365) s expressed COX-1 and COX-2 and the SCCF2 cells had increased COX-2 mRNA expression |
366) SEM showed that experimental group cells had more fat-like cells, whose volum |
367) lyzed by coculture experiments using U937 cells labeled with 2,7-bis(2-carboxyethyl) |
368) , but the number of vascular and muscular cells labeled with the human cell-specific |
369) herent differential propensities of these cells may restrict their clinical outcome. |
370) It has been hypothesized that developing cells may self-organize into tissue-specif |
371) In this context, mesenchymal stem cells play a crucial role as they are attr |
372) Mast cells play a vital role in hypersensitivit |
373) After an incubation period of 2 weeks, cells present in silica-containing hydroge |
374) an increase in the activity of deterrent cells present in tarsal chemosensilla of l |
375) However, identifying and sorting these cells remains a challenge in the absence o |
376) ffects of scaffold permeability on seeded cells remains largely unknown during tissu |
377) oenvironmental stiffness and that stromal cells such as adipocytes play a critical r |
378) e governed by interaction between several cells such as bone-forming osteoblasts, os |
379) In MCF-7 cells, the compounds were able to decrease |
380) For rainbow trout and human cells, the immunotoxic effects of QDs were |
381) idamycin suppressed Huh7 tumor initiating cells via GSK3β/β-catenin pathway. |
382) ranslated to in vivo targeted delivery of cells via the circulation in a variety of |
383) n ideal method for identifying subsets of cells without the need for markers by usin |
384) of mouse induced pluripotent stem (miPS) cells without using feeder-cells and adhes |
385) Human adipose tissue-derived regenerative cells (ADRCs) can be isolated easily and a |
386) ted human amniotic fluid mesenchymal stem cells (AFMSCs) as feeder cells to support |
387) uman bone marrow-derived mesenchymal stem cells (BM-MSCs) and human adipose tissue-d |
388) NKL) signaling helps putative cancer stem cells (CSC) to maintain their stemness. |
389) on's jelly (WJ) MSCs and dental pulp stem cells (DPSCs) were highly proliferative as |
390) ne or CMs with surface-seeded endothelial cells (ECs; CM/EC modules) were injected i |
391) e the potential of human endometrial stem cells (EnSCs) to form urinary bladder epit |
392) the cellular behaviour of hepatocyte-like cells (HLCs) on the surface of the galacto |
393) For SaBP, human mesenchymal stem cells (HMSCs), umbilical cord vein endothe |
394) Oral keratinocyte cells (HaCaT) were exposed to 25 μM alen |
395) proliferation of intermediate progenitor cells (IPCs) was affected. |
396) saline (PBS) and bone marrow mononuclear cells (MNCs) were injected as negative and |
397) ntal and clinical use of mesenchymal stem cells (MSCs), focusing mainly on the treat |
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