戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 by measuring their affinities for m(7)GDP by fluorimetry.
2 lcium, using multifrequency phase-modulation fluorimetry.
3 in fura-2-loaded cells using dual wavelength fluorimetry.
4 nerves at 20 Hz and were monitored by fura-2 fluorimetry.
5 tal reflection mid-infrared spectroscopy and fluorimetry.
6 rformance Liquid Chromatography coupled with fluorimetry.
7 domain stability using differential scanning fluorimetry.
8 protein substrates and differential scanning fluorimetry.
9 dependent manner using differential scanning fluorimetry.
10  or Streptococcus pneumoniae was assessed by fluorimetry.
11 Orp1 using confocal microscopy and multiwell fluorimetry.
12 circular dichroism and differential scanning fluorimetry.
13 nt inhibitor missed by differential scanning fluorimetry.
14  by mass spectrometry, spectrophotometry and fluorimetry.
15 cted by EMSA, steady-state, and stopped-flow fluorimetry.
16 s of H/D exchange) and differential scanning fluorimetry.
17 em and BODIPY-diacylglycerol was detected by fluorimetry.
18 fusion of dyes was assessed by microscopy or fluorimetry.
19 lular Ca2+ level were monitored using Fura-2 fluorimetry.
20 .3, and 92 microm, pH 10.0) were measured by fluorimetry.
21 mpared with those from differential scanning fluorimetry, a commonly used primary screening technique
22             The use of differential scanning fluorimetry allowed rapid evaluation of ligand-induced t
23  mass spectrometry and differential scanning fluorimetry also demonstrate the unique structural dynam
24                        Differential scanning fluorimetry analyses confirmed the binding of YjhC to th
25 N15-34 heterodimer and differential scanning fluorimetry analyses show that PCH mutations cause therm
26 dditionally, extensive Differential Scanning Fluorimetry analysis combined with cryo- and ambient-tem
27 ociation were determined by a combination of fluorimetry and 2D NMR exchange spectroscopy (EXSY).
28 1, as measured by both differential scanning fluorimetry and circular dichroism.
29 g molecular logic operations, as verified by fluorimetry and colorimetry.
30 doxorubicin accumulation was determined with fluorimetry and correlated with the imaging and tissue-c
31 sorption spectroscopy, differential scanning fluorimetry and cryo-crystallography, we identified comp
32 -induced aggregation of FcepsilonRI, we used fluorimetry and flow cytometry to quantitatively monitor
33                          Using voltage-clamp fluorimetry and gating current analysis, we demonstrate
34     To this end, using differential scanning fluorimetry and hydrogen-deuterium exchange mass spectro
35 gment-based screen via differential scanning fluorimetry and in silico structure-based screening, eac
36                  Using differential scanning fluorimetry and isothermal titration calorimetry, we cha
37    BLG-LA complex formation was monitored by fluorimetry and it was observed that a moderate heat tre
38  have used Forster resonance energy transfer fluorimetry and kinetic modeling to characterize the lig
39 of the biosynthetic reaction was followed by fluorimetry and reverse-phase, paired-ion high pressure
40                        Differential scanning fluorimetry and saturation transfer difference-nuclear m
41                          Herein we have used fluorimetry and transmission electron microscopy to prov
42 bitory potential using differential scanning fluorimetry and various cellular assays.
43 ace plasmon resonance, differential scanning fluorimetry), and mass spectrometry to clarify the impac
44 es and lengths of mismatches were assayed by fluorimetry, and in many instances, our MismatCHA design
45 ngle light scattering, differential scanning fluorimetry, and isothermal calorimetry, to characterize
46             Using NMR, differential scanning fluorimetry, and microscale thermophoresis, we determine
47 g limited proteolysis, differential scanning fluorimetry, and native mass spectrometry in the presenc
48  have used protein engineering, stopped-flow fluorimetry, and rapid acid quenching techniques to eluc
49 anthroline) were studied by crystallography, fluorimetry, and UV-visible spectroscopy.
50  fluorescence microscopy and automated plate fluorimetry (APF) are coupled with facile husbandry to f
51 We report a label-free differential scanning fluorimetry approach to determine PFAS-BSA binding over
52 te the utility of this differential scanning fluorimetry assay as a rapid high-throughput approach fo
53                      A differential scanning fluorimetry assay showed that recombinant SDs can bind t
54 ing a protein-adaptive differential scanning fluorimetry assay.
55 amics simulations, and differential scanning fluorimetry assays and describe for the first time a str
56  reported inhibitor in differential scanning fluorimetry assays.
57 s were identified in a differential scanning fluorimetry-based screen of an in-house library of 755 c
58 smon resonance and nanodifferential scanning fluorimetry biophysical profiles.
