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1 iction rules have been developed but need to be further validated.
2 linical utility and prognostic value need to be further validated.
3 nostic indicator in the management of cancer is further validated.
4          The relevance to human NASH and HCC was further validated.
5 g03055671 at TNFSF10 (P = 1.67 x 10-8) genes was further validated.
6 nical detection of primary SS once they have been further validated.
7 y undescribed antiviral ISGs, TAP1 and BMP2, were further validated.
8 ration count, and TP53 and CDKN2A/B deletion were further validated.
9 n via alteration of the Tsc2-mTor-Eif4e axis was further validated across MIA rodent models.
10            The optimal setup for our purpose was further validated against a set of serum samples fro
11                                   The models were further validated against seven new MeONPs.
12 ic variants identified by these methods have been further validated and functionally investigated in
13 us erythematosus area and severity index has been further validated and utilized in a number of studi
14 h poor HRQOL identified in this study should be further validated, and could be used in clinical prac
15 was associated with poor outcomes and should be further validated as a standard end point of chemoimm
16 nes in cancer cells, whose products may then be further validated as potential biomarkers.
17                                       MEGF10 was further validated as an ADAM17 substrate using ADAM1
18 d in a model-specific microarray dataset and were further validated as suitable reference genes in an
19 pper pillars with different orientations and is further validated at the atomic scale by recourse to
20 ntial expression of selected candidate genes was further validated at protein level and analyzed for
21                                  The results were further validated at the macroscale using prepacked
22 racting proteins in the progression of NSCLC are further validated by proteomics data.
23              These tentative criteria should be further validated by correlations with clinical trial
24 wever, the model's generalizability needs to be further validated by external datasets.
25              However, these findings need to be further validated by further research.
26 scopy technique used, which can subsequently be further validated by more quantitative AFM force spec
27 ase their affinity and stability, which will be further validated by the bioassays in the future.
28            Furthermore, top DE circRNAs have been further validated by RT-qPCR using divergent primer
29                          These advances have been further validated by successful phase 2 and phase 3
30 y the photophysical properties, and this has been further validated by the time-dependent density fun
31 ys known to be associated with anti-PD1, and is further validated by 6 CRISPR gene sets associated wi
32                  Flexibility of the approach is further validated by additional designs of angle-swit
33             SRA-mediated protection from CIH is further validated by adoptive transfer of SRA(+) hepa
34                          The developed model is further validated by both in vitro data on isolated c
35                                    The model is further validated by demonstrating our ability to can
36                                    The model is further validated by independent data sets from addit
37 ribute more than tethered ends to HSI, which is further validated by specifically designed match frag
38                                          BSP is further validated by substantiated biological discove
39        The correctness of CLPred predictions is further validated by the case studies of Sox transcri
40                                         This is further validated by the photophysical properties of
41                       Moreover, the approach is further validated by tracking, for over 80 years, the
42 ionship between inhibitors and Ca(2+), which was further validated by (19)F NMR spectroscopy showing
43                                This response was further validated by a dematin-specific antibody and
44 affinity of NMK-T-057 toward gamma-secretase was further validated by a fluorescence-based gamma-secr
45 tion using sequence similarity networks that was further validated by a structural analysis.
46                                 The approach was further validated by an observed reduction in Euclid
47                                    The model was further validated by an open test on 12 additional i
48  in determining galectin-ligand interactions was further validated by analysis of galectin-3 interact
49                        The mechanistic model was further validated by applying it to a test set of su
50 r of ERalpha transcriptional activity, which was further validated by assessment of direct transcript
51                                   IsoResolve was further validated by case studies of genes with isof
52                          The resulting model was further validated by chemical synthesis of a novel i
53                                   The method was further validated by comparing the CpG methylation p
54                                    The model was further validated by comparison with reported respon
55                               The ISS system was further validated by demonstrating effectiveness in
56     Biological applicability of the platform was further validated by demonstrating increase in endop
57                                         This was further validated by depleting gamma interferon (IFN
58                                   The method was further validated by detecting genomic DNA with high
59                                 The approach was further validated by determining the relative merope
60         The efficacy of the BSA-based method was further validated by direct comparison with commerci
61 identified targets associated with RA, which was further validated by experimental studies.
