REDWOOD CITY, Calif., Nov. 22, 2021 (GLOBE NEWSWIRE) -- Codexis, Inc. (NASDAQ: CDXS), a leading enzyme engineering company enabling the promise of synthetic biology, today announced that two of the ...
Homocystinuria is a genetic disorder in which the body cannot break down a particular amino acid. The disorder passes from parents to children in an autosomal recessive manner, which means that two ...
An unusual homocysteine-containing compound, 5-amino-4-imidazolecarboxamide-5′-S-homocysteinylriboside, was isolated from the urine of a child with homocystinuria and detected in the urines of six ...
Homocystinuria is the most common inborn error of sulfur amino acid metabolism. It is most commonly caused by cystathionine beta-synthase (CBS) deficiency, which is ...
LEXINGTON, Mass.--(BUSINESS WIRE)--Orphan Technologies, a company dedicated to helping patients control their homocysteine levels, today announced that OT-58 for the treatment of cystathionine beta ...
HCU is a rare autosomal recessive inherited sulfur amino acid metabolism disorder primarily caused by a cystathionine beta-synthase deficiency (CBS). HCU patients have a broad spectrum of age (older ...
Denovo Sciences Inc, a pioneer in AI-driven drug discovery based on synthetic data, Weill Cornell Medicine-Qatar (WCM-Q), and Sidra Medicine are engaging in a collaboration to identify and develop ...
In a new paper, researchers describe finding the gene that causes Mexican cavefish to lose their vision. The same gene responsible for this evolutionary change in the fish is also responsible for ...
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