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1                                              CAT enhanced MET-stimulated FAK activation and synergist
2                                              CAT promoted Nrf2 nuclear translocation and HO-1 gene ex
3                                              CAT scores increase at exacerbation and reflect severity
4                                              CAT-1 ubiquitination and endocytosis in phorbol ester-st
5                                              CAT-1-HA-GFP was stably expressed in porcine aorthic end
6                                              CAT-ANX scores were strongly related to the probability
7 6); worse scores for mMRC (0.23; P = 0.004), CAT (1.8; P = 0.003), SGRQ (4.5; P = 0.003), and SF-12 P
8 tion of CAT-1, a functional mutant of CAT-1 (CAT-1-HA-GFP) was generated in which a hemagglutinin ant
9           Cationic amino acid transporter 1 (CAT-1) is responsible for the bulk of the uptake of cati
10 lated a human monoclonal antibody to IL-17A (CAT-2200) that can potently neutralize the effects of re
11     The purpose of this study was to build a CAT for patients with HF.
12                               In contrast, a CAT fixes measurement uncertainty and allows the number
13  survive Cm treatment when coinfected with a CAT-expressing strain.
14 cluster-anion-templated (CAT) assembly of a {CAT} subset{Mo24 Fe12 } macrocycle forms a giant ca. 220
15                         Crystallization of A-CAT in the presence of MgATP yielded structures with AMP
16 ium myosin-II heavy chain kinase-A (termed A-CAT).
17 .32 min(-1), respectively, and showed that A-CAT can use ADP to phosphorylate peptides and proteins.
18          Biochemical assays confirmed that A-CAT hydrolyzed ATP, ADP, and AMP with kcat values of 1.9
19            Our results suggest that aberrant CAT-tailed protein aggregation results from a defect in
20           Chloramphenicol acetyltransferase (CAT) activity varied greatly between strains, but there
21 on of the chloramphenicol acetyltransferase (CAT) gene is driven by a functional 895-bp fragment of t
22 apped and chloramphenicol acetyltransferase (CAT) reporter constructs were used to identify a 1.2 kb
23 used to a chloramphenicol acetyltransferase (CAT) reporter has been used to study the parameters infl
24 ed to use chloramphenicol acetyltransferase (CAT), as chloroplasts are particularly vulnerable to chl
25 nt bacteria expressing Cm acetyltransferase (CAT) are present.
26  N-terminal CAT coupled to a C-terminal ADO (CAT-ADO) prevents H(2)O(2) inhibition by converting it t
27 iver tumor models using a combination of AKT-CAT or AKT-NRAS(G12V) .
28  DDC treatment altered the morphology of AKT-CAT tumors and caused loss of lipid droplets.
29                Transcriptome analysis of AKT-CAT tumors revealed that cellular growth and proliferati
30 conversion and accelerated the growth of AKT-CAT tumors.
31 lar carcinomas further demonstrated that AKT-CAT tumors generated in the context of chronic liver inf
32                                          AKT/CAT and MET/CAT combination induced microscopic tumor fo
33          Activated AKT and beta-catenin (AKT/CAT) genes were hydrodynamically codelivered using the S
34 analysis, we compared the primary murine AKT/CAT and MET/CAT tumors to a panel of 53 human HCCs and d
35                            Conversion of AKT/CAT tumor cells to frank HCC during passage was associat
36 works identified in primary and passaged AKT/CAT tumors were steatosis and lipid metabolic pathways,
37                                  Primary AKT/CAT tumor cells were steatotic (fatty) hepatocellular ad
38 nsitivity to NEM distinguishes generally all CAT and y(+)LAT isoforms.
39 the seven cysteine residues conserved in all CAT isoforms did not lead to NEM insensitivity of hCAT-2
40  express the arginine transporters CAT-1 and CAT-2B, and that the majority of newly diagnosed patient
41 indings show how coactivation of the AKT and CAT pathways in hepatocytes can efficiently model develo
42 veral cancer cell lines, OLIG but not BA and CAT inhibited respiration.
43 the effect of additional cryoprotectants and CAT on fresh sperm motility.
