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1 CCT also indicated a sloped correlation to error (correl
2 CCT and corneal power measured using Orbscan II, Pentaca
3 CCT appears to significantly affect the error by up to 4
4 CCT chaperonin further binds and disassembles subcomplex
5 CCT decreased from 644 +/- 67 mum before DMEK to 557 +/-
6 CCT decreased significantly over time.
7 CCT did not show a significant change after 6 months up
8 CCT is efficacious on global cognition, select cognitive
9 CCT was also found to be significantly associated with I
10 CCT was determined bilaterally using handheld ultrasound
11 CCT was measured at baseline, then at 2 weeks and 1, 3,
12 n containing tailless complex polypeptide 1 (CCT), revealed a robust interaction between PDCD5 and CC
13 x chaperonin containing t-complex protein 1 (CCT) was identified, and subsequent studies showed that
14 ludes cytosolic chaperonin containing TCP-1 (CCT; also called TRiC) and its cochaperone phosducin-lik
15 ) (P = .7); Kmin: -0.25 +/- 1.25 D (P = .2); CCT: -16.38 +/- 37 mum (P = .01); GAT-IOP: +1.0 +/- 2.3
17 ssess the intrasession repeatability of ACD, CCT, PCT at different nasal and temporal locations, WTW,
18 issue altered, derived from [PTA = (FT + AD)/CCT], where FT = flap thickness, AD = ablation depth, an
24 year after the rejection episodes, BSCVA and CCT in these eyes remained unchanged when compared with
27 age corneal curvature was flatter by 4 D and CCT was reduced by 83 mum (P < 0.0001, for all), postope
33 and molecular analyses indicate that GCT and CCT operate in parallel to gibberellic acid, a phytohorm
35 ount by future studies investigating IOP and CCT as risk factors or diagnostic tests for glaucoma in
37 corneal edema, or corneal dystrophy, IOP and CCT readings were available for 3251 Chinese, 3232 Malay
38 ed to investigate the association of IOP and CCT with potential risk factors and genetic ancestry.
40 acam HR exhibited significantly lower Km and CCT measurements (P < .001, for all); however, no signif
45 l single nucleotide polymorphisms (SNPs) and CCT using linear regression, adjusting for age, gender a
52 ere wasn't significant difference of average CCT between the ethnic groups (P = 0.3) and gender (P =
54 rate of change were associated with baseline CCT (ss = -0.1 to -0.09 and -0.011, respectively, all P
57 e we report an additional connection between CCT and actin by identifying one of the CCT subunits, CC
58 ally significant inverse correlation between CCT and pO2 in the anterior chamber angle (P = .048).
59 es unique insight into the interplay between CCT and a cochaperone to orchestrate the folding of a pr
61 The eukaryotic chaperonin TRiC (also called CCT) is the obligate chaperone for many essential protei
63 ty of anterior chamber depth (ACD), central (CCT) and peripheral corneal thickness (PCT), white-to-wh
67 Mediator CDK8 module encoded by CENTER CITY (CCT; Arabidopsis MED12) and GRAND CENTRAL (GCT; Arabidop
68 ly associated with age (scaled coefficients: CCT 0.62, p < 0.0001; age -0.55, p <0.0001; r2 = 0.25).
69 ciated with age and AL (scaled coefficients: CCT 0.89, p < 0.0001; DCT IOP 0.46, p < 0.01; age - 0.60
70 eronin containing TCP1 or TCP1-Ring complex (CCT/TRiC chaperonin), a complex known to function in pro
71 s of the chaperonin containing TCP1 complex (CCT) were found to interact with V-ATPase for the first
75 enerated knock-in mice in which the critical CCT domain Leu502 residue required for high affinity rec
76 CTP:phosphocholine cytidylyltransferase (CCT) interconverts between an inactive soluble and activ
84 h keratoconus that had serial evaluation for CCT, following CXL, using high-definition optical cohere
86 ol and are consistent with a direct role for CCT in translocation of LF through the protective antige
87 y process, the Gbeta-CCT and the PhLP1-Gbeta-CCT complexes, were isolated and analyzed by a hybrid st
88 n the Gbetagamma assembly process, the Gbeta-CCT and the PhLP1-Gbeta-CCT complexes, were isolated and
90 d pachymetry determined significantly higher CCT values than Orbscan IIz (P<0.001), Visante (P<0.001)
92 ray crystallographic study of a single human CCT subunit in the context of a hexadecameric complex ca
96 USP and HD-OCT showed better agreement in CCT readings at all visits, and may better estimate the
99 1 region, which regulate normal variation in CCT, may play a role in the thinning associated with ker
101 riable linear regression analysis, increased CCT was significantly associated with younger age, male
103 a significant association between increased CCT and younger age, male sex, and higher IOP but not gl
105 flux is reduced by compromise of individual CCT subunits, various disease-relevant autophagy substra
107 , while the mean difference between J0, J45, CCT, and ACD measurements was 0.07 D, -0.016 D, -5.05 mu
108 d a complex with CCT and beta-tubulin, a key CCT-folding substrate, and specifically inhibited beta-t
112 of the minimum angle of resolution [logMAR]; CCT, 554.1+/-39.1 mum at last visit before rejection vs.
