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Standardized dosing may not be appropriate for everyone

These are fundamentally different experimental conditions

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This means the vote did not: Immediately add the substances to the 503A Bulks List Authorize pharmacies to begin compounding them based only on the committee vote Complete the FDA drug approval process Establish that products containing the substances have undergone FDA review for safety, quality, or benefit Create a pathway for 503B outsourcing facilities to produce the substances for office use The scope of this meeting is specifically the Section 503A Bulks List

We postulate that NAD + /NADH disequilibrium in the gdh3 / gdh3 mutant led to a different proline catabolism in the mutant compared to the wild-type strain