ライフサイエンスコーパス: multipotent stem cell

1 ls, demonstrating that the crypt contained a multipotent stem cell.

2 s (GEPs), including those of the presumptive multipotent stem cell.

3 rypts, that has been proposed to contain the multipotent stem cell.

4 rived from the adult mouse small intestine's multipotent stem cell.

5 n under some circumstances and may represent multipotent stem cells.

6 opmental backup functions are reminiscent of multipotent stem cells.

7 DGCR8 to reprogram adult somatic cells into multipotent stem cells.

8 em cells and may play similar roles in other multipotent stem cells.

9 s robust identification and isolation of the multipotent stem cells.

10 broadly permissive chromatin established in multipotent stem cells.

11 for lineage choice and differentiation from multipotent stem cells.

12 for ASC expansion provide a large number of multipotent stem cells.

13 g been proposed to depend on the activity of multipotent stem cells.

14 n in vitro model of SMC differentiation from multipotent stem cells.

15 which has recently been suggested to contain multipotent stem cells.

16 embryonic day 7.5 with a lack of detectable multipotent stem cells.

17 urons and glia are often derived from common multipotent stem cells.

18 nferring mitotic responsiveness to EGF among multipotent stem cells.

19 ulates multiple committed progenitors and/or multipotent stem cells.

20 ferentiation of white adipose tissue-derived multipotent stem cells (ADMSCs) into lipid-accumulating,

21 Hence, multipotent stem cells alter their properties over time

22 ts of the mouse stomach are descended from a multipotent stem cell and undergo an orderly migration-a

23 s, which contain a heterogeneous mix of both multipotent stem cells and more restricted progenitor po

24 A challenge has been to obtain multipotent stem cells and/or progenitors that can gener

25 throughout adult life due to the presence of multipotent stem cells and/or unipotent progenitor cells

26 testinal crypts contain more than one active multipotent stem cell, and that these cells can be retai

27 the origins and behaviors of pluripotent and multipotent stem cells, and their therapeutic potential.

28 Epidermal lineage commitment occurs when multipotent stem cells are specified to three lineages:

29 opulation of granule-free cells included the multipotent stem cell as well as committed precursors of

30 mary epithelial cell hierarchy contains both multipotent stem cell as well as lineage-limited duct an

31 differentiation of human bone marrow-derived multipotent stem cells (bmMSC) over periods of up to sev

32 of the follicle outer root sheath (ORS) and multipotent stem cells (bulge), the compartments which n

33 Neural crest cells are highly multipotent stem cells, but it remains unclear how their

34 We traced the origin of these cells to basal multipotent stem cells capable of generating both GABAer

35 ither frozen, nor fresh hAFSCs cultivated in multipotent stem cell culture conditions expressed OCT4A

36 arts receiving equal volumes of saline or BM multipotent stem cells delivered in the same manner, the

37 We investigated whether these multipotent stem cells derived from bone marrow could be

38 four principal cell types deriving from one multipotent stem cell: enterocytes, goblet, enteroendocr

39 ompanies the IL-3-mediated commitment of the multipotent, stem cell factor (SCF)-dependent EML cell l

40 Although our data argue against a multipotent stem cell for smooth and striated muscle cel

41 sible, autologous source of undifferentiated multipotent stem cells for therapeutic application.

42 to defects in the proliferative capacity of multipotent stem cells found in the bulge.

43 In skin, multipotent stem cells generate the keratinocytes of the

44 on, these clonally expanded human BM-derived multipotent stem cells (hBMSCs) do not appear to belong

45 Recently, multipotent stem cells in Drosophila malpighian tubules

46 aryocyte differentiation apparent from early multipotent stem cells in myelofibrosis and associated a

47 hat when normal SG homeostasis is perturbed, multipotent stem cells in the bulge can be mobilized to

48 ition by causing proliferation of quiescent, multipotent stem cells in the hair follicle bulge region

49 gle miRNA that can efficiently differentiate multipotent stem cells into a specific lineage or regula

50 e of soluble cues directs differentiation of multipotent stem cells into discrete populations of spec

51 directed differentiation of pluripotent and multipotent stem cells into mesodiencephalic dopaminergi

52 uring the development and differentiation of multipotent stem cells into specialised cell types remai

53 gnals and early molecular events that commit multipotent stem cells into the adipocyte lineage are no

54 that KLF2 does not affect the commitment of multipotent stem cells into the preadipocytic lineage bu

55 Terminal differentiation of multipotent stem cells is achieved through a coordinated

56 n the present study we tested the ability of multipotent stem cells isolated from adult muscle to sur

57 Our results suggest that multipotent stem cells isolated from adult muscle, which

58 Pluripotent or multipotent stem cells isolated from human embryos or ad

59 readily attainable source of proliferating, multipotent stem cells, its potential for use in regener

60 t population of central nervous system (CNS) multipotent stem cells known as oligodendrocyte progenit

61 The neural crest is a multipotent stem cell-like population that is induced du

62 The vertebrate body forms from a multipotent stem cell-like progenitor population that pr

63 Neural crest cells are a population of multipotent stem cell-like progenitors that arise at the

64 The neural crest (NC) is a population of multipotent stem cell-like progenitors that arise at the

65 The neural crest is a multipotent, stem cell-like population that migrates ext

66 prevent neurons from dedifferentiating to a multipotent, stem cell-like state.

