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MicroRNA induced cardiac reprogramming in vivo: evidence for mature cardiac myocytes and improved cardiac function.

Circulation research | 2015

A major goal for the treatment of heart tissue damaged by cardiac injury is to develop strategies for restoring healthy heart muscle through the regeneration and repair of damaged myocardium. We recently demonstrated that administration of a specific combination of microRNAs (miR combo) into the infarcted myocardium leads to direct in vivo reprogramming of noncardiac myocytes to cardiac myocytes. However, the biological and functional consequences of such reprogramming are not yet known.

Pubmed ID: 25351576 RIS Download

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Associated grants

  • Agency: NHLBI NIH HHS, United States
    Id: HL73219
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL093470
  • Agency: NHLBI NIH HHS, United States
    Id: R01-HL093470
  • Agency: NHLBI NIH HHS, United States
    Id: HL72010
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL073219
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL081744
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL81744
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL072010

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Gene Expression Omnibus (GEO) (tool)

RRID:SCR_005012

Functional genomics data repository supporting MIAME-compliant data submissions. Includes microarray-based experiments measuring the abundance of mRNA, genomic DNA, and protein molecules, as well as non-array-based technologies such as serial analysis of gene expression (SAGE) and mass spectrometry proteomic technology. Array- and sequence-based data are accepted. Collection of curated gene expression DataSets, as well as original Series and Platform records. The database can be searched using keywords, organism, DataSet type and authors. DataSet records contain additional resources including cluster tools and differential expression queries.

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