ライフサイエンスコーパス: growth potential

1 tributable to a difference in intrinsic axon growth potential.

2 nd Shh(-/-);Gli3(-/-) lungs exhibit enhanced growth potential.

3 quately addressed and provided the child has growth potential.

4 lls were compared in terms of their in vitro growth potential.

5 tep in HMEC acquisition of uniform unlimited growth potential.

6 03X) caused dramatic protection from loss of growth potential.

7 are compromised in their differentiative and growth potential.

8 pulation doublings without any diminution in growth potential.

9 static cancer cells without decreasing their growth potential.

10 tic potential without interfering with their growth potential.

11 in concert to modify an individual's genetic growth potential.

12 regulate genes important in regulating cell growth potential.

13 ics balancing leaf persistence against plant growth potential.

14 corresponding to time-of-day effect on axon growth potential.

15 on may occur in part by de-repressing latent growth potential.

16 cy must be distinguished from modest genetic growth potential.

17 as essential for their anchorage-independent growth potential.

18 m resilience, but it also signifies untapped growth potential.

19 nitor cells that expand uniformly with equal growth potential.

20 tic twin pairs naturally matched for genetic growth potential.

21 he fetus to reach its genetically determined growth potential.

22 ufficient to enhance tumor cell survival and growth potential.

23 ich balances leaf construction costs against growth potential.

24 because all existing graft materials have no growth potential.

25 whether it can be altered to enhance axonal growth potential.

26 in the inflamed gut in order to maximize its growth potential.

27 activity as a critical regulator of neuronal growth potential.

28 ve carbonate budget states and reducing reef growth potential.

29 concerns over reef carbonate production and growth potential.

30 ereby the fetus fails to achieve its genetic growth potential.

31 molog (PTEN) is deleted to enhance intrinsic growth potential.

32 declines are now suppressing Caribbean reef growth potential.

33 e to growth inhibitors and lack of intrinsic growth potential.

34 butes to the age-related decline of the axon growth potential.

35 rogenitor cell population to preserve future growth potential.

36 ith good clinical status fail to reach their growth potential.

37 ss and increase cancer cell survivorship and growth potential.

38 TX/96), to measure in vitro reassortment and growth potentials.

39 in genomic sequence, iPSCs acquire unlimited growth potential, a characteristic shared with cancer ce

40 agenomes to explore environmental drivers of growth potential, a fundamental aspect of bacterial life

41 nd/or Slug has been correlated with invasive growth potential, a property primarily attributed to the

42 ter inhabited by a population, the lower its growth potential, a relationship presumably molded by na

43 On the basis of growth potential, ability to re-initiate ES cultures and

44 to constrain links between reef ecology and growth potential across more than 400 tropical western A

45 and single-cell amplified genomes to survey growth potential across the range of prokaryotic diversi

46 pediatric patients because these grafts show growth potential after transplant, reducing or eliminati

47 type growth kinetics with subsequent loss of growth potential after which survivors are generated via

48 nic cells displayed unlimited stem-cell-like growth potential and a stable phenotype in culture.

49 Wind energy has significant growth potential and applicability on a global scale, bu

50 al traits beyond the acquisition of enhanced growth potential and decreased cell death.

51 he brain cell-secreted factors altered their growth potential and drove them toward a state of quiesc

52 steal cell populations were tested for their growth potential and for expression of conventional mark

53 d cancer stem cell (CSC) phenotypes based on growth potential and gene expression signatures that rep

54 ablish a correlation between diminished axon growth potential and histone 4 (H4) hypoacetylation.

55 Whether disturbed reefs can recover their growth potential and how rapidly, are thus critical rese

56 er, the signalling pathways that enhance the growth potential and induce spontaneous axon regeneratio

57 sed in keratinocytes with long-term in vitro growth potential and is coexpressed with high levels of

58 entify macroecological patterns in bacterial growth potential and link growth rates to soil carbon cy

59 ssages when the majority of cells lost their growth potential and neared senescence but p21 levels de

60 e cells with CD154 and IL-21, and determined growth potential and phenotypes in vitro.

