ライフサイエンスコーパス: early differentiation

1 cells, which undergo a binary choice during early differentiation.

2 ly regulated activation of NF-kappaB but not early differentiation.

3 for a specific task related to stemness and early differentiation.

4 or cell cycle progression, pluripotency, and early differentiation.

5 sion of developmental genes and induction of early differentiation.

6 numbers of inactivated X chromosomes during early differentiation.

7 nvolved in the LESC maintenance and/or their early differentiation.

8 ature of Earth's heterogeneous accretion and early differentiation.

9 vitro, along with upregulation of markers of early differentiation.

10 ell fusion, none of the treatments prevented early differentiation.

11 kely because of an ASC-sensitive block(s) in early differentiation.

12 competence is acquired only gradually during early differentiation.

13 t are repressed in ESCs and derepressed upon early differentiation.

14 xpressed gene in the vascular lineage during early differentiation.

15 of involucrin, consistent with promotion of early differentiation.

16 etylation also alters gene expression during early differentiation.

17 yonic mammalian hair cells but not for their early differentiation.

18 During early differentiation (14 hours to 1 day after BrdU), re

19 th-defying phenotype of KCs does not require early differentiation; 5) NF-kappaB is one regulator of

20 to identify 69 genes altered by IRF-8 during early differentiation (62 up-regulated and 7 down-regula

21 -regulated opposition to pluripotency during early differentiation, a process highly distinct from st

22 ast, contains cells that are maturing toward early differentiation and are likely transit-amplifying

23 entifies ICSBP as a factor critical for both early differentiation and final maturation of DCs.

24 express the transcription factor MafB during early differentiation and maintain calbindin expression

25 Yet, the genetic mechanisms underlying early differentiation and patterning of the cerebellum a

26 Early differentiation and regular spacing of the precoci

27 ses define a specific role for both genes in early differentiation and survival of the placodally der

28 ling promoted osteoprogenitor proliferation, early differentiation, and commitment to the osteoblasti

29 e-specific matrix genes that are silenced in early differentiation are expressed during the terminal

30 Controls of stem cell maintenance and early differentiation are known in several systems.

31 immature T-ALLs are characterized by a very early differentiation arrest and show unique genetic and

32 Therefore, early differentiation between SLC34A1 (NaPi-IIa) and CYP

33 nsable for osteoblast lineage commitment and early differentiation but also blocks osteoblast maturat

34 rvoirs showed that strong coupling supported early differentiation but required a higher number of ba

35 ed intrinsically in the germ cells for their early differentiation, but is required in the germ cells

36 ars is thought to hold clues to the planet's early differentiation, but until now no meteoritic regol

37 promoting ESC attachment, proliferation, and early differentiation, compared to native EB and decellu

38 Characterization of an early differentiation defect, the multiple-R8 phenotype,

39 se of only approximately 15% decrease during early differentiation despite global changes in gene exp

40 aging and gene expression profiling to study early differentiation dynamics spontaneously occurring w

41 nd various other features of this important, early differentiation event.

42 am of egl-5 to direct HSN cell migration, an early differentiation event.

43 n through the cell cycle and that these very early differentiation events do not require the accumula

44 ce promotes proliferation of osteoblasts and early differentiation events like production of alkaline

45 Studying these early differentiation events may help to identify specif

46 tive surfaces; conidia germinate and undergo early differentiation events, but appressorium maturatio

47 phocyte precursors and suggest a sequence of early differentiation events.

48 e undergo distinct expression changes during early differentiation events.

49 6-cell cysts, bridging the expression of the early differentiation factor Bam with late markers such

50 n, probably by inhibiting the translation of early differentiation factors, whereas niche signals pre

51 f adult hippocampal newborn cells die during early differentiation from intermediate progenitors (IPC

52 involved in epidermal differentiation, with early differentiation genes (KRT1, KRT10, DSC1, DSG1) be

53 that distinguish tonsil BCs from tonsil PCs (early differentiation genes [EDGs]), and tonsil PCs from

54 The molecular mechanisms controlling SM early differentiation have been studied extensively.

55 With early differentiation, hPSC proliferation slows, energy

56 The effects of Nodal on early differentiation illustrate how hESCs can augment m

57 2F2 in the activation of neural genes during early differentiation in humans.

