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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.
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
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
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.
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
37 ribute more than tethered ends to HSI, which is further validated by specifically designed match frag
42 ionship between inhibitors and Ca(2+), which was further validated by (19)F NMR spectroscopy showing
44 affinity of NMK-T-057 toward gamma-secretase was further validated by a fluorescence-based gamma-secr
48 in determining galectin-ligand interactions was further validated by analysis of galectin-3 interact
50 r of ERalpha transcriptional activity, which was further validated by assessment of direct transcript
56 Biological applicability of the platform was further validated by demonstrating increase in endop
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.
67 than was AD8 Env-SERINC5 interactions, which was further validated by immunoprecipitation assays.
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
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
79 d eIF2gamma in HCV IRES-mediated translation was further validated by ribozymes directed against addi
83 ate the complex model of PmrD-PmrA(N), which was further validated by site-directed spin labeling exp
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
97 s in functional response and gene expression were further validated by an in vitro proliferation assa
100 e analogs (LAMe and C3) as inhibitors, which were further validated by binding studies and co-crystal
102 er cell lines, determined by MSO microarray, were further validated by bisulfite nucleotide sequencin
104 lts of this microarray platform and analysis were further validated by comparing gene expression patt
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
114 er of cancer-specific splicing switch events were further validated by laser capture microdissection.
117 he key metabolites involved in wound healing were further validated by multiple reaction monitoring-b
119 tent and face validity whereby the questions were further validated by other gastroenterologists.
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
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
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
135 genomic associations with drug efficacy have been further validated (e.g. with clopidogrel and warfar
137 2D with equally optimized performance, which was further validated experimentally using light-trappin
142 ing any cardiovascular or renal outcome, has been further validated for patients with diabetes, renal
153 37 OTs are found in cancer genes and 23 OTs are further validated in five human cell lines by target
157 e oxygenation-associated coagulopathy should be further validated in large-scale prospective clinical
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
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
174 ity, and its association with psoriasis risk was further validated in an additional case-control 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
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
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
197 ifferential expression and network analyses, were further validated in an independent cohort includin
200 me activity assays, and the in vitro results were further validated in cell culture experiments.
207 rted significant SNPs (P value < 1 x 10(-7)) were further validated in two additional independent lun
209 n sites, notably R158, R282, and R283, which were further validated in various cancer cell lines.
212 The gene that showed the highest correlation was further validated on an independent set of specimens
218 lthough the methodology performance needs to be further validated, results support the applicability
224 The confirmed device's high performance is further validated through its integration in three di
226 alterations after JQ1 treatment; each miRNA was further validated through BRD4 binding to its predic
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
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
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
243 In the present studies, the Yale CQ method was further validated using 2 SPECT gamma cameras and 2
245 ll reduction in HIF transcriptional response was further validated using a hypoxia response element (
248 their potential use as preneoplastic markers was further validated using an independent model of prem
252 the WDXRF data for six of the cumin samples was further validated using inductively coupled plasma-a
254 he function of expressed olfactory receptors was further validated using MDL12330A, which can specifi
257 P-2 gene which exhibited highest prevalence, was further validated using RNase R assay and Sanger seq
259 site P-gp pocket as the preferred one, which was further validated using site-directed mutagenesis ex
261 idated) and 0.989 (conventional); this model was further validated using test compounds from two inhi
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
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
275 rm overlaps with respect to DEG lists, which were further validated using qRT-PCR assays on selected
278 As related to metastasis, such as HAND2-AS1, were further validated using RNAi-based loss-of-function
284 ing the first year, but the effect needed to be further validated when PPIs were shifted to on-demand
286 acy of our target ROI and cutoff value could be further validated with PET-autopsy data from large-sc
293 ed with clinical stages and prognosis, which was further validated with two independent cohorts of ES
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.