ライフサイエンスコーパス: cell number

1 r5-positive intestinal stem cell tracing and cell number.

2 stored blastocyst development, hatching, and cell number.

3 of primary CD4(+) T cells up to 300-fold in cell number.

4 We obtained high quality data from small cell number.

5 ease early in life, without affecting T(reg) cell number.

6 d symmetric divisions that increase the seam cell number.

7 rtion of animals showing an increase in seam cell number.

8 Drosophila VGSC, reduces neuroblast progeny cell number.

9 lineages, with a concomitant reduction in T cell number.

10 that leads to reliable results, unbiased by cell number.

11 Heat flow increased over time with cell number.

12 vation is known to affect both cell size and cell number.

13 ess of the differences in geometry and total cell number.

14 om loss of islet cell size rather than islet cell number.

15 isconnect between bioluminescence signal and cell number.

16 al activity at the critical period increased cell number.

17 ability of the data obtained with the lowest cell number.

18 adult gonadectomy has no effect on CRFR1-GFP cell number.

19 and informative as the analysis of a larger cell number.

20 le knockout mice show a partial rescue in DP cell number.

21 mplifying cells, which together determine RM cell number.

22 challenges for precious samples with limited cell number.

23 r than cell-intrinsically, to control VGluT3 cell number.

24 dex of blastocysts and increased their total cell number.

25 he total cell surface area rather than total cell number.

26 ng organ development to determine final leaf cell number.

27 s repressor complex, leading to reduced leaf cell number.

28 ves terminal differentiation, limiting final cell numbers.

29 rease in INPs and overall neuroblast progeny cell numbers.

30 stimulated to divide to maintain tissue-wide cell numbers.

31 mall lymph nodes with marked reductions in B cell numbers.

32 s tumor associated inflammation and CD8(+) T cell numbers.

33 which effectively increased DN CD38(hi) NKT cell numbers.

34 in which growth rates scale positively with cell numbers.

35 to a greater extent, germinal center (GC) B cell numbers.

36 e B cells, resulting in reduced peripheral B cell numbers.

37 regulatory circuitry in samples with limited cell numbers.

38 n-presenting capacity of DCs and increased T-cell numbers.

39 e cytokine secretion levels and regulatory T cell numbers.

40 d that NKG2D deficiency affects peripheral B cell numbers.

41 sory hair cells has been hampered by limited cell numbers.

42 nction, promoting increases in gingival Th17 cell numbers.

43 sed marginal zone and decreased follicular B cell numbers.

44 ons were observed between asthma and B- or T-cell numbers.

45 ns between LLP2A signal and macrophage and T cell numbers.

46 n in BAL and BW samples, while requiring low cell numbers.

47 ared to controls despite normal peripheral B cell numbers.

48 g memory Treg cells, but not higher IgE(+) B-cell numbers.

49 lood vessel growth and circulating red blood cell numbers.

50 organization by TSA-seq, we reduced required cell numbers 10- to 20-fold for TSA-seq by deliberately

51 llergic sensitization had higher memory Treg cell numbers 12.3% (95% CI 4.2; 21.0), (11.1% (95% CI 3.

52 d higher total B and CD27(+) IgA(+) memory B-cell numbers (15.2% [95% CI 3.2; 28.7], 22.5% [95% CI 3.

53 The osteoclast cell numbers (-32.45%, P = 0.01) and surface (-32.58%, P

54 2, MYBL2, NEK2, NIPA2, and TCEB3) decreasing cell number, activating p16/p21, and undergoing morpholo

55 gy and neurodegeneration but reduced Iba1(+) cell numbers, all of which could not be rescued by addit

56 terial and nematode abundance, but bacterial cell numbers also declined under warming, demonstrating

57 gene expression profiles indicates that low cell number analysis is as dependable and informative as

58 This increase in orexin cell number and activity persisted during protracted wit

59 hoea, OVA-specific antibody production, mast cell number and activity, inflammatory gene expression i

60 ts reveal specific abnormalities in myogenic cell number and behavior associated with SPEG deficiency

61 e reporter is that the luciferase expressing cell number and bioluminescence signal are linearly prop

62 chanisms underlying the relationship between cell number and body size remain poorly understood.

