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pharmacology
A quantity of scientific publications steadily grows from year to year, this implyies that the QSRR enormous advantage and potential in chemistry, biology, and pharmacology.
      
Conditions under which Rhodococcus cells convert BSS to 17β-hydroxyandrost-4-ene-3-one (testosterone), commonly used in pharmacology, were determined.
      
This provided a theoretical basis for the development of a new trend in pharmacology.
      
Problem of controls in physiology and pharmacology: Psychophysiological and morphofunctional effects of chronic saline administr
      
The applicability of these immunosensors to solving various analytical problems in medicine and pharmacology in particular, was demonstrated.
      
The proposed technique can be used in pharmacology and medical practice.
      
The results obtained can be used to develop procedures for determining Analgin and in pharmacology and medicine to improve the stability of Analgin-containing formulations.
      
Molecular constructions on the basis of polyribonucleotides could be used as sensing elements with adjustable properties in biosensor technology, nanobiotechnology, and molecular pharmacology.
      
Bile Acids: chemistry, biosynthesis, analysis, chemical and metabolic transformations and pharmacology
      
α1 - adrenolytic activities of pyridoindole derivatives recently synthesized in the Institute of Experimental Pharmacology, Slovak Academy of Sciences, were measured.
      
This review is intended to focus on the composition of oat and its therapeutic potential in the pharmacology that supports its use to cure various maladies.
      
This expands the application of the model to pharmacology, in which the influence of the mechanical action of the heart and its oxygen consumption is of major interest.
      
The basic pharmacology of dihydropyridine Ca-agonists published so far (BAY k8644, CGP 28-392, H 160/51, YC 170, and 202-791) is described.
      
Pharmacology of angiotensin receptors and AT1 receptor blockers
      
These studies have already provided valuable information concerning the nature, biophysics, pharmacology and regulation of human cardiac ionic currents in normal and diseased tissues.
      
This study extends the characterisation of ESCM as a preparation for studying receptor pharmacology, and indicates that the β1AR is the predominant subtype mediating increases in contraction rate in murine ESCM.
      
Clinical pharmacology studies have shown that the catechol-O-methyltransferase inhibitor tolcapone increases the bioavailability area under the plasma concentration-time curve (AUC) and the plasma elimination half-life (t1/2) of levodopa.
      
Pharmacology and immunology of botulinum toxin serotypes
      
Clinical pharmacology and therapeutic use of COMT inhibition in Parkinson's disease
      
In vivo studies on receptor pharmacology of the human eccrine sweat gland
      
 

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