67 sitive abl PTK in a growth factor dependent, multipotent stem cell line (FDCP-Mix) in which growth is

68 myeloid progenitor cell line (EPRO) with the multipotent stem cell line from which it was derived (EM

69 er gene expression, and differentiation of a multipotent stem cell line.

70 vital for the differentiation of ES cells to multipotent stem cells, little is known regarding the ro

71 Differentiation of multipotent stem cells occurs through the highly coordin

72 Basal cells are multipotent stem cells of a variety of organs, including

73 Adipocytes arise from multipotent stem cells of mesodermal origin, which also

74 c factor (CNTF) acts instructively to switch multipotent stem cells of the CNS to an astrocytic fate.

75 keratinocytes in the same way as it affects multipotent stem cells of the skin.

76 m cells that do not necessarily overlap with multipotent stem cells of the tissue of origin.

77 T-IPs did not include multipotent stem cells or molecular evidence of T cell-r

78 number of DiI-labeled, clonally expanded BM multipotent stem cells, or the same volume of phosphate-

79 Modern clonality studies have confirmed the multipotent stem-cell origin of the neoplastic process i

80 ion in times of stress with maintenance of a multipotent stem cell pool over decades of life.

81 ll (cNCC) mesenchyme, a highly proliferative multipotent stem cell population that forms orofacial co

82 embryonic stem cells, but their function in multipotent stem cell populations is poorly understood.

83 Our study provides evidence that single multipotent stem cells positioned throughout the mature

84 The multipotent stem cells proliferate or differentiate into

85 Rare multipotent stem cells replenish millions of blood cells

86 anatomical site that contains a reservoir of multipotent stem cells (SCs) that can maintain normal ti

87 at exfoliated human deciduous tooth contains multipotent stem cells [stem cells from human exfoliated

88 trated that these undifferentiated cells are multipotent stem cells, suggesting that local signaling

89 Neural crest (NC) cells are multipotent stem cells that arise from the embryonic ect

90 rise via a hierarchical scheme starting with multipotent stem cells that become increasingly restrict

91 dipose-derived stem cells (hASCs), which are multipotent stem cells that can be differentiated into f

92 Neural crest cells (NCCs) are multipotent stem cells that can differentiate into multi

93 Mesenchymal stem cells (MSCs) are multipotent stem cells that can differentiate into vario

94 Muscle side population (SP) cells are rare multipotent stem cells that can participate in myogenesi

95 e neural crest is an embryonic population of multipotent stem cells that form numerous defining featu

96 Multipotent stem cells that generate both neurons and gl

97 opoietic stem cells (HSCs) are self-renewing multipotent stem cells that generate mature blood lineag

98 human colorectal epithelium is maintained by multipotent stem cells that give rise to absorptive, muc

99 ne neural progenitor cells (NPCs), which are multipotent stem cells that give rise to cells in the ce

100 ural crest cells (CNCCs) are a population of multipotent stem cells that give rise to craniofacial bo

101 C-MSCs), originating in Wharton's jelly, are multipotent stem cells that home to damaged tissues and

102 ugh Nestin is widely considered a marker for multipotent stem cells, these Nestin-expressing progenit

103 ineage of the main olfactory epithelium-from multipotent stem cells through neuronal progenitors to m

104 and mesodermal tissue type specification of multipotent stem cells throughout the formation of the e

105 s requires the commitment of pluripotent and multipotent stem cells to distinct differentiation pathw

106 f the repopulating ability and plasticity of multipotent stem cells to regenerate lost or diseased ti

107 his signaling pathway inhibits expression of multipotent stem cell transcription factors in spleen.

108 he RPESC as an accessible, human CNS-derived multipotent stem cell, useful for the study of fate choi

109 racterize the generation of glial cells from multipotent stem cells we have cultured neuroepithelial

110 pported recombination in all of their active multipotent stem cells were located adjacent to "control

111 cretory cells clonally dedifferentiated into multipotent stem cells when they were cultured ex vivo w

112 Multipotent stem cells, which normally gave rise to neur

113 The mesenchymal cell is a multipotent stem cell with the capacity to give rise to

114 Multipotent stem cells with neural crest-like properties