ライフサイエンスコーパス: transit time

1 roups (45 and 30 mg), except for DCE CT mean transit time.

2 als without CCSVI, without any delay in mean transit time.

3 al pressure multiplied by the hyperemic mean transit time.

4 ness, with the compliant cells having faster transit time.

5 inversely reduced the erythrocyte capillary transit time.

6 bacter hepaticus, influence small intestinal transit time.

7 including distention of colon and slowed GI transit time.

8 he antro-duodenum and also reduces oro-cecal transit time.

9 tanol by the enterocyte nor small intestinal transit time.

10 d gastric emptying, and increased intestinal transit time.

11 no significant difference in cardiopulmonary transit time.

12 d there was a prolongation of the TC biliary transit time.

13 ributes to establishing their lymphoid organ transit time.

14 ow, relative cerebral blood volume, and mean transit time.

15 f capillary geometry and fMLP-stimulation on transit time.

16 er breast size was associated with increased transit time.

17 ted, primarily by an effect on arteriovenous transit time.

18 r pores represents more than one-half of the transit time.

19 atively correlated with the gastrointestinal transit time.

20 rtic elastic modulus and increased the pulse transit time.

21 , and that isoprenoid stepping ensures short transit times.

22 uses are the major factor contributing to LN transit times.

23 on of polysomes and an increase in ribosomal transit times.

24 unterparts in both topological mechanism and transit times.

25 s rolling interactions and prolongs monocyte transit times.

26 neutrophils, prolonging their lung capillary transit times.

27 ament mass was the primary driver of network transit times.

28 layers, offering the prospect of ultra-fast transit times.

29 ntrols (p = 0.43)--or total gastrointestinal transit time--1.6 days (range 0.5-2.9) in patients and 2

30 ood volume (6-33% decrease), and tissue mean transit time (10-54% increase) were observed in the gray

31 fe (0.79 +/- 0.25 days; 19 hours) and marrow transit time (5.80 +/- 0.42 days).

32 ileum filling also decreased as small bowel transit time accelerated and the meal reached the termin

33 mall intestine and a slower gastrointestinal transit time allow the bacterial lactase to be active, d

34 mize these modified spirals suggest equating transit times along the inner and the outer track of the

35 Mean transit time and blood volume fraction were comparable b

36 Brain perfusion (mean transit time and blood volume fraction) was comparable b

37 quantitative voxel based thresholds for mean transit time and cerebral blood volume (CBV).

38 atal necrosis in an 8-month-old infant, mean transit time and cerebral blood volume were low relative

39 l lesions, striatal flow was normal but mean transit time and cerebral blood volume were low, consist

40 mulations of runoff generation, stream water transit time and evaporation-transpiration partitioning.

41 ment session, the animals were tested for GI transit time and galactose absorption, and fecal weight

42 (Slc10a2, Slc51a) and increases in whole gut transit time and intestinal permeability.

43 was accompanied by more rapid intrarenal dye transit time and slight increase in renal extraction rat

44 The transit time and the size of each cell were accurately m

45 -doubling time, shorten the duration of G(1) transit time and/or G(1)-S transition, and transform NIH

46 dramatically shortening the duration of G(1) transit time and/or G1-S transition, and transforms NIH3

47 No significant correlation was found between transit times and age, sex, weight, and height.

48 al completion rates, gastric and small bowel transit times and diagnostic yield were analyzed.

49 Cardiopulmonary transit times and dispersions (full widths at half maxim

50 Transit times and FWHM values for the patients with hear

51 Cardiopulmonary transit times and FWHM values were significantly prolong

52 nists stimulate intestinal motility, shorten transit times and in a pilot trial accelerated transit i

53 s characterized by higher loss rates, faster transit times and lower throughput, suggesting that neur

54 is a new method for ambulatory assessment of transit times and motility throughout the gastrointestin

55 d newborn pigs, and changes in arteriovenous transit times and retinal arteriolar and venular diamete

56 eters from the vesicle and by monitoring the transit times and the number of released molecules that

57 Dynamical (e.g., velocimetry and transit timing) and statistical methods have confirmed a

58 coefficient, tissue oxygen saturation, mean transit time, and blood volume fraction in the cortex an

59 group); local brain oxygen saturation, mean transit time, and blood volume fraction were subsequentl

60 Laxation response, oral-cecal transit time, and central opioid withdrawal symptoms wer

61 luation of glomerular filtration rate, renal transit time, and differential renal function.