63 t enrichment analysis predicts hematopoietic cell number and cell infiltration are modulated by CR1(l

64 of positional fluctuations in dictating stem cell number and dynamics, and we discuss the applicabili

65 motes the age-related reduction of satellite cell number and function and contributes to sarcopenia.

66 Stem cell number and function have been identified as potenti

67 an provide high-throughput quantification of cell number and function in BAL and BW samples, while re

68 as associated with significantly improved NK-cell number and function, lower viral infections, and lo

69 have been associated with a decline in stem cell number and function.

70 rd the injury site promoted rapid changes in cell number and generated shifts in tension at cellular

71 Ngn3 and NeuroD1 L3740 also increased the L-cell number and GLP-1 levels and improved glucose tolera

72 ere of higher quality than C-IVF in terms of cell number and hatching ability.

73 hibit neuroprotective function by increasing cell number and neurites, as shown by indirect coculture

74 ng a cell model, we show that 4HNE decreases cell number and oxidative phosphorylation (control, 388.

75 ic inflammatory skin disorder, and both mast cell number and PAMP1-20 concentrations (agonist of the

76 evolved multicellular life cycles, with both cell number and propagule size varying among isolates.

77 ps were confirmed by a greater TRAP-positive cell number and reabsorption surface on both the pressur

78 -1 with an antibody increased KLRG1(+) ILC-2 cell number and reduced disease burden.

79 n, E2F target gene expression, and epidermal cell number and shape in e2fb mutant and overexpression

80 NTHi infection increased the total cell number and significantly decreased the proportion o

81 evelopment much evidence indicates that both cell number and the cell fates generated by each neurobl

82 emonstrate a direct correlation between stem cell number and time to bone fracture union in a human p

83 therefore contribute independently to final cell number and to mosaic order.

84 essing ventral tegmental area (VTA) dopamine cell number and volume and expression of tyrosine hydrox

85 ans with misspecified identity and increased cell number and, furthermore, causes defects in apical m

86 Antibiotic treatment reduces EC cell numbers and 5-HT levels in naive C57BL/6 mice, whic

87 (-/-)) and Myd88 (-/-) mice express lower EC cell numbers and 5-HT levels, whereas treatment with TLR

88 king PKC-theta had reduced ILC2 numbers, TH2 cell numbers and activation, airway hyperresponsiveness,

89 od counts (CBC), antibody binding of RBCs, T cell numbers and activation, hematopoietic progenitor ch

90 CVC increased liver T-cell numbers and attenuated Il-2 expression without an e

91 cells results in substantially reduced T(FR) cell numbers and consequently elevated GC responses.

92 anaphylaxis, likely due to reduction in mast cell numbers and depletion of pre-formed inflammatory me

93 nstrated a positive correlation between Treg-cell numbers and epidermal BMP7 expression in cutaneous

94 death and division to maintain overall stem cell numbers and epithelial tissue homeostasis.

95 c deletion of CD28 caused a reduction in TFR cell numbers and function, which resulted in increased g

96 nce, but increased IL-22 in vivo decreased T cell numbers and functions in the liver and lymphoid tis

97 e demonstrate that epidermal flanks modulate cell numbers and geometry of their fusing fronts to achi

98 cells resulted in a marked reduction in TFH cell numbers and IgE antibody levels, but type 2 cytokin

99 hematopoietic stem cells severely reduced B cell numbers and impaired B cell development in a hemato

100 We observed low NK cell numbers and impaired NK cell maturation, suggesting

101 Despite severely diminished MAIT cell numbers and impaired phenotype in circulation, peri

102 creased pulmonary monocyte-derived dendritic cell numbers and increased IFN-gamma-dependent expressio

103 ol showed strongly decreased adaptive immune cell numbers and increased neutrophils, accompanied by h

104 evelopment of septic shock by maintaining NK cell numbers and integrity.

105 TH2 cell numbers and levels of their cytokines, IL-4 and IL-

106 ocus on pathways that raise systemic myeloid cell numbers and modulate immune cell phenotypes, review

107 the alteration of beta-cell identity, islet cell numbers and morphology, and gene expression by disr

108 ced myelin thickness, mature oligodendrocyte cell numbers and mRNA levels of myelination-related gene

109 RP3-II, but not of HRP3-I, increased Schwann cell numbers and myelination in PNS neuron-glia co-cultu

110 ll-specific deletion of Shp1 had normal iNKT cell numbers and peripheral distribution.

