A gas chromatographic procedure for detection of pathological organic aciduria

MR1-restricted mucosal-associated invariant T (MAIT) cells respond to mycobacterial vaccination and infection in nonhuman primates.

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Activation of the mitochondrial caspase pathway and subsequent calpain activation in monkey RPE cells cultured under zinc depletion.

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Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I).

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Infant mice with glutaric acidaemia type I have increased vulnerability to 3-nitropropionic acid toxicity.

Journal of inherited metabolic disease·2006

Development of pathogenic concepts in glutaryl-CoA dehydrogenase deficiency: the challenge.

Journal of inherited metabolic disease·2004

Animal models for glutaryl-CoA dehydrogenase deficiency.

Journal of inherited metabolic disease·2004

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Measurement of stable isotope ratios of halogenated organic compounds by liquid chromatographic, high-temperature combustion isotope ratio mass spectrometry.

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Related Experiment Videos

A gas chromatographic procedure for detection of pathological organic aciduria

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MR1-restricted mucosal-associated invariant T (MAIT) cells respond to mycobacterial vaccination and infection in nonhuman primates.

Activation of the mitochondrial caspase pathway and subsequent calpain activation in monkey RPE cells cultured under zinc depletion.

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