59 attering, MS analysis, differential scanning fluorimetry, CD, SDS-PAGE, and immunoblotting with confo
60        Using nanoscale differential scanning fluorimetry, chemical denaturation, and mass photometry,
61                      Experiments using pulse fluorimetry confirmed an increase in the interstitial co
62 e, NAD hydrolysis, and differential scanning fluorimetry data, contribute to a comprehensive characte
63 s, monitored in real time using stopped flow fluorimetry, demonstrate simultaneous binding and bendin
64 olid-phase microsphere assay coupled to flow-fluorimetry detection, based on the Luminex xMap technol
65 ity measurements using differential scanning fluorimetry, differential scanning calorimetry, and elec
66  calorimetry (ITC) and differential scanning fluorimetry (DSF) analyses demonstrate that the recombin
67 e thermal stability by differential scanning fluorimetry (DSF) and capsid dynamics by matrix-assisted
68 ical assays, including differential scanning fluorimetry (DSF) and nuclear magnetic resonance (NMR) s
69 Microbalance (QCM) and Differential Scanning Fluorimetry (DSF) are consistent with our single molecul
70  of measurements using Differential Scanning Fluorimetry (DSF) as an inexpensive, high throughput scr
71 iety of proteins, that differential scanning fluorimetry (DSF) can be used to determine and optimize
72 ctrometry (HDX-MS) and differential scanning fluorimetry (DSF) experiments to determine how anti-CRIS
73                        Differential scanning fluorimetry (DSF) is a rapid and inexpensive screening m
74                        Differential scanning fluorimetry (DSF) is a technique that reports protein th
75 tency, suggesting that differential scanning fluorimetry (DSF) is a useful orthogonal measure of inhi
76  order parameters, and differential scanning fluorimetry (DSF) to explore conformational entropy chan
77 minary screening using differential scanning fluorimetry (DSF), (ii) validation by NMR spectroscopy a
78                        Differential scanning fluorimetry (DSF), also known as ThermoFluor or Thermal
79 osedimentation assays, differential scanning fluorimetry (DSF), and binding energy calculations, we d
80 STD) NMR spectroscopy, differential scanning fluorimetry (DSF), DNA-encoded library selection, and in
81 l-molecule drugs using differential scanning fluorimetry (DSF), we found 15 compounds that decreased
82                                 Thioflavin T fluorimetry estimates rapid and near-stoichiometric coas
83                                 Stopped-flow fluorimetry experiments demonstrated that the priming re
84 tures derived from the differential scanning fluorimetry experiments indicated a significant differen
85 ination reactions, and differential scanning fluorimetry experiments, we identified active site featu
86                                 Stopped flow fluorimetry for the forward reaction gave a saturable fl
87     Equilibrium constants were determined by fluorimetry from 10 to 20 degrees C by nonlinear curve f
88  Fragment screening by differential scanning fluorimetry has been performed to discover new chemical
89           From a STAT3 differential scanning fluorimetry high-throughput screen, we identified compou
90             Polarography, spectrophotometry, fluorimetry, high-performance liquid chromatography, and
91 iophysical techniques (differential scanning fluorimetry, homogeneous time-resolved fluorescence, and
92                        Differential scanning fluorimetry identified clear preferences in these FGFs f
93                                 Stopped flow fluorimetry illuminated the conformational dynamics invo
94               We apply differential scanning fluorimetry in combination with scattering upon thermal
95 ant implications for the use of variable Chl fluorimetry in ecophysiological studies of coral stress
96 meabilities were measured using stopped-flow fluorimetry in SM vesicles with entrapped carboxyfluores
97 recordings in COS-7 cells, and voltage-clamp fluorimetry in Xenopus oocytes, both heterologously expr
98 imited proteolysis and differential scanning fluorimetry indicate that RIG-I is in an extended and fl
99 ic techniques, such as differential scanning fluorimetry, intrinsic tryptophan fluorescence, circular
100              Pulse-amplitude-modulated (PAM) fluorimetry is widely used in photobiological studies of
101 re explored using nano differential scanning fluorimetry, isothermal titration calorimetry, and 12 X-
102 on-coupled proteomics, differential scanning fluorimetry, isothermal titration calorimetry, and X-ray
103                              A new sensitive fluorimetry method for the simple and rapid measurement
104 odology employing nano-differential scanning fluorimetry (nanoDSF), presenting distinct advantages ov
105 erface using nanoscale differential scanning fluorimetry, NMR water-ligand observed via gradient spec
106  plasmon resonance and differential scanning fluorimetry of TCA intermediates and potential metabolit
107 were observed with 4-s time resolution using fluorimetry of TorA-green fluorescent protein mutant 3*
