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However, the human 4-N-trimethylaminobutyraldehyde dehydrogenase has so far not been identified.
Over 400 million people have an inherited condition called glucose-6-phosphate dehydrogenase deficiency.
We could find no reference to caution in people at risk of glucose-6-phosphate dehydrogenase deficiency.
Lactate dehydrogenase levels are generally used to monitor disease activity.
Women also produce less of the enzyme dehydrogenase, which helps in breaking down alcohol.
This mitochondrial enzyme is associated with the 3-methyl-2-oxobutanoate dehydrogenase complex.
The effect of Gerovital H3 on the glucose-6-phosphate dehydrogenase activity.
The cytosolic together with the mitochondrial glycerol-3-phosphate dehydrogenase work in concert.
Hydrogen atoms are removed under the influence of the enzyme dehydrogenase.
The E1-catalyzed process is the rate-limiting step of the whole pyruvate dehydrogenase complex.
Activity of the 2-oxoglutarate dehydrogenase complex is decreased in many neurodegenerative diseases.
This enzyme is also called 2,4-diaminopentanoic acid C4 dehydrogenase.
One example is the case of Pyruvate dehydrogenase complex.
The protein encoded by this gene is a member of the alcohol dehydrogenase family.
There are three different enzyme components in the pyruvate dehydrogenase complex.
Dangerous levels of methemoglobinemia only occur in patients with glucose-6-phosphate dehydrogenase deficiency.
This protein belongs to the aldehyde dehydrogenase family of proteins.
We present a case illustrating the particular caution necessary in subjects at risk of glucose-6-phosphate dehydrogenase deficiency.
In our patient it seems probable that the low concentrations reflected the glucose-6-phosphate dehydrogenase deficiency.
The first box shows the overall isocitrate dehydrogenase reaction.
Alcohol dehydrogenase is a dimer with a mass of 80 kDa.
There is no crystal structure available for sarcosine dehydrogenase.
This gene encodes one subunit of the 2-oxoglutarate dehydrogenase complex.
An example of this occurring is the relationship between glyceraldehyde-3-phosphate and the enzyme glyceraldehyde-3-phosphate dehydrogenase.
The first process is catalyzed by enzymes called carbon monoxide dehydrogenase.