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1 f the valve was demonstrated by performing a Lowry protein assay in the device, wherein fluid flow wa
2      Concentrations of sulfide, ammonia, and Lowry-reactive substances were measured over 48 h.
3  classic spectrophotometric methods (Biuret, Lowry, Bradford and Markwell) were applied to evaluate t
4 ting as hydride donors, but also as Bronsted-Lowry acids.
5 on reactions, and reactions between Bronsted-Lowry acids and bases.
6 -walled carbon nanotubes (SWNTs) in Bronsted-Lowry acids.
7 ch performs a role in the theory of Bronsted-Lowry acids and bases that is similar to the role of the
8 etween intermediate(s) and solvent (Bronsted-Lowry base) is known to drive the reaction, the gas-phas
9 ent (ka) by fluorophotometry, [protein]Ac by Lowry assay, corneal endothelial cell morphology by spec
10                  One study, based on Coffin- Lowry cells defective in RSK2, reported that RSK2 was th
11                                       Coffin-Lowry Syndrome (CLS) is an X-linked mental retardation c
12                          Cells from a Coffin-Lowry syndrome patient (deficient in RSK2) or expressing
13 phosphorylation response is normal in Coffin-Lowry cells.
14  implicated in the pathophysiology of Coffin-Lowry syndrome.
15  a good animal model for the study of Coffin-Lowry syndrome.
16                                 Since Coffin-Lowry syndrome and neonatal lactic acidosis are associat
17 l S6 kinase 2 (Rsk2), a model for the Coffin-Lowry syndrome (CLS), exhibit a significant delay in gro
18 ctivating mutations in humans lead to Coffin-Lowry syndrome, our results imply that alterations in GP
19 s of RSK2 activity in humans leads to Coffin-Lowry syndrome, which is manifested by mental retardatio
20  whose diagnosis was later revised to Coffin-Lowry syndrome.
21                                 Differential Lowry protein assay (DLA) of the thiolated Ig reactant a
22 terfaces was also confirmed using a modified Lowry assay that prevents interference from Metrizamide
23            Values for the Lowry and modified Lowry methods varied by 20-50% from control protein valu
24 tho-diphenols; the Lowry assay, the modified Lowry assay, and a new method including a calculation to
25 bound phenols) as determined by the modified Lowry method.
26 gestion, as measured by the disappearance of Lowry-reactive substances and the appearance of ammonia.
27 nce of covalently bound ortho-diphenols; the Lowry assay, the modified Lowry assay, and a new method
28                               Values for the Lowry and modified Lowry methods varied by 20-50% from c
29                     Color development of the Lowry protein assay was tracked over time for bovine ser
30 he differences in response obtained with the Lowry assay in the presence and absence of copper.
31 is assumes that the phenol response with the Lowry assay is not affected by copper.

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