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It has been shown that stem cells/progenitors from AF can contribute to functional recovery of both glomerular and tubular compartment and preliminary investigations have demonstrated their use for renal tissue engineering.
It has recently been shown that stem cell populations exist in "niches"—specific anatomical locations that regulate how the stem cells participate in tissue generation, maintenance and repair [26], [27].
However, studies have been shown that stem cells are also capable of protecting or stimulating the regeneration of damaged DA neurons in host [ 21, 22].
It has been shown that stem cell niches in Arabidopsis are hypersensitive to DNA damage, and an even a low dose of DNA damage can trigger programmed cell death selectively in these stem cells (Fulcher and Sablowski 2009).
The field of adipose-derived MSC therapy (ADMSC) is a rapidly growing area of research, and it has been shown that stem cells have an affinity for damaged joint tissue; recent in vivo studies have confirmed that stem cells have the ability to localize and participate in the repair of damaged joint structures, including cruciate ligaments, menisci, and cartilage lesions [ 6].
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It has been shown that stems with diaphyseal edges or fins have greater primary stability than round stems, particularly with respect to rotational stability [ 9, 13].
Students and educators, according to Wozniak, need to be shown that Stem subjects are not just about memorising formulas but are about creating things – turning ideas into reality.
It was shown that stem cell released factors (e.g. VEGF and IL-8) stimulate angiogenesis and activate Wnt signaling, promoting the healing of diabetic ischemic ulcers.
Although the mdx mouse diaphragm muscle is a membranous structure and, therefore, presents difficulties in direct intervention, it was shown that stem cell implantation via local application to this muscle generated moderate muscle reorganisation.
It has been shown that Pancreatic Stem Cells (PSCs) share many features with skin stem cells.
In some cases (bronchioalveolar stem cells, prostate luminal epithelial stem cells, intestinal crypt stem cells), by means of genetic lineage-marking it has been shown that normal stem cells are the cells of origin for corresponding types of cancer (Barker et al. 2009; Kim et al. 2005; Wang et al. 2009; Zhu et al. 2009).
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