ライフサイエンスコーパス: stem cell identity

1 h Wnt responsive and Wnt dependent to define stem cell identity.

2 et gene) is a master regulator of intestinal stem cell identity.

3 ted a remarkably dynamic view of pluripotent stem cell identity.

4 entral in regulating epidermal and embryonic stem cell identity.

5 the niche, a microenvironment that specifies stem cell identity.

6 milieu may be important determinants of the stem cell identity.

7 ls "drifting away" from the niche and losing stem cell identity.

8 nd that neither WUS nor CLV3 is a marker for stem cell identity.

9 sions can repopulate the niche and revert to stem cell identity.

10 ng of maintenance and loss of pluripotential stem cell identity.

11 asymmetrically, with one daughter retaining stem cell identity.

12 ovel WUS-independent CLV1 pathway regulating stem cell identity.

13 an essential regulatory network to maintain stem cell identity.

14 nknown which molecular factors endow cambium stem cell identity.

15 tivation and the transcriptional programs of stem cell identity.

16 ulatory regions for key master regulators of stem cell identity.

17 consequently, enable the cell to maintain a stem cell identity.

18 transcriptional repressor maintaining muscle stem cell identity.

19 emories play an important part in regulating stem cell identities.

20 gest that the MR does not inherently dictate stem cell identity, although its stereotypical inheritan

21 s the JAK-STAT signaling that is crucial for stem cell identity and activity, comparatively little is

22 s SOX2 play critical roles in the control of stem cell identity and are dysregulated in many human ca

23 croenvironments, or "niches", which regulate stem cell identity and behavior.

24 g the expression of genes that contribute to stem cell identity and by reprogramming the expression o

25 V1) receptor kinase in Arabidopsis regulates stem cell identity and differentiation through its repre

26 Wnt signalling is known to be important for stem cell identity and epithelial regeneration in severa

27 ulators of proteome complexity that regulate stem cell identity and function.

28 tein SALL4 plays a vital role in maintaining stem cell identity and governing stem cell self-renewal

29 ays essential roles in maintaining embryonic stem cell identity and in controlling cellular different

30 ons regulate developmental genes involved in stem cell identity and lineage choice.

31 Intestinal epithelial stem cell identity and location have been the subject of

32 panded cells retain phenotypic and molecular stem cell identity and mediate improved durable, multili

33 re, we show that IAA33 maintains root distal stem cell identity and negatively regulates auxin signal

34 es auxin gradients in filaments to determine stem cell identity and overall plant form.

35 Stem cell identity and plasticity are controlled by mast

36 s a potent resource for the investigation of stem cell identity and regulation from functional as wel

37 Regulatory factors controlling stem cell identity and self-renewal are often active in

38 regulatory genes important for hematopoietic stem cell identity and self-renewal in human leukemia ce

39 tinct fate upon division: one cell retaining stem cell identity and the other cell destined to differ

40 ting the APC/C inhibitor Emi1 causes loss of stem cell identity and trophoblast differentiation of mo

41 bility may have an equally important role in stem-cell identity and function.

42 and cell death, (4) metabolic regulation of stem cell identity, and (5) metabolic requirements of th

43 ironment, in accordance with the notion that stem cell identities are contextual and not determined b

44 Pathways that regulate epigenetic control of stem cell identity are critical to the molecular etiolog

45 hematopoietic stem cells (HSCs) to maintain stem cell identity are not fully understood.

46 that Brn2, an important regulator of neural stem cell identity, associates with condensed chromatin

47 us, asymmetric division is not necessary for stem-cell identity but rather is a tool that stem cells

48 that Polycomb Group (PcG) proteins maintain stem cell identity by repressing differentiation genes,

49 REST plays a key role in safeguarding muscle stem cell identity by repressing multiple non-muscle lin

50 ng information that prevents self-renewal of stem cell identity by the germ cell they enclose.

51 We further show that stem cell identity correlates with the mode of MR inheri

52 Stem cell identity depends on the integration of extrins

53 patterning, eye and wing morphogenesis, and stem cell identity determination.

54 et of mRNAs, including mRNAs that encode the stem cell identity factors SOX2 and PAX6, and components

55 ed to post-transcriptional repression of key stem cell identity factors, thereby promoting exit from

56 The precisely timed repression of the stem cell identity gene WUSCHEL (WUS) by the floral home

57 ibitors ARR7 and ARR15, and induction of the stem cell identity gene WUSCHEL Furthermore, plastid str

58 pressive histone modifications, we show that stem cell identity genes are silenced during differentia

59 ops involving the phytohormone cytokinin and stem cell identity genes.

60 tate by looking for coordinate expression of stem cell identity genes.

61 size of the organizing center that maintains stem cell identity in neighboring cells.

62 ing in the activation of CAIL expression and stem cell identity in only a narrow domain.

63 d lesional skin reveals changes in epidermal stem cell identity in OTULIN-deficient keratinocytes pri

64 athway activity, that perpetuates intestinal stem cell identity in response to Wnt/R-spondin stimulat

65 AIL) transcription factors to define cambium stem cell identity in the Arabidopsis root.

66 that CrCLV3 promotes cell proliferation and stem cell identity in the gametophyte meristem.

67 The Wnt signaling pathway controls stem cell identity in the intestinal epithelium and in m

68 is that the existing SCN actively suppresses stem cell identity in the PZ.

69 istem that is essential for specification of stem-cell identity in overlying cells.

70 This loss of stem cell identity is not associated with defects in the

71 ell types, but their function in maintaining stem cell identity is unclear.

72 issues following damage(5-9), revealing that stem-cell identity is an induced rather than a hardwired

73 d, because p63 and p73 are now implicated in stem cell identity, neurogenesis, natural immunity and h

74 s and traffic to adjoining cells to activate stem-cell identity non-autonomously.

75 etric division: daughter cells either retain stem cell identity or initiate differentiation.

76 es daughter cells that either maintain their stem cell identity or undergo differentiation to form ma

77 Maintenance of stem-cell identity requires proper regulation of enhance

78 ncover that mitochondrial dynamics regulates stem cell identity, self-renewal, and fate decisions by

79 e represents a conserved mechanism promoting stem cell identity that evolved in the common ancestor o

80 in leaf primordia, causing a proliferative, stem cell identity to persist in these cells.

81 cell domain to the meristem tip and promotes stem cell identity, together with CLV3 expression, gener

82 valuable resource for exploring pluripotent stem cell identity versus cell fitness, and offer a fram

83 ana, WUSCHEL (WUS) is a key factor promoting stem cell identity, whereas the CLAVATA (CLV1, CLV2, and

84 er cell remains in the niche and self-renews stem cell identity, whereas the other, displaced away, i