ライフサイエンスコーパス: minus

1 was attenuated in the presence of NF1 (exoA-minus).

2 s depth range (that is, its mean buoyancy is minus 0.5 per cent), although this anomaly may be concen

3 model (SRTM) with distribution volume ratio minus 1 (DVR - 1) for 60- and 90-min scans.

4 Pancreas SUV ratio minus 1 (SUVR-1) (20-30 min; spleen as reference region)

5 ate of <40% for isolates with an MIC plus or minus 1 doubling dilution of the intermediate breakpoint

6 ction), fructose storage (fructose ingestion minus (13)C-fructose oxidation), fructose conversion int

7 of 214 dialysis patients (mean age 62.6{plus minus}15.0; 32% female).

8 ally normal subjects was set as 45 mum (mean minus 2 standard deviations).

9 selected the activation differences (1-back minus 2-back) in the lateral and medial prefrontal corti

10 degrees Celsius occurs within 20 seconds at minus 20 degrees Celsius and within 30 seconds at minus

11 t tertile (66.9{plus minus}5.8% vs 92.4{plus minus}3.3%).

12 20 degrees Celsius and within 30 seconds at minus 30 degrees Celsius, consuming only 3.8 per cent an

13 studies in approximately the same area (plus/minus 5 degrees of original scan location).

14 those within the highest tertile (66.9{plus minus}5.8% vs 92.4{plus minus}3.3%).

15 mparing the change in mean response (90 days minus 7 days) between the 3 treatment groups using a gro

16 26), executive function (Trail-Making Test B minus A; range, -290 to 290), and spatial ability (Card

17 an, the net benefit (absolute risk reduction minus absolute risk increase) was positive for 46% of pa

18 at blood collection for premenopausal women) minus age at menarche, subtracting years of oral contrac

19 at blood collection for premenopausal women) minus age at menarche, years of oral contraceptive (OC)

20 andomly distributed throughout the bacteria, minus an excluded volume about the chromosomal DNA.

21 age-adjusted axial length difference (ALD) (minus and plus denotes myopia and hypermetropia, respect

22 as increased system emissions from charging minus avoided emissions from discharging.

23 baseline scores and recovery (outcome scores minus baseline scores).

24 The effect of treatment (LDX minus baseline vs placebo minus baseline) on these behav

25 Using the change score (peak at induction minus baseline) for bleeding on probing and probing dept

26 of treatment (LDX minus baseline vs placebo minus baseline) on these behavioral and neural markers o

27 2 y; glucose change was defined as follow-up minus baseline.

28 roscopy and site-directed mutagenesis at the minus beta2 side converge in indicating that the limited

29 ontrol) or mFOLFOX6 plus SIRT (SIRT) plus or minus bevacizumab.

30 hted averages, where net inputs equal inputs minus biomass removal) despite relatively low P inputs.

31 that noncyloplegic refraction tends to over minus by 1 to 2 D.

32 The risk difference (no co-trimoxazole group minus co-trimoxazole group) was -0.0319 (-0.075 to 0.011

33 The mean difference (closed loop minus control) in the percentage of time that the blood

34 r score difference between groups (binocular minus control) was -0.3 (95% CI: -2.2 to 1.5, P = 0.71,

35 fined as the cost of implementing the bundle minus cost savings from fewer infections.

36 ing by about 30 000 annually (new infections minus deaths).

37 ensitometry differences (adjacent arterioles minus DH [DeltaA] or venules minus DH [DeltaV]).

38 cent arterioles minus DH [DeltaA] or venules minus DH [DeltaV]).

39 V genes were also identified, mostly for the minus DNA strand within the EBNA locus, a major locus re

40 e expression of EBV genes from both plus and minus DNA strands; 42 of these pA sites are commonly use

41 Fkh1- and Fkh2-domain-swap-minus (dsm) mutations are functional as transcription fa

42 ded velocities toward either the microtubule minus (dynein) or plus (most kinesins) end.

43 iction error was defined as refractive error minus emmetropia.

44 In Drosophila, extended minus end growth depended on Patronin, and Patronin redu

45 Therefore, we hypothesized minus end growth might be particularly important beyond

46 To determine whether minus end growth populated new dendrites with microtubul

47 t Patronin facilitates sustained microtubule minus end growth, which is critical for populating dendr

48 nd zebrafish neurons, we observed persistent minus end growth, with runs lasting over 10 min.

49 is the only myosin known to move toward the minus end of actin filaments.

