aldose reductase inhibitors in diabetic peripheral neuropathy.
It is interesting to note that individuals with a deficiency in 5 alpha reductase do not develop androgenetic alopecia.
Efficacy of 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors for prevention of stroke.
glutathione reductase reaction a hydride ion is transferred from the bound coenzyme NADPH to the flavin ring system of FAD.
inhibitor of 5 alpha reductase.
Azelaic acid was also shown to be a potent inhibitor of 5 alpha reductase.
A variety of changes were identified that are common to HMG-CoA reductase inhibitors, viz.
nitrate reductase and emissions of nitrous oxide from soils.
nitrite reductase diversity under the L. perenne and fallow treatments.
Complex II = Succinate dehydrogenase complex; succinate; ubiquinone oxidoreductase; coenzyme Q reductase.
quinone reductase in mouse liver cells.
Two of the compounds also led to a fourfold boost in production of a detoxifying enzyme called quinone reductase in mouse liver cells.
Saw Palmetto inhibits the enzyme 5-alpha reductase, which in turn reduces the amount of DHT produced.
More importantly the easily understandable rules provided insights which were directly comparable to the relevant literature concerning the binding site of dihydrofolate reductase.
Other organisms can use fumarate reductase for ATP production by anaerobic respiration.
Kinetic an crystallographic analysis of the key active site acid/base arginine in a soluble fumarate reductase.
Identification of the active site acid/base catalyst in a bacterial fumarate reductase: a kinetic and crystallographic study.
Structural and mechanistic mapping of a unique fumarate reductase.
reductase inhibitors carry out their work by blocking the production of the main hormone responsible for prostate enlargement.
reductase gene, also take up mercury from the soil (Rugh C.L et al.
reductase inhibitor activity.
reductase enzyme to stop it converting testosterone to dihydrotestosterone.
reductase domain binds FMN, FAD and NADPH.
Substrate binding to this site is thought to affect enzyme activity by altering the relative positions of the two subunits of ribonucleotide reductase.
The new compound showed weak activity against aldose reductase.
During the initial glutathione reductase reaction a hydride ion is transferred from the bound coenzyme NADPH to the flavin ring system of FAD.
Initial results suggest a shift in nitrite reductase diversity under the L. perenne and fallow treatments.
In the male fetus, an enzyme, 5 alpha reductase, converts testosterone to dihydrotestosterone.
The second group, the 5-alpha reductase inhibitors carry out their work by blocking the production of the main hormone responsible for prostate enlargement.
A good example of this, which will be discussed elsewhere on this site, is the intersex condition, five alpha reductase deficiency.
Yellow poplar saplings, expressed with the bacterial mercuric reductase gene, also take up mercury from the soil (Rugh C.L et al.
Rosuvastatin accounts for greater than 90% of the circulating HMG-CoA reductase inhibitor activity.
Certain combinations of minerals, herbs and vitamins bind with the 5-alpha reductase enzyme to stop it converting testosterone to dihydrotestosterone.
The C-terminal or reductase domain binds FMN, FAD and NADPH.
For example, the hormone DHT (dihydrotestosterone) forms from the natural enzyme 5-Alpha Reductase.
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