44 in photosynthesis, that is, LH, EnT, ET, and CAT, define the structure of this review with the only f
45  significantly higher than those for FAS and CAT.
46 physical association-dissociation of GLO and CAT, in response to environmental stress or stimuli, see
47 th 1-standard deviation higher SOD, GPx, and CAT activities were 1.07 (95% confidence interval (CI):
48         Overall, activities of SOD, GPx, and CAT were not associated with CHD among women who were ge
49                                 SOD, GR, and CAT activities in red blood cell lysate and saliva and M
50                                  The HPX and CAT domains are rotated with respect to one another comp
51 icate that dihydrogen activation by QCAT and CAT tweezers is carried out in a pairwise manner, and PH
52 28,484 persons were followed in the SCIT and CAT groups, respectively.
53 A along with decreased activities of SOD and CAT were significantly (p<0.01) ameliorated by SP2.
54 and IL-8, and increased IL-10, GSH, SOD, and CAT levels.
55 re differences between transport of tENT and CAT compared to cENT through laboratory columns containi
56                          Rather, the WGR and CAT domains function together to recruit PARP-2 to sites
57              Thus, combining the antioxidant CAT-SKL with erlotinib targeted both CSCs and bulk cance
58                                   In assays, CAT-ADO turns over 225 times versus three times for the
59                             Study 1 assessed CAT score before and after 8 weeks of outpatient pulmona
60 ed pulmonary function who were asymptomatic (CAT score, <10) and whether those with symptoms had diff
61                 However in cancer cells, BA, CAT, and knockdown of the major ANT isoforms, ANT2 and A
62                                     Baseline CAT scores are elevated in frequent exacerbators.
63 acerbators had significantly higher baseline CAT scores than infrequent exacerbators (19.5 +/- 6.6 vs
64     There was an inverse correlation between CAT scores and observational clinical human reliability
65        The observed interaction site between CAT-2200 and IL-17A is consistent with data from hydroge
66 ATS and the surrounding tissues, mediated by CAT, can explain the complex auxin transport kinetics we
67                                          CAG-CAT-Tbx20 transgenic mice were generated for Cre-depende
68 long with the CAR coexpressing catalase (CAR-CAT), performed superior over CAR T cells as they showed
69                                Moreover, CAR-CAT T cells exerted a substantial bystander protection o
70 duced oxidative stress when admixed with CAR-CAT T cells.
71 gkrekic acid (BA), and carboxyatractyloside (CAT), and the F1FO-ATP synthase inhibitor, oligomycin (O
72                                    Catalase (CAT) mitigated stress and maintained viability and sperm
73  glutathione peroxidase (GPx), and catalase (CAT) activities with the risk of CHD.
74 xidant capacity (TEAC) levels, and catalase (CAT) and glutathione peroxidase (GPx) activities.
75 ), glutathione reductase (GR), and catalase (CAT) as well as levels of free radical damage marker mal
76     Cholesterol oxidase (ChOx) and catalase (CAT) were co-immobilized on a graphene/ionic liquid-modi
77 ), superoxide dismutase (SOD), and catalase (CAT).
