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

5 ) but not MBTS (P=0.40) subjects (pre-Fontan minus 14-month mean, -3.25+/-8.24% versus 0.99+/-8.80%;

6 (prespecified equivalence limits of plus or minus 2 days) in the intention-to-treat population.

7 (the cutoff point: the mean SNFL in controls minus 2 standard deviations).

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

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

10 20 degrees Celsius and within 30 seconds at minus 30 degrees Celsius, consuming only 3.8 per cent an

11 gram at a 50 per cent state of charge and at minus 30 degrees Celsius, delivering 6.4-12.3 times the

12 0.9% saline (placebo) every 28 days (plus or minus 5 days) for 1 year.

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

14 we found that Sox9 engages TUBB3 promoter at minus 980 base pairs from the transcriptional start site

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

16 resholded statistical T maps (hypometabolism minus amyloid burden), resulting from voxel-based statis

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

18 scabiosa, 14 from Sonchus asper, 17 from A. minus and 11 from T. officinale.

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

20 Comparison of minus and plus NESs identified structural and sequence d

21 replication strategy allows TBSV to separate minus- and plus-strand syntheses in time and regulate as

22 nd TUA2 was defined as total urinary arsenic minus arsenobetaine and arsenocholine.

23 3-year progression-free survival rate (ABVD minus AVD) was 1.6 percentage points (95% CI, -3.2 to 5.

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

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

26 < 0.05), and the changes in M/I (detraining minus baseline) correlated directly with changes in CD i

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

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

29 red for generating the major non-functional 'minus beta' isoform, which skips exons 7 and 8.

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

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

32 tes (orders Perissodactyla + Cetartiodactyla minus cetaceans) were merged with host trait data and IU

33 avorable outcome (experimental group [21.0%] minus control group [17.2%]) in the modified intention-t

34 At age 2 years, the difference (intervention minus control) in BMI (calculated as weight in kilograms

35 Unadjusted differences (intervention minus control) in Z scores were 0.05 for weight-for-age

36 Difference spectra (mutant minus control) of all the mutants showed an increase in

37 tex (ACC) that signal the net value (benefit minus cost) of rewards that will be received oneself and

38 erfusion-defined penumbra volume at baseline minus CT infarct volume at 24-48 h).

39 and FA/B(-*) and by the characteristic light-minus-dark absorbance difference spectrum in the QY regi

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

41 Cin8Kin switched frequently between plus and minus directionality along single MTs, demonstrating tha

42 rands - asymmetric DNA methylation; plus and minus DNA stands - symmetric DNA methylation) in MeDIP-S

43 where DNA methylation predominates (plus or minus DNA strands - asymmetric DNA methylation; plus and

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

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

46 Fire alone (minus elephants) had negligible effects on gecko density

47 iction error was defined as refractive error minus emmetropia.

48 siently relocalize to sites marked by the MT minus end binding protein PTRN-1/Patronin.

49 r satellites become stuck at the microtubule minus end near the centrosome.

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

51 transports intracellular cargoes towards the minus end of microtubules (MTs).

52 ion interface of FtsZ, the equivalent of the minus end of tubulin.

53 ermis, NOCA-1 functions redundantly with the minus end protection factor Patronin/PTRN-1 to assemble

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

55 Live-cell imaging reveals minus end-directed dynein-dynactin motility along microt

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

57 The minus end-directed microtubule motor cytoplasmic dynein

58 , using proteomic profiling, we identify the minus end-directed microtubule motor protein HSET as a d

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

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

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

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

63 ng of nuclear congression and identified two minus end-directed motors operating in parallel in this

64 ongression depends on the cooperation of two minus end-directed motors.

65 ergo either diffusive, or highly processive, minus end-directed movements along microtubules.

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

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

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

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

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

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

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

73 ons in Myo6, the gene encoding the (F-actin) minus end-directed unconventional myosin, myosin VI, cau

74 Cytoplasmic dynein drives the majority of minus end-directed vesicular and organelle motility in t

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

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

77 drites, given that they have a population of minus end-distal microtubules not present in axons?

