This lysosomal storage disease is treated by reducing complex sphingolipid accumulation with the glucosylceramide synthase inhibiter miglustat. O Type 1 diabetes Gaucher disease Krabbe disease Fabry disease
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- Ethylhydroceuprin (optochin) is a specific inhibitor of S. pneumoniae and its mechanism is: a. ATPase b. ABC transporters c. ATP synthase d. tRNA synthetase e. Any of these answers thank you!D-Gluconic acid is formed from D-Glucoge Select one:a. By substitutonb. By oxydationc. By esterificationd. By reductionThe enzyme that catalyzes the conversion of glucose to mannose is classified as aa. Isomeraseb. Hydrolasec. Transferased. Lyasee. Ligase
- Gluconeogenesis involves using glucose to synthesize amino acids. TRUE/FALSEIn Alzheimer’s disease, nerve cell death is associated with the accumulation of aggregates of misfolded protein. Compare this process with the onset of diabetes mellitus.A 9 year old mentally retarded girl with a protuberant abdomen, short stature, coarse facial features and cloudy corneas. skeletal malformations include dysostosis Multiplex and Bullet shaped middle phalanx .what is the enzyme deficient in this patient? A)Iduronate sulfatase B) beta - Galactosidase C)alpha - L- Iduronidase D) beta - Glucuronidase
- By definition, essential amino acids are not synthesized by an organism. Arginine is classified as an essential amino acid in infants, even though it is part of the urea cycle. Explain.Which of these enzymes is needed to maintain a steady pool of methylene THF used in pyrimidine synthesis and cancer cells proliferation? Group of answer choices Phosphoglyceratedehydrogenase Glyceraldehydegehydrogenase Glycine decarboxylase ThymidylatesynthaseArgininosuccinic aciduria is a condition that results when the urea-cycle enzyme argininosuccinase is deficient. Argininosuccinate is present in the blood and urine. Suggest how this condition might be treated while still removing nitrogen from the body.
- Suggest an explanation for the fact that the amount of glycogen in type I glycogen-storage disease (von Gierke disease) is increased.prpc is a normal protein of our neuronal cell membrane that is sensitive to protease action (ie can be broken down by protease) true or false?An allosteric regulator of glycogen synthase is: UDP-glucose. cAMP. glucose 1-phosphate. ATP. glucose 6-phosphate.