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1 r when an enzyme binds to an aggregate using hydrogen-deuterium exchange mass spectrometry.
2 ntent is supported by circular dichroism and hydrogen-deuterium exchange mass spectrometry.
3 unfolding process of sIGPS was monitored by hydrogen-deuterium exchange mass spectrometry.
4 sion chromatography, circular dichroism, and hydrogen-deuterium exchange mass spectrometry.
5 protomers is evident in the N197Q mutant by hydrogen-deuterium exchange mass spectrometry.
6 sed by circular dichroism, fluorescence, and hydrogen-deuterium exchange mass spectrometry.
7 ray ionization native mass spectrometry, and hydrogen-deuterium exchange mass spectrometry.
8 ans of time-resolved electrospray ionization hydrogen-deuterium exchange mass spectrometry.
9 sing a combination of biochemical assays and hydrogen-deuterium exchange mass spectrometry.
10 which this antibody binds, we have employed hydrogen-deuterium exchange mass spectrometry.
11 e mapped these regulatory interactions using hydrogen-deuterium exchange mass spectrometry.
12 donuclease active site of APE1, as mapped by hydrogen-deuterium exchange mass spectrometry.
13 nescence resonance energy transfer and amide hydrogen/deuterium exchange mass spectrometry.
14 ed dimer were ascertained by high-resolution hydrogen/deuterium exchange mass spectrometry.
15 p and C-terminally truncated E2p proteins by hydrogen/deuterium exchange mass spectrometry.
16 face is validated by peptide mapping through hydrogen/deuterium exchange mass spectrometry.
17 d in recent years due to the introduction of hydrogen/deuterium exchange mass spectrometry.
18 can analysis, site-directed mutagenesis, and hydrogen/deuterium exchange-mass spectrometry.
21 revious limited tryptic digestion result and hydrogen-deuterium exchange mass spectrometry analyses p
23 ck (residues 775-818) using a combination of hydrogen-deuterium exchange mass spectrometry and isothe
25 terized homotypic interactions of TcpB using hydrogen/deuterium exchange mass spectrometry and hetero
26 2200 and IL-17A is consistent with data from hydrogen/deuterium exchange mass spectrometry and mutage
28 tegrating complementary structural data from hydrogen/deuterium exchange mass spectrometry and previo
29 ions targeted by 24E9 Fab were identified by hydrogen/deuterium exchange mass spectrometry and reveal
32 MHC-peptide hydrogen bonding as measured by hydrogen-deuterium exchange mass spectrometry, and incre
33 ystallography, small-angle X-ray scattering, hydrogen-deuterium exchange mass spectrometry, and mutat
34 isolation of neutralization escape mutants, hydrogen/deuterium exchange mass spectrometry, and X-ray
35 proprotein convertase 1/3 using a histidine hydrogen-deuterium exchange mass spectrometry approach.
37 RIalpha complex, probed by peptide array and hydrogen/deuterium exchange mass spectrometry, brings to
39 nger in association with RPL11, we conducted hydrogen-deuterium exchange mass spectrometry, computati
40 Hydrogen-deuterium exchange mass spectrometry corroborat
42 ength monomeric structure of the protein, on hydrogen-deuterium exchange mass spectrometry data, and
43 Hydrogen-deuterium exchange mass spectrometry demonstrat
44 n entropy observed in the course of the ECT, hydrogen-deuterium exchange mass spectrometry demonstrat
45 Hydrogen-deuterium-exchange mass spectrometry demonstrat
46 Hydrogen/deuterium exchange mass spectrometry demonstrat
49 tron microscopy (cryo-EM) and enhanced amide hydrogen-deuterium exchange mass spectrometry (DXMS) to
51 asic processing sites of PE by peptide amide hydrogen-deuterium exchange mass spectrometry (DXMS).
53 mbines rigid-body computational docking with hydrogen/deuterium exchange mass spectrometry (DXMS).
54 tive signaling intermediate I2 with enhanced hydrogen/deuterium exchange mass spectrometry (DXMS).
