ライフサイエンスコーパス: differentiation stage

1 nto aberrant pharyngeal cells (Morphogenesis/Differentiation stage).

2 each pathway depends on the T cell type and differentiation stage.

3 lationship of these effects with chondrocyte differentiation stage.

4 s not active in transformed cells of a later differentiation stage.

5 te slightly before the mesenchymal stem cell differentiation stage.

6 rentiation data, and in line with a sample's differentiation stage.

7 iffusive state of CaV1.2 irrespective of the differentiation stage.

8 itional methods that are used to identify HC differentiation stage.

9 at the late of the commitment stage and the differentiation stage.

10 NAs and Oil-red O-staining at the end of the differentiation stage.

11 orms associated with various cell growth and differentiation stages.

12 and CD94/NKG2A contribute to define discrete differentiation stages.

13 s of a single-cell type rather than distinct differentiation stages.

14 ore proliferative keratinocytes in disturbed differentiation stages.

15 sis of murine B cells at specific activation-differentiation stages.

16 g is not restricted to certain cell types or differentiation stages.

17 of primary mouse MKs representing successive differentiation stages.

18 cells from activated precursors in distinct differentiation stages.

19 epithelial beta-catenin depletion during the differentiation stage also led to variable enamel defect

20 that CD45+ hematopoiesis peaks at late D14EB differentiation stages, although low-level CD45- erythro

21 y delivering IL-1 signaling during the early differentiation stage and integrating IL-23 signaling to

22 ns with SPIB occupancy, signatures of B-cell differentiation stage and potential pathogenetic mechani

23 istinct keratin (K) species as a function of differentiation stage and proliferative status, we used

24 dicate that CD8alphaalpha on T cells marks a differentiation stage and that it likely functions as a

25 + or CD8+ T cell lineages, varies with their differentiation stage and tissue localization, and canno

26 The level of JAM-C expression defines B-cell differentiation stages and allows the classification of

27 Methylation appears to change at specific differentiation stages and overlap with changes in trans

28 ween WT and Dicer KO iNKT cells at different differentiation stages and predicted to be targeted by t

29 cel growth: a proliferative stage, a stomata differentiation stage, and a cell elongation stage.

30 but the proportions of CD8(+) cells, T cell differentiation stage, and expression of costimulatory m

31 tors, including cell type, proliferation and differentiation stage, and extracellular stimuli.

32 ells depending on their tissue of origin and differentiation stage, and it affects their capacity to

33 t studies, we examined whether cellular age, differentiation stage, and/or tissue origin of primary c

34 s stages, change phenotypes by acting during differentiation stages, and facilitate new growth by act

35 ession signatures defining various lineages, differentiation stages, and signaling pathways.

36 o the presence of many cell types at various differentiation stages, and stringent medium and growth

37 The differentiation stage- and tissue-specific MHC-bound pep

38 ter region (bcr) protein, as well as several differentiation stage- and tissue-specific self-antigens

39 xpressed during the immediate-early and late differentiation stages are Chlamydia-specific and have e

40 To identify the differentiation stage at which ZBP-89 repression of the

41 t a correlation of ABCG2 gene expression and differentiation stage both in human and HCC derived cell

42 s levels of cortisol decreased CLDN1 in late differentiation stage but not in the early stage.

43 molecularly distinct diseases, differing in differentiation stage (cell of origin), oncogenic mechan

44 I large, PreBII small, immature B) and their differentiation-stage characteristic gene expression pro

45 The molecular programs underlying the differentiation stage consist of highly regulated expres

46 ility of chicken ccn2 mRNA is regulated in a differentiation stage-dependent manner in chondrocytes.

47 growth factors that act in a cell type- and differentiation stage-dependent manner.

48 Differentiation stage divides allergen-specific CD4(+) T

49 ey determinants of the dedifferentiation and differentiation stages during reprogramming.

50 c cell lines corresponding to the same early differentiation stages express abundant NELL2 mRNA.

51 nance of these cholinergic neurons after the differentiation stage have not been fully elucidated.

52 with mouse hematopoietic cells at different differentiation stages: hematopoietic stem cells, progen

53 T lymphocytes with respect to their in vivo differentiation stages identifies a distinct subset of C

54 ects appear to be highly associated with the differentiation stage in stem/progenitor pools.

55 on an osteoblast-derived protease at a late differentiation stage in this culture model just prior t

56 le of distinct TNFRs in initial and terminal differentiation stages in mTECs.

57 ucing functions in lymphocytes, precisely at differentiation stages in which V(D)J recombination occu

58 hat maintaining cell-cell contact during the differentiation stage, in combination with growth factor

59 Late differentiation stages, in contrast, showed extensive de

60 ognosis acute myeloid leukemia is increased, differentiation-stage inappropriate expression of the Ab

61 f a luteinized theca cell lineage at various differentiation stages including CD133(+), CD44(+), and

62 their response is governed primarily by the differentiation stage, independently of killer cell Ig-l

63 ing from early-activated to isotype-switched differentiation stages is both temporally and spatially

64 Early differentiation stages mainly displayed enhancer demethy

65 We analyzed the effect of differentiation stage of freshly isolated, mouse liver c

66 eveloping spinal cord have been focused on a differentiation stage of GRP cells.