62                                   The method was further validated by histones isolated from histone
63                            Conversion of LC3 was further validated by immunoblotting.
64 nt in human peritendinous scar tissue, which was further validated by immunofluorescent staining for
65  response, inflammation, and survival, which was further validated by immunohistochemical staining.
66 1 with distant metastasis in TNBC (P = 0.01) was further validated by immunohistochemistry.
67 than was AD8 Env-SERINC5 interactions, which was further validated by immunoprecipitation assays.
68                                  Versatility was further validated by implementing the biosensors in
69                                 The platform was further validated by isolating CTCs from blood sampl
70  3, one of these novel interacting partners, was further validated by isothermal titration calorimetr
71 -mir hairpins against the target gene, which was further validated by knocking down two additional ES
72                                    The model was further validated by mapping onto it a diverse set o
73             The performance of the apparatus was further validated by measuring rapid H/D exchange ki
74  involvement of the oxidative stress pathway was further validated by measuring the levels of the PAC
75 unotherapy in BC with lung metastasis, which was further validated by multiplex immunofluorescence an
76 urse of metal bioaccumulation in oysters and was further validated by predicting the bioaccumulation
77                      The developed procedure was further validated by recovery studies by comparing w
78                                         This was further validated by reduced levels of Kif7 at cilia
79 d eIF2gamma in HCV IRES-mediated translation was further validated by ribozymes directed against addi
80 ision for subsequent RNA-Seq analysis, which was further validated by RT-qPCR and RNA FISH.
81                                   The method was further validated by showing that the 3D printed mat
82 on of TGF-beta3-mediated protein endocytosis was further validated by silencing of clathrin.
83 ate the complex model of PmrD-PmrA(N), which was further validated by site-directed spin labeling exp
84                                  This result was further validated by stem-loop real-time reverse tra
85             The utility of spectral counting was further validated by studying the negative effect of
86         The predictive quality of the models was further validated by successful prediction of the in
87                                   The method was further validated by TaqMan reactions.
88 ent with the observed carbon efficiency, and was further validated by testing for agreement with gas
89 rable environment for both cell types, which was further validated by the expression of AF tissue-spe
90        The negative regulatory role of Dok-1 was further validated by the expression of small interfe
91                              The methodology was further validated by the observation of reduction in
92                         The current approach was further validated by the quantification of Arg in su
93 ctivated, and the altered expression of CDK1 was further validated by Western analysis.
94  (pentose phosphate and pyruvate metabolism) was further validated by western blot analysis.
95                           Pathway activation was further validated by Western blot analysis.
96                                         This was further validated by WNT5a-siRNA transfection assay
97 s in functional response and gene expression were further validated by an in vitro proliferation assa
98                                      Results were further validated by analysis of a prospectively co
99                                These results were further validated by assessing the translation effi
100 e analogs (LAMe and C3) as inhibitors, which were further validated by binding studies and co-crystal
101                      The CvGal ligand models were further validated by binding, inhibition, and compe
102 er cell lines, determined by MSO microarray, were further validated by bisulfite nucleotide sequencin
103          The molecular concentration changes were further validated by commonly accepted chemical ext
104 lts of this microarray platform and analysis were further validated by comparing gene expression patt
105                             These surrogates were further validated by demonstrating that established
106 lecules containing fluorine, binding results were further validated by direct observations of the bou
107 translational modifications within the cells were further validated by fluorescence and proteomic ana
108 tionships activated in erythropoiesis, which were further validated by genome-wide TR4 binding studie
109  the pathways identified in the trajectories were further validated by high-level quantum chemistry c
110                              Microarray data were further validated by immunoblotting and by choleste
111                                 The findings were further validated by immunohistochemistry (IHC) sta
112                           Candidate variants were further validated by in vitro assays.
113                                Selected CNVs were further validated by independent methods using qPCR
114 er of cancer-specific splicing switch events were further validated by laser capture microdissection.
115                                These results were further validated by mathematical simulations.
116                            Satisfying models were further validated by MCCV.
117 he key metabolites involved in wound healing were further validated by multiple reaction monitoring-b
118                         CARM1 selective hits were further validated by orthogonal methods.
119 tent and face validity whereby the questions were further validated by other gastroenterologists.
