"After taking hair or skin cells from patients with Fanconi anemia, the investigators corrected the defective gene in the patients' cells using gene therapy techniques pioneered in Verma's laboratory. They then successfully reprogrammed the repaired cells into induced pluripotent stem (iPS) cells ... The resulting FA-iPS cells were indistinguishable from human embryonic stem cells and iPS cells generated from healthy donors."Reprogramming cells like computers - like I said, cool.
Tuesday, June 2, 2009
ASC and disease
Pretty cool development reported by Science Daily.