67 In regenerative medicine applications, the differentiation stage of implanted stem cells must be op

68 of latent gene expression, depending on the differentiation stage of the cell.

69 rocess that varies according to the type and differentiation stage of the phagocyte.

70 Our data provide evidence that the differentiation stage of the starting cell has a critica

71 Depending on the differentiation stage of the target cell, the local envi

72 ach enables identifying the lineage-specific differentiation stages of hematopoietic cells on biomate

73 X was strongly increased during the terminal differentiation stages of human and mouse erythroblasts,

74 ansition from the proliferative to the early differentiation stages of myogenesis.

75 ion is a general characteristic of the early differentiation stages of rodent trophoblast, given that

76 acterial genes involved in the infection and differentiation stages of symbiosis, we obtained genes e

77 iate-early genes) and secondary (late genes) differentiation stages of the cycle.

78 potent stem cell (iPSC)-derived cells at two differentiation stages on peripheral nerve regeneration.

79 virtually all responding cells regardless of differentiation stage or profile of cytokine secretion,

80 PD1(+) T cells likely represent a particular differentiation stage or trafficking ability rather than

81 adation of RNA regardless of cell line type, differentiation stage, or passage number.

82 onregulatory and Treg populations of defined differentiation stages purified ex vivo from circulating

83 orced expression of polysialic acid in early differentiation stages reduces myotube formation and del

84 cending (inside-out) placement, common early differentiation stage (regardless of size, location, cor

85 me T(H)17/T(H)1 population at early and late differentiation stages, respectively, whereas the CCR6(-

86 We observed differentiation stage-restricted egress of thymocytes fr

87 That LPS-response genes in B cells also have differentiation stage-restricted expression suggests tha

88 l LPS-response genes were also found to have differentiation stage-restricted expression within the B

89 cell lymphoma specimens two specific B cell differentiation stage signatures of germinal center B ce

90 but could be beneficial during the prolonged differentiation stage.SIGNIFICANCE STATEMENT Increasing

91 This impairment is differentiation stage specific, since germinal center B

92 Our results demonstrated differentiation stage-specific and dose-dependent roles

93 vel of transcriptional activation to produce differentiation stage-specific B cell responses.

94 tigations did not determine the mechanism of differentiation stage-specific CYBB and NCF2 transcripti

95 that Cux/CDP regulates cell-type-restricted, differentiation stage-specific Emu enhancer activity by

96 ferentiated mouse erythroleukemia mediates a differentiation stage-specific exon 16 splicing switch t

97 eloped a novel algorithm that leverages both differentiation stage-specific expression data and large

98 nregulating the targeted gene in tissue- and differentiation stage-specific fashion.

99 Therefore, mechanisms involved in differentiation stage-specific HoxA10 tyrosine phosphory

100 nation codons into selected transcripts in a differentiation stage-specific manner, supporting the hy

101 ity are tightly controlled in a temporal and differentiation stage-specific manner.

102 e c-Fos, and they change their expression of differentiation stage-specific markers after treatment w

103 This differentiation stage-specific mechanism reflects a basi

104 This result was accomplished through a differentiation stage-specific reduction of apoptosis in

105 Using Ontogenet, we found differentiation stage-specific regulators of mouse hemat

106 Moreover, differentiation stage-specific splicing "switches" may a

107 onal complex stability requires an erythroid differentiation stage-specific splicing switch promoting

108 studies identified distinct brown adipocyte differentiation stage-specific, NRRE-1-protein complexes

109 Appropriate differentiation-stage-specific application of Gsk3 inhib

110 Also, we found that differentiation-stage-specific ARIH2 transcription was r

111 s, we show that MLL4 exhibits cell-type- and differentiation-stage-specific genomic binding and is pr

112 lineage, the mechanisms of apoptosis may be differentiation-stage-specific.

113 novo-derived motif signatures at all of the differentiation stages studied (ie, hematopoietic stem c

114 Bmp signaling by Bmpr1a depletion during the differentiation stage switched differentiation of crown

115 pared with M-ERRgammaWT myocytes at the same differentiation stage, the glucose oxidation rate was re

116 As and miRNA signatures allows specific cell-differentiation stages to be identified, and is a powerf

117 e expression profile is linked to the memory differentiation stage, we analyzed the degree of polyfun

118 d memory CD8(+) T cells from a wide range of differentiation stages were capable of significantly inh

119 d whether surface phenotypes associated with differentiation stages were predictably associated with

120 es are needed to facilitate correlating cell differentiation stage with location in the culture syste

121 The TRA subsets aligned along progressive differentiation stages within the mature mTEC subset and