about
Monoamine related functional gene variants and relationships to monoamine metabolite concentrations in CSF of healthy volunteersAssociations of the A66G Methionine Synthase Reductase Polymorphism in Colorectal Cancer: A Systematic Review and Meta-AnalysisGenetic epidemiology: some special contributions of birth cohortsHeterosis: emerging ideas about hybrid vigourPhenylethanolamine N-methyltransferase (PNMT) gene and early-onset Alzheimer diseaseVariants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autismAssociation of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disordersThe Integration of Genetic Propensities into Social-Control Models of Delinquency and Violence among Male YouthsRegional meta-analysis of published data supports linkage of autism with markers on chromosome 7.Association between 5-HT2A, TPH1 and GNB3 genotypes and response to typical neuroleptics: a serotonergic approachADHD and Disruptive Behavior scores - associations with MAO-A and 5-HTT genes and with platelet MAO-B activity in adolescentsImproving the prediction of treatment response in depression: integration of clinical, cognitive, psychophysiological, neuroimaging, and genetic measures.PICK1 Genetic Variation and Cognitive Function in Patients with Schizophrenia.The Association of the COMT V158M Polymorphism with Endometrial/Ovarian Cancer in HNPCC Families Adhering to the Amsterdam Criteria.Smoking as a product of gene-environment interactionGenetic diversity in cytokines associated with immune variation and resistance to multiple pathogens in a natural rodent population.Parent-child DRD4 genotype as a potential biomarker for oppositional, anxiety, and repetitive behaviors in children with autism spectrum disorderSingle nucleotide polymorphism in gene encoding transcription factor Prep1 is associated with HIV-1-associated dementia.Association between the 5-HT6 receptor C267T polymorphism and response to antidepressant treatment in major depressive disorder.Catecholamine storage vesicles: role of core protein genetic polymorphisms in hypertension.A neuronal nitric oxide synthase (NOS-I) haplotype associated with schizophrenia modifies prefrontal cortex function.Positional cloning, association analysis and expression studies provide convergent evidence that the cadherin gene FAT contains a bipolar disorder susceptibility allele.An evolutionary perspective on epistasis and the missing heritabilityDo dopamine gene variants and prenatal smoking interactively predict youth externalizing behavior?A functional variant of the serotonin transporter gene (SLC6A4) moderates impulsive choice in attention-deficit/hyperactivity disorder boys and siblings.Association of ADHD, tics, and anxiety with dopamine transporter (DAT1) genotype in autism spectrum disorder.Genetic Variation of the Mu Opioid Receptor (OPRM1) and Dopamine D2 Receptor (DRD2) is Related to Smoking Differences in Patients with Schizophrenia but not Bipolar DisorderDopaminergic, serotonergic, and oxytonergic candidate genes associated with infant attachment security and disorganization? In search of main and interaction effectsGenetic polymorphisms and obesity influence estradiol decline during the menopause.Haptoglobin phenotype modifies serum iron levels and the effect of smoking on Parkinson disease riskDRD2 polymorphisms modulate reward and emotion processing, dopamine neurotransmission and openness to experienceThe search for genenotype/phenotype associations and the phenome scan.Posttraumatic Brain Injury Cognitive Performance Is Moderated by Variation Within ANKK1 and DRD2 Genes.Interaction between smoking and functional polymorphism in the TGFB1 gene is associated with ischaemic heart disease and myocardial infarction in patients with rheumatoid arthritis: a cross-sectional study.Extensive additivity of gene expression differentiates subspecies of the house mouse.Enterovirus RNA in peripheral blood may be associated with the variants of rs1990760, a common type 1 diabetes associated polymorphism in IFIH1.Genetic dissection of heterosis using epistatic association mapping in a partial NCII mating designAssociation of the Neuronal Cell Adhesion Molecule (NrCAM) Gene Variants with Personality Traits and Addictive Symptoms in Methamphetamine Use Disorder.Identification of candidate polymorphisms on stress oxidative and DNA damage repair genes related with clinical outcome in breast cancer patients.IFNG genotype and sex interact to influence the risk of childhood asthma
P2860
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P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Molecular heterosis: a review
@ast
Molecular heterosis: a review
@en
Molecular heterosis: a review
@nl
type
label
Molecular heterosis: a review
@ast
Molecular heterosis: a review
@en
Molecular heterosis: a review
@nl
prefLabel
Molecular heterosis: a review
@ast
Molecular heterosis: a review
@en
Molecular heterosis: a review
@nl
P3181
P356
P1476
Molecular heterosis: a review
@en
P2093
D E Comings
J P MacMurray
P3181
P356
10.1006/MGME.2000.3015
P407
P577
2000-09-01T00:00:00Z