50 rt of many intracellular cargoes towards the minus end of microtubules (MTs).

51 es accumulation of organelles at the plus or minus end of microtubules, respectively.

52 studied so far exclusively move towards the minus end of the microtubule(3).

53 anation for why all dyneins move towards the minus end of the microtubule.

54 ich the microtubule plus end grows while the minus end shrinks, is observed in cells; however, the un

55 in to transport KIF1C toward the microtubule minus end, and KIF1C to transport dynein toward the micr

56 tact microtubule network and the microtubule minus end-binding protein, Patronin.

57 LIS1) in the interaction of end tracking and minus end-directed human dynein complexes with these sit

58 nusual structure, Trkin encodes a functional minus end-directed kinesin that specifically colocalizes

59 Cytoplasmic dynein is a minus end-directed microtubule motor that transports int

60 Cytoplasmic dynein is an enormous minus end-directed microtubule motor.

61 esin-14s are commonly known as nonprocessive minus end-directed microtubule motors that function main

62 abE engage myosin-5 as well as plus end- and minus end-directed microtubule motors, providing an expe

63 ingle microtubules, but reverts to canonical minus end-directed motility when anchored on the surface

64 plored how the balance between plus end- and minus end-directed motors, as well as the influence of m

65 They implicate cortical domains where minus end-directed motors, such as dynein, are activated

66 on antagonistic activities of plus end- and minus end-directed motors.

67 We propose that the minus end-directed stepping action of Cut7 is selectivel

68 r domains with their neighbors inhibit their minus end-directed stepping action, but not their plus e

69 r Klp2, a kinesin-14, converts Cut7 from net minus end-directed to net plus end-directed stepping.

70 h greater crowding converting the motor from minus end-directed to plus end-directed stepping.

71 This minus end-directed transport is largely unaffected by ge

72 bule-dependent motors, we establish that the minus end-directed transport of SVs requires the dynein/

73 decreases dynein binding to APC to stimulate minus end-directed transport, which could modulate endoc

74 s KlpA without the tail is nonprocessive and minus end-directed.

75 o which the motor domain binds, KlpA becomes minus end-directed.

76 tors can move toward the microtubule plus-or-minus end.

77 HSET maintains its protective minus-end activity even when challenged by a known micro

78 that microtubule rotational diffusion about minus-end attachment points contributes to kinetochore c

79 otubule-binding domain and is independent of minus-end binders gamma-TuRC, CAMSAP1, and KANSL1/3.

80 distribution and interacts with microtubule minus-end binding protein CAMSAP2.

81 Memo1 deficiency leads to disrupted MT minus-end CAMSAP2 distribution, initiation of aberrant M

82 Thus, NuMA may serve as a mitosis-specific minus-end cargo adaptor, targeting dynein activity to mi

83 es tubulin off-rate to specifically suppress minus-end catastrophe.

84 tial regulation of microtubule stability and minus-end clustering.

85 1, the heavy chain of the cytoplasmic dynein minus-end directed microtubule motor, in a genetic scree

86 but not KIF13B undergoes a tug-of-war with a minus-end directed motor.

87 we present cryo-EM structures of the unique minus-end directed myosin VI motor domain in rigor (4.6

88 microtubule gliding assays in both plus- and minus-end direction.

89 provide novel insight into the mechanisms of minus-end dynamics, essential for our understanding of m

90 vitro reconstitution approach to investigate minus-end dynamics.

91 erminant of the difference between plus- and minus-end dynamics.

92 CAMSAP/Patronins regulate microtubule minus-end dynamics.

93 We find that minus-end lifetimes are not defined by the mean size of

94 umerous studies have observed a role for the minus-end microtubule motor dynein in HIV-1 infection, t

95 ueled macromolecular machines that power all minus-end microtubule-based transport processes of molec

96 t spindle poles, we hypothesized that the MT minus-end motor dynein mediates ER concentration around

97 ctional (ncd), the other known Drosophila MT minus-end motor, nor Klp61F, a MT plus-end motor that ge

98 ER-MT association that is independent of MT minus-end motors is required for proper ER partitioning

99 rds the plus-end, and C-kinesins towards the minus-end of microtubules.

100 Msp300 recruits the microtubule minus-end protein Patronin, a calmodulin-regulated spect

101 tubulin conformations to enable microtubule minus-end recognition.

102 sential for our understanding of microtubule minus-end regulation in cells.

103 at a homozygous knockdown mouse model for MT minus-end regulator calmodulin-regulated spectrin-associ

104 s, and signaling pathways control MT length, minus-end spacing, and coverage.