111 Immune cell numbers and phagocytic activity were evaluated by f

112 w cells into young animals reduced satellite cell numbers and promoted satellite cells to switch towa

113 ental developmental mechanism for regulating cell numbers and sculpting developing organs.

114 lymerase II and transcription factors on low cell numbers and single cells.

115 ugmented upon TPC1 inhibition, although mast cell numbers and size were diminished.

116 tion between absolute natural killer T (NKT) cell numbers and the subsequent development of MODS.

117 ues are negatively correlated with CD4+CD38+ cell numbers and total CD4+ T cell counts in patients wi

118 TAC-seq (scATAC-seq) allow analyses of small-cell-number and single-cell samples, but their signals r

119 I, 17% to 85% versus CI, 20% to 70% of total cell number) and CD138 (TI, 1% to 73% versus CI, 12% to

120 All NK expansions achieved the required cell number, and 11 of 13 patients enrolled received all

121 rowth indicated by higher cell viability and cell number, and inhibited cell injury indicated by lowe

122 on in islet density, decreased relative beta-cell number, and presence of amyloid deposits.

123 , decreased T cell infiltration, increased B cell numbers, and decreased macrophage recruitment.

124 After challenge, symptoms, Treg cell numbers, and forkhead box protein 3 (Foxp3), TH2 an

125 ytic treatment reduces p16(INK4a)-expressing cell numbers, and inhibits Wnt activation and hyperplasi

126 , reduced autoantibody production and plasma cell numbers, and normalized B and T cell subsets.

127 etween visual field sensitivity and ganglion cell number are reviewed.

128 Methods for quantifying cell numbers are already available (e.g., fluorescence i

129 NK cell numbers are increased in the blood of PD patients a

130 ne cells, especially when sample volumes and cell numbers are limited.

131 Although total CD4(+)FOXP3(+) Treg cell numbers are reduced, frequencies are maintained in

132 r application in experimental settings where cell numbers are restricted, such as in vivo infections

133 Stat1(-/-) mice however have normal CD4(+) T cell numbers as innate STAT1 signaling is required for t

134 uction correlated with reduced invariant NKT cell numbers as well as lower IL-23 levels.

135 reased cell recruitment with higher CD4(+) T cells numbers as well as increased IFN-gamma and TNF-alp

136 In HG patients, total B-cell numbers, as well as IgA + and IgG + switched memory

137 cline may be caused by a decrease in cardiac cell number because of increased cell death or by a redu

138 Variations in cell numbers between baseline, placebo and Q-GRFT treate

139 Like osteoblast cell numbers, BMP-2 expressions were also elevated in lu

140 ntage, defect depth percentage, implantation cell number, body weight, tissue source, and the type of

141 cells and decreases hematopoietic progenitor cell numbers both in vivo and in vitro.

142 which was not associated with reductions in cell number but with the extracellular accumulation of c

143 group (n = 30) grafts contained similar beta-cell numbers but included isolates that were cultured fo

144 etion of Nur77 had no effect on CD4(+)CD8(+) cell numbers but reversed the loss of mature CD4(+) thym

145 xist in the absence of changes in microglial cell number, but with putative evidence of microglial an

146 and miR-145 transfection decreased cervical cell number by increasing apoptosis and decreasing cell

147 ere run with moderate levels of O. cf. ovata cell numbers (ca. 10(5) cells.L(-1)) and total toxin in

148 of clodronate effectively reduced total BALF cell numbers, CCR2(+) immature macrophages, and eosinoph

149 plasticity and show that temperature-induced cell number changes are controlled by Wnt- and TGF-beta

150 Often, as total cell number changes, stem cell number changes proportionally in a phenomenon calle

151 Often, as total cell number changes, stem cell number changes proportion

152 eg, Treg-memory, and CD27(+) IgA(+) memory B-cell numbers compared to children without atopic disease

153 This question is central to morphogenesis, cell number control, and homeostasis.

154 During exacerbation, peripheral blood Th2 cell numbers correlated with ACQ6 and AQLQ scores, while

155 For some IEL subpopulations, the decrease in cell numbers could be attributed to apoptosis and reduce

156 We therefore generated a high depth, high cell number dataset to determine the effect of reduced s

157 tor proliferation was reduced and progenitor cell number declined, leading to interruption in the sup

158 e Chlamydomonas reinhardtii as a function of cell number density and light stimulus using high spatio

159 Tissue stiffness correlated variably with cell number density, oligodendrocyte interconnectivity,

160 The age-related recovery of the T-cell number depended on a homeostatic peripheral prolife

161 the analysis of secreted compounds from low cell numbers down to a single cell.

