O-demethyltramadol

solute carrier family 22 member 1 ; Homo sapiens







3 Article(s)
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1 27082504 SLC22A1/OCT1 Genotype Affects O-desmethyltramadol Exposure in Newborn Infants. 2016 Aug 2
2 27541716 Loss-of-function polymorphisms in the organic cation transporter OCT1 are associated with reduced postoperative tramadol consumption. 2016 Nov 4
3 21562485 Genetically polymorphic OCT1: another piece in the puzzle of the variable pharmacokinetics and pharmacodynamics of the opioidergic drug tramadol. 2011 Jul 3