105 anization, i.e., polymer length, number, and minus-end spacing, is regulated and how it impinges on a

106 from Naegleria gruberi (NgCKK), which lacks minus-end specificity.

107 Both NuMA's minus-end-binding and dynein-dynactin-binding modules ar

108 Here, we identified Patronin, a minus-end-binding protein, for its crucial and dose-sens

109 However, a requirement of MT minus-end-binding proteins in dendrite-specific pruning

110 led-coil domains from a plus-end-directed or minus-end-directed kinesin fused to streptavidin.

111 Further, our results show that the minus-end-directed kinesin-14 HSET/KIFC1 suppresses tubu

112 the role of tetrameric Kif25, a microtubule minus-end-directed kinesin-14 motor, in preventing prema

113 Cytoplasmic dynein is the primary minus-end-directed microtubule motor protein in animal c

114 is a molecular motor that drives nearly all minus-end-directed microtubule-based transport in human

115 t approximately equal fractions of plus- and minus-end-directed motility along microtubules.

116 whether the mechanism of the unconventional minus-end-directed motility differs fundamentally from t

117 However, the functional necessity of minus-end-directed movement along actin is unclear as th

118 een found to naturally exhibit long-distance minus-end-directed processive motility on single microtu

119 terminal microtubule-binding tail to achieve minus-end-directed processivity on single microtubules o

120 dynein is the primary motor for microtubule minus-end-directed transport and is indispensable to euk

121 lus ends leading, so "mal-oriented" MTs with minus-end-out are transported toward the cell body while

122 gery, we detected equal numbers of plus- and minus-end-out microtubule orientations throughout the de

123 dynein, targeted to cortical actin, removes minus-end-out microtubules from axons.

124 reduction of Patronin lowered the number of minus-end-out microtubules.

125 out, indicating low Patronin normally limits minus-end-out microtubules.

126 ch is critical for populating dendrites with minus-end-out microtubules.

127 our study demonstrates that Patronin orients minus-end-out MT arrays in dendrites to promote dendrite

128 tronin mutant neurons significantly restored minus-end-out MTs in dendrites and thereby rescued dendr

129 uggesting that Patronin stabilizes dendritic minus-end-out MTs.

130 Dendrite microtubules are polarized with minus-end-out orientation in Drosophila neurons.

131 while dendrites contain microtubules with a minus-end-out orientation.

132 ents entry into dendrites and thus maintains minus-end-out polarity within proximal dendrites.

133 , and Patronin reduction disrupted dendritic minus-end-out polarity.

134 , however, do not readily enter, maintaining minus-end-out polarity.

135 in made terminal dendrites almost completely minus-end-out, indicating low Patronin normally limits m

136 and increased average lifetimes of plus- and minus-end-stabilizing caps.

137 their astral microtubules, remotely from the minus-end.

138 ansport of lysosomes toward the microtubules minus-end.

139 ression resulted in a drastic decrease of MT minus ends and a concomitant increase of plus-end-out MT

140 n which CAMSAP2 anchors KIFC3 at microtubule minus ends and immobilizes microtubule arrays in dendrit

141 o transport diverse cargo toward microtubule minus ends and to organize and position microtubule arra

142 mixed polarity into a configuration in which minus ends are away from the chromosomes, enabling forma

143 Microtubule minus ends are inherently more stable than plus ends des

144 us ends are highly dynamic in neurons, while minus ends are often capped and stable.

145 This structure reorganizes so that minus ends are sorted to the periphery of the array, for

146 Microtubule minus ends are thought to be stable in cells.

147 Minus ends extended into growing dendrites in the presen

148 Although minus ends grow slower, their lifetimes are similar to t

149 endent manner or moving processively towards minus ends in an adaptor protein-dependent manner.

150 translocation of peroxisomes to microtubule minus ends indicates that mammalian Hook proteins activa

151 Dynamic organization of microtubule minus ends is vital for the formation and maintenance of

152 ddaCs distribute the minus ends of microtubules (MTs) to dendrites but the pl

153 We find that gammaTuRC stably caps the minus ends of microtubules that it nucleates stochastica

154 tubule lattice and to the shrinking plus and minus ends of microtubules.

155 approach close to and cross-bridge with the minus ends of non-KMTs, which form a framework that inte

156 locate from the microtubule plus ends to the minus ends, and this relocation requires LIS1 and its bi

157 suppresses depolymerization at both plus and minus ends, rather than sliding microtubules within the

158 icrotubules are forced backward toward their minus ends, resulting in buckling.

