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2 species of nonmodel treefrogs and developed a pipeline that allowed us to assemble their complete amino acid and nucleoti
3 defined rate constants and, thus, K(d) of their interaction-allowed us to assess ACTIS accuracy by comparing the determin
6 Finally, the generated genotypes have allowed us to check inversion functional effects, validating
7 OMA-selective neuron, we discovered a population code that allowed us to classify action exemplars irrespective of the v
9 ansfer efficiencies measured by fluorescence depolarization allowed us to construct a two-dimensional proximity correlati
10 mple design based on the low concentration of nanoparticles allowed us to demonstrate the capability of TOF-SIMS to spati
11 n the communication center of the functional regions, which allowed us to design a selective inhibitor, MPH-220.
12 habitat preference results, based on longitudinal GPS data, allowed us to determine ideal habitat ratios (grassland:open
13 atomic force microscopy (HS-AFM) and kinetic modeling which allowed us to determine that septin filament assembly was a d
15 one- and two-dimensional NMR spectroscopy experiments have allowed us to determine the predominant tautomeric structure
19 sfection of three spectrally-distinct fluorescent reporters allowed us to evaluate different transfection methods and rev
20 Our three-step electrochemical procedure also allowed us to evaluate the Ni valence involved with the diffe
21 Using these newly generated viruses allowed us to examine the expression of CHPK in infected chic
22 overall increase in the number of studies in the field has allowed us to expand the database more than 5-fold.
24 nucleotide polymorphisms was applied to 290 isolates, which allowed us to identify 25 additional cases related to the out
25 rmediates and iterative rounds of site-directed mutagenesis allowed us to identify 4 of 413 residues from TrpB that are c
26 potent stem cell (iPSC) clones derived from 100 individuals allowed us to identify differentially expressed genes between
29 cule photophysical studies of these biocompatible nanotubes allowed us to identify the optimal luminescence properties in
30 enzymes were localized in the plant Golgi apparatus, which allowed us to identify the SmFucTs involved in core fucosylat
31 Repeated injection of HoxB8 progenitors also allowed us to maintain stable circulating HoxB8 neutrophil co
32 e chromosome X, combined with the ultra-long nanopore data, allowed us to map methylation patterns across complex tandem
35 , because its fluorescence is sensitive to viscosity, Coupa allowed us to precisely localize sites of mitochondria-lysoso
36 mation on moose location further strengthened our model and allowed us to predict microbe occurrences with ~90% accuracy.
37 re, combined with small-angle X-ray scattering (SAXS), also allowed us to predict the general position of the Dimerizatio
38 The immobile Holliday junction sequence allowed us to produce crystals that provided unprecedented at
41 Steered molecular dynamics simulations allowed us to rationalize the results in terms of key interac
45 and both the c-Jun/JunB and imiquimod psoriasis mouse model allowed us to study the therapeutic mechanism of this drug.
49 Furthermore, the use of diamond nanoparticles in phantoms allowed us to tune the T1 value of the phantoms which open th
50 kp1 protein in Arabidopsis and that the fertile ask1 mutant allowed us to uncover a comprehensive set of SCF functions.