120                     These laboratory results were further validated by performing a small field study
121                                      Results were further validated by plating and sequencing of indi
122                                         They were further validated by pull-down/immunoblotting exper
123 a by using whole genome cDNA microarrays and were further validated by quantitative real-time PCR ana
124  The expressional difference of IL8 and MMP9 were further validated by real-time quantitative RT-PCR
125                            The above results were further validated by real-time reverse transcriptio
126                       The microarray results were further validated by RT-PCR and phenotypic analyses
127                               These findings were further validated by Sanger sequencing, segregation
128 ell-type ratio in tension and opposite xylem were further validated by spatial transcriptomics and me
129 ites were identified using photolabeling and were further validated by the docking simulation: one at
130                                  The methods were further validated by their ability to efficiently r
131    Several differentially expressed proteins were further validated by tissue microarray immunohistoc
132 ue (R(2) = 0.87 and 0.88, respectively), and were further validated by using a training/test set appr
133 selected DEGs related to Alzheimer's disease were further validated by western blot and real-time PCR
134                                        These were further validated by Western blotting using specifi
135 genomic associations with drug efficacy have been further validated (e.g. with clopidogrel and warfar
136 brain CpGs associated with AD, some of which are further validated experimentally.
137 2D with equally optimized performance, which was further validated experimentally using light-trappin
138 s; this novel concept of differential wiring was further validated experimentally.
139                                   The models were further validated experimentally against seven inde
140  and internal TF activity exploration, which were further validated experimentally.
141 ped 3105 SSRs in eight rice varieties, which were further validated experimentally.
142 ing any cardiovascular or renal outcome, has been further validated for patients with diabetes, renal
143                               This criterion was further validated for content and convergence.
144                             This correlation was further validated for IL-1beta by immunodetection in
145 root ganglia (DRG) after nerve injury, which was further validated for its mouse homolog.
146                                 This variant was further validated for opposite association in two be
147                                 The equation was further validated for secondary organic material (SO
148                                   The system was further validated for studying cancer cell transmigr
149 C8 substrates from human cell lysates, which were further validated for catalytic turnover.
150                           Selected compounds were further validated for inhibition of ZIKV infection
151                                   Four genes were further validated for protein, including LMO4, whic
152                             If these results are further validated in a similar population, they coul
153  37 OTs are found in cancer genes and 23 OTs are further validated in five human cell lines by target
154                         These broad patterns are further validated in similar studies of nonmammalian
155                        These results need to be further validated in a larger cohort.
156 t platelet inhibition, yet this will need to be further validated in additional studies.
157 e oxygenation-associated coagulopathy should be further validated in large-scale prospective clinical
158                       If these results could be further validated in patients, the novel DHI might em
159                                     This has been further validated in minimally invasive techniques
160                                           It is further validated in 39 independent test samples [thi
161  the proposed mechanism of ASMase regulation is further validated in a model of UV radiation.
162  vitro cytotoxic effect on malignant T cells is further validated in a xenograft model.
163 e suppression of cardiac remodelling by SIKE is further validated in rats and monkeys.
164                                 The approach was further validated in (13)C-glucose feeding experimen
165                              The IPSET model was further validated in 2 independent cohorts including
166                             This association was further validated in 25,042 IBD cases and 34,915 con
167 and multivariate Cox regression analyses and was further validated in 42 primary neuroblastomas using
168  blocking DR1301-restricted MBP presentation was further validated in a binding assay using an analog
169                        The four-analyte test was further validated in a blind binary code study by us
170  cells characterized by PDGFRbeta expression was further validated in a cohort of human PanNET.
171 th the metabolic status of obese individuals was further validated in a cross-sectional cohort of 381
172 e protein-folding-associated toxicity, which was further validated in a model of ER-stress-induced re
173                                         This was further validated in a mouse model of smoke exposure
174 ity, and its association with psoriasis risk was further validated in an additional case-control coho
175                         The test performance was further validated in an independent 304-patient coho
176 estational time irrespective of breed, which was further validated in an independent cohort of sows,
177 -17 cells using a decomposition analysis and was further validated in an independent prospective coho
178 h the percentage of ALDH1+ tumor cells; this was further validated in an independent set of tissue ar
179     The efficacy and safety of this approach was further validated in an ovarian cancer model with ty
180 nt study, the functional role of XRCC5 in AD was further validated in animals and humans.
