Unknown,Transcriptomics,Genomics,Proteomics

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Gene expression data from undifferentiated mouse embryonal carcinoma cell strains (MOE430A and MOE430B)


ABSTRACT: Gene expression profiles of undifferentiated mouse embryonal carcinoma cell strains (P19, P19CL6, and 4 P19CL6 sublines) were obtained, using Affymetrix GeneChip Mouse Genome 430A and 430B. Heart diseases such as cardiac infarction damage cardiomyocytes and consequently lead to significant loss of the contractile capacity of the heart. To repair functions of the injured heart, a great deal of research has attempted to develop regenerative medicine using pluripotent stem cell-based cardiomyocytes as cell therapy products. However, the efficiency of the current methods available for the cardiac differentiation of stem cells is insufficient for clinical settings. A comprehensive understanding of the mechanism involved in the cardiac differentiation of stem cells is necessary to improve the differentiation efficiency. To identify genes assosiated with cardiomyogenic potential, we isolated P19CL6 cell sublines possessing distinct properties in cardiomyogenesis and comprared their transcriptome profiles with those of mouse embryonal carcinoma P19 and P19CL6 cells. Total RNA isolated from undifferentiated EC cell strains (P19 cells, P19CL6 cells, and 4 P19CL6 sublines) using Affymetrix chips MOE430A and MOE430AB. CEL files unavailable.

ORGANISM(S): Mus musculus

SUBMITTER: Yoji Sato 

PROVIDER: E-GEOD-26875 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

AW551984: a novel regulator of cardiomyogenesis in pluripotent embryonic cells.

Yasuda Satoshi S   Hasegawa Tetsuya T   Hosono Tetsuji T   Satoh Mitsutoshi M   Watanabe Kei K   Ono Kageyoshi K   Shimizu Shunichi S   Hayakawa Takao T   Yamaguchi Teruhide T   Suzuki Kazuhiro K   Sato Yoji Y  

The Biochemical journal 20110701 2


An understanding of the mechanism that regulates the cardiac differentiation of pluripotent stem cells is necessary for the effective generation and expansion of cardiomyocytes as cell therapy products. In the present study, we have identified genes that modulate the cardiac differentiation of pluripotent embryonic cells. We isolated P19CL6 cell sublines that possess distinct properties in cardiomyogenesis and extracted 24 CMR (cardiomyogenesis-related candidate) genes correlated with cardiomyog  ...[more]

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