This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Summary of the specific aims of the project.
The specific aims of the project were:
Aim 1. Define the role of DNA methylation- and histone acetylation-mediated regulation of genes in the differentiation of human embryonic stem cells (hESC) into vascular smooth muscle cells (VSMC).
Aim 2. Define the role of DNA methylation- and histone acetylation-mediated regulation of genes in the differentiation of human embryonic stem cells (hESC) into endothelial cells (EC).

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Research Centers in Minority Institutions Award (G12)
Project #
5G12RR003034-24
Application #
7959158
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
2009-06-01
Project End
2010-05-31
Budget Start
2009-06-01
Budget End
2010-05-31
Support Year
24
Fiscal Year
2009
Total Cost
$112,959
Indirect Cost
Name
Morehouse School of Medicine
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
102005451
City
Atlanta
State
GA
Country
United States
Zip Code
30310
Piano, Ilaria; Baba, Kenkichi; Claudia Gargini et al. (2018) Heteromeric MT1/MT2 melatonin receptors modulate the scotopic electroretinogram via PKC? in mice. Exp Eye Res 177:50-54
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