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1 of a decline in the restorative capacity of tissue stem cells.
2 nd germ cells are continuously maintained by tissue stem cells.
3 believed to originate from transformation of tissue stem cells.
4 s and in its possible derivation from normal tissue stem cells.
5 ce for unprecedented transdifferentiation of tissue stem cells.
6 d the potential plasticity of HSCs and other tissue stem cells.
7 about the possible totipotency of some adult tissue stem cells.
8 ritical for the proper regulation of various tissue stem cells.
9 type, characteristic of development-involved tissue stem cells.
10 ells that have molecular programs resembling tissue stem cells.
11 ce of cancer cells with properties of normal tissue stem cells.
12 ing that these cells have features of normal tissue stem cells.
13 ons, with a focus on the regulation of adult tissue stem cells.
14 ial in part through its rejuvenation of aged tissue stem cells.
15 arguably the most extensively characterized tissue stem cells.
16 ypes are transcriptionally similar to normal tissue stem cells.
17 research in cell adhesion, inflammation, and tissue stem cells.
18 s have been shown to originate in epithelial tissue stem cells.
19 rine cells in vivo, suggesting that they are tissue stem cells.
20 t or by endogenous DNA-replication errors in tissue stem cells.
21 least some BCCs can arise from hair follicle tissue stem cells.
22 ion or infection usually first occurs in the tissue stem cells.
23 nd tissue because they do not develop ground tissue stem cells.
24 ing and plasticity, features associated with tissue stem cells.
25 are slow cycling in vivo, a known feature of tissue stem cells.
26 he early oncologic processes and the role of tissue stem cells.
27 nt spheroids previously shown to derive from tissue stem cells.
28 agenic events that generate cancers in human tissue stem cells.
33 similarities and differences between normal tissue stem cells and cancer stem cells (CSCs) have been
34 nts have excess cell divisions in the ground tissue stem cells and endodermis, indicating IRK functio
37 prime instigators of a functional decline of tissue stem cells and of mitochondrial dysfunction that
38 along with the distinctive scarcity of adult tissue stem cells and the complexities of their niches i
41 utrient-sensing pathways active in mammalian tissue stem cells and their relevance to normal and canc
43 mming, and hematopoietic and skeletal muscle tissue stem cells, and we discuss the implications for r
47 ent lineage-tracing studies, we propose that tissue stem cells are routinely lost and replaced in a s
51 om bone marrow stem cells (BMSC) and adipose tissue stem cells (ASC) of humans and rhesus macaques we
52 arabiosis rejuvenates the performance of old tissue stem cells at some expense to the young, but whet
53 atogonial stem cells (SSCs) are unique among tissue-stem cells because they undergo ROS-dependent sel
56 ave challenged this paradigm by showing that tissue stem cells can differentiate to unexpected cell l
62 function in mouse models, indicating that a tissue stem cell defect may underlie the pathophysiology
63 elopment, the vascular precursors and ground tissue stem cells divide to renew themselves and produce
67 al organoids-3D spheroids derived from adult tissue stem cells-enable investigation of epithelial phy
72 named antiviral Dicer (aviD), that protects tissue stem cells from RNA viruses-including Zika virus
73 a hallmark of dyskeratosis congenita, impair tissue stem cell function in mouse models, indicating th
76 have some phenotypic similarities with adult tissue stem cells, has been suggested to contribute to t
79 the past decades, studies of pluripotent and tissue stem cells have uncovered a range of metabolic pr
81 ntegral to the regulation of energy balance, tissue/stem cell homeostasis, and disease pathogenesis.
84 m1 expression identifies distinct connective tissue stem cells in both the bone (OCR stem cells) and
85 indicating that a similar process occurs in tissue stem cells in dyskeratosis congenita patients.
86 yos and second asymmetric division of ground tissue stem cells in early-heart embryos are abnormally
89 lls to send mitogenic signals to neighboring tissue stem cells in response to estrogen and progestero
90 ayed the ability of mTert-driven GFP to mark tissue stem cells in testis, bone marrow (BM), and intes
92 tophagy genes in the regulation of different tissue stem cells, including neural stem/progenitor cell
93 hown to promote self-renewal in a variety of tissue stem cells, including neuronal stem cells and hem
94 at lncRNAs exert critical functions in adult tissue stem cells, including skin, brain, and muscle, as
95 nfection, mutation, or epigenetic change-the tissue stem cell is involved in the generation of cancer
96 t to which cancer stem cells resemble normal tissue stem cells is a critical issue if targeted therap
98 rentiation of specific cell types from adult tissue stem cells is a major challenge in developmental
99 tion in stem cell biology is how the fate of tissue stem cells is initially determined during develop
103 that supports expansion of several types of tissue stem cells, is a candidate therapeutic target for
104 n patterns of vascular precursors and ground tissue stem cells, likely via the YDA-MKK4/5 cascade, du
109 ly reprograms and splits into a mixed ground tissue/stem cell niche fate and a vascular precursor fat
110 pled receptor-5 (LGR5) is expressed in adult tissue stem cells of many epithelia, and its overexpress
111 esis are that (a) tumors originate in either tissue stem cells or their immediate progeny through dys
112 lls must be phenotypically similar to normal tissue stem cells or whether they can retain the identit
114 arises from the transformation of a resident tissue stem cell, our results show that EMT can produce
117 mportantly, in contrast to its role in other tissue stem cells, PRC1 negatively regulates the cell cy
118 illustrate immunologic regulation of a core tissue stem cell program after damage and support a role
119 , estradiol, and progesterone, via increased tissue stem cell proliferation to prepare for impending
120 rate subphyla, collectively demonstrate that tissue stem cells rather than pluripotent blastema cells
122 AML1 is a transcription factor implicated in tissue stem cell regulation and belongs to the small Run
124 The role of the immune system in regulating tissue stem cells remains poorly understood, as does the
125 These observations establish that adult tissue stem cells reside within the CD62L(+) Tcm cell co
135 evealed substantial upregulation of an adult tissue stem-cell signature, activated Wnt signalling, an
136 ese results indicate that, similar to normal tissue stem cells, subsets of CSCs in some tumours conta
137 echanistic insight into the dynamics between tissue stem cell subtypes and demonstrates that p63 regu
141 ogenase (15-PGDH) is a negative regulator of tissue stem cells that acts via enzymatic activity of ox
142 s whether malignancy arises in self-renewing tissue stem cells that suffer oncogene activation or in
143 dult mammalian tissues, could regulate adult tissue stem cells through modulating niche signaling and
144 tudies reveal that IL-17 can directly act on tissue stem cells to promote tissue repair and tumorigen
145 Although oncogenic mutations predispose tissue stem cells to tumor initiation, the rate-limiting
147 acquired oncogenic mutations, we discuss how tissue stem cells undergoing malignant transformation ac
148 ssue-resident and recruited immune cells and tissue stem cells underlying tissue adaptation to enviro
149 rns, which separated them clearly from other tissue stem cells with lower developmental potency.