61 d cold treatment alone had minimal affect on growth potential and resulted in ~1% flowering.

62 pha(+)Sca-1(+) (PalphaS) MSCs have augmented growth potential and robust tri-lineage differentiation

63 und that EZH2 expression correlates with NPC growth potential and that EZH2 is the dominant H3K27 met

64 nse to climate change is dependent on innate growth potential and the discrepancy between the two opt

65 nate budgets are declining, threatening reef growth potential and thus capacity to track rising sea-l

66 and the suppression of anchorage-independent growth potential and tumor formation in nude mice.

67 La cells and have lost anchorage-independent growth potential and tumorigenicity.

68 kade with an anti-EGFL7 antibody reduced the growth potential and viability of AML cells.

69 e heterodimer, the two halves have different growth potentials and assemble into hexamers.

70 Engineered HSPCs displayed altered in vitro growth potentials and induced acute leukemias following

71 ncluding 6-fold less scarring, 40% increased growth potential, and 4-fold more hypertrophic chondrocy

72 The transformed phenotype, growth potential, and actin cytoskeleton of 749r-1 cells

73 vironmental exposures that can limit genetic growth potential appear to have lessened, and variation

74 chemosensory neurons to foods with distinct growth potentials are amplified by prior consumption of

75 red axons must overcome their poor intrinsic growth potential as well as the inhibitory environment o

76 5 cells, resulted in a profound reduction in growth potential, as determined by the colony formation

77 These cells show increased growth potential at 33 degrees C, but on shift to the no

78 rapid growth might lead to an exhaustion of growth potential before progression to clonal immortalit

79 inventory costs and significantly increases growth potential but necessitates active phloem loading.

80 y intraclonal heterogeneity and hierarchy of growth potential, but also plasticity of cellular differ

81 imulates germination not by enhancing embryo growth potential, but by weakening the micropylar region

82 ly acceptable level without sacrificing bone-growth potential, but COX-associated inflammation appear

83 Inosine augments neurons' intrinsic growth potential by activating Mst3b, a component of the

84 mechanosensing of the increase in embryonic growth potential by GA action.

85 g the nymphal stage showed higher population growth potential compared to the group supplemented acro

86 oducibly isolated and had markedly increased growth potential compared to uninfected cells; HTLV-2 tr

87 rongly enhanced and Wnt-dependent clonogenic growth potential compared to virtually identical populat

88 immediate temperature, accumulated heat, and growth potential comprised a daily leaf-growth model.

89 tumour has reached the limit of its present growth potential due to cell competition that either res

90 th the mTORC1/4E-BP/eIF4E axis inhibited the growth potential endowed by accumulation of multiple dri

91 We find that growth potential, estimated from codon usage statistics,

92 steps resulting in acquisition of unlimited growth potential, evasion of apoptosis and non-responsiv

93 phenotypically distinct cells with enhanced growth potential exist within the normal arterial media,

94 to come, this work illustrates the power and growth potential for association studies of human ageing

95 t-pubertal growth stage due to the remaining growth potential for the pre-pubertal patients.

96 re at risk of not reaching their full airway growth potential in adolescence and early adulthood, sug

97 xamined for their levels of gene expression, growth potential in cell culture, and virulence in mice.

98 ed that equine MaSCs (eMaSCs) maintain their growth potential in culture for an indefinite period, wh

99 gotes exhibited a slight decrease in overall growth potential in culture.

100 ilability of t(6)A-modified tRNA, determines growth potential in eukaryotic cells.

101 g carcinoma cells (3LL) have more aggressive growth potential in IL-10 transgenic mice compared with

102 od, whereas canine MaSCs (cMaSCs) lose their growth potential in long term cultures.

103 sed to CC had no alteration of cell shape or growth potential in monolayer culture, however, a statis

104 itment and endows B cells with extraordinary growth potential in response to external proliferation a

105 on and resulted in a concomitant increase in growth potential in response to M-CSF.

106 e side effects of selection, both broadening growth potential in some conditions and narrowing it in

107 oning lesion to stimulate intrinsic neuronal growth potential in the absence of substrate modificatio

108 mediates PI3K-dependent augmentation of the growth potential in the PNS.