62 celeration time of mitral E velocity, A wave transit time, and end diastolic volume/pressure ratio wa

63 cimens were initially positive regardless of transit time, and incubation yielded another 19 positive

64 on of multipolar spindles, increases mitotic transit time, and induces micronucleation in response to

65 culate tissue blood flow, blood volume, mean transit time, and permeability-surface area product.

66 ment of tumor blood flow, blood volume, mean transit time, and permeability-surface area product.

67 ntral venous pressure, prolonged fluorescein transit time, and the presence of any retinal ischemia w

68 ct, we measured exhaled H2 and CH4, oro-anal transit time, and the severity of psychological and gast

69 imulus-induced changes in mean arteriovenous transit times, and arteriolar and venular diameters, fro

70 Appetite, gastric-emptying and orocecal transit times, and selected endocrine responses were mon

71 han filament orientation in reducing average transit times, and transport properties were optimized i

72 The short transit time ( approximately 4.5 s) between electrochemi

73 ficantly smaller than the arteriolar-venular transit time ( approximately 500 ms), indicating an arte

74 of capillary geometry and fMLP on neutrophil transit time are presented as a simple dimensionless exp

75 Predicted transit times are consistent with previous experimental

76 ons between bacterial species abundances and transit times are diet dependent.

77 Cell transit times are inferred to be proportional to the ins

78 on, raptor levels, cell size, and cell cycle transit times are not diminished in these cells.

79 cifically UbcH7 in the regulation of S phase transit time as well as in cell proliferation.

80 ysis and fluorescence detection and the fast transit times (as low as 10 ns) of the fluorescent molec

81 arent occupancy states exceeded the expected transit times assuming simple diffusion by orders of mag

82 The oral-cecal transit times at baseline for subjects in the methylnalt

83 IGE patients exhibited prolonged arterial transit time (ATT) in the left superior temporal gyrus.

84 ns, more rapid gastric-emptying and orocecal transit times, attenuated insulin and glucagon-like pept

85 --that newly arrived cargo exhibits a lag or transit time before exiting the Golgi.

86 in cell cycle regulatory gene expression and transit times between normal and chronic myeloid leukemi

87 power broadening, collisional broadening and transit time broadening.

88 , probiotics significantly reduced whole gut transit time by 12.4 h (95% CI: -22.3, -2.5 h) and incre

89 Visual analysis and mean transit time calculation were performed on the rest and

90 elevated cerebral blood volume and high mean transit time/cerebral blood flow and cerebral blood volu

91 in SM/ICC-GCKO mice, which had increased gut transit time compared with controls.

92 a, gastroparesis, prolonged gastrointestinal transit time, constipation and difficulty with defecatio

93 Transit time correlated directly with LV end-diastolic a

94 ended to take the heterogeneity of capillary transit times (CTH) into account.

95 rointestinal transit time (TGTT) and colonic transit time (CTT) were measured in mice lacking D2, D3,

96 as to determine normative ranges for colonic transit time (CTT), Patient Assessment of Constipation-S

97 d cells with various target cell ratios, the transit time delay increased approximately linearly with

98 Thus, from the transit time delay we can identify target cells and quan

99 correlation and compared the results to mean transit time derived using bolus tracking.

100 Gut transit time did not change in SM-GCKO or ICC-GCKO mice

101 However, transit time did not correlate strongly with age, body s

102 tions, calcium balance, and gastrointestinal transit time did not decrease as fiber intake increased.

103 ipid secretion and taurocholate (TC) biliary transit time during high ASBT activity.

104 etics of fluid phase endocytic flux (uptake, transit time, efflux).

