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phenyl butyrate

National Institutes of Health

Papers overview

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2014
2014
Hereditary tyrosinemia type I (HT1) is a rare disease caused by a deficiency of fumarylacetoacetate hydrolase (FAH) in the… 
2011
2011
Objective: Ornithine transcarbamylase (OTC) deficiency is the most common urea cycle disorder. In our case, we discussed the… 
2007
2007
o-Hydroxybutyrophenone(o-HBP) was prepared by Fries rearrangement of phenyl butyrate(PB) in the presence of AlCl3.The influence… 
2006
2006
Purpose: Angiogenesis is required for tumor progression and represents a rational target for therapeutic intervention.Histone… 
2006
2006
OBJECTIVE To elucidate effects of histone deacetylase inhibitors on cell cycle of leukemia cell lines and investigate its… 
1985
1985
Two purified carboxylesterases that were isolated from a rat liver microsomal fraction in a Norwegian and a German laboratory… 
1975
1975
A comparative study of the kinetic be,avior of horse, sheep, chicken, pig, and ox liver carboxylesterases is reported. The… 
1967
1967
A study was undertaken to establish an experimental procedure whereby accurate rates of enzyme-catalyzed substrate hydrolysis…