322) eNOS) in human umbilical vein endothelial cells (HUVECs) to evaluate the involvement |
323) esion of human umbilical vein endothelial cells (HUVECs) together with the stimulati |
324) res with human umbilical vein endothelial cells (HUVECs). |
325) Human mesenchymal stem cells (hMSCs) adhered, proliferated and di |
326) s the use of adult human mesenchymal stem cells (hMSCs) as an alternative to autolog |
327) Human mesenchymal stem cells (hMSCs) or autologous bovine NP cell |
328) Cells exposed to Pb(2+) also increased pro |
329) alyze cultures of human gastric carcinoma cells exposed to 10 μM lead nitrate. |
330) cessary for gastrin gene transcription in cells exposed to Pb(2+) . |
331) The cells have been shown to circulate in reci |
332) ystems of endothelial and osteoblast-like cells have shown evidence of BTE efficacy |
333) uggest that bone marrow (BM)-derived stem cells have therapeutic efficacy in neonata |
334) Cardiac progenitor cells isolated from adult rats were seeded |
335) urface markers and gene profiling of stem cells isolated from different sources, viz |
336) Fibroblast-like cells isolated from the olfactory bulb of |
337) 2 O2 ; 1, 10, 25, and 50 µM) of the gill cells showed a significant increase in the |
338) The SaOS-2 cells showed an increased growth if silica |
339) The cells showed positive chemotaxis towards C |
340) Using stem cells, we can recapitulate this process an |
341) importance of NO expression by the seeded cells, we created TEBV using autologous AS |
342) ell cycle dynamics in cortical progenitor cells, we generated cerebral cortex-specif |
343) Adipose-derived stem cells (ASCs), as a fascinating cell source |
344) ring strategies with adipose-derived stem cells (ASCs), the focus of this study was |
345) s of the ceramics and bone marrow stromal cells (BMSCs) into the bone defect (mandib |
346) entiation of bone marrow mesenchymal stem cells (BMSCs) on the composite scaffold we |
347) in which human endothelial colony-forming cells (ECFCs) and human mesenchymal progen |
348) d (CB)-derived endothelial colony-forming cells (ECFCs) fulfil these requirements. |
349) res of UCB haematopoietic stem/progenitor cells (HSCs) for the treatment of blood-re |
350) In liver sinusoids, hepatic stellate cells (HSCs) locate the outer surface of m |
351) e incorporation into DNA of proliferating cells after 4 h (70% of control) and 48 h |
352) CSLM showed a visual increase of dead cells after PDT. |
353) ct the differentiation rate of adult stem cells by regulating mitochondrial metaboli |
354) ted to increase the numbers of transfused cells by stimulating normal granulocyte do |
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