78 terozygous db/m+, db/db, and db/db catalase (CAT)-transgenic (Tg) mice were used for DNA chip microar
79 seed oil diet up-regulated hepatic catalase (CAT) (activity and expression), superoxide dismutase (SO
80 idant enzyme activities, including catalase (CAT), superoxide dismutase (SOD), and glutathione peroxi
81 r, which was fabricated by loading catalase (CAT) onto l-lysine/multiwalled carbon nanotube (PLL/f-MW
82 D) activity, associated with lower catalase (CAT) and ascorbate peroxidase (APX) activities, leading
83 ation in the enzymatic activity of catalase (CAT) and superoxide dismutases (SOD) and cellular levels
84 stigated whether overexpression of catalase (CAT) in renal proximal tubular cells (RPTCs) could preve
85 P via studies of the activities of catalase (CAT), superoxide dismutase (SOD), and glutathione peroxi
86 ies of superoxide dismutase (SOD), catalase (CAT) and peroxidase (POD) decreased at a later time peri
87 ion of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione reductas
88 uch as superoxide dismutase (SOD), catalase (CAT), glutathione-s-transferase (GST) and non-enzymatic
89  liver superoxide dismutase (SOD), catalase (CAT), reduced glutathione (GSH) and glutathione peroxida
90 50 1A (CYP1A), vitellogenin (Vtg), catalase (CAT), Cu/Zn-superoxide-dismutase (Cu/Zn-SOD), and glutat
91 e to different sizes of CeO2 while catalase (CAT) activity was not affected by either size of CeO2 th
92 that GLO physically interacts with catalase (CAT) in rice leaves, and that the interaction can be der
93 upplementing exhausted assays with catalase (CAT) restored ADO activity, demonstrating that inhibitio
94 ative electron transfer (ET), and catalysis (CAT), which serve as a blue print for the rational desig
95 ix is then presented to the MMP-1 catalytic (CAT) domain in a distinct orientation.
96         The core binding (CB) and catalytic (CAT) domains of IntDOT interact with core-type sites adj
97 nal domains-Trp-Gly-Arg (WGR) and catalytic (CAT).
98 y rely on flexibility between the catalytic (CAT) and hemopexin-like (HPX) domains.
99 ions of conserved residues in the catalytic (CAT) domain or residues predicted by homology modeling t
100 NT) and DNA assay (tENT), and Catellicoccus (CAT) by DNA assay.
101 utively active AKT-1 (AKT) and beta-catenin (CAT), followed by induction of chronic liver inflammatio
102 and l-ornithine are transported by cationic (CAT) and y(+)L (y(+)LAT) amino acid transporters.
103 aluated 14 patients with DM using the CDASI, CAT-BM, and PGA scales.
104                               In conclusion, CAT overexpression in the RPTCs ameliorated maternal dia
105  of db/db mice compared with db/m+ and db/db CAT-Tg mice and in RPTs of streptozotocin-induced diabet
106 that {CAT} subset{Mo24 Fe12 } with different CATs gives the compounds 1-4 for CAT=Anderson {FeMo6 } (
107 e composed of a C-terminal catalytic domain (CAT), a central Trp-Gly-Arg (WGR) domain and an N-termin
108 NA damage interface to the catalytic domain (CAT).
109 rocess of self-signalling that occurs during CAT self-fusion have recently been revealed by live-cell
110 vities (ethoxyresorufin-O-deethylase (EROD), CAT, SOD, and GR) were also determined.
111                        In 152 exacerbations, CAT scores rose from an average baseline value of 19.4 +
112 th carboxy-terminal Ala and Thr extensions ("CAT tails").
113  'Fast Approximate Tree Classification' (FAT-CAT) web server provides a novel approach to ortholog id
114 l, plant and animal proteins demonstrate FAT-CAT's high precision at separating orthologs and paralog
115 ns from across the Tree of Life, enables FAT-CAT to predict orthologs and assign function for most se
116                                      The FAT-CAT phylogenetic placement is used to derive a functiona
117                                      The FAT-CAT web server is available at http://phylogenomics.berk
118 s(olate)) to give Fe(THO).Fe(SO4) (DMA)3, Fe-CAT-5, Ti(THO).(DMA)2, Ti-CAT-5, and V(THO).(DMA)2, V-CA
119                              Accordingly, Fe-CAT-5 exhibits ultrahigh proton conductivity (5.0 x 10(-
120  and are either a 2-fold interpenetrated (Fe-CAT-5 and Ti-CAT-5) or noninterpenetrated (V-CAT-5) poro
121 rystal X-ray diffraction structure of the Fe-CAT-5 shows bound sulfate ligands with DMA guests residi
122 h different CATs gives the compounds 1-4 for CAT=Anderson {FeMo6 } (1), Keggin {PMo12 } (2), Dawson {
123 ach person-day of follow-up was assessed for CAT exposure, and outcomes were defined by using diagnos
124  also report evidence that the mechanism for CAT-SKL inhibition of CSCs may depend on antioxidant-ind
125            In addition, FAK was required for CAT-induced cyclin D1 expression in a kinase-independent
126 ncrease in H2O2 when GLO is dissociated from CAT.