159 y capture and stabilize existing microtubule minus ends, which then template new microtubule growth.

160 nise specific tubulin conformations found at minus ends.

161 icles, and macromolecules toward microtubule minus ends.

162 , proteins, and viruses, towards microtubule minus ends.

163 main also depolymerizes microtubule plus and minus ends.

164 ) that exhibit biased localization toward MT minus ends.

165 The number of growing plus, but not minus, ends increased in dendrites with reduced KT, CPC,

166 Because astral MT minus-ends are anchored by centrosomes at spindle poles,

167 This includes release of MT minus-ends from the centrosome, leading to PCM dispersio

168 NuMA is recruited to new minus-ends independently of dynein and more quickly than

169 NuMA localization to minus-ends involves a C-terminal region outside NuMA's c

170 How dynein becomes enriched at minus-ends is not known.

171 dels of microtubule growth, we conclude that minus-ends of KMTs have selectively detached and depolym

172 mediated intracellular transport towards the minus-ends of microtubules.

173 anched MTs preferentially originate near the minus-ends of pre-existing MTs.

174 cargo adaptor, targeting dynein activity to minus-ends to cluster spindle microtubules into poles.

175 ynein pulls on mammalian spindle microtubule minus-ends, and this localized activity at ends is predi

176 lation to show that NuMA targets dynactin to minus-ends, localizing dynein activity there.

177 rotubules in 3D and identify their plus- and minus-ends.

178 in display specific, steady-state binding at minus-ends.

179 ninferiority margin of -2.75 (50% of placebo minus escitalopram), so noninferiority could not be clai

180 ss was defined as the transpulmonary (airway minus esophageal) pressure during end-inspiratory pause

181 id-latitude net precipitation (precipitation minus evapotranspiration, at 30 degrees N to 50 degrees

182 stimated for 2000 to 2014 as observed deaths minus expected deaths (estimated from 1999 mortality rat

183 The mean observed minus expected duration of mechanical ventilation across

184 er performing units as ICUs with an observed minus expected duration of mechanical ventilation greate

185 erforming units as ICUs that had an observed minus expected duration of mechanical ventilation less t

186 nal reward prediction error (RPE), or actual minus expected reward.

187 erences in diversification rates (speciation minus extinction) between habitats are often weak and in

188 factors promote diversification (speciation minus extinction) in clades.

189 In good memory performers (R-hits minus false alarm), the coupling was stronger in R than

190 and from the balance method (oral d3-alpha-T minus fecal d3-alpha-T excreted).

191 t month 12, the difference between study eye minus fellow eye improvement in group 2 patients of 0.53

192 t month 18, the difference between study eye minus fellow eye improvement in our acute group 2 gene t

193 The ability of this gL-minus Gag recombinant RRV to infect, persist, and elicit

194 serves as a chemoattractant for mating-type minus gametes but repels plus gametes.

195 en cilia of mating type plus and mating type minus gametes mediated by adhesion receptors SAG1 and SA

196 both the control and test samples, Cognitor Minus gave NPVs of 99% and 100% respectively.

197 ference in means (awake-regional anaesthesia minus general anaesthesia) of 0.23 (95% CI -2.59 to 3.06

198 t pregnancy (delivery date of next pregnancy minus gestational age at birth).

199 ps (number of impacts, 6 vs 41 [lower impact minus higher impact = 35; 95% CI, 21-51; P < .001]; line

200 ear acceleration, 99g vs 1112g [lower impact minus higher impact= 1013; 95% CI, 621 - 1578; P < .001]

201 9 radian/s2 vs 65016 radian/s2 [lower impact minus higher impact= 57427; 95% CI , 31123-80498; P < .0

202 reased atmospheric CO(2) (DeltaC(a) = future minus historic CO(2)) compensates for increased physiolo

203 ), or (4) profit function - i.e. carbon gain minus hydraulic risk.

204 The TLCPD (IOP minus ICP) was calculated for the sitting and supine pos

205 an arterial blood pressure at midbrain level minus ICP, was unchanged (from 70 +/- 12 mmHg to 67 +/-

206 5b was transfected into fibroblasts plus and minus IL-13 to see if this miR plays a role.

207 The RNFL thickness difference (fellow eye minus injected eye) was significantly correlated with th

208 protein, ferritin, and apoferritin (ferritin minus iron) were measured over the wavelength range of 4

209 nd reported percentage reduction in IPD as 1 minus IRR.