162 f diabetes caused by reduced pancreatic beta-cell number (due to destruction or defective development

163 show that PIEZO1 is important in regulating cell number during CNS development.

164 g promotes faster regeneration and increases cell number during homeostasis.

165 Some clusters increase in cell number during late larval stages, whereas others do

166 is limited by the need for relatively large cell numbers, especially when studying post-translationa

167 Here, we study how increased cell number evolved in the vertebrate central nervous sy

168 In mammals, cardiac growth by cell number expansion changes to growth by cardiomyocyte

169 ire months of culture to generate sufficient cell numbers for feasibility studies in a lab setting an

170 A decrease in NK cell numbers from systemic circulation was observed conc

171 We found that firstly, cell number has a much more profound effect than sequenc

172 T(reg) cell function and decreases in T(reg) cell numbers have been observed in patients with autoimm

173 luates the impact of intravascular bacterial cell numbers (ie, the level of bacteremia), in patients

174 nction of position, and thus functional stem cell number in each organ.

175 gly suggest that an early deficiency in beta-cell number in infants with CF may contribute to the dev

176 s as an additional mechanism for restricting cell number in nutrient-fluctuating environments.

177 development, which affect the terminal seam cell number in opposing directions.

178 the birth rate of tumor cells increases with cell number in the regime of small population size.

179 four weekly IVIs increased the photoreceptor cell number in the retinae of Rho(P23H/+) mice compared

180 arrier eventually enabling OA to image small cell numbers in a complete organism in vivo.

181 that conditions associated with reduced MZ B cell numbers in adult mice cause increased cDC2 occupanc

182 flammation/gliosis and increased neural stem cell numbers in areas of tissue injury.

183 sonance imaging (MRI), and higher peak CAR-T cell numbers in blood, but not cerebrospinal fluid (CSF)

184 by gut but not skin dysbiosis, and reduced T cell numbers in both sites.

185 secreting bacteria also reduced inflammatory cell numbers in bronchoalveolar lavage (BAL).

186 ed to a marked reduction of eosinophil and T cell numbers in bronchoalveolar lavage fluid compared wi

187 ciations of higher Treg and CD27(+) IgA(+) B-cell numbers in children with food-allergic sensitizatio

188 sequencing platforms, sequencing depths and cell numbers in designing scRNA-seq experiments, so as t

189 on, the ability of MACS to isolate increased cell numbers in less time than FACS may prove valuable i

190 ) mice and a continued reduction in CD4(+) T cell numbers in mesenteric lymph nodes.

191 enhanced CD4 TFH and germinal center (GC) B cell numbers in naive mice and hastened islet allograft

192 a systemic reduction in natural killer (NK) cell numbers in SRalpha-tTA/Tet-O-MYC(ON) mice bearing M

193 Expression of CD44 and apoptotic cell numbers in tendon tissue from patients with long he

194 oved lung compliance, and increased CD8(+) T cell numbers in the airways.

195 proliferative zone and an increase in goblet cell numbers in the colon crypts of Zfp36(DeltaIEC) mice

196 ease in cellularity of Peyer's Patches while cell numbers in the lamina propria and intraepithelial l

197 ion, and an increase in intraepithelial mast cell numbers in the lung.

198 cells (ILC2s) and monocyte-derived dendritic cell numbers in the mediastinal lymph nodes, and increas

199 Plasma cell numbers in the nasal mucosa increased during treatm

200 ads to splenic atrophy and contraction of NK cell numbers in the periphery through a modulated expres

201 ased IL-12-producing hapten-primed dendritic cell numbers in the skin-draining lymph nodes.

202 entiated T cells in the thymus and altered T cell numbers in the spleens of A20 mutant mice.

