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glycogen storage disease xi
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Galactose metabolism
Homo sapiens (human)
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LDHA
Lactate dehydrogenase is an AU-rich element-binding protein that directly interacts with AUF1
Genomic organization of human lactate dehydrogenase-A gene
A conditional knockout resource for the genome-wide study of mouse gene function
Mouse library set to be knockout
ALDOA
Interaction of the dissociable glycerol-3-phosphate dehydrogenase and fructose-1,6-bisphosphate aldolase. Quantitative analysis by an extrinsic fluorescence probe
Fructose-bisphosphate aldolase a is a potential metastasis-associated marker of lung squamous cell carcinoma and promotes lung cell tumorigenesis and migration.
Hemolytic anemia and severe rhabdomyolysis caused by compound heterozygous mutations of the gene for erythrocyte/muscle isozyme of aldolase, ALDOA(Arg303X/Cys338Tyr).
Sweet siblings with different faces: the mechanisms of FBP and F6P aldolase, transaldolase, transketolase and phosphoketolase revisited in light of recent structural data.
ENO3
Recurrent rhabdomyolysis due to muscle ����-enolase deficiency: very rare or underestimated?
PGM1
Conservation of functionally important global motions in an enzyme superfamily across varying quaternary structures
A metabolic hypothesis of cell growth and death in pancreatic cancer
The glycosylation of phosphoglucomutase is modulated by carbon source and heat shock in Saccharomyces cerevisiae
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