108                Importantly, we also employed fluorimetry of vacuoles loaded with cDCFDA, a pH-sensiti
109                  Using differential scanning fluorimetry on a CHIL protein from Vitis vinifera (VvCHI
110                        Differential scanning fluorimetry or differential scanning calorimetry is comm
111                         Isothermal titration fluorimetry over the pH range of 4.5 to 9.0 is used to m
112 ured peptide scaffold, GGG, we have employed fluorimetry, potentiometry, and calorimetry to determine
113                                              Fluorimetry results revealed that quercetin could bind t
114              Pulse amplitude modulated (PAM) fluorimetry revealed significant differences in the phot
115 s, gel filtration, and differential scanning fluorimetry revealed that polyphosphate binds to and des
116       Furthermore, the Differential Scanning Fluorimetry screen of a kinase panel demonstrated the va
117                        Differential scanning fluorimetry showed a stabilizing effect of the substrate
118 raterminal Ca2+ stores either because fura-2 fluorimetry showed extremely low Ca2+ elevation (approxi
119                        Differential scanning fluorimetry showed interaction of the isolated periplasm
120                        Differential scanning fluorimetry showed that both molecules bind to the alpha
121                        Differential scanning fluorimetry shows a destabilizing effect induced by PGRN
122                        Differential scanning fluorimetry shows that uL6 of F. johnsoniae is intrinsic
123                                Voltage-clamp-fluorimetry studies also indicated that in L529I, NS1643
124                     In differential scanning fluorimetry studies, BTK bound to pirtobrutinib exhibite
125 est followed by those from RT-qPCR, and last fluorimetry, suggesting that a portion of virus may be p
126 by various techniques (differential scanning fluorimetry, surface plasmon resonance, and microscale t
127             We show by differential scanning fluorimetry that the N-linked glycans thermodynamically
128 nning calorimetry, and differential scanning fluorimetry, the most significant impact of the mutation
129 ed trypsin hydrolysis, differential scanning fluorimetry, thermal denaturation, and CD analyses suppo
130 mission EM, CD, atomic force microscopy, and fluorimetry to analyze the structural transitions of ref
131 e distinctive but complementary methods: (1) fluorimetry to assess physical collection, (2) RT-qPCR t
132                       We used micromodulated fluorimetry to examine the effect of cystoliths on photo
133  nuclear in origin and suggested by in vitro fluorimetry to have been caused by K3 thiol arylation.
134 were next evaluated by differential scanning fluorimetry to identify compounds that must bind to NC o
135                               Using scanning fluorimetry to map proteins (a proxy for cells) and F420
136 d bending reaction steps, using stopped-flow fluorimetry to observe changes in resonance energy trans
137 gs, cysteine accessibility and voltage clamp fluorimetry to probe the relationships between voltage s
138 cence polarization and differential scanning fluorimetry to quantify changes caused by 75 cancer-asso
139 es in protein-adaptive differential scanning fluorimetry to screen the Aurora collection of 300+ fluo
140                                        Using fluorimetry to simultaneously measure four mitochondrial
141 sfer, AlphaScreen, and differential scanning fluorimetry) to measure binding affinity; and crosslinki
142 ragment, discovered by differential scanning fluorimetry, to an in vivo MAT2a tool inhibitor is discu
143           We have used differential scanning fluorimetry together with site-directed mutagenesis of r
144 h gold standard clinical assays and standard fluorimetry tools showed that the sensor can accurately
145 bitors was screened by differential scanning fluorimetry using a recombinant TcK2 encompassing the ki
146                        Differential scanning fluorimetry, utilizing external fluorescent probes, is a
147                        Differential scanning fluorimetry was employed to analyze the stabilization of
148             Finally, intrinsic and extrinsic fluorimetry was used for examining the HMP protective ro
149                  Here, differential scanning fluorimetry was used in a medium-throughput screen to id
150                                  Single cell fluorimetry was used to monitor caffeine-induced oscilla
151                  Using differential scanning fluorimetry, we determined that the SBP for an ABC trans
152                           Using quantitative fluorimetry, we found that labeled TTC showed vastly sup
153                   Using kinetic stopped-flow fluorimetry, we show that FAST(M) allows simultaneous re
154 mass spectrometry, and differential scanning fluorimetry, we showed that zinc binds to this TDP-43 do
155  24 hours at 5 degrees C and quantified with fluorimetry) were measured 48 hours after treatment and
156 ) have now been investigated by stopped-flow fluorimetry, which allowed a pre-steady-state analysis t

 
Page Top