78 in-5 acting normally restrains the number of minus end-distal microtubules that are transported into

79 hinner and contained a greater proportion of minus end-distal microtubules, suggesting that kinesin-5

80 The discovered minus end-tracking property of the TubRC complex expands

81 All stalks point towards the microtubule minus end.

82 llows Kar3 to bias translocation towards the minus end.

83 lar movement of cargo toward the microtubule minus end.

84 the velocity of dynein-dependent microtubule minus-end (towards the nucleus) movement of EGF and BDNF

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

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

87 hile CAMSAP3/Marshalin is a microtubule (MT) minus-end binding protein that regulates MT networks.

88 including a recently described family of MT minus-end binding proteins called calmodulin-regulated s

89 er of the Patronin/Nezha/CAMSAP family of MT minus-end binding proteins, suppresses dapk-1 epidermal

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

91 1, the heavy chain of the cytoplasmic dynein minus-end directed microtubule motor, in a genetic scree

92 es (MTs) are substrates upon which plus- and minus-end directed motors control the directional moveme

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

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

95 ariable central domain cooperate to suppress minus-end dynamics in vitro and that both regions are re

96 ter and dynein on chromosome arms provides a minus-end force.

97 mains of CAMSAP and Patronin are involved in minus-end localization.

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

99 We propose a model whereby minus-end microtubule stabilization mediated by a functi

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

101 otubule length, disrupted astral microtubule minus-end organization, and increased levels of the pola

102 s is mediated by dyneins translocating along minus-end out microtubules.

103 -dependent aberrant long spindle microtubule minus-end protrusions that push the properly segregated

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 kinesin-5 Cin8 was shown to switch from fast minus-end- to slow plus-end-directed motility upon bindi

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

108 -binding domain and recruits the microtubule minus-end-binding protein, Patronin, to form cortical nc

109 dynein is a molecular motor responsible for minus-end-directed cargo transport along microtubules (M

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

111 analysed the motility of the six members of minus-end-directed kinesin-14 motors in the moss Physcom

112 HIP) (FHF) complex, which interacts with the minus-end-directed microtubule motor dynein and its acti

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

114 nsisting of the plus-end tracker EB1 and the minus-end-directed molecular motor Kinesin-14 is suffici

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

116 e (MT) motor protein responsible for most MT minus-end-directed motility.

117 is controlling the switch between plus- and minus-end-directed motility.

118 Kip2, helping it overcome dynein's intrinsic minus-end-directed motility.

119 ative actions of the bipolar kinesin-5 and a minus-end-directed motor, which then pulls the sliding M

120 However, in the SAC model, minus-end-directed motors bind the minus ends of MTs as

121 -directed motors are balanced by forces from minus-end-directed motors that pull spindle poles togeth

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

123 This effect is observed only for microtubule minus-end-moving LDs.

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

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

126 r than non-uniform microtubules, uniparallel minus-end-out microtubules are the signature of dendrite

127 wth, microtubules display mixed polarity and minus-end-out microtubules push the tip of the axon, con

128 In dendrites, the minus-end-out microtubules were generally more stable an

129 rity orientations with both plus-end-out and minus-end-out oriented microtubules.

130 ur results show that cortical dynein slides 'minus-end-out' microtubules from the axon, generating un

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

132 ansport of lysosomes toward the microtubules minus-end.

133 he cell cortex in the steady state and at MT minus ends after injury.

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

135 iding a key piece to the puzzle of how these minus ends are formed and stabilized.

136 After their depletion, minus ends are not sorted outward at the early stages of

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

138 cytoplasmic fluid and on microtubules whose minus ends are tethered to the cortex.

139 MTs is balanced by depolymerization of their minus ends at the poles, producing poleward flux, while

140 are driven by the clustering of microtubule minus ends by dynein.

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

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

143 c field by designing a charged surface of MT minus ends labeled with dsDNA via a streptavidin-biotin

144 Proteins residing at the plus and minus ends of microtubules have been thought not to comm

145 l isoforms, are motors that move towards the minus ends of microtubules.

146 transports many cellular cargoes towards the minus ends of microtubules.

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

148 AC model, minus-end-directed motors bind the minus ends of MTs as cargo and transport them poleward a

149 more central role as nuclei migrate towards minus ends of polarized microtubule networks.

