of morphine responses in mice reveals a QTL on

نویسنده

  • Clarissa Parker
چکیده

In this study we identified a quantitative trait locus (QTL) on mouse Chromosome 7 associated with locomotor activity and rearing post morphine treatment. This QTL was revealed after correcting for the effects of another QTL peak on Chromosome 10 using composite interval mapping. The positional candidate genes are and . Several other genes within Syt9 Ppfibp2 the interval are linked to neural processes, locomotor activity, and the defensive response to harmful stimuli. This article is included in the gateway. INCF 1,2 3,4 5

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Analysis of morphine responses in mice reveals a QTL on

In this study we identified a quantitative trait locus (QTL) on mouse Chromosome 7 associated with locomotor activity and rearing post morphine treatment. This QTL was revealed after correcting for the effects of another QTL peak on Chromosome 10 using composite interval mapping. The positional candidate genes are and . Several other genes within Syt9 Ppfibp2 the interval are linked to neura...

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Analysis of morphine responses in mice reveals a QTL on Chromosome 7

In this study we identified a quantitative trait locus (QTL) on mouse Chromosome 7 associated with locomotor activity and rearing post morphine treatment. This QTL was revealed after correcting for the effects of another QTL peak on Chromosome 10 using composite interval mapping. The positional candidate genes are Syt9 and Ppfibp2. Several other genes within the interval are linked to neural pr...

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Analysis of morphine responses in mice reveals a QTL on Chromosome 7 [version 2; referees: 2 approved]

In this study we identified a quantitative trait locus (QTL) on mouse Chromosome 7 associated with locomotor activity and rearing post morphine treatment. This QTL was revealed after correcting for the effects of another QTL peak on Chromosome 10 using composite interval mapping. The positional candidate genes are and . Several other genes within Syt9 Ppfibp2 the interval are linked to neural p...

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تاریخ انتشار 2017