Source:http://linkedlifedata.com/resource/pubmed/id/20728443
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
18
|
pubmed:dateCreated |
2010-9-27
|
pubmed:abstractText |
We analyzed the mRNA diversity of genes after inducing neuronal differentiation in human NT2 teratocarcinoma cells using all-trans retinoic acid (RA). DNA microarray analyses of cells treated with RA identified 358 RA-responsive genes. mRNA diversity analysis revealed that 274 genes produced multiple protein-coding transcripts by alternative splicing. Among these 274 genes, we chose 26 genes that showed AS in their C-terminus and 12 transcription factor genes for further analysis. By using transcript-specific primers, we performed quantitative real-time PCR analysis to examine the expression profiles of all the protein-coding transcripts. Consequently, we identified genes which showed different RA-induced changes in the expression of their protein-coding transcripts.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Sep
|
pubmed:issn |
1873-3468
|
pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
|
pubmed:issnType |
Electronic
|
pubmed:day |
24
|
pubmed:volume |
584
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
4041-7
|
pubmed:meshHeading |
pubmed-meshheading:20728443-Alternative Splicing,
pubmed-meshheading:20728443-Cell Line, Tumor,
pubmed-meshheading:20728443-Gene Expression,
pubmed-meshheading:20728443-Humans,
pubmed-meshheading:20728443-Neurogenesis,
pubmed-meshheading:20728443-Oligonucleotide Array Sequence Analysis,
pubmed-meshheading:20728443-Pluripotent Stem Cells,
pubmed-meshheading:20728443-Transcription, Genetic,
pubmed-meshheading:20728443-Transcription Factors,
pubmed-meshheading:20728443-Tretinoin
|
pubmed:year |
2010
|
pubmed:articleTitle |
Alternative splicing of genes during neuronal differentiation of NT2 pluripotential human embryonal carcinoma cells.
|
pubmed:affiliation |
Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|