105 had low cerebral blood flow, prolonged mean transit time, elevated cerebral blood volume and high me

106 receptor (TCR)-independent factors to the LN transit time, exposing the divergent surveillance strate

107 Transit time flow (TTF) probes may be useful for predict

108 Two methods, transit time flow measurement and intraoperative fluores

109 h amniotic and vascular catheters and with a transit-time flow probe around a femoral artery.

110 h amniotic and vascular catheters and with a transit-time flow probe around a femoral artery.

111 A transit-time flow probe was placed on the ascending aort

112 otic and femoral vascular catheters and with transit-time flow probes around the contra-lateral femor

113 Coronary artery flow was measured with a transit time flowmeter during baseline, pharmacological

114 flow (RBF) was measured using an ultrasonic transit-time flowmeter and a non-cannulating V-shaped pr

115 ference was observed in mean cardiopulmonary transit time for SonoVue or Levovist (9.1 seconds +/- 2.

116 n was consistent with a longer half-ribosome transit time for the synthesis of apoB in MTP-inhibited

117 The slow diffusion also led to much longer transit times for barrier crossing, allowing transition

118 tein-coding sequence, consistent with longer transit times for ribosomes translating longer coding se

119 These results combined with longer transit times for the T = 4 capsids indicated that the c

120 lower arterial fraction and higher vascular transit time, fractional volume of the vascular space, a

121 Lymph transit time from hand to axilla, ttransit, was 9.6+/-7.

122 Aortic pulse wave transit time from the root of the subclavian artery to a

123 ir effects on sentinel node localization and transit times from injection to arrival at the sentinel

124 ity (BCVA), area of CNP, retinal fluorescein transit time (FTT), and an evaluation for rubeosis iridi

125 Total GI transit time, galactose absorption, zonulin levels in pl

126 minal ultrasound, and total gastrointestinal transit time (GITT) determined with radio-opaque markers

127 A prolonged gastric transit time has been recognized as a risk factor for in

128 The inverse of the hyperemic mean transit time has been shown to correlate with absolute f

129 found in the first 75% of capsule endoscopy transit time have a high probability of being found on o

130 Capillary transit time heterogeneity remained unchanged, suggestin

131 cited changes in capillary volume, such that transit time heterogeneity remained unchanged.

132 above baseline levels indicated hepatic vein transit time (HVTT).

133 ability, as determined by alterations in RBC transit time in a microfluidic channel assay, as well as

134 dependent in part on having spent sufficient transit time in NRP stage 1.

135 e laxation and reverse slowing of oral cecal-transit time in subjects taking high opioid dosages.

136 2)+/- lines also exhibit a faster cell cycle transit time in the absence of RA.

137 proliferation, which resulted from decreased transit time in the G(0)/G(1) phase of cell cycle.

138 Substitution of this marrow transit time in the heavy water analysis gave a better-d

139 The MS group showed prolonged mean transit time in the periventricular NAWM, as compared wi

140 on in tumors and normal tissue, and for mean transit time in tumors; however, permeability values did

141 rations of microbial metabolites and digesta transit time in woodrats (Neotoma spp.).

142 al heterogeneity of blood flow and capillary transit times in both mucosa and muscularis, with relati

143 BC adhesion, but overswelling prolonged sRBC transit times in capillary-sized microchannels.

144 rated by a 3-fold increase in ribosomal mean transit times in cell-free extracts from hibernators (ac

145 Transit times in patients and control subjects were comp

146 Transit times in patients with heart disease, including

147 A new method to define and to measure transit times in the step mode ETOF experiments was deve

148 tributions of flow and capillary erythrocyte transit times in two segments of small intestine in anes

149 f curvature has a significant effect on cell transit time, in addition to minimum capillary radius an

150 blocked the 81% shortening of distal colonic transit time induced by CRF.

151 kly, and spending approximately 1/3 of their transit time interacting with MHCII on DC.

