コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ial in part through its rejuvenation of aged tissue stem cells.
2 arguably the most extensively characterized tissue stem cells.
3 ypes are transcriptionally similar to normal tissue stem cells.
4 research in cell adhesion, inflammation, and tissue stem cells.
5 s have been shown to originate in epithelial tissue stem cells.
6 rine cells in vivo, suggesting that they are tissue stem cells.
7 ce of cancer cells with properties of normal tissue stem cells.
8 least some BCCs can arise from hair follicle tissue stem cells.
9 ion or infection usually first occurs in the tissue stem cells.
10 nd tissue because they do not develop ground tissue stem cells.
11 ing that these cells have features of normal tissue stem cells.
12 ing and plasticity, features associated with tissue stem cells.
13 are slow cycling in vivo, a known feature of tissue stem cells.
14 he early oncologic processes and the role of tissue stem cells.
15 nt spheroids previously shown to derive from tissue stem cells.
16 agenic events that generate cancers in human tissue stem cells.
17 of a decline in the restorative capacity of tissue stem cells.
18 nd germ cells are continuously maintained by tissue stem cells.
19 believed to originate from transformation of tissue stem cells.
20 s and in its possible derivation from normal tissue stem cells.
21 ce for unprecedented transdifferentiation of tissue stem cells.
22 d the potential plasticity of HSCs and other tissue stem cells.
23 about the possible totipotency of some adult tissue stem cells.
27 similarities and differences between normal tissue stem cells and cancer stem cells (CSCs) have been
29 prime instigators of a functional decline of tissue stem cells and of mitochondrial dysfunction that
32 utrient-sensing pathways active in mammalian tissue stem cells and their relevance to normal and canc
34 mming, and hematopoietic and skeletal muscle tissue stem cells, and we discuss the implications for r
36 ent lineage-tracing studies, we propose that tissue stem cells are routinely lost and replaced in a s
38 om bone marrow stem cells (BMSC) and adipose tissue stem cells (ASC) of humans and rhesus macaques we
39 arabiosis rejuvenates the performance of old tissue stem cells at some expense to the young, but whet
40 ave challenged this paradigm by showing that tissue stem cells can differentiate to unexpected cell l
44 function in mouse models, indicating that a tissue stem cell defect may underlie the pathophysiology
49 a hallmark of dyskeratosis congenita, impair tissue stem cell function in mouse models, indicating th
52 have some phenotypic similarities with adult tissue stem cells, has been suggested to contribute to t
56 ntegral to the regulation of energy balance, tissue/stem cell homeostasis, and disease pathogenesis.
58 m1 expression identifies distinct connective tissue stem cells in both the bone (OCR stem cells) and
59 indicating that a similar process occurs in tissue stem cells in dyskeratosis congenita patients.
62 lls to send mitogenic signals to neighboring tissue stem cells in response to estrogen and progestero
63 ayed the ability of mTert-driven GFP to mark tissue stem cells in testis, bone marrow (BM), and intes
65 tophagy genes in the regulation of different tissue stem cells, including neural stem/progenitor cell
66 hown to promote self-renewal in a variety of tissue stem cells, including neuronal stem cells and hem
67 at lncRNAs exert critical functions in adult tissue stem cells, including skin, brain, and muscle, as
68 nfection, mutation, or epigenetic change-the tissue stem cell is involved in the generation of cancer
69 t to which cancer stem cells resemble normal tissue stem cells is a critical issue if targeted therap
70 rentiation of specific cell types from adult tissue stem cells is a major challenge in developmental
71 tion in stem cell biology is how the fate of tissue stem cells is initially determined during develop
74 that supports expansion of several types of tissue stem cells, is a candidate therapeutic target for
75 pled receptor-5 (LGR5) is expressed in adult tissue stem cells of many epithelia, and its overexpress
76 esis are that (a) tumors originate in either tissue stem cells or their immediate progeny through dys
77 lls must be phenotypically similar to normal tissue stem cells or whether they can retain the identit
79 arises from the transformation of a resident tissue stem cell, our results show that EMT can produce
82 rate subphyla, collectively demonstrate that tissue stem cells rather than pluripotent blastema cells
84 AML1 is a transcription factor implicated in tissue stem cell regulation and belongs to the small Run
94 evealed substantial upregulation of an adult tissue stem-cell signature, activated Wnt signalling, an
95 ese results indicate that, similar to normal tissue stem cells, subsets of CSCs in some tumours conta
96 echanistic insight into the dynamics between tissue stem cell subtypes and demonstrates that p63 regu
98 s whether malignancy arises in self-renewing tissue stem cells that suffer oncogene activation or in
99 dult mammalian tissues, could regulate adult tissue stem cells through modulating niche signaling and
100 rns, which separated them clearly from other tissue stem cells with lower developmental potency.
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。