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Polymorphisms and a rare missense mutation that impair CaMKK2 function are associated with bipolar disorder Whole exome sequencing and genetic association studies have uncovered a link between bipolar disorder and loss-of-function polymorphisms and mutations in human CAMKK2

Estrogen replacement suppresses a prostaglandin H synthase-dependent vasoconstrictor in rat mesenteric arteries

Beads were then washed twice with 300 l of IP lysis buffer

Jones, Ghassemzadeh 2018)

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This could potentially result in the overestimation of GSSG and thus lower GSH:GSSG values