• progenitor
  • $3.52 million Directing hES Derived Progenitor Cells into Musculoskeletal Lineages , David W. Rowe, principal investigator, UConn Health Center and UConn. (uconn.edu)
  • ethical
  • Last month, a separate group of scientists conducted a peer review evaluating all the applications, and ranked each proposal for the state stem cell panel with respect to ethical and scientific merit. (uconn.edu)
  • research
  • These techniques will be able to provide safe and stable seeding cells for research and clinical application. (diva-portal.org)
  • The disbursements are the first made under Connecticut's 10-year, $100 million commitment to fund stem cell research, as authorized by Gov. M. Jodi Rell and the General Assembly in 2005. (uconn.edu)
  • Eight Connecticut-based universities and non-profit institutes submitted 70 research proposals totaling $65 million to the state stem cell panel. (uconn.edu)
  • The plan calls for $1 billion in research funding (about half for work on stem cells) and the creation of a post for a science and technology director. (scienceblogs.com)
  • cycle
  • $200,000 Cell Cycle and Nuclear Reprogramming by Somatic Cell Fusion , Winfried Krueger, principal investigator, UConn Health Center. (uconn.edu)
  • Department
  • $200,000 Quantitative Analysis of Molecular Transport and Population Kinetics of Stem Cell Cultivation in a Microfluidic System , Tai-Hsi Fan, principal investigator, Department of Mechanical Engineering. (uconn.edu)
  • However
  • However, in pluripotent stem cells of primates including humans, it is not easy to grow the cells while maintaining the cell-specific properties, i.e., undifferentiation status and pluripotency (multipotency). (patentsencyclopedia.com)
  • However, the passage process in culture in coexistence with feeder cells is complicated, and many of substances for maintaining undifferentiation status are expensive. (patentsencyclopedia.com)
  • presence
  • In vitro, in the presence of VEGF(165), hAC133(+) cells only adopted a venous and microvascular EC phenotype, while hMAPCs differentiated into both arterial and venous ECs, possibly because hMAPCs expressed significantly more sonic hedgehog (Shh) and its receptors as well as Notch 1 and 3 receptors and some of their ligands. (cun.es)