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・ Beta-galactoside alpha-2,3-sialyltransferase
・ Beta-galactoside alpha-2,6-sialyltransferase
・ Beta-galactoside permease
・ Beta-galactoside transacetylase
・ Beta-galactosyl-N-acetylglucosaminylgalactosylglucosyl-ceramide beta-1,3-acetylglucosaminyltransferase
・ Beta-globin co-transcriptional cleavage ribozyme
・ Beta-glucan
・ Beta-glucan-transporting ATPase
・ Beta-glucogallin O-galloyltransferase
・ Beta-glucogallin—tetrakisgalloylglucose O-galloyltransferase
・ Beta-glucosidase
・ Beta-glucoside kinase
・ Beta-glucuronidase
・ Beta-Hexachlorocyclohexane
・ Beta-Hydride elimination
Beta-Hydroxy beta-methylbutyric acid
・ Beta-Hydroxybutyric acid
・ Beta-Hydroxybutyryl-CoA
・ Beta-keratin
・ Beta-ketoacyl-(acyl-carrier-protein) synthase III
・ Beta-ketoacyl-ACP synthase
・ Beta-ketoacyl-acyl-carrier-protein synthase I
・ Beta-ketoacyl-acyl-carrier-protein synthase II
・ Beta-ketodecanoyl-(acyl-carrier-protein) synthase
・ Beta-ketothiolase deficiency
・ Beta-L-arabinosidase
・ Beta-L-rhamnosidase
・ Beta-lactam Ring Records
・ Beta-lactamase
・ Beta-lactamase inhibitor protein


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Beta-Hydroxy beta-methylbutyric acid : ウィキペディア英語版
Beta-Hydroxy beta-methylbutyric acid

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β-Hydroxy β-methylbutyric acid (HMB), or β-hydroxy β-methylbutyrate, is a metabolite of the essential amino acid leucine and is synthesized in the human body. Its part in protein synthesis was discovered by Steven L. Nissen at Iowa State University.〔 It has been used in scientific studies to purportedly increase muscle mass and decrease muscle breakdown. Nissen held the original patent on the metabolite as a nutritional supplement. It was discovered in pigs and small quantities can also be found in grapefruit, alfalfa, and catfish. As a supplement it is usually sold as the calcium salt calcium beta-hydroxy-beta-methylbutyrate.
Research published in the ''Journal of Applied Physiology'' has shown that HMB may have an effect on increasing muscle weight and strength. A review in ''Nutrition & Metabolism'' provides an in depth and objective analysis of HMB research.

The same study lists as HMB's proposed mechanisms of action the following:
* Increased sarcolemmal integrity via conversion to HMG-CoA
* Enhanced protein synthesis via the mTOR pathway
* Depression of protein degradation through inhibition of the ubiquitin pathway
The human body produces about 0.2-0.4 grams per day. Standard doses in research studies have been 1.5 to 3.0 grams per day, usually divided into two doses. Toxicity at these doses is unlikely, as the no-observed-adverse-event-level (NOAEL) in rats is between 2.48 to 2.83 g/kg BW per day, roughly equivalent to 70 to 100 g/day in humans.
==References==


抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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