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P743: the pivotal role of glutaminolysis in myelodysplastic syndrome (mds): a novel strategy for the targeted therapy of mds

14000 Rs

Hereditary spastic paraplegia is a common phenotypic finding in ARG1 deficiency, P5CS deficiency and HHH syndrome: three inborn errors of metabolism caused by alteration of an interconnected pathway of glutamate and urea cycle metabolism

Nitric oxide and mitochondrial respiration in the heart

Just as important, the trial results were produced under a prescription drug used as directed a research-use-only context is not the same setting, and the trial numbers cannot be assumed to transfer to it

The cancelled Phase I trial was not buried by a regulator