80) Human bone marrow-derived mesenchymal stem |
81) rce of growth factors shown to facilitate human bone growth. |
82) of dedifferentiated fat cells (DFATs) and human bone marrow mesenchymal stem cells ( |
83) The hypothesis of this work was that human bone marrow-derived mesenchymal stem |
84) somes do not have any cytotoxic effect on human bone marrow-derived mesenchymal stem |
85) We tested both human bone marrow-derived mesenchymal stem |
86) m cell fraction (STRO-1 positive cell) of human bone marrow. |
87) ecting "opening a bottle" was explored in human subjects by electromyographic (EMG) |
88) nce and absence of a medical condition in human subjects is often modelled as an out |
89) Here, we assessed in healthy human subjects whether PFC subareas have d |
90) us controlled testing of interventions on human subjects. |
91) re analyzed in postmortem tissues from 20 human subjects. |
92) s of topical sildenafil on PrU healing in human subjects. |
93) gh recidivism and poor study retention in human subjects. |
94) Human umbilical cord blood (hUCB) has been |
95) Human umbilical vessels have been recogniz |
96) MSCs were isolated from human umbilical cord or adipose tissue. |
97) lial nitric oxide (NO) synthase (eNOS) in human umbilical vein endothelial cells (HU |
98) vestigated the role of CIT in adhesion of human umbilical vein endothelial cells (HU |
99) s in stem cell mono- and co-cultures with human umbilical vein endothelial cells (HU |
100) Whereas endothelium-denuded human umbilical veins (HUVs) have been suc |
101) ssed their in vitro antitumor activity in human cancer cell lines (HTLA-230 neurobla |
102) lso showed potential cytotoxicity against human cancer cell lines with IC50 ranging |
103) ; it is known to inhibit proliferation of human cancer cells. |
104) Lastly, in a murine and human cancer model, the SPIIF was able to |
105) pHO) is known to occur in both canine and human cancer patients. |
106) itive and specific biomarkers for several human cancer types. |
107) Human hepatocytes that were cocultured dir |
108) Primary human hepatocytes represent an important c |
109) em for pharmacological studies on primary human hepatocytes under defined serum-free |
110) tabolic activity and stability of primary human hepatocytes was studied in this bior |
111) Thus, coculture of human hepatocytes with MSCs demonstrates b |
112) es, but few studies currently use primary human hepatocytes. |
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