127 was diminished when exposed to effluent from CAT-column.
128 o affinity optimization was used to generate CAT-2200 from a parental lead antibody using random muta
129 thin the catalase and myeloperoxidase genes (CAT and MPO) has been studied in relation to asthma; how
130 umulation likely results from SA-induced GLO-CAT dissociation.
131                                   In the GLO-CAT complex, GLO-mediated H2O2 production during photore
132 a chimera carrying the backbone of human (h) CAT-2 and the protein domain of SLC7A14 corresponding to
133           Fish oil diet up-regulated hepatic CAT (activity and expression), paraoxonase-1 (PON-1) exp
134 DPPH and ORAC methods) and an heterogeneous (CAT method) system.
135                                       All HF-CAT scales demonstrated good construct validity through
136  showed a more precise measurement of all HF-CAT scales over a larger range than comparable static to
137                             The resulting HF-CAT was administered to 100 patients with ancillary HF (
138                                       The HF-CAT assessment took 3:09+/-1:52 minutes to complete and
139                                       The HF-CAT scales identified significant differences between pa
140 escent protein [GFP]-Tg [controls] and Hoxb7/CAT-GFP-Tg, which overexpress CAT in RPTCs) were studied
141 liorated in male offspring of diabetic Hoxb7/CAT-GFP-Tg dams via the Nrf2-HO-1 defense system.
142 is oocytes established that indeed all human CATs (including the low affinity hCAT-2A), but neither y
143  reduced electrocatalytically by immobilized CAT to obtain a sensitive amperometric response to chole
144                              The immobilized CAT retained its bioactivity with a high protein loading
145                              The immobilized CAT shows a couple of reversible and well-defined cyclic
146                   Study 3 assessed change in CAT score at baseline and at 12 months in stable outpati
147                   Study 2 assessed change in CAT score at discharge and after 3 months in patients ad
148 hs (mean 0.6, 95% CI -0.4 to 1.5), change in CAT score correlated significantly with change in SGRQ s
149                                    Change in CAT score from baseline to exacerbation onset was signif
150                               Mean change in CAT score from hospital discharge to 3 months after disc
151            Although no significant change in CAT score was identified after 12 months (mean 0.6, 95%
152                           The mean change in CAT score with pulmonary rehabilitation was -2.5 (95% CI
153  the 3'-SL resulted in an 83-98% decrease in CAT activity.
154 ntil day 14, concordant with the decrease in CAT score.
155  minimum clinically important improvement in CAT score.
156      Our results suggest that an increase in CAT protein dynamics underlies the DNA-dependent activat
157 but did not protect against the reduction in CAT activity or the increased cellular levels of GSH.
158                    At exacerbation, rises in CAT score were significantly associated with falls in FE
159 d the interrelationships between variants in CAT and MPO, ambient air pollutants, and acute respirato
160 t the letter "A" is coded in the same way in CAT and ACT.
161  metastasis, indicating that hypoxia-induced CAT enhances cell release rather than early organ coloni
162                                 Internalized CAT-1-HA-GFP was accumulated in early, recycling, and la
163 uterized Adaptive Testing-Anxiety Inventory (CAT-ANX).
164 uterized Adaptive Test-Depression Inventory (CAT-DI), that decreases patient and clinician burden and
165 en shown to inhibit system y(+) (most likely CAT-1), but not system y(+)L.
166 substrates without Ltn1p-accessible lysines, CAT-tailing enabled degradation by exposing lysines sequ
167 D is sufficient for binding to an isolated M-CAT-like DNA element, multimeric forms are deficient for
168 the RBP-Jkappa NOTCH effector and a single M-CAT motif within these regions.
169  a tail-tail configuration in CRM5 and the M-CAT motif in CRM7 are necessary for enhancer function.