150 This force on minus ends represents a newly uncovered chromosome trans

151 MT tracks, whereas in the SAFE model, all MT minus ends that reach the pole are depolymerized by kine

152 t new minus ends within seconds, reanchoring minus ends to the spindle and delivering them to poles.

153 in/dynactin are specifically enriched at new minus ends within seconds, reanchoring minus ends to the

154 Rather than walking toward minus ends, dynein remains associated with plus ends due

155 MA's friction being lower when moving toward minus ends, EB1's lower toward plus ends, and PRC1's exh

156 Free microtubule minus ends, found in many differentiated cells, contribu

157 hows how mammalian CAMSAP proteins stabilize minus ends, providing a key piece to the puzzle of how t

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 , proteins, and viruses, towards microtubule minus ends.

161 main also depolymerizes microtubule plus and minus ends.

162 lectrophoretic mobilities measured for their minus ends.

163 ocessively tracked shrinking, depolymerizing minus ends.

164 ) that exhibit biased localization toward MT minus ends.

165 icles, and macromolecules toward microtubule minus ends.

166 family members also bind specifically to MT minus-ends and protect them against kinesin-13-induced d

167 ir abilities to suppress tubulin addition at minus-ends and to dissociate from MTs.

168 ion in axons and accumulation of microtubule minus-ends at axon tips.

169 /Patronin family all localize to and protect minus-ends but have evolved distinct effects on MT dynam

170 that both regions are required to stabilize minus-ends in Drosophila S2 cells.

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

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

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

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

175 ter polymerization dynamics at the plus- and minus-ends of microtubules.

176 punctae that moved processively towards the minus-ends of the cytoplasmic MTs.

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

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

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

180 , thereby creating stretches of decorated MT minus-ends.

181 with polymerization and tracks along growing minus-ends.

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

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

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

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

186 a drops to 37% with the use of precipitation minus evapotranspiration (P-E), a measure that represent

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

188 The mean observed minus expected duration of mechanical ventilation across

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

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

191 Mean observed minus expected duration of mechanical ventilation was th

192 ntly (p < 0.01) poorer performance (observed minus expected duration of mechanical ventilation, > 0.5

193 ntly (p < 0.01) better performance (observed minus expected duration of mechanical ventilation, < -0.

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

195 The net yield (revenue minus expenditure) was calculated for each vaccine.

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

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

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

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

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

201 Elephant exclusion alone (minus fire) had negligible effects on gecko density.

202 lence in mean between groups (awake-regional minus general anaesthesia 0.169, 95% CI -2.30 to 2.64).

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

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

205 9 radian/s2 vs 65016 radian/s2 [lower impact minus higher impact= 57427; 95% CI , 31123-80498; P < .0

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

207 intraobserver, and interimage variability (1 minus intraclass correlation coefficient) and agreement

208 Noninvasive hemoglobin monitoring minus laboratory hemoglobin differences showed an intrac

209 onservative treatments such as occlusion and minus lenses.

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

211 oplast DNA methylation levels in plus versus minus mating type gametes followed by chloroplast DNA hy

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

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

214 WS (median SWS after diuretic administration minus median SWS before diuretic administration) were co

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

216 ground carbon uptake (growth and recruitment minus mortality) by approximately 76% per year, mostly b

217 in) are 15-times more frequent than in pilus-minus mutant cells (0.2 events/min), indicating the pili

218 he same for wild-type cells (12 s) and pilus-minus mutant cells (13 s), suggesting the pili do not pl

219 of the effects of wild-type fungus and a DON minus mutant derivative.

220 The oxalate-minus mutants accumulated fumaric acid, produced functio

221 Here, we generated oxalate-minus mutants of S. sclerotiorum using two independent m

222 The oxalate-minus mutants retained pathogenicity on plants, but thei

223 ost tissue enhanced virulence of the oxalate-minus mutants, whereas supplementing with oxalate did no

224 fX complex using membranes prepared from LH2-minus mutants.

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

226 es and can be assigned to the sub-class of C-minus OBPs.