55 ys11-linked diubiquitin, in combination with hydrogen-deuterium exchange mass spectrometry, enable us
56 We then use hydrogen-deuterium exchange mass spectrometry experiment
57 of ERK2 recognition by MKP3, we carried out hydrogen/deuterium exchange mass spectrometry experiment
59 n of homology modeling, immunoprecipitation, hydrogen-deuterium exchange mass spectrometry (H/DXMS),
63 Here, we use comprehensive mutagenesis and hydrogen deuterium exchange mass spectrometry (HDX-MS) t
64 e specific intent of using the particles for hydrogen-deuterium exchange mass spectrometry (HDX MS) e
65 cific chemical modifications within the CDR, hydrogen-deuterium exchange mass spectrometry (HDX MS) w
68 ns between beta2AR and beta-arrestin 1 using hydrogen-deuterium exchange mass spectrometry (HDX-MS) a
70 tructural integrity of therapeutic proteins, hydrogen-deuterium exchange mass spectrometry (HDX-MS) i
71 ticle (SMALP) technology can be coupled with hydrogen-deuterium exchange mass spectrometry (HDX-MS) t
77 combined traditional analytical methods with hydrogen/deuterium exchange mass spectrometry (HDX MS),
79 f ion-mobility mass spectrometry (IM-MS) and hydrogen/deuterium exchange mass spectrometry (HDX-MS) a
80 ted with protein interactions can be done by hydrogen/deuterium exchange mass spectrometry (HDX-MS) b
82 gher-order structure information provided by hydrogen/deuterium exchange mass spectrometry (HDX-MS) i
84 Analysis of disulfide-bonded proteins by hydrogen/deuterium exchange mass spectrometry (HDX-MS) r
88 ody by using the complementary approaches of hydrogen/deuterium exchange mass spectrometry (HDX-MS),
89 rate mesoporphyrin (MPIX) and backbone amide hydrogen/deuterium exchange mass spectrometry (HDX-MS).
90 ha and a spectrum of oncogenic mutants using hydrogen/deuterium exchange mass spectrometry (HDX-MS).
91 inked IgG1 ADCs and the corresponding mAb by hydrogen/deuterium exchange mass spectrometry (HDX-MS).
92 mains one of the most serious limitations of hydrogen/deuterium exchange-mass spectrometry (HDX-MS),
95 with Alzheimer's disease as determined using hydrogen-deuterium exchange-mass spectrometry (HX-MS) co
96 proteolytic activity that is very useful for hydrogen/deuterium exchange mass spectrometry (HX-MS).
98 plasmon resonance, analytical rheology, and hydrogen-deuterium exchange mass spectrometry (HXMS), we
99 al properties of proteins can be probed with hydrogen/deuterium exchange mass spectrometry (HXMS).
101 ge is shown to increase the dynamic range of hydrogen/deuterium exchange mass spectrometry in terms o
106 ensive integrated approach of cross-linking, hydrogen-deuterium exchange mass spectrometry (MS), elec
107 Library screening, other approaches, such as hydrogen/deuterium exchange mass spectrometry (MS) and X
108 peptides, examined through crystallographic, hydrogen-deuterium exchange mass spectrometry, mutagenes
109 an cAMP signaling, by a combination of amide hydrogen/deuterium exchange mass spectrometry, peptide a
110 Computational docking combined with amide hydrogen/deuterium exchange mass spectrometry provided a
111 ioluminescence resonance energy transfer and hydrogen/deuterium exchange mass spectrometry reaffirms
114 tructures of the muPA:nanobody complexes and hydrogen-deuterium exchange mass spectrometry revealed m
119 ther with molecular dynamics simulations and hydrogen-deuterium exchange mass spectrometry, reveals h
124 ction based on biophysical measurements with hydrogen-deuterium exchange/mass spectrometry, surface p
125 titive enzyme-linked immunosorbent assay and hydrogen-deuterium exchange mass spectrometry that 7 of
128 d fluorescence polarization measurements and hydrogen-deuterium exchange mass spectrometry to define
132 ize this mechanism, we applied peptide amide hydrogen-deuterium exchange mass spectrometry to probe c
133 identification, native mass spectrometry and hydrogen-deuterium exchange mass spectrometry to show th
134 ium unfolding of wild-type alpha(1)-AT using hydrogen-deuterium/exchange mass spectrometry to charact
136 In this study, we have used peptide amide hydrogen/deuterium exchange mass spectrometry to probe t
141 te E2-containing complexes, peptide-specific hydrogen/deuterium exchange mass spectrometry was used t
143 using differential scanning fluorimetry and hydrogen-deuterium exchange mass spectrometry, we show h
144 hosphodiesterase8 (PDE8), monitored by amide hydrogen-deuterium exchange mass spectrometry, we show p
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