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Kainate selectively depressed and 6-cyano-7-nitroquinoxaline-2,3-dione 6-cyano-7-nitroquinoxaline-2,3-dione 6-cyano-7-nitroquinoxaline-2,3-dione 6-cyano-7-nitroquinoxaline-2,3-dione 6-cyano-7-nitroquinoxaline-2,3-dione 6-cyano-7-nitroquinoxaline-2,3-dione
(RS -alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid, a selective quisqualate RS -alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionich kainate and quisqualate RS -alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionicf aspaRS -alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic
Rather, it is the drive to initiate and maintain walking-related behaviors that is selectively depressed in stung cockroaches, with minimal or no interference to other behaviors [10].
Alongside these potential reasons (higher expression or activity of thrombin), Jones and colleagues found that antithrombin activity is selectively depressed in rheumatoid arthritis synovial fibroblasts [ 6].
We have previously shown that in conscious dogs with DM that: 1) baseline CBF was significantly decreased, 2) endothelium-dependent (ACh) coronary vasodilation were impaired, and 3) reflex cholinergic NO-dependent coronary vasodilation was selectively depressed.
Jones and coworkers [ 11] found that antithrombin activity is selectively depressed in RA synovial fluid as compared with that in osteoarthritis, although the concentration of the antithrombin thrombin complex was significantly increased.
Similar(53)
These results suggest that a 5-lipoxygenase product selectively enhances aspartate release and a cyclooxygenase product selectively depresses glutamate release.
In addition, barbiturates selectively depress transmission at the sympathetic ganglia, which may contribute to decreased blood pressure following their administration.
Consonant with this, DCG-IV, a type 2/3 mGluR agonist reported to selectively depress mossy fiber transmission [40], [50], [51], reduced the frequency of SPWs at concentrations that depressed the occurrence of large miniature EPSCs.
We conclude that subclinically depressed individuals selectively process pain-related stimuli, and this processing bias could enhance their vulnerability to develop pain symptoms.
The main mechanism is that the adsorbate-induced charges could change the schottky barrier height, following by selectively enhancing or depressing the electrochemical responses of different charged analytes.
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