152 c acid, and 15% dairy fat), small-intestinal transit time, intestinal cholesterol absorption, biliary

153 ed to mouth-to-caecum (MCTT) and large bowel transit times (LBTTs) in 4 groups of 8 individuals: (1)

154 logy and includes such factors as intestinal transit time, length of remnant bowel, presence of intac

155 than did those on blood flow and tracer mean transit time maps (r approximately 0.6), likely as a res

156 he difference between lesion volumes on mean transit time maps and DW images, divided by DW lesion vo

157 rithm identifies hypoperfused tissue in mean transit time maps by simultaneously minimizing the mean

158 en predictions of the model and the measured transit times may be explained by lymphocytes undergoing

159 Transit times measured with MR imaging may help in discr

160 er, along with in vivo blood T1 and arterial transit time measurements.

161 PMN transit time (median) in group 1 (n = 11) was 3.34 ms, i

162 ates (hundreds per second), and single cargo transit times (milliseconds).

163 absolute cerebral blood flow (CBF), and mean transit time (MTT) (referenced to an arterial input func

164 e (BV), and lower (>0.30 and >0.39) for mean transit time (MTT) and permeability surface area product

165 Parameter maps for mean transit time (MTT) and plasma flow (PF) were evaluated q

166 The parenchymal mean transit time (MTT) is theoretically superior to other me

167 rain perfusion: hypoperfusion volume on mean transit time (MTT) map decrease >30% from baseline to 2-

168 ion (PV), distribution volume (DV), and mean transit time (MTT) of gadopentetate dimeglumine.

169 lomerular filtration rate (GFR) and the mean transit time (MTT) of the tracer for the vascular compar

170 n CBF, cerebral blood volume (CBV), and mean transit time (MTT) were determined between hemispheres i

171 Blood flow (BF), blood volume (BV), mean transit time (MTT), and capillary permeability-surface a

172 Blood flow (BF), blood volume (BV), mean transit time (MTT), and permeability-surface area produc

173 Blood flow (BF), blood volume (BV), mean transit time (MTT), and permeability-surface area produc

174 Distribution volume (DV), mean transit time (MTT), and portal fraction (PF) of blood in

175 e tissue blood flow (BF), blood volume, mean transit time (MTT), and vascular permeability-surface ar

176 Blood flow, blood volume, mean transit time (MTT), permeability-surface area product, e

177 blood volume (BV), blood flow (BF), and mean transit time (MTT), were calculated at the primary site.

178 meters, pulmonary blood flow (PBF), and mean transit time (MTT).

179 (CBF), cerebral blood volume (CBV), and mean transit time (MTT).

180 ing Blood Flow (BF), Blood Volume (BV), Mean Transit Time (MTT)] and permeability parameters [includi

181 eased renal vascular resistance (measured by transit time nanoprobes) and urinary excretion of kidney

182 w folders exhibit topological mechanisms and transit times nearly identical with those of their Go-li

183 y, and also agrees with the transition-state transit time observed in slower folding proteins by sing

184 These data are consistent with a ribosomal transit time of 3.2 min for serum-deprived cells and 1.6

185 ity imaging revealed a significantly shorter transit time of 4 hours for the D4 cells upon in vivo bl

186 ore label appeared at the skin surface and a transit time of 4-5 weeks.

187 minary study suggests that analysis of liver transit time of a bolus of ultrasound contrast agent pro

188 st duration was consistent with the expected transit time of a single molecule through the laser beam

189 t cells were retarded by the magnetic field; transit time of a target cell (bound with magnetic beads

190 x at a rate of approximately 1.7 mm/d with a transit time of approximately 6 days.

191 ing protein signaling axis is inhibited, the transit time of EGF receptor through early endosomes are

192 itogenic signals are enhanced due to delayed transit time of EGFR through early endosomes, and cells

193 ces endosomal maturation, which shortens the transit time of EGFR through early endosomes, thereby li

194 The transit time of fX activated on the reaction chamber was

195 ndent slow rolling drastically increases the transit time of leukocytes rolling through an inflamed t

196 letely explained by the approximately 30 min transit time of Pol II across the alpha2-Mlocus.

197 ftware, it is possible to calculate the mean transit time of room-temperature saline injected down a

198 The transit time of sucrose through a sieve tube is found to

199 ery after chemobleaching (FRAC) to probe the transit time of the Kir2.1 K+ channel to reach the cell

200 amplitude, change in volume, reflecting the transit time of the ligand through the protein, followed

201 ow neutrophil mitotic pool and shortened the transit time of the postmitotic pool (control, mean = 6.