109 or negatively enrich for cells with enhanced growth potential in these assays.

110 mine whether clonogenic cells with long-term growth potential in vitro persist in vivo and give rise

111 tion in which a newborn fails to achieve its growth potential, increasing the risk of perinatal morbi

112 ia and neuroblastoma, can be induced to lose growth potential irreversibly and terminally differentia

113 Intrinsic neurite growth potential is a key determinant of neuronal regene

114 Tumor regrowth indicates that clonogenic growth potential is continually maintained, but the dete

115 Cell growth potential is determined by the rate of ribosome b

116 Axon growth potential is highest in young neurons but diminis

117 human fetal cortical plate, where the axonal growth potential is highest, and are lost in mature adul

118 lecular mechanisms underlying this unlimited growth potential is of broad interest for tooth regenera

119 path to carcinogenesis, the key to unlimited growth potential lies in overcoming the steady loss of t

120 ic cell types also prove to be restricted in growth potential, not identical to the corresponding pos

121 r culture on stromal layers, we assessed the growth potential of 70 cases of newly diagnosed B-lineag

122 striction (IUGR) is a failure to achieve the growth potential of a fetus that is promised by the gene

123 nt of CDC2 but not CDK2 protein; a decreased growth potential of Adp21WAF1/CIP1-infected cells demons

124 A broadly known method to stimulate the growth potential of axons is to elevate intracellular le

125 cultured glioma cells secrete glutamate, the growth potential of brain tumors has not yet been linked

126 We also demonstrated the growth potential of C. formicarius on these two host pla

127 sformation and in elevating the survival and growth potential of cancer cells.

128 uences both the contractile activity and the growth potential of cardiac myocytes.

129 ns has been attributed to a loss of inherent growth potential of cells and to inhibitory signals asso

130 of historical and future young-of-year (YOY) growth potential of Chinook salmon (Oncorhynchus tshawyt

131 As a consequence, the stem cell growth potential of cultured SUV39H2-deficient canine ke

132 es deleterious effects of Lig4 deficiency on growth potential of embryonic fibroblasts (MEFs) and gen

133 Growth potential of embryos isolated from seeds pretreat

134 In a cross-sectional study, the number and growth potential of eosinophil-lineage-committed progeni

135 r alterations responsible for the aggressive growth potential of epidermal growth factor receptor (EG

136 ng an experimental condition for testing the growth potential of functioning heart in the absence of

137 es suggested that E. faecalis suppressed the growth potential of GBS in SBM.

138 Cell proliferation assay revealed a higher growth potential of GM3 KO MEFs.

139 he above findings suggest that the increased growth potential of human lens epithelial cells by Ad12-

140 cifically attenuates proliferation and tumor growth potential of human melanoma cells expressing BRAF

141 e investigated separately effects of SHAM on growth potential of isolated embryos as well as on endos

142 d help to explain the compromised health and growth potential of LBW female piglets.

143 romosome number of 51 to 65, we assessed the growth potential of leukemic cells from 129 children wit

144 ent in establishing infection, impairing the growth potential of lung epithelial cells and thereby sl

145 s a negative regulator of the metastatic and growth potential of malignant cells and strongly suggest

146 y important for cell proliferation and tumor growth potential of melanoma cells expressing mutant NRA

147 tion inhibited tumorigenesis by reducing the growth potential of melanoma cells.

148 rtially accounts for the different postnatal growth potential of molars and incisors.

149 rming assays demonstrated an increase in the growth potential of monocyte progenitors and a significa

150 alysis was able to qualitatively predict the growth potential of mutant strains in 86% of the cases e

151 lymphoma (BL) cells and to contribute to the growth potential of other B-cell lymphoma-, gastric carc

152 llular metabolism and cell division with the growth potential of the cell.

153 during the diauxic switch and the long-term growth potential of the cell.

154 nly increased after a significant decline in growth potential of the culture.