170 ensional (3D) extended metal catecholates (M-CATs) was synthesized by combining the appropriate metal
171 l lung expression of the anti-oxidant marker CAT and decreased expression of the pro-oxidant marker N
172                              AKT/CAT and MET/CAT combination induced microscopic tumor foci by 4 week
173  compared the primary murine AKT/CAT and MET/CAT tumors to a panel of 53 human HCCs and determined th
174 Fak in an oncogenic (c-MET/beta-catenin, MET/CAT)-driven HCC model.
175 C) upon in vivo passage, whereas primary MET/CAT tumors emerged directly as frank HCC.
176 , Fak deficiency significantly repressed MET/CAT-induced tumor development and prolonged survival of
177 t and prolonged survival of animals with MET/CAT-induced HCC.
178 the Cutaneous Assessment Tool-Binary Method (CAT-BM), with the Physician Global Assessment (PGA) as t
179 lational up-regulation of a particular mRNA, CAT-1; however, a detailed, transcriptome-wide understan
180 suppress Gpr132 gene expression via a muscle CAT element in the Gpr132 gene.
181  Sentence Completion (SSC), category naming (CAT) and verbal fluency (FAS), in localizing the Wernick
182                                        A new CAT for patients with HF was built using modern psychome
183  (compared with the reference category of no CAT) and survival analysis was conducted.
184 sperm motility (P<0.05), but the addition of CAT mitigated these effects (P>0.05), producing a mean 2
185           Regardless, the simple addition of CAT to present-day procedures will significantly improve
186 ration is very high, whereas the affinity of CAT for H2O2 (measured Km approximately 43 mM) is extrao
187                      The epistatic effect of CAT and MPO variants was most evident in communities exh
188 wever, the function of CAT tails and fate of CAT tail-modified ('CATylated') NCs has remained unknown
189                     However, the function of CAT tails and fate of CAT tail-modified ('CATylated') NC
190  be useful in the clinical interpretation of CAT data, particularly in response to intervention studi
191 -regulation of CAT-1, a functional mutant of CAT-1 (CAT-1-HA-GFP) was generated in which a hemaggluti
192 RQC component Rqc1p, and that the process of CAT tailing enables robust ubiquitination of the nascent
193 mechanisms of PKC-induced down-regulation of CAT-1, a functional mutant of CAT-1 (CAT-1-HA-GFP) was g
194                 Here we examined the role of CAT-tailing in nascent-chain degradation in budding yeas
195 ctivation also resulted in ubiquitination of CAT-1.
196                                   The use of CATs to judge specialist technical performance before em
197 type were more likely to show no activity on CAT (P < 0.05).
198 did not collapse DeltaPsi until OLIG, BA, or CAT was added.
199 e indicate that sulphide generated by CSE or CAT/MST or from thiosulphate is unlikely to contribute t
200 nesis resulted from delivery of AKT, MET, or CAT alone.
201 ols] and Hoxb7/CAT-GFP-Tg, which overexpress CAT in RPTCs) were studied from the prenatal period into
202 tudy 1, 565 of 675 (84%) patients had paired CAT scores.
203 200 patients recruited, 164 (82%) had paired CAT scores.
204 200 patients recruited, 147 (74%) had paired CAT scores.
205 e CAT; we included only patients with paired CAT scores in the analysis.
206                      Among elderly patients, CAT-related LGIE and UGIE are clinically relevant risks
207                                          PEG-CAT contacting only the detector vessel blocked FMD in t
208 resence of polyethylene glycol catalase (PEG-CAT).
209 +) channel opening in an iberiotoxin- or PEG-CAT-sensitive fashion in cell-attached patches but had l
210     Physiological parameters, SOD, POD, PPO, CAT activity, free proline, soluble protein and MDA cont
211 tional cohort of elderly veterans prescribed CAT.
212                               Pretransformed CAT thymocytes had increased DNA damage at the transloca
213 re transfected with polymorphic APP promoter-CAT fusion clones.
214     Etomoxir treatment significantly reduced CAT and GLUT4 mRNA transcription in adipose tissue, but
215 berrant proteins, a phenomenon that requires CAT-tail addition to the nascent peptides by Rqc2.
