
by: Basrur PK, et al.
Published: (1991-08-01) -
Down Syndrome Cognitive Phenotypes Modeled in Mice Trisomic for All HSA 21 Homologues.
by: Pavel V Belichenko, et al.
Published: (2015-01-01) -
Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction
by: Sandra Chantot-Bastaraud, et al.
Published: (2017-07-01)