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Absence of the sulfate transporter SAT-1 has no impact on oxalate handling by mouse intestine and does not cause hyperoxaluria or hyperoxalemia

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Tirzepatide has fewer injection site reactions

Loss-of-function missense mutations as well as single nucleotide polymorphisms in the genes encoding K ir 4.1 and AQP4 (which is selectively astroglial and operates in concert with K ir 4.1) are linked to epilepsy in humans

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