Cultured human retinal pigment epithelial (RPE) cells of different passages (P0 and P3) were used as a model system to examine changes in gene expression in proliferating RPE cells by polymerase chain reaction (PCR)-based differential expressed mRNA analysis (DEmRNA-PCR). DEmRNA-PCR showed enhanced
Quantifying the activation of the small molecular weight G-protein ras
β Scribed by Katharine Chapman; David J. Hall
- Publisher
- The American Society for Biochemistry and Molecular Biology
- Year
- 2005
- Tongue
- English
- Weight
- 110 KB
- Volume
- 33
- Category
- Article
- ISSN
- 1470-8175
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