181 rvival in 126 HPSCC and LSCC patients, which was further validated in another cohort of head and neck
182 already established for DESI-MS imaging, and was further validated in cancer margin assessments using
183 ghly disease-specific antibody (C9RANT), and was further validated in carriers using repeat-primed po
184 ho) RD experiments in studying slow exchange was further validated in characterizing an exchange as s
185  connection within the JAK/STAT pathway, and was further validated in characterizing perturbed signal
186  The prognostic accuracy of the 5-gene score was further validated in European and US patients with h
187            The potential of this formulation was further validated in nonhuman primates, where high l
188                              This conclusion was further validated in permanent cell lines expressing
189                                 This finding was further validated in the same sample set by stem-loo
190       The prognostic value of the IHC4 score was further validated in the second separate cohort.
191               Prognostic value of the models was further validated in the TCGA data set, and, as obse
192 was upregulation of miRNA-194 (miR-194) that was further validated in vitro and in vivo.
193 sis, nevus biology, and fibrogenic signaling was further validated in vivo by the demonstration of st
194  the acetylation-dependent regulation of p53 was further validated in vivo by using a knock-in mouse
195           The necessary function of NK cells was further validated in vivo through selected antibody
196                        Selected combinations were further validated in a neutropenic murine pneumonia
197 ifferential expression and network analyses, were further validated in an independent cohort includin
198                            The major results were further validated in an independent cohort of cross
199                 Successfully replicated SNPs were further validated in beta-blocker treated participa
200 me activity assays, and the in vitro results were further validated in cell culture experiments.
201                           Maturation effects were further validated in cortical organoids, spinal mot
202                           These observations were further validated in doxycycline-inducible CC10-IL-
203                   The findings in cell lines were further validated in human prostate cancer tissues.
204                               These findings were further validated in mice bearing transplantable MT
205                                These results were further validated in the GOGO subsets without radio
206                     SNPs with P < 1 x 10(-3) were further validated in the OncoArray study of oral an
207 rted significant SNPs (P value < 1 x 10(-7)) were further validated in two additional independent lun
208                     Main biological findings were further validated in two independent cohorts.
209 n sites, notably R158, R282, and R283, which were further validated in various cancer cell lines.
210                             The bioreporters were further validated in vetch (Vicia hirsuta), produci
211                                 Our approach is further validated on modified D0(3)-CSRO detected in
212 The gene that showed the highest correlation was further validated on an independent set of specimens
213                        This pPIB frame range was further validated on the extended AD and FTLD cohort
214                   This successful prediction was further validated on three structurally diverse comp
215                                  The results were further validated on a soft benchmark by comparing
216                                  The results were further validated on an independent cohort of relap
217                            These classifiers were further validated on an independent high-risk ALL c
218 lthough the methodology performance needs to be further validated, results support the applicability
219          Although certain findings remain to be further validated, the present study substantiates Du
220                                Model results are further validated through close agreement between co
221            Its efficacy and generalizability are further validated through cross-family and cross-typ
222                                       Models are further validated through Monte Carlo experiments in
223                             Reported results are further validated through well-known biological sign
224      The confirmed device's high performance is further validated through its integration in three di
225               In vivo off-target deamination is further validated through target site deep sequencing
226  alterations after JQ1 treatment; each miRNA was further validated through BRD4 binding to its predic
227                     This experimental result was further validated through DFT calculations showing t
228 sterification under salt stressed conditions was further validated through in vitro experiments in wh
229 d serial analysis of gene expression results were further validated through immunohistochemical analy
230 markers and the model robustness/performance were further validated through internal 7-fold cross-val
231 athways and species-specific pathways, which were further validated through the use of single cell da
232 vealed the top 10 predictive features, which were further validated through XGBoost's internal featur
233                         Present results must be further validated to substantiate use of (68)Ga-DOTAT
234                   Nine of the novel partners were further validated to bind syndecan-4 in HEK293 cell
235 l PEM water electrolysers, and its stability was further validated under industrial testing condition
236 t maps with limited data availability, which are further validated using an established mouse inner-e
237                                These results are further validated using likelihood and Akaike weight
238       Significantly dysregulated metabolites are further validated using pure standards and targeted
239                           These markers will be further validated using a large clinical cohort.
240 t lenient significance levels, which need to be further validated using larger samples in the future.
