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Published in 2020 at "Molecular genetics and metabolism"
DOI: 10.1016/j.ymgme.2020.05.003
Abstract: Propionic acidemia (PA) and methylmalonic acidemia (MMA) are autosomal recessive disorders of propionyl-CoA (P-CoA) catabolism, which are caused by a deficiency in the enzyme propionyl-CoA carboxylase or the enzyme methylmalonyl-CoA (MM-CoA) mutase, respectively. The functional…
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Keywords:
primary hepatocytes;
coa coa;
coa;
tca cycle ... See more keywords
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Published in 2021 at "Molecular genetics and metabolism"
DOI: 10.1016/j.ymgme.2021.03.001
Abstract: Propionic Acidemia (PA) and Methylmalonic Acidemia (MMA) are inborn errors of metabolism affecting the catabolism of valine, isoleucine, methionine, threonine and odd-chain fatty acids. These are multi-organ disorders caused by the enzymatic deficiency of propionyl-CoA…
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Keywords:
hst5040;
mma;
small molecule;
coa coa ... See more keywords
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Published in 2022 at "Frontiers in Cardiovascular Medicine"
DOI: 10.3389/fcvm.2022.855118
Abstract: Objectives Effective management of aortic coarctation (CoA) affects long-term cardiovascular outcomes. Full appreciation of CoA hemodynamics is important. This study aimed to analyze the relationship between aortic shape and hemodynamic parameters by means of computational…
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Keywords:
coa;
coarctation;
coa coa;
study ... See more keywords