216                                         SOD, CAT, GST, GSH, vitamin E and C levels were high in combi
217 ioxidant enzymes, such as Cu/Zn-SOD, Mn-SOD, CAT, GR, and guaiacol peroxidase, were also determined i
218 parameters, such as antioxidant status (SOD, CAT, GPX and GSH) and lipid peroxidation was also studie
219                                  Strikingly, CAT-expressing pneumococci in mouse lungs were outcompet
220 sferase/mercaptopyruvate sulphurtransferase (CAT/MST) pathway caused an increase in HPV similar to th
221 leads to down-regulation of the cell surface CAT-1.
222  after bronchodilator use) and had symptoms (CAT score, >/=10) had a higher risk of respiratory exace
223 ition of C-terminal alanine-threonine tails (CAT-tails), and a Cdc48 hexamer is recruited to extract
224                   The third key DIMM target, CAT-4 (CG13248), has not previously been associated with
225 e describe that the cluster-anion-templated (CAT) assembly of a {CAT} subset{Mo24 Fe12 } macrocycle f
226 ifunctional protein comprising an N-terminal CAT coupled to a C-terminal ADO (CAT-ADO) prevents H(2)O
227 IVE To develop a computerized adaptive test (CAT) for depression, called the Computerized Adaptive Te
228 ve Pulmonary Disease (COPD) Assessment Test (CAT) is an eight-item questionnaire designed to assess a
229                    The COPD Assessment Test (CAT) is responsive to change in patients with chronic ob
230  function, dyspnea and COPD assessment test (CAT) scores) were also measured at those time points.
231 pnea Scale (mMRC), the COPD Assessment Test (CAT), St. George's Respiratory Questionnaire (SGRQ), 12-
232 ory symptoms using the COPD Assessment Test (CAT; scores range from 0 to 40, with higher scores indic
233 as a surrogate for the COPD Assessment Test [CAT] >/=10 vs <10) in addition to COPD exacerbations in
234 techniques used for computer adaptive tests (CATs) may be able to address these problems.
235      Using this approach, we determined that CAT tailing is mechanistically distinct from canonical t
236                         We hypothesized that CAT scores at exacerbation relate to exacerbation severi
237 ion of clathrin heavy chain, indicating that CAT-1-HA-GFP internalization requires clathrin-coated pi
238                                 We show that CAT processes Cm intracellularly but not extracellularly
239                                We show that {CAT} subset{Mo24 Fe12 } with different CATs gives the co
240                                          The CAT can reliably assess technical performance in laparos
241                                          The CAT provides a reliable score of exacerbation severity.
242                                          The CAT-DI provided excellent discrimination throughout the
243                                          The CAT-HF (Cardiovascular Improvements With MV-ASV Therapy
244                                          The CAT/ChOx/GR-IL/GCE showed excellent analytical performan
245 daptive Testing-Depression Inventory and the CAT-ANX, comorbid major depressive disorder and generali
246 g construct validity, both the CDASI and the CAT-BM were significant predictors of the PGA scales.
247            This was partially blocked by the CAT antagonist aspartate (1 mm) and also by PAG.
248        Moreover, HPV was not affected by the CAT antagonist aspartate and was blocked rather than enh
249 lled in the London COPD cohort completed the CAT at baseline (stable state), exacerbation, and during
250        In all the high MO conformations, the CAT and HPX domains are not in tight contact, and the re
251  structural distortions that destabilize the CAT.
252 nificantly related to the time taken for the CAT score to return to baseline (rho = 0.42, P = 0.012).
253 mum clinically important improvement for the CAT to range between -1.2 and -2.8 with receiver operati
254        We aimed to identify the MCID for the CAT using anchor-based and distribution-based methods.
255 of measurement) to estimate the MCID for the CAT; we included only patients with paired CAT scores in
256 and this chain is properly positioned in the CAT domain active site for subsequent hydrolysis.
257                         Back-rotation of the CAT and HPX domains to the X-ray closed conformation rel
258 iochemical data and homology modeling of the CAT domain suggest that Arg-285 is the missing Arg I res
259 e of the minimum important difference of the CAT is 2 points.