113 gressors were older, had significantly lower CCT and baseline IOPs, and were more likely to have pseu
114 Orbscan II measured significantly lower CCT compared with Pentacam (20 mum; P < .0005) and Galil
121 gular TA was detected in 72 eyes (90%); mean CCT was 492+/-62.10 mum; postoperative endothelial cell
135 traocular distances using SS-OCT were 6 mum (CCT), 16 mum (ACD), 14 mum (AD), 13 mum (LT), 14 mum (VD
139 her insight into the genetic architecture of CCT and illustrate that the use of minority groups in GW
142 s, and little is known about the efficacy of CCT in people with mild cognitive impairment or dementia
144 CCTepsilon conversely reflect the levels of CCT oligomer, our results suggest that CCTepsilon provid
147 of EV was significantly higher than that of CCT (P = 0.003), whereas a combination of both factors i
148 accuracy, significantly better than that of CCT, in differentiating actively rejecting from clear gr
149 1, 2016, for randomized controlled trials of CCT in older adults with mild cognitive impairment or de
150 1, 2016, for randomized controlled trials of CCT in older adults with mild cognitive impairment or de
151 ying surprisingly that the effect of loss-of-CCT activity on mutant ATXN3 or huntingtin oligomerizati
153 perative and intraoperative parameters, only CCT and EV were identified as significant factors, predi
155 o relationship between corneal hysteresis or CCT and quantitative measures of optic disc cupping, sug
157 r stages based on PET/CT, but not CXR/MRI or CCT/MRI, were associated with significant differences in
158 in T-complex 1 (TCP-1) ring complex (TRiC or CCT for chaperonin containing TCP-1) have been shown to
159 the mammalian cytosolic chaperonin TRiC (or CCT), primarily through its DNA binding domain (AML1-175
161 ts, requiring the TCP1 Ring Complex (TriC or CCT) chaperonin and five tubulin-specific chaperones, tu
163 ryo-electron microscopy studies of the PDCD5.CCT complex suggested a possible mechanism of inhibition
164 corneal thickness at the 6-o'clock position, CCT, and CV were significantly smaller in the torsional
168 For each 10-microm increase in preoperative CCT, the odds of developing corneal decompensation incre
169 iding whether to perform a triple procedure, CCT remains a less effective, but adequate, alternative.
172 led that increased VCDR (P = 0.003), reduced CCT (P = 0.045), and reduced superior and inferior retin
175 trieved from five RCTs and two retrospective CCTs and subsequently pooled into meta-analyses; however
183 aspin, Pph3, the chaperonin containing TCP1 (CCT) and 25 other proteins--define a novel intranuclear
185 g the Dmin, e.g., collision cell technology (CCT) and analyte isotope selection, are also discussed.