203 lfurimonas, which typically occurs with high cell numbers in the vicinity of sulfidic environments.

204 sruption of Vascular Patterning, and reduced cell numbers in vascular bundles.

205 , cytokine profiles and Th-1, Th-2 and Th-17 cells numbers in each mating type treated mice showed th

206 lease (CUT&RUN) method to profile TFs in low cell numbers, including single cells and individual pre-

207 In AS mice, the bright(tdT) cell number increased and presented differential express

208 In anoxic incubations, Methylobacter cell numbers increased almost two orders of magnitude wi

209 d; however, standardization to total granule cell numbers indicated that the two groups of wild-caugh

210 ure temperature, although their average seam cell number is comparable at 20 degrees .

211 Control of cell number is crucial to define body size during animal

212 The cell number is determined by the balance between cell pr

213 However, islet cell number is maintained and insulin secretion is unaff

214 egrees C min(-1)) that a reduction in viable cell number is observed following slow rates of warming

215 tly affect developmental mechanisms in which cell number is the strongest determinant of body size.

216 Although Phlpp1 deficiency increased TRAP(+) cell numbers, it suppressed actin-ring formation and bon

217 Cell viability, cell number, lactate dehydrogenase (LDH) activity, cell

218 ecause of inherent obstacles including small cell numbers, large cell-type heterogeneity, complex ana

219 Importantly, this increase in cell number leads to an increase in body size only in a

220 GC area was smaller and plasmablasts/plasma cell numbers lower in anti-BAFF-treated rats, which was

221 han invertebrates, and an increase in neural cell number may have contributed to the sophisticated an

222 Strategies to increase beta-cell number must not only tackle the difficult challenge

223 d that in the absence of BD(L), the absolute cell number of CD4(+)Foxp3(+) T regulatory cells (Treg),

224 t despite a reduction in peripheral CD8(+) T cell numbers of ~50% in MHCI hemizygous mice, MHCI level

225 r proportions, number of genes expressed per cell, number of marker genes and their fold change, and

226 e the effect of reduced sequencing depth and cell number on the ability to accurately identify CD4+ T

227 t this time also negatively predicted DCX(+) cell numbers on an individual level, while hens that acq

228 ly, absence of CD4 help caused reductions in cell numbers only among terminally differentiated cells

229 cells using Lysm-cre did not impact myeloid cell number or function.

230 es mellitus (PNDM) is caused by reduced beta-cell number or impaired beta-cell function.

231 ngle gene mutations reducing pancreatic beta cell number or impairing beta cell function.

232 ity structure can be analyzed by quantifying cell numbers or by quantifying biomass for individual po

233 ass I antigen presentation or diminish CD4 T-cell numbers or impair their function.

234 eal any major changes in staining intensity, cell number, or forebrain puncta counts.

235 each groups, which is in appropriate to the cell numbers (P < 0.0001).

236 HIV coinfection significantly increased T cell numbers (P = 0.017) and shifted cells from an intra

237 cells, with increased cell size and reduced cell number per leaf blade with incrementing ploidy.

238 Together, we conclude that localized cell number plays a key role in dictating cellular behav

239 rgic activity or reducing starburst amacrine cell numbers prevents invasion of endothelial cells into

240 e non-invasively, yielding information about cell number, proliferation, or metabolism.

241 The cell number ratio of the two metabolic phenotypes is fou

242 tant mice had reduced mature oligodendrocyte cell numbers, reduced myelin thickness and impaired axon

243 icantly reduced leukemic stem and progenitor cell numbers, reduced regeneration of leukemic long-term

244 ution in hierarchical tissues by considering cell number regulation that acts on cell division rates

245 s, but showed no differences in regulatory T-cell numbers relative to patients without IRAEs.

246 res of M. salina resulted in decreased algal cell numbers, relative to uninfected controls, and gener

247 Although Lgr5-positive intestinal stem cell numbers remained constant in Msi1-overexpressing ti

248 ll ensembles increased in size, whereas odor-cell numbers remained stable.

249 We hypothesized that this reduction in new cell numbers resulted from impaired proliferation, which

250 e and map compacted heterochromatin from low-cell number samples.

