
My research is primarily directed at understanding the mechanisms by which human embryonic stem cells maintain pluripotency and to find out ways to prolong the pluripotent state of hESCs in vitro. My studies indicate that noggin, a BMP4 antagonist, is effective in preventing spontaneous differentiation in hESC culture on Matrigel for up to two weeks. The current research is focused at finding out the involvement of various signal transduction pathways involved in maintenance of pluripotency by noggin. Another recent project is a xenobiotic stimulation of human embryonic stem cells to differentiatethem in to kidney lineage by using embryonic kidney conditioned media. I am also involved in finding out the nature of heteromeric protein complex formed by Egr, Nab and CBP on the LH beta promoter in gonadotrophs.
