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Wolfram syndrome-1 (WS1) is primarily caused by mutations in the WFS1 gene encoding the ER-resident wolframin protein, presenting with diabetes mellitus, optic atrophy, neurological deficits, and hearing impairment [173]

Bernhardt ML, Kong BY, Kim AM, OHalloran TV, Woodruff TK (2012) A zinc-dependent mechanism regulates meiotic progression in mammalian oocytes

In receptor pharmacology, retatrutide serves as the reference balanced tri-agonist

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These approaches expand the experimental toolbox available to researchers probing peptide pharmacokinetics and distribution

De wetenschap doet veel onderzoek naar glutathion