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Serotonin Plasma Membrane Transport Proteins (Latest Articles)
Latest indexed articles for 'Serotonin Plasma Membrane Transport Proteins'
Articles 1 to 10 of 200:
Gene-environment interactions and depression.
2 Nov 2009
rec_pub_19887661-gene-environment-interactions-depression.htm
Gene-environment interactions and depression.
2 Nov 2009
rec_pub_19887659-gene-environment-interactions-depression.htm
30 Oct 2009
CONTEXT: The 5-HTTLPR polymorphism in the promoter region of the serotonin transporter gene (SLC6A4) has been found to moderate several categories of emotional response after stressful life events. Previous studies generally focused on its effect on ...
rec_pub_19884608-interactive-effect-stressful-life-events-serotonin-transporter-5.htm
6 Oct 2009
Stereodefined trisubstituted cyclopropanes bearing naphthyloxy, thiophenyl, and (N-methylamino)methyl groups were synthesized in enantiopure form employing asymmetric cyclopropanation of (E)- and (Z)-allylic alcohols as the key step. In vitro assays ...
rec_pub_19791802-synthesis-1-1-1-naphthyloxy-2-thiophenyl-2.htm
29 Sep 2009
3,4-Methylenedioxymethamphetamine (MDMA) is a drug of abuse worldwide and a selective serotonin (5-HT) neurotoxin. An important factor in the risk of drug abuse and relapse is stress. Although multiple parallels exist between MDMA abuse and stress, ...
rec_pub_19824774-mdma-pretreatment-leads-mild-chronic-unpredictable-stress-induced.htm
22 Sep 2009
Sequential structural modifications of the aryloxypropanamine template (e.g., atomoxetine, 2) led to a novel series of 1-(3-amino-2-hydroxy-1-phenyl propyl)-1,3-dihydro-2H-benzimidazol-2-ones as selective norepinephrine reuptake inhibitors (NRIs). ...
rec_pub_19722525-1-3-3-amino-2-hydroxy-1-phenyl-propyl-1-3-dihydro-2h-benzimidazol-2.htm
Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease.
21 Sep 2009
OBJECTIVE: Huntington disease (HD) is an autosomal dominant neurodegenerative disorder caused by a CAG repeat expansion in the HD gene (HTT). We aimed to assess whether interaction between CAG repeat sizes in the mutant and normal allele could ...
rec_pub_19776381-normal-mutant-htt-interact-affect-clinical-severity-progression.htm
Huntington disease: a tale of two genes.
21 Sep 2009
rec_pub_19776377-huntington-disease-tale-two-genes.htm
14 Sep 2009
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder, caused by a polyglutamine expansion in the huntingtin protein (htt). Increasing evidence suggests that transglutaminase (TGase) plays a critical role in the ...
rec_pub_19759302-striatal-expression-calmodulin-fragment-improved-motor-function.htm
[Serotonin receptor gene polymorphism and analgesic sensitivity]
30 Aug 2009
There are gene polymorphisms changing the expression or activation of the serotonin (5-HT) receptors, which are associated with pain. This review showed an availability of 5-HT2A receptor gene polymorphism in analgesic sensitivity. To search gene ...
rec_pub_19764436-serotonin-receptor-gene-polymorphism-analgesic-sensitivity.htm
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