187 ith chromatin via their conserved C-terminal CCT (CONSTANS, CONSTANS-like, and TIMING OF CAB EXPRESSI
188 lose resemblance to the SPAK/OSR1 C-terminal CCT/PF2 domain, which is required for physical interacti
189 SPAK possesses a conserved carboxy-terminal (CCT) domain, which recognises RFXV/I motifs present in i
190 re PT/INR, conventional coagulation testing (CCT) is performed, which is time-consuming and requires
194 In this issue, Trinidad et al. show that CCT/TRiC is a chaperone required for p53 folding, thus p
195 entified, and subsequent studies showed that CCT is required for efficient delivery of LF and related
207 diated in vivo by an interaction between the CCT domain in SPAK and RFXV/I domains in WNK3 and NKCC1/
213 ntified a network of proteins, including the CCT complex, USP7, Aurora kinase, Nedd4, and Trim24, tha
214 o define the physiological importance of the CCT domain, we generated knock-in mice in which the crit
216 as therefore to evaluate the accuracy of the CCT measurements performed by three different observers,
217 ween CCT and actin by identifying one of the CCT subunits, CCTepsilon, as a component of the myocardi
218 ow that an interaction with a subunit of the CCT/TCP-1 ring complex (TRiC) chaperonin complex is invo
222 affect stress granules differently, with the CCT complex inhibiting stress granule assembly, while th
227 OLMaster 700, and central corneal thickness (CCT) and anterior chamber depth (ACD) values obtained fr
229 astigmatism (TA), central corneal thickness (CCT) and endothelial cell density 12 months postoperativ
230 MAR, keratometry, central corneal thickness (CCT) and higher-order aberrations (HOAs) over a 6 mm pup
234 s thickness (LT), central corneal thickness (CCT) and white-to-white (WTW) distance were measured by
237 aracteristics and central corneal thickness (CCT) from the Infant Aphakia Treatment Study (IATS) pati
245 teresis, IOP, and central corneal thickness (CCT) were measured; optic disc photographs were analyzed
247 eadings (mean-K), central corneal thickness (CCT), and anterior and posterior elevation at the apex a
248 r pressure (IOP), central corneal thickness (CCT), and baseline vertical cup-to-disc ratio (VCDR).
250 flat keratometry, central corneal thickness (CCT), and thinnest corneal thickness (TCT) measurements
251 tometry readings, central corneal thickness (CCT), anterior chamber depth (ACD), lens thickness (LT),
252 istances, such as central corneal thickness (CCT), aqueous depth (AD), anterior chamber depth (ACD),
253 ween baseline CH, central corneal thickness (CCT), average intraocular pressure (IOP), and rates of R
254 al zone 2-10 mm), central corneal thickness (CCT), best spectacle-corrected visual acuity (BSCVA), an
255 l acuity (BSCVA), central corneal thickness (CCT), endothelial cell density (ECD) and complication ra
256 l acuity (BSCVA), central corneal thickness (CCT), endothelial cell density (ECD), and need for regra
257 ll density (ECD), central corneal thickness (CCT), graft survival rate, and postoperative complicatio
258 try (Kmax, Kmin), central corneal thickness (CCT), intraocular pressure with Goldmann applanation ton
259 ics, preoperative central corneal thickness (CCT), IOP (using noncontact tonometry), manifest refract
260 i with POAG, with central corneal thickness (CCT), vertical cup-to-disc ratio (VCDR) and with diabete
261 essure (IOP), and central corneal thickness (CCT), while adjusting for potentially confounding factor
264 t refraction (D), central corneal thickness (CCT, micrometers) and endothelial cell density (ECD).
265 c data (age, sex, central corneal thickness [CCT], intraocular pressure [IOP], refraction, medication
266 TG (510.79 +/- 44.37 mum) groups had thinner CCT than PXG (520.48 +/- 38.95 mum), PACG (524.00 +/- 37
271 dicate that computerized cognitive training (CCT) is a safe and efficacious intervention for cognitio
273 sfers (UCTs) and conditional cash transfers (CCTs) on birth registration, vaccination uptake, and sch
277 etero-oligomeric eukaryotic chaperonin, TRiC/CCT, which contributes to its biosynthesis and activity
278 d by circadian clock, ATP-dependent TCP/TRiC/CCT chaperonin and mitochondrial electron transport chai
280 all visits, and may better estimate the true CCT following CXL as compared to dual Scheimpflug tomogr
290 nuclear foci and physically associating with CCT, suggesting an evolutionarily conserved biological f
295 ependent, and does not further increase with CCT knockdown in autophagy-defective cells/organisms, im
296 eins mutated to prevent the interaction with CCT show conformational instability and acquire an abili
297 the Gbeta fold, disrupting interactions with CCT and releasing a PhLP1-Gbeta dimer for assembly with
298 he structures show that Gbeta interacts with CCT in a near-native state through interactions of the G
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