58 sassembly in the control of Hh signaling and early differentiation in muscle cells.

59 ratinocyte proliferation, stratification, or early differentiation in skin.

60 CPCs undergoing early differentiation in vitro increase levels of CaMKII

61 adhesion, adherens junction composition, and early differentiation in vivo and in vitro.

62 d of endothelial cells expressing markers of early differentiation, including VEGFR2 (Flk1), Tal1/SCL

63 embryonic stem cells (hESCs) in response to early differentiation, induced by retinoic acid, versus

64 adipocytes to PGF2alphaEA/bimatoprost during early differentiation inhibits adipogenesis.

65 The constancy of Zn/Fe(T) during early differentiation involving olivine requires that Fe

66 rom stem cell self-renewal to overt signs of early differentiation is a poorly understood but importa

67 bitors (p15, p16, p21, and p27), a marker of early differentiation (keratin 1), mediators of apoptosi

68 inal differentiation program, stimulating an early differentiation marker (keratin 1) and suppressing

69 suggests that 9-O-acetylation appears as an early differentiation marker as cells mature from the DP

70 number of basal keratinocytes expressing the early differentiation marker keratin 1 (K1).

71 tors unexpectedly increased the synthesis of early differentiation marker protein delta-crystallin in

72 d by expression of the gene encoding for the early differentiation marker, Myogenin.

73 Early differentiation markers are abundantly expressed i

74 Expression of early differentiation markers is RBP-Jkappa-independent

75 Induction of p21WAF1/Cip1 expression and early differentiation markers occur through two differen

76 NOTCH3 (N3) transcription, inducing HES5 and early differentiation markers such as involucrin (IVL) a

77 rogram characterized by normal expression of early differentiation markers such as myogenin and p21,

78 s encoding general cell growth functions and early differentiation markers was not affected, suggesti

79 D34(+) cells were equivalent with respect to early differentiation markers, and following culture, th

80 ein levels of some cell cycle regulators and early differentiation markers.

81 Activated Notch1 also induces expression of 'early' differentiation markers, while suppressing the la

82 derlying the switch between self-renewal and early differentiation may be acting in these two pools.

83 reas the transition between self-renewal and early differentiation modes of the network underlies the

84 ates the role of Akt and Clk1 kinases in the early differentiation of 3T3-L1 cells to adipocytes.

85 ess exposure increased the proliferation and early differentiation of adult neural progenitor cells.

86 correlates temporally and spatially with the early differentiation of angioblasts into the endothelia

87 s of osteogenesis prematurely and led to the early differentiation of bone.

88 search is needed to develop tools that allow early differentiation of bvFTD from primary psychiatric

89 We studied the early differentiation of calcium release units, which me

90 o create a precise genetic definition of the early differentiation of cap mesenchyme progenitors.

91 clear kinase that plays an essential role in early differentiation of cardiomyocytes.

92 ide evidence to show that MAIT cells promote early differentiation of CCR2-dependent monocytes into m

93 d and sufficient for maturation, but not for early differentiation of CMs.

94 Accurate, early differentiation of dementias will become increasin

95 host dendritic cells (DCs) and that there is early differentiation of donor-derived DCs, even after t

96 ets, provides insight into the formation and early differentiation of Earth.

97 clusions, indicating involvement of MYO5B in early differentiation of epithelial cells.

98 e conclude that stat92E is necessary for the early differentiation of follicle cells and for proper g

99 an effect on the generation, migration, and early differentiation of granule cells.

100 expression of Wnt3a in the neocortex induced early differentiation of IPs into neurons and the accumu

101 s play a role in efficient commitment and/or early differentiation of most T progenitors.

