Post Profile

Autologous Induced Pluripotent Stem Cells And Gene Repair Therapy For Treatment Of Familial Hypercholesterolemia

Study shows, for the first time, the successful reprogramming of diseased human hepatocytes into induced pluripotent stem cells (iPSC).1 Results also found differentiation into mature hepatocytes was more efficient than that with fibroblast-derived iPSCs. The generation of diseased hepatocyte-derived human iPSC lines provides a good basis for the study of liver disease pathogenesis...
read more


Related Posts

New Method To Produce Blood Cells From Stem Cells Could Yield A Purer, Safer Cell Therapy

Health : Medical News Today

A new protocol for reprogramming induced pluripotent stem cells (iPSCs) into mature blood cells, using just a small amount of the patient's own blood and a readily available cell type, is reported on in the current issue of STEM CEL...

Reprogramming patients' cells offers powerful new tool for studying, treating blood diseases

Health : Medical News Today

CHOP researchers advance stem cell studies in a childhood leukemia and diamond blackfan anemia First produced only in the past decade, human induced pluripotent stem cells (iPSCs) are capable of developing into many or even all huma...

New Study Sheds Light On Cellular Reprogramming

Health : Medical News Today

Mature cells can be reprogrammed to pluripotency and thus regain the ability to divide and differentiate into specialized cell types. Although these so-called induced pluripotent stem cells (iPS cells) represent a milestone in stem ...

Reprogramming Patients' Cells Offers Powerful New Tool for Studying, Treating Blood Diseases

Health : Newswise Medical News

Scientists reprogrammed skin cells from patients with rare blood disorders into human induced pluripotent stem cells, highlighting the great promise of iPSCs in advancing understanding of and eventually treating such diseases.

Medical News Today: Cure for mitochondrial diseases steps closer with stem cell breakthrough

Health : Medical News Today

A new study shows how scientists used two complementary cell reprogramming methods to create mutation-free lines of stem cells from human patients with mitochondrial diseases.


Copyright © 2016 Regator, LLC