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He did for awhile, then I got nervous about it and made him stop

Human OPRM1 and murine Oprm1 promoter driven viral constructs for genetic access to mu-opioidergic cell types

The most common genetic mutation causing SCD is the A to T transversion in the HBB gene on chromosome 11, leading to a substitution of valine for glutamic acid in the sixth codon [4] of the -globin protein chain and the production of sickle hemoglobin S (HbS)

NF-kappaB activation in sarcoidosis

Yarmohammadi F, Wallace Hayes A, Najafi N, Karimi G (2020) The protective effect of natural compounds against rotenone-induced neurotoxicity

2015;128(4):418-25.e5