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1 ions, in particular deuterium oxide (D2 O or heavy water).
2 by growing C. elegans in the presence of 70% heavy water.
3 gG4 dimer formation at high concentration in heavy water.
4 estimates of the melting points of light and heavy water.
5 ferent when mineralization is carried out in heavy water.
6 ing a 7-day metabolic labeling protocol with heavy water.
7 y-one patients with suspected NAFLD ingested heavy water ((2) H2 O, 50-mL aliquots) two to three time
8 n the incorporation of deuterium ((2)H) from heavy water ((2)H(2)O) into the deoxyribose moiety of pu
9 f the incorporation of deuterium ((2)H) from heavy water ((2)H(2)O) into the deoxyribose moiety of pu
10 he incorporation of deuterium ((2)H(2)) from heavy water ((2)H(2)O) into tubulin dimers and polymers
12 for estimating protein dynamics in vivo with heavy water ((2)H(2)O) using matrix-assisted laser desor
13 logical limitations have hampered the use of heavy water ((2)H(2)O), a convenient, universal biosynth
19 tope labelling of microbial populations with heavy water (a passive tracer) and (15) N ammonium in co
20 stitution of this marrow transit time in the heavy water analysis gave a better-defined blood half-li
22 LB/c controls were labeled continuously with heavy water, and splenic B cells and dendritic cells wer
28 tional spectra of cold, composition-selected heavy water clusters, D(+)(D2O)n, can be exploited to ca
29 ique was developed to measure the density of heavy water confined in a nanoporous silica matrix in a
30 d the ability to differentiate the origin of heavy water, confirming that deuterium incorporation was
31 rational sum-frequency generation spectra of heavy water (D(2)O) near a monolayer graphene electrode,
33 Employing a sonic spray, we atomized the heavy water (D(2)O, 99.9 atom % D) solution of three cla
36 Relative ion abundances of the light- and heavy-water digestion products, which are separated by 2
38 glyceride gain, mice were first administered heavy water for 5 weeks to label adipose triglycerides w
39 sed concentration, decreased temperature and heavy water from 8% to 25% in all buffers except for hig
40 entially labeled peptides in the presence of heavy water (H(2)(18)O), and performed LC/MS/MS analysis
44 uantification of deuterium assimilation from heavy water into single bacterial cells to check the inf
47 he bioinformatics aspects of the analysis of heavy water labeled mass spectral data, available softwa
48 that measures fractional gluconeogenesis by heavy water labeling and gas chromatographic-mass spectr
49 ty of isotope ratio mass spectrometry with a heavy water labeling approach to capture the full range
59 gue impurities (HOD/H(2)O) on the surface of heavy water microdroplets, implying possible future deve
62 ng data in healthy adult subjects using both heavy water (n = 4) and deuterium-labeled glucose (n = 9
63 to be strictly observed in the operation of heavy-water nuclear power plants is the mandatory regula
66 a readily accessible amount, could provide a heavy-water output comparable to that of modern plants.
70 ange of NaCl concentrations and in light and heavy water revealed that the X-ray radius of gyration (
73 n of the circadian clock: when mutants drank heavy water to lengthen the period, these aspects of the
74 he density data we obtained for the confined heavy water under these conditions are valuable to large
75 oods harvested from a hydroponic system with heavy water, vitamin A activity of stable isotope-labele
76 The increased second-order rate constant in heavy water was expected from ordering of this loop over
77 in the THz spectrum of deuterated glycine in heavy water, which allow us to separate the distinct mod
78 nged by stable isotope labeling studies with heavy water, which yielded estimates in excess of 3 days
79 was exposed to Ringer solution made up from heavy water, whose solvent isotope effect should reduce
80 e is digested with RNase T1 in 18O-labeled ("heavy") water with the 18O being incorporated at the 3'-