155 Thus, as the growth potential of the environment decreases, cells app

156 eurotrophin 3 during exercise, the increased growth potential of the exercise-conditioned animals req

157 in the heterozygote mice matches the limited growth potential of the great majority of TSC hamartomas

158 he number of susceptible cells influence the growth potential of the virus?

159 splantation experiments designed to test the growth potential of these lesions.

160 these interactions can explain the unlimited growth potential of these tumors.

161 ctors on the spatiotemporal distribution and growth potential of Trichodesmium for the last glacial m

162 pecific niche signals can restore metastatic growth potential of tumor cells lacking one of the oncog

163 vels of ROS associated with the uncontrolled growth potential of tumor cells.

164 al and, thereby, the cell shape and invasive growth potential of tumor cells.

165 ted and soil was rehydrated to determine the growth potential of underground adventitious buds.

166 gside mutation co-occurrence to quantify the growth potential of variants within individuals.

167 Leaf surface temperatures and growth potentials of plants growing under well-watered c

168 nucleation mechanisms are discussed and the growth potentials of the nuclei are also analyzed and di

169 rum IGF-1 levels, but this neither predicted growth potential or skeletal integrity nor defined growt

170 f certain neuronal populations that retain a growth potential over time, and lead to functional impro

171 of Pak1 regulation of anchorage-independent growth, potential Pak1 regulation of invasiveness, and a

172 ytokines and demonstrate that this increased growth potential precedes polyploidization of the cultur

173 ory factors in the lesion scar and poor axon growth potential prevent axon regeneration.

174 tion to survey the distribution of microbial growth potential, regardless of cultivation status.

175 thereby offering a unique system to uncover growth potential regulators.

176 gnificantly reduced capacity to enhance cell growth potential relative to BL cells expressing wild-ty

177 ying this EBER-dependent enhancement of cell growth potential remain to be elucidated.

178 t a fraction of adult mouse hepatocytes have growth potential similar to that of hematopoietic stem c

179 xons are double conditioned to enhance their growth potential, some traverse the lesion core and expr

180 ein (MEZ) results in an irreversible loss in growth potential, suppression of tumorigenic properties

181 os from dormant seeds, however, had a lesser growth potential than those from nondormant seeds.

182 poietic cells leads to functional defects in growth potential that may be of consequence to leukemic

183 merase-deficient cells began to show loss of growth potential, the cells arrested in G2/M and showed

184 ut is most often competitively excluded; and growth potential, the innate capacity for growth at the

185 ic effect most closely related to population growth potential; the colder the winter inhabited by a p

186 roximal-distal growth axes with two types of growth potential: they can be indeterminate, in which ca

187 be crucial for acquisition of the unlimited growth potential thought to be critical for malignant pr

188 control system, suggest that the cell trades growth potential to avert the potential toxicity associa

189 cl-2 is an oncogene that confers deregulated growth potential to B lymphocytes through its ability to

190 Enhanced expression of MYCN confers growth potential to neuroblastoma cells, and a direct li

191 er a complete SCI in rats improves intrinsic growth potential to result in axon regeneration out of a

192 o confer anchorage independence and invasive growth potential to transformed cells.

193 undaries promotes the homogenization of zinc growth potential, to achieve uniform nucleation and grow

194 ively active Rheb to enhance their intrinsic growth potential, transplanted a growth supporting perip

195 at exerts its detrimental, highly aggressive growth potential upon escape from cell-cycle blockade, a

196 This extension of the in vitro growth potential was accomplished without any of the obv

197 We also observe that growth potential was negatively correlated with the rela

198 Embryo growth potential was quantified by incubating decoated e

199 te index of each site, which is a measure of growth potential, was varied to represent different leve

200 y, the strongest environmental predictors of growth potential were productivity indicators, such as d

201 PCR in aggressive MPM cells attenuated their growth potential, whereas EPCR silencing in nonaggressiv

202 Axons differ in their growth potential: whereas during development, axons rapi

203 changes have driven major reductions in reef growth potential, which have declined from an average 4.

204 SAC unleashes cyanobacterial growth potential with 0.1 g/L/hour biomass productivity

205 tween target cell availability and the virus growth potential with a combination of experimental and