Evidence for association of two variants of the nociceptin/orphanin FQ receptor gene OPRL1 with vulnerability to develop opiate addiction in Caucasians.
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Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disordersAsparagine synthetase deficiency detected by whole exome sequencing causes congenital microcephaly, epileptic encephalopathy and psychomotor delay.The genetics of the opioid system and specific drug addictionsGenetic Deletion of the Nociceptin/Orphanin FQ Receptor in the Rat Confers Resilience to the Development of Drug Addiction.Nociceptin/orphanin FQ receptor gene variation is associated with smoking status in Japanese.
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Evidence for association of two variants of the nociceptin/orphanin FQ receptor gene OPRL1 with vulnerability to develop opiate addiction in Caucasians.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on April 2010
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Evidence for association of tw ...... piate addiction in Caucasians.
@en
Evidence for association of tw ...... piate addiction in Caucasians.
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type
label
Evidence for association of tw ...... piate addiction in Caucasians.
@en
Evidence for association of tw ...... piate addiction in Caucasians.
@nl
prefLabel
Evidence for association of tw ...... piate addiction in Caucasians.
@en
Evidence for association of tw ...... piate addiction in Caucasians.
@nl
P2093
P2860
P1433
P1476
Evidence for association of tw ...... piate addiction in Caucasians.
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P2093
David A Nielsen
Dmitri Proudnikov
Douglas Londono
Judith A Briant
P2860
P356
10.1097/YPG.0B013E32833511F6
P407
P577
2010-04-01T00:00:00Z