WebD CBLC-mediated monoubiquitination of lysine residues in AURKA. Flag-tagged wild-type (WT) or mutant (K23R, K63R, K69R, K99R, K117R, K141R, K227R, K250R, and K258R) AURKA constructs were ... WebFeb 2, 2024 · Methylmalonic aciduria and homocystinuria, CblC type (OMIM #277400) is the most common disorder of cobalamin intracellular metabolism, an autosomal recessive disease, whose biochemical hallmarks are hyperhomocysteinemia, methylmalonic aciduria and low plasma methionine. Despite being a well-recognized disease for pediatricians, …
CBLC: saiba o que é, para que serve e como funciona - Onze
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Methylmalonic acidemia with homocystinuria
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