202 f intracellular transport of Muc-1 indicated transit times of 21 +/- 15 min from the rough endoplasmi

203 00 msec was demonstrated, revealing arterial transit times of 750, 950, and 1100 msec to consecutive

204 In comparison, transit times of a nontarget cell remained nearly the sa

205 hod employs Node-Pore Sensing to measure the transit times of cells as they interact with a series of

206 ological systems have been demonstrated, the transit times of fertilizer N in the pedosphere-hydrosph

207 ytochalasin did not affect the mean cellular transit times of FITC-GC (2.8 and 2.5 minutes for contro

208 e reaction chamber was prolonged relative to transit times of nonreacting tracers or preformed fXa.

209 4 and 39 minutes per orbit; in addition, the transit times of the inner body display an alternating v

210 The inferred midnight transit times of the three bulges, using the rotation ra

211 stribution, residual water contents, crystal transit times) of clasts produced by key eruptions.

212 ll deformability, but the dependence of pore transit time on cell properties is not well understood.

213 culiar, power-law logarithmic dependences of transit time on ligand concentration.

214 volume (SE = 80%; SP = 97%), Increased mean transit time on PCT was predictive of the tissue at risk

215 high amounts of dietary fiber do not change transit time or defecation frequency if they are already

216 ther flow characteristics, such as capillary transit time or RBC velocity, also vary significantly ov

217 s is the relative invariance of single cargo transit times out to large size (even as macroscopic tra

218 treatment (P = 0.03), prolonged fluorescein transit time (P = 0.0001), and the presence of some capi

219 /IMR, where TmnBase referred to nonhyperemic transit time; PaBase and PdBase, the nonhyperemic aortic

220 al blood flow, distribution volume, and mean transit time) parameters were calculated by placing regi

221 lues were determined for esophageal transit (transit time, percentage emptying at 10 s), liquid-only

222 ermine tissue blood flow, blood volume, mean transit time, permeability, and hepatic arterial fractio

223 Blood flow, mean transit time, permeability, and hepatic arterial fractio

224 avitational effects) implied by the observed transit times permit the planetary masses to be measured

225 including gastric acidification, intestinal transit time, presence of gastric lipase, sample/digesti

226 divided by the inverse of the hyperemic mean transit time provides an index of microcirculatory resis

227 s, tautp, and the distribution of individual transit times, PTP(t).

228 Pulse transit time (PTT) is being widely pursued for cuff-less

229 that substrate molecules spend most of their transit time randomly moving in the central pore of the

230 A longer PMN pore transit time reflects increased PMN rigidity.

231 time ASL sequences to assess alterations of transit time, reproducibility and quantification of cere

232 nated by the deformability of cells, and the transit time required for the fully deformed cell to tra

233 blood flow, cerebral blood volume, and mean transit time, respectively.

234 significant retardation of small-intestinal transit times (resulting in increased cholesterol absorp

235 Probiotics may improve whole gut transit time, stool frequency, and stool consistency, wi

236 investigate the effect of probiotics on gut transit time, stool output, and constipation symptoms in

237 Transit time studies were performed using 10 radiopaque

238 F(V), volume of distribution V(D), and blood transit time tau were determined.

239 F(V), volume of distribution V(D), and blood transit time tau.

240 Total gastrointestinal transit time (TGTT) and colonic transit time (CTT) were

241 r portal flow, distribution volume, and mean transit time than did the background liver (all P < .05)

242 We show that stiffer cells have longer transit times than less stiff ones and that cell size si

243 aphy allows determination of cardiopulmonary transit times that are significantly prolonged in heart

244 The high pH, simple gut structure, and fast transit times that typify caterpillar digestive physiolo

245 correlation function of these data indicated transit times that were consistent with the observed ele

246 the pulmonary microcirculation affect their transit time, their tendency to contact and interact wit

247 a particular state is related to the average transit time through that state.

