Article ID Journal Published Year Pages File Type
8349937 Pharmacology Biochemistry and Behavior 2018 28 Pages PDF
Abstract
These results reinforce the validity of type III Nrg1+/− mice for schizophrenia research and suggest that loss of function of type III Nrg1 may not be responsible for the exaggerated response to acute D9-THC observed in heterozygous Nrg1 TM mice. This highlights the importance of careful consideration of Nrg1 isoform type differences.
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Life Sciences Biochemistry, Genetics and Molecular Biology Biochemistry
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