210 ted as critically hypoperfused tissue volume minus ischaemic core volume.

211 Noninvasive hemoglobin monitoring minus laboratory hemoglobin differences showed an intrac

212 ency reactivation phenotype to that of a LAT-minus [LAT(-)] virus, while similar recombinant viruses

213 e right 2D:4D, the left 2D:4D, and the right minus left 2D:4D) were neither predictors of pre-exercis

214 naive patients with liver metastases plus or minus limited extrahepatic metastases were randomly assi

215 D) was defined as recipient MELD score at LT minus lowest MELD score within the preceding 30 days.

216 a transpulmonary pressure gradient (mean PAP minus mean PAWP) <12 mm Hg, and pulmonary vascular resis

217 c pulmonary pressure gradient (diastolic PAP minus mean PAWP) <7 mm Hg, a transpulmonary pressure gra

218 nd +84% between Org-M and Min-F (i.e., Org-M minus Min-F).

219 Instruction compliance (R-hits minus NR-hits) was significantly related to negative cou

220 The FI and FI minus number of patients lost to follow-up of RCTs suppo

221 was 8.0 (95% CI, 5.0-9.0) and the median FI minus number of patients lost to follow-up was 1.0 (95%

222 ardial revascularization using the FI and FI minus number of patients lost to follow-up.

223 event rate), the delta gap (predicted delta minus observed delta), and the predicted number needed t

224 The event-rate gap (predicted event rate minus observed event rate), the delta gap (predicted del

225 The R-based pipeline uses Fluorescence Minus One (FMO) controls or distinct population differen

226 We derived Euclidean Norm Minus One g (ENMO), Low-pass filtered ENMO (LFENMO), Mea

227 erence between both strategies (standardized minus open) was -4.9% (95% CI [-12.5%; 2.6%]).

228 ed inorganic N (DIN) mass reductions (inflow minus outflow) were greater in the Dry Basin than in the

229 ce interval (CI) for the difference (EGP-437 minus PA 1%) was less than -10%.

230 ositive end-expiratory pressure, DeltaP [PIP minus PEEP], tidal volume, dynamic compliance [Cdyn]) or

231 e found that 56% of the terrestrial surface, minus permanent ice and snow, currently has low human im

232 exercise time increment between groups (PCI minus placebo 16.6 s, 95% CI -8.9 to 42.0, p=0.200).

233 left) of the XDF motif and the Phe rotamer (minus, plus, trans).

234 hrough beta-oxidation in muscle mitochondria minus/plus pharmacological or genetic inhibition of redo

235 The effect of PSEs (minus PNEs) on brain activation in right insula was posi

236 sitively correlated with the effect of PSEs (minus PNEs) on number of puffs taken from a cigarette (r

237 The driving pressure (plateau pressure minus positive end-expiratory pressure) has been suggest

238 expansion is therefore hygroscopic expansion minus post-gel shrinkage.

239 e posttest HR, and HR difference (resting HR minus posttest HR) were measured and musculoskeletal pai

240 Initial AFP <400 ng/mL and AFP fall (initial minus pre-LDLT) >2000 ng/mL predicted better RFS; Grade

241 Subtraction maps (contrast-enhanced CT minus precontrast CT) were calculated after motion corre

242 up mortality in power calculations (observed minus predicted difference, -6.7% +/- 9.8%; p < 0.01).

243 calculated (stable postoperative refraction minus predicted refraction).

244 and overlapping seasonal differences (post- minus preintervention change) between control and interv

245 3 years (treatment group difference of BLRc minus R&R, 12%; 95% CI, -1% to 25%).

246 criteria; treatment group difference of BLRc minus R&R, 5%; 95% CI, -2% to 13%).

247 &R group (treatment group difference of BLRc minus R&R, 9%; 95% confidence interval [CI], -6% to 23%)

248 -breath washout data) and resistance at 5 Hz minus resistance at 20 Hz measured by using impulse osci

249 cueing task (response time difference: left minus right target trials).

250 Further, gL-minus RRV elicits cellular immune responses that are pre

251 ction of the CD20(+) subpopulation by the gL-minus RRV.

252 large mammals; and (3) (with an appropriate minus sign) sloths undertaking suspended locomotion acro

253 nked viral polymerase from the 5' end of the minus strand [(-)strand] of viral relaxed circular DNA (

254 , an RC DNA species with a covalently closed minus strand but an open plus strand (closed minus-stran

255 equal proportions on the plus strand and the minus strand of the host genome.