241 s ligand-induced dimerization of HYB(DeltaC) is further validated using analytical ultracentrifugatio
242                              This phenomenon is further validated using the patient-derived explant (
243   In the present studies, the Yale CQ method was further validated using 2 SPECT gamma cameras and 2
244  with the LPS concentration logarithm, which was further validated using a Griess reagent kit.
245 ll reduction in HIF transcriptional response was further validated using a hypoxia response element (
246                                         Data was further validated using a validation cohort; and was
247                                The structure was further validated using an anti-iC3b mAb that was sh
248 their potential use as preneoplastic markers was further validated using an independent model of prem
249                 Up-regulation of these genes was further validated using combinations of real-time re
250             Stress-induced modulation of Pr1 was further validated using glutamate-sensitive murine h
251                                    The model was further validated using independent data obtained fr
252  the WDXRF data for six of the cumin samples was further validated using inductively coupled plasma-a
253                                   The result was further validated using knockdown of DvABCB1 by RNAi
254 he function of expressed olfactory receptors was further validated using MDL12330A, which can specifi
255                                    The model was further validated using N. tabacum cell extracts or
256                                         This was further validated using NanoLuc-Based Protein Comple
257 P-2 gene which exhibited highest prevalence, was further validated using RNase R assay and Sanger seq
258                     The umami taste of GK-15 was further validated using sensory evaluation, which su
259 site P-gp pocket as the preferred one, which was further validated using site-directed mutagenesis ex
260 selective, expression-dependent RNA transfer was further validated using synthetic reporters.
261 idated) and 0.989 (conventional); this model was further validated using test compounds from two inhi
262                                 This finding was further validated using transgenic p16-3MR mice, whi
263                              Our methodology was further validated using two consistency checking tec
264 leotide polymorphisms (SNPs), 6,257 of which were further validated using a tiling microarray.
265                                     Findings were further validated using an independently-collected
266 Positive samples identified in the screening were further validated using autoantibody titer quantifi
267  of chemical exposure on two affected miRNAs were further validated using breast cancer human cell li
268              The effects of CLEC12A blocking were further validated using CLEC12A knockout (KO) anima
269 y Ford Hospital (United States); the results were further validated using data from the Toronto Gener
270 nal changes in diet-exposed fecal microbiota were further validated using gut chemostat cultures and
271 otrophic factor and C-reactive protein (CRP) were further validated using immunoassay in two independ
272                                         Data were further validated using next-generation sequencing
273                                 Our findings were further validated using phospho-specific Western bl
274                                These results were further validated using publicly available datasets
275 rm overlaps with respect to DEG lists, which were further validated using qRT-PCR assays on selected
276                               Selected genes were further validated using real time PCR (RT-PCR).
277              Top differently regulated genes were further validated using real-time quantitative poly
278 As related to metastasis, such as HAND2-AS1, were further validated using RNAi-based loss-of-function
279                             The CoMFA models were further validated using two separate test sets: one
280         Significant associations in RhinoGen were further validated using virus-induced wheezing illn
281                           The flavonoid mQTL was further validated via the use of transient and stabl
282                                These results were further validated via immunogold electron microscop
283                            These transcripts were further validated via qRT-PCR.
284 ing the first year, but the effect needed to be further validated when PPIs were shifted to on-demand
285 future work, these potential biomarkers will be further validated with a larger patient cohort.
286 acy of our target ROI and cutoff value could be further validated with PET-autopsy data from large-sc
287                                   The method is further validated with blood and plasma samples.
288                                    The model is further validated with independent data sets collecte
289                             This observation was further validated with clinical specimens and functi
290                                Our framework was further validated with functional analysis and augme
291                     The stability of crystal was further validated with least gyration radius (209 +/
292                     This domain organization was further validated with single-chain protein construc
293 ed with clinical stages and prognosis, which was further validated with two independent cohorts of ES
294                                      Results were further validated with channelrhodopsin 2-assisted
295 sm pathways was significantly altered, which were further validated with genes in glucose metabolism
296 ibition of in-vitro assembled fibrils, which were further validated with orthogonal assays including
297  were statistically analyzed and the results were further validated with peripheral blood mononuclear
298 and toxicity of alpha-syn by our novel assay were further validated with the in vivo experiments.
299                Our most promising candidates were further validated with the use of targeted quantita
300                                   The method is further validated within a cohort of congenital heart

 
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