251 Transcriptome data in single-cell and small-cell-number samples are more continuous and often less n

252 oliferation and survival, circulating tumour cell number, seeding of cancer cells in distant organs a

253 Whereas in smokers B-cell numbers slightly increased, robust increases in B-c

254 Reduced cell number spleen ILC2s could be differentiated from NI

255 Regulatory T (Treg)-cell numbers strongly increase during psoriatic skin inf

256 ion are independent of changes in epithelial cell number, suggesting that the size of the thymus is r

257 t inhibiting TRPM7 activity increases T(reg) cell numbers, suggesting that it may be a therapeutic ta

258 Experimentally reducing Ocn(+) cell numbers suppresses the neutrophil response and lung

259 cytes constitute a smaller fraction of total cell number than previously estimated in the normal adul

260 tly greater negative effect on Synechocystis cell numbers than Chlorella (P < 0.0001).

261 e evidence that the major changes in ovarian cell number that regulate D. melanogaster ovariole numbe

262 attended by significant upregulation of Tfh cell numbers that altogether might explain the observed

263 In larvae, mpeg1+ cell numbers then increased showing two distinct types i

264 pt organoid proliferation and increased stem cell numbers through pSTAT3 activation in Paneth cells.

265 eneration, the therapeutic expansion of beta-cell number to reverse diabetes, is an important goal.

266 s a homeostatic sensor to control epithelial cell numbers, triggering extrusion and apoptosis in crow

267 However, the impact of sequencing depth and cell numbers, two important factors in scRNA-seq, has no

268 x (bHLH) transcription factor, increase seam cell number variability.

269 However, cervical CD4+ T-cell number was associated with HSV-2 infection and a di

270 Osteoblast cell number was higher and osteoclast and inflammatory c

271 ully developed Arabidopsis thaliana embryos, cell number was not affected either in single or double

272 However, a rebound in the cell number was observed after the prolonged exposure ex

273 In PD, dopaminergic amacrine cell number was reduced between 58% and 26% in different

274 e physiological age-related decline of the T-cell number was slower in pDGS patients compared with ag

275 nistically, we showed that the increase in T cell numbers was associated with superior tissue homing

276 Increase in KLRG1(+) ILC-2 cell numbers was attributed to an intrinsic defect in PD

277 tigate the mechanism of the decrease in stem cell number, we analyzed the Notch signaling pathway.

278 Th) T cell activity, and natural killer (NK) cell number were measured by flow cytometry.

279 The total blastocyst cell numbers were counted, and the fragmentation rate an

280 In addition, memory T cell numbers were decreased in modified avian influenza

281 nd increases in bronchoalveolar lavage fluid cell numbers were detected a lower doses and volumes, si

282 , the individual atopic diseases, and immune cell numbers were determined.

283 Furthermore, CD28(null) CD8 T-cell numbers were increased in Amish children, with high

284 M(+) (70-80%), but IgA(+) (and not IgG(+)) B-cell numbers were increased in LFs from severe COPD comp

285 r was higher and osteoclast and inflammatory cell numbers were lower in the P group compared to C, L-

286 Total splenic DC cell numbers were modestly increased but differentiation

287 Catecholamine effects on immune cell numbers were mostly similar to cortisol in directio

288 Despite this, beta-cell numbers were only slightly reduced in older animals

289 However, peritoneal mast cell numbers were significantly lower in infected mice,

290 By 7 wk, colitis score and colon CD4(+) T cell numbers were similar in Cre(+) and Cre(-) mice desp

291 TI, 1% to 73% versus CI, 12% to 69% of total cell number) were predominantly expressed.

292 red the proliferative cell cycle and grew in cell number when treatment was terminated.

293 olog results in reduction in pancreatic beta-cell number which we demonstrate to be due to increased

294 3 in mice significantly reduces HCRT and MCH cell numbers, while knock-down of a Peg3 ortholog in zeb

295 st, the rate of decline in thymic epithelial cell numbers with age was radiation-sensitive only in ma

296 noma cells were seeded at different starting cell numbers with growth and reduction kinetics monitore

297 2 inactivation leads to a robust increase in cell number, with local disorganization of the cytoskele

298 ectively no impact of warming rate on viable cell number within the range of warming rates examined (

299 ns that result in an exponential increase of cell number without changing the overall size of the emb

300 raries with a 2.5-fold reduction in required cell numbers without sacrificing performance compared to