Morphological and immunocytochemical characteristics indicate the yield of early progenitors and represent a quality control for human
mesenchymal stem cell culturing.
Differences between in vitro viability and differentiation and in vivo bone - forming efficacy of human
mesenchymal stem cells cultured on PCL - TCP scaffolds.
Not exact matches
Despite a lack of rigorous clinical trials to test safety or efficacy, a ban of the treatment by health authorities, and a lack of peer review by the scientific community, the privately funded Stamina Foundation has been using
cultured mesenchymal stem cells that have been exposed to putative conditions that favour neuronal differentiation to treat different diseases in severely or terminally ill patients.
«The resulting hydrogel composed of physically self - assembled CarHC polymers exhibited a rapid gel - sol transition on light exposure, which enabled the facile release / recovery of 3T3 fibroblasts and human
mesenchymal stem cells (hMSCs) from 3D
cultures while maintaining their viability.»
Bartosz Balana (Ravens, TUD)-- «Influence of
culture conditions on differentiation and bioelectrical properties of human
mesenchymal stem cells» (2005)
Mesenchymal stem cells inhibit and stimulate mixed lymphocyte
cultures and mitogenic responses independently of the major histocompatibility complex.
Serum free
cultured bone marrow
mesenchymal stem cells as a platform to characterize the effects of specific molecules.
Differential osteogenicity of multiple donor - derived human
mesenchymal stem cells and osteoblasts in monolayer, scaffold - based 3D
culture and in vivo.
Bone marrow - derived
mesenchymal stem cells (BM - MSCs) are obtained by isolating mononucleated
cells from a marrow aspirate by centrifugation on a density gradient, followed by adherent
cell expansion in tissue
culture.
Dr. Masayo Yumoto, team leader of Regenerative Medicine Research & Planning Division, Rohto Pharmaceutical Co., Ltd., has been holding a leadership role in the joint research lab at the Institute of Medical Sciences, University of Tokyo, to develop next generation
cell culture method using human
mesenchymal stem cells.
Cell Culture, Cryopreservation, thawing and processing of Human, Pig and Rat
Mesenchymal Stem Cells and also performed their differentiated them into Adipogenic, Osteogenic and Chondrogenic c
Cells and also performed their differentiated them into Adipogenic, Osteogenic and Chondrogenic
cellscells.