248 equence cleavage position that regulates its transit time through the endoplasmic reticulum and diffe

249 rom these carbohydrates during their limited transit time through the gut.

250 ubstrate in solution that is slower than the transit time through the membrane, a situation that can

251 sulting in significantly shortened leukocyte transit times through venules.

252 olesterol absorption caused small intestinal transit time to return to normal.

253 e oligonucleotides accelerated their S phase transit time to that of CD3-activated PBTs.

254 ipermissive temperatures, carboxypeptidase Y transit time to the vacuole was slower in Sec(-) cells c

255 out to calibrate the devices by relating the transit times to the known D values of Ru(NH3)6(2+) in a

256 and static images were analyzed to determine transit times to the sentinel node, the number of nodes

257 ing regulates EGFR signaling response by the transit-time to late endosomes where it is switched-off

258 hane anaesthesia with vascular catheters and transit-time ultrasonic flow probes around a carotid art

259 Direct PV transit-time ultrasonography (US) and fluorescent micros

260 19-24 kg) were instrumented chronically with transit time ultrasound flow probes on both external ili

261 s enter and leave the LN more slowly, with a transit time unaffected by the absence of MHCI molecules

262 women with intractable constipation and slow transit time underwent colectomy and 6 women who underwe

263 e-contrast MR imaging and that measured with transit-time US (mean difference, -3.5 mL/min/100 g; 95%

264 r volume flow consisted of measurements with transit-time US flowmetry.

265 positive correlation was found between mean transit time values and disability scales in patients wi

266 ed for both continuous and pulsed radiation; transit time values for the ion chambers included in thi

267 ntinuous monitoring by Kepler, the method of transit timing variations (TTVs) has blossomed as a new

268 a period P(b) = 33.6 days and exhibits large transit timing variations indicative of a perturber.

269 Here we report transit timing variations of the four planets in the Kep

270 y induced deviations from a constant period (transit timing variations) also shows no significant sig

271 The transit-time variations depend on the mass of the additi

272 ed on gender differences in gastrointestinal transit time, visceral sensitivity, central nervous syst

273 The mean arterial transit time was 1538 msec +/- 123 (standard deviation)

274 Median transit time was 17.5 min (range, 1 min to 18 h) after i

275 ted by MTS-1, and the total gastrointestinal transit time was assessed by radiopaque markers and abdo

276 trol values by using two-tailed t tests, and transit time was correlated with standard LV functional

277 vascular volume, and the renal arteriovenous transit time was determined with an intravenous microbub

278 , interval from biopsy, or tumor location on transit time was found.

279 Transit time was influenced by breast size.

280 In 11 autoregulating preparations, proximal transit time was likewise unchanged from the control val

281 With six different volumes, bubble transit time was linearly related to volume (r=.91).

282 Median gastric transit time was lower after erythromycin compared to do

283 Total gut transit time was measured to monitor the functional cons

284 Mean colonic transit time was similar in both groups at baseline and

285 Transit time was the same between groups.

286 Arterial elastic modulus and pulse wave transit time were assessed using ultrahigh frequency ult

287 e (CBV), cerebral blood flow (CBF), and mean transit time were assessed with dynamic susceptibility c

288 e cerebral blood flow and tracer mean tissue transit time were computed, as were maps of apparent dif

289 men was traced, and the net transit area and transit time were noted.

290 higher arterial fraction and lower vascular transit time were observed for HCCs (P < 0.05).

291 Transit times were calculated as the ratio of capillary

292 Transit times were measured.

293 Orocecal transit times were not significantly different for place

294 Median small bowel transit times were similar in both groups (236 min versu

295 iolabeled meal, their gastric and intestinal transit times were studied with a gamma camera.

296 lf-life, but parameters, particularly marrow transit time, were poorly defined.

297 deformability is measured by evaluating the transit time when each individual RBC squeezes through a

298 host functions such as gastrointestinal (GI) transit time, which in turn can further affect the micro

299 e rolling through E-selectin results in long transit times, which are essential for efficient leukocy

300 d day 5), blood kinetics (day 6), and marrow transit time while on drug (days 6 to 14).