260 cus of this study was the development of the CAT-DI.
261 ation through a local destabilization of the CAT.
262 mical and electrocatalytic properties of the CAT/PLL/f-MWCNT biosensor, offering a new idea for the d
263 tatistically longer completion time than the CAT-BM by about 1.5 minutes.
264                        We therefore used the CAT animal model to obtain mechanistic insights into the
265  absences was elevated for children with the CAT (G/G) and MPO (G/A or A/A) genes (relative risk = 1.
266 stal structure of IL-17A in complex with the CAT-2200 Fab at 2.6 A resolution in order to provide a d
267 inal, Ala- and Thr-containing extension-the 'CAT tail'.
268              Complex antithrombotic therapy (CAT) prescribed to elderly patients increases the risk o
269 ated Carboxy-terminal Alanine and Threonine (CAT) tail elongation-can be recapitulated in vitro with
270 g a carboxyl-terminal alanine and threonine (CAT) tail through a noncanonical elongation reaction.
271 uated by calibrated automated thrombography (CAT) using protein S-deficient plasma.
272                                        Thus, CAT-tails do not serve as a degron, but rather provide a
273 ed activation of beta-catenin in thymocytes (CAT mice) induces lymphomas that depend on recombination
274 Fe(SO4) (DMA)3, Fe-CAT-5, Ti(THO).(DMA)2, Ti-CAT-5, and V(THO).(DMA)2, V-CAT-5 (where DMA = dimethyla
275 er a 2-fold interpenetrated (Fe-CAT-5 and Ti-CAT-5) or noninterpenetrated (V-CAT-5) porous anionic fr
276 y the lower conductivity values found for Ti-CAT-5 (8.2 x 10(-4) S cm(-1) at 98% RH and 25 degrees C)
277 scillatory recruitment of signal proteins to CAT tips that are communicating and growing towards each
278  were identified by CAZyme Analysis Toolkit (CAT).
279                                Tralokinumab (CAT-354) is an IL-13-neutralising human IgG4 monoclonal
280 ysis and chloramphenicol acetyl transferase (CAT) reporter assays indicate that EGR-1 transactivates
281                         GLUT4 and transgenic CAT mRNA were measured.
282 er of the collective-to-amoeboid transition (CAT), promoting the dissemination of amoeboid-moving sin
283 cally the Collective-to-Amoeboid Transition (CAT).
284 m, which we term connective auxin transport (CAT).
285 e inducible cationic amino acid transporter (CAT)2, ODC, and iNOS were measured in macrophages and H
286 titutively express the arginine transporters CAT-1 and CAT-2B, and that the majority of newly diagnos
287 bfamily of cationic amino acid transporters (CATs) due to sequence homology, may represent system c.
288 ns receiving conventional allergy treatment (CAT; nasal steroids or oral antihistamines) were compare
289 ured by the conjugated autoxidizable triene (CAT) assay.
290  regulatory element sufficient to upregulate CAT protein levels (but not RNA) upon AdoMetDC inhibitio
291 g ability of each variant was assessed using CAT reporter gene assays, real-time semiquantitative rev
292 (THO).(DMA)2, Ti-CAT-5, and V(THO).(DMA)2, V-CAT-5 (where DMA = dimethylammonium).
293 CAT-5 and Ti-CAT-5) or noninterpenetrated (V-CAT-5) porous anionic framework.
294 ains essential for activation (Zn1, Zn3, WGR-CAT).
295 m of information throughout the plant, while CAT acts locally, allowing tissues to modulate and be mo
296 en bromide-activated resin column bound with CAT was used to remove H(2)O(2) from the donor vessel.
297  95% CIs) associated with SCIT compared with CAT adjusted for age, sex, vocational status, and income
298 vational study, receiving SCIT compared with CAT was associated with lower risk of autoimmune disease
299                               Treatment with CAT-SKL-a re-engineered protein form of the antioxidant
300  10% dimethylformamide (DMF) with or without CAT did not (P>0.05).

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