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

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

229 Measures: The RMSE of the residuals (fitted minus observed values) for the 3 regression models was u

230 n ions by SSM linearly depend on time to the minus one-fourth.

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

232 cells with reduced microvilli ("microvillus-minus," or MVM) but retaining normal tight junctions.

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

234 mate [95% IE] 59-68) and IPD caused by PCV13 minus PCV7 serotypes declined by 93% (91-94), by July, 2

235 o declined by 12-32% and IPD caused by PCV13 minus PCV7 type IPD declined by 58-72%, depending on age

236 ypes against which PCV7 has no effect (PCV13 minus PCV7).

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

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

239 difference between groups (solanezumab group minus placebo group) in the change from baseline was -0.

240 d treatment difference at week 9 (citalopram minus placebo) was -0.93 (95% CI, -1.80 to -0.06), P = .

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

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

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

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

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

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

247 Medical school losses (costs minus revenues) increased by $6018 (95% CI, $5506-$6629)

248 identified by computational analysis of ribo-minus RNA generated from human umbilical venous endothel

249 total precipitation minus total sublimation minus runoff) and a dynamic term.

250 ry site, alpha4 threonine 126 located on the minus side of alpha4 that contributes to the accessory s

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

252 ntion-to-treat population (safety population minus sites excluded with Good Clinical Practice violati

253 s loaded with OVA alone (PNSN(OVA)), plus or minus soluble CpG 1826.

254 s hepatic steatosis at nonenhanced CT (liver minus spleen CT attenuation < 1 HU) without evidence of

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

256 First, the minus strand is synthesized by the viral replicase compl

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

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

259 ation as a result of cytidine deamination of minus-strand DNA transcripts.

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

261 y simple process that involves complementary minus-strand RNA [(-)RNA] synthesis and subsequent (+)RN

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

263 had little or no effect on the formation of minus-strand strong-stop cDNA but caused a significant r

264 egration site sequences into plus-strand and minus-strand subpopulations, and use this to identify th

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

266 ol extracts from Centaurea scabiosa, Arctium minus, Taraxacum officinale, Centaurea nigra and Cirsium

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

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

269 e calculated vaccine effectiveness (VE) as 1 minus the adjusted odds ratio for vaccination.

270 ng >5 days; where LOS was the discharge date minus the admission date plus 1) among 33,920 patients w

271 the amount from the seventh to the ninth day minus the amount from the first to the third day, divide

272 ucted by nonlinear least square fitting of 1 minus the change in R2*divided by R2*at baseline as a fu

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

274 s the ACC signal the net value (the benefits minus the costs) of rewards that others will receive?

275 l tissue from fish transferred to SW plus or minus the deiodinase inhibitor, iopanoic acid, revealed

276 Vaccine efficacy was defined as 1 minus the hazard ratio or the incidence-rate ratio, mult

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

278 4-14) and defined vaccine effectiveness as 1 minus the incidence rate ratio, expressed as a percentag

279 ession model are defined as the observations minus the modeled values.

280 rm and calculated vaccine effectiveness (one minus the odds ratio of vaccination) by comparing infant

281 n does a random patient in the control group minus the probability of the opposite situation.

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

283 nces (rate of the end point in those with AF minus the rate in those without AF per 1000 person-years

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

285 baseline, the false-positive result rate (1 minus the specificity rate) for Lung-RADS was 12.8% (95%

286 lated as the maximum possible residence time minus the sum of residence time of source organs, assumi

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

288 ydraulic safety margin (stem water potential minus the water potential at which 50% of conductivity i

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

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

291 the CRM1 groove in the opposite orientation (minus) to that of previously studied NESs (plus).

292 e mass balance (that is, total precipitation minus total sublimation minus runoff) and a dynamic term

293 ); Pc = 9 x 10(-5)); and Trail Making Test B minus Trail Making Test A (P = .002; Pc = .02).

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

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

296 ll-length and internal RNA transcripts of U3-minus vectors are reduced in the nuclei of transfected c

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

298 viral RNA extracted from immature (protease-minus) virions.

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

300 onsoon (ISM) rainfall differences (with dust minus without dust) change from -9% to 23% of long-term