102 We explored the early differentiation of naive CD4 T helper (Th) cells i

103 Thus, the early differentiation of naive diabetogenic T cells into

104 velopment and suggest that TWH regulates the early differentiation of neural progenitors.

105 1), which is localized in the nucleus during early differentiation of odontoblasts, is able to bind s

106 The early differentiation of olfactory structures and the pe

107 en postulated to play a critical role in the early differentiation of oligodendrocytes (OLs) in addit

108 est that proliferation, cell cycle exit, and early differentiation of primary lens fiber cells are re

109 a mutation in valentino (val), which blocks early differentiation of rhombomeres 5 and 6 in the hind

110 the nuclear localization of SOX9 during the early differentiation of Sertoli cells and the determina

111 sfer to inductive medium and potentiates the early differentiation of some cells.

112 Prox motif and TBK1 were dispensable for the early differentiation of TFH cells.

113 promoter based upon the role of keratin 4 in early differentiation of the esophageal squamous epithel

114 veal a novel role for mesodermal Fgf8 on the early differentiation of the NC along the parasympatheti

115 hese two genes has specific consequences for early differentiation of the primary olfactory pathway-w

116 studies imply that Sox9 is required for the early differentiation of the prostate bud epithelia.

117 ial cell types and could also be involved in early differentiation of the skeleton and kidney.

118 e TGF-beta-triggered pathways that drive the early differentiation of these cell populations.

119 in the steps of cell fate determination and early differentiation of various retinal cell types.

120 To compare the role of FAS during early differentiation or survival of Tmem in chronic inf

121 These results suggest that during the early differentiation process CD4 T cells acquire a mixe

122 of s-process neodymium in the Earth, and not early differentiation processes.

123 l a developmental clock characteristic of an early differentiation program common to all EBs, further

124 uggesting that TopIIbeta is not required for early differentiation programming but is specifically re

125 in the regulation of keratinocyte growth and early differentiation, rather than terminal differentiat

126 Microarray analysis at various times during early differentiation reveal that mesoderm- and endoderm

127 ion, tubular organization and elongation and early differentiation) revealed signaling pathways poten

128 lterations in their generation, survival, or early differentiation, since all occurred normally in in

129 Upon early differentiation, SMAD2/3 signaling is decreased wh

130 ive ascending (inside-out) placement, common early differentiation stage (regardless of size, locatio

131 ells by delivering IL-1 signaling during the early differentiation stage and integrating IL-23 signal

132 eukemic cell lines corresponding to the same early differentiation stages express abundant NELL2 mRNA

133 Early differentiation stages mainly displayed enhancer d

134 the transition from the proliferative to the early differentiation stages of myogenesis.

135 xpression is a general characteristic of the early differentiation stages of rodent trophoblast, give

136 ast, forced expression of polysialic acid in early differentiation stages reduces myotube formation a

137 genesis, while Six genes appear to act in an early differentiation step during thymus/parathyroid mor

138 if treated with patterning molecules at very early differentiation steps before neural induction.

139 During early differentiation steps, the ES cell factor Tbx3 ass

140 ation, while P2X5 and P2X7 receptors control early differentiation, terminal differentiation and deat

141 1 is required to maintain Oct4 expression at early differentiation time points.

142 two TLE genes expressed most dynamically in early differentiation, TLE3 and TLE4.

143 in each head segment, we have examined their early differentiation using Alcian labeling of cartilage

144 A remarkable general feature of early differentiation was a resolution of complexity thr

145 induction of scd1 expression by cAMP during early differentiation was distinct from that observed du

146 s suggest that TLE activity is essential for early differentiation where it acts to suppress the plur

147 regulated independent of pluripotency during early differentiation, which is distinct from what occur

148 myogenic regulatory proteins shifted toward early differentiation with increased erythropoietin rece

149 gulatory network to balance self-renewal and early differentiation within the "mitotic region," which

150 AT12 protein was found expressed in the root early differentiation zone, where its abundance was modu