Human catechol-O-methyltransferase: cloning and expression of the membrane-associated form
about
Cloning and functional expression of human kynurenine 3-monooxygenaseInteraction between GABA(A) receptor beta subunits and the multifunctional protein gC1q-RCloning and functional expression of a soluble form of kynurenine/alpha-aminoadipate aminotransferase from rat kidneyMolecular cloning and nucleotide sequence of a cDNA encoding hydroxyindole O-methyltransferase from chicken pineal glandProgesterone-mediated regulation of catechol-O-methyl transferase expression in endometrial cancer cells.Genetic contribution of catechol-O-methyltransferase variants in treatment outcome of low back pain: a prospective genetic association study.Executive functions and selective attention are favored in middle-aged healthy women carriers of the Val/Val genotype of the catechol-o-methyltransferase gene: a behavioral genetic studyHaplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia.Vitamin D inhibits proliferation of human uterine leiomyoma cells via catechol-O-methyltransferaseInfluence of GABA(A) receptor α subunit isoforms on the benzodiazepine binding siteGene-sex interactions in schizophrenia: focus on dopamine neurotransmission.Polymorphism of the catechol-O-methyltransferase gene in Han Chinese patients with psoriasis vulgaris.Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome.Modulation of the COMT Val(158)Met polymorphism on resting-state EEG power.Duplication of the pepF gene and shuffling of DNA fragments on the lactose plasmid of Lactococcus lactis.The enzymatic activities of brain catechol-O-methyltransferase (COMT) and methionine sulphoxide reductase are correlated in a COMT Val/Met allele-dependent fashion.Genetic Risk Score Predicts Late-Life Cognitive Impairment.Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder.Pharmacogenetic tools for the development of target-oriented cognitive-enhancing drugs.COMT Val158Met polymorphism is associated with blood pressure and lipid levels in general families of Bama longevous area in China.Progesterone regulates catechol-O-methyl transferase gene expression in breast cancer cells: distinct effect of progesterone receptor isoformsA point mutation in the gamma2 subunit of gamma-aminobutyric acid type A receptors results in altered benzodiazepine binding site specificity.Impact of interacting functional variants in COMT on regional gray matter volume in human brain.Pharmacogenetic insights into codeine analgesia: implications to pediatric codeine use.Variation in the COMT gene: implications for pain perception and pain treatment.Imaging genetics of schizophrenia.Presynaptic dopaminergic function: implications for understanding treatment response in psychosis.Pharmacology of recombinant gamma-aminobutyric acidA receptors rendered diazepam-insensitive by point-mutated alpha-subunits.Manic symptom severity correlates with COMT activity in the striatum: A post-mortem study.COMT haplotypes suggest P2 promoter region relevance for schizophrenia.On the benzodiazepine binding pocket in GABAA receptors.Subtle changes in residue 77 of the gamma subunit of alpha1beta2gamma2 GABAA receptors drastically alter the affinity for ligands of the benzodiazepine binding site.Expression of functional membrane-bound and soluble catechol-O-methyltransferase in Escherichia coli and a mammalian cell line.Sex-specific effects of COMT Val158Met polymorphism on corpus callosum structure: A whole-brain diffusion-weighted imaging study.Structural correlates of COMT Val158Met polymorphism in childhood ADHD: a voxel-based morphometry study.Proximity-accelerated chemical coupling reaction in the benzodiazepine-binding site of gamma-aminobutyric acid type A receptors: superposition of different allosteric modulators.Production of rat soluble and membrane-bound catechol O-methyltransferase forms from bifunctional mRNAs.Human catechol O-methyltransferase genetic variation: gene resequencing and functional characterization of variant allozymes.Association between COMT (Val158Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study.Role of COMT in ADHD: a systematic meta-analysis.
P2860
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P2860
Human catechol-O-methyltransferase: cloning and expression of the membrane-associated form
description
1991 nî lūn-bûn
@nan
1991 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Human catechol-O-methyltransfe ...... f the membrane-associated form
@ast
Human catechol-O-methyltransfe ...... f the membrane-associated form
@en
Human catechol-O-methyltransfe ...... the membrane-associated form.
@nl
type
label
Human catechol-O-methyltransfe ...... f the membrane-associated form
@ast
Human catechol-O-methyltransfe ...... f the membrane-associated form
@en
Human catechol-O-methyltransfe ...... the membrane-associated form.
@nl
prefLabel
Human catechol-O-methyltransfe ...... f the membrane-associated form
@ast
Human catechol-O-methyltransfe ...... f the membrane-associated form
@en
Human catechol-O-methyltransfe ...... the membrane-associated form.
@nl
P2093
P2860
P356
P1476
Human catechol-O-methyltransfe ...... f the membrane-associated form
@en
P2093
P2860
P304
P356
10.1073/PNAS.88.4.1416
P407
P577
1991-02-01T00:00:00Z