256 f the plus strand in RC DNA, suggesting that minus-strand closing can occur before plus-strand proces

257 Reverse genetics based on a tandem minus-strand complementary DNA genome copy under the con

258 minus strand but an open plus strand (closed minus-strand RC DNA [cM-RC DNA]) was detected by this ap

259 Most interviral recombinants are minus-strand recombinant RNAs, and the junction sites ar

260 binding the viral polymerase NS5 to initiate minus-strand RNA synthesis.

261 ous viral progeny from infected cells, viral minus-strand RNA, plus-strand RNA, and proteins that are

262 nscription of the incoming virion-associated minus-strand RNA, thereby preventing the synthesis of vi

263 ligo(U) stretch at the 5' end of coronavirus minus-strand RNAs, it is tempting to speculate (but rema

264 anidine hydrochloride (GuHCl) (which targets minus-strand synthesis to produce double-stranded RNA) w

265 ished that HCV dsRNA contained genome-length minus strands.

266 d by analysing reads generated from plus and minus strands.

267 rediction error (postoperative SE refraction minus target refraction) was -0.19+/-0.72 D.

268 There was minimal mean difference (eFick minus Td = -0.02 L/min/m2, or -0.4%) but wide 95% limits

269 an time from start of incubation to Cognitor Minus test was 27.1 hours.

270 The Cognitor Minus test was performed on one set >12 hours incubation

271 The Cognitor Minus test, performed on blood culture samples after 12

272 ome sequencing of bladder cancer cells {plus minus} tet-on ZFP36L1 was performed.

273 ups (difference in median of oral vitamin D3 minus that of UVB: 1.5 mg/dL; 95% CI: -5.0, 7.0 mg/dL).

274 e expected number of assessments for a visit minus the actual number of assessments received for that

275 test-negative design, VE was estimated as 1 minus the adjusted odds ratio from a logistic regression

276 FD area measurements in the total scan area minus the area of GA (Pearson r = 0.747; P < 0.001) than

277 e in Hb level, calculated as the nadir level minus the baseline level (range, -5.8-0 g/dL; mean, -1.8

278 ing net canopy C export (NCE, photosynthesis minus the C cost of leaf growth and maintenance) as a fi

279 sured children (defined as the reimbursement minus the cost of care) were compared across hospital ty

280 ures of annual profit: gross profit (revenue minus the cost of goods sold); earnings before interest,

281 day 7 level (calculated as the day 14 level minus the day 7 level) was 0.03 g/dL (range, -0.25-0.32

282 Vaccine effectiveness was defined as 1 minus the hazard ratio comparing vaccinated with unvacci

283 sing Cox regression, with VE calculated as 1 minus the hazard ratio.

284 RR was calculated as the maximal HR achieved minus the HR at: 30-s (HRR30), 1-min (HRR1), 2-min (HRR2

285 4-14) and defined vaccine effectiveness as 1 minus the incidence rate ratio, expressed as a percentag

286 accine effect was leaky, calculated mVE as 1 minus the Mantel-Haenszel relative risk of vaccine on in

287 Method 1 estimates R as 1 minus the proportion of cases that are imported.

288 nergy balance (equal to daily energy intakes minus the REE), and survival were recorded.Of 390 enroll

289 he relative abundance of positive correlates minus the sum of the relative abundance of negative corr

290 novel variable, remaining D2B as 90 minutes minus the time between hospital arrival and catheterizat

291 ulated as the value in the nonsedation group minus the value in the sedation group.

292 from Artemisia tridentata ssp. Spiciformis, minus their chloroplast targeting regions, are 71% ident

293 uding all participants assigned to treatment minus those who withdrew due to a non-treatment-related

294 veal that microtubule organizing centers use minus to plus-end directed remote control to individuali

295 The net cost, calculated as revenue minus total cost, was $1685 with dalbavancin versus $75

296 evaluating the efficacy of chemotherapy plus/minus trastuzumab suggested that the magnitude of trastu

297 The difference between involved minus uninvolved serum free light chains (dFLC) has been

298 vagal villus afferent distributions (control minus VAGX) paralleled control distributions, but were s

299 he difference in success rates (ceftobiprole minus vancomycin/aztreonam) >-10%.

300 DB motility and suggest that an imbalance of minus versus plus end-directed microtubule motility in n

301 ed m(6)A residues on the IAV plus (mRNA) and minus (vRNA) strands and used synonymous mutations to ab