Pages that link to "Q34396807"
Jump to navigation
Jump to search
The following pages link to Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2 (Q34396807):
Displaying 50 items.
- Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome (Q24314765) (← links)
- Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial syndrome (Q24317602) (← links)
- Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility (Q24679438) (← links)
- No evidence of association between Catechol-O-Methyltransferase (COMT) Val158Met genotype and performance on neuropsychological tasks in children with ADHD: a case-control study (Q24794008) (← links)
- Can we observe epigenetic effects on human brain function? (Q26827275) (← links)
- The role of the catechol-O-methyltransferase (COMT) gene in personality and related psychopathological disorders (Q26863407) (← links)
- Chromosomal microdeletions: dissecting del22q11 syndrome (Q28206335) (← links)
- 22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome (Q28217633) (← links)
- Catechol-O-methyltransferase Val158Met polymorphism is associated with somatosensory amplification and nocebo responses (Q28542991) (← links)
- The Role of Human Aldo-Keto Reductases in the Metabolic Activation and Detoxication of Polycyclic Aromatic Hydrocarbons: Interconversion of PAH Catechols and PAH o-Quinones (Q28712007) (← links)
- Detoxication of structurally diverse polycyclic aromatic hydrocarbon (PAH) o-quinones by human recombinant catechol-O-methyltransferase (COMT) via O-methylation of PAH catechols (Q28742535) (← links)
- Meta-Analysis of the COMT Val158Met Polymorphism in Major Depressive Disorder: Effect of Ethnicity (Q30277686) (← links)
- Polymorphisms in genes encoding dopamine signalling pathway and risk of alcohol dependence: a systematic review (Q30834350) (← links)
- Linkage studies of catechol-O-methyltransferase (COMT) and dopamine-beta-hydroxylase (DBH) cDNA expression levels (Q30843348) (← links)
- Treatment of cognitive deficits associated with schizophrenia: potential role of catechol-O-methyltransferase inhibitors (Q31116328) (← links)
- New, selective catechol-O-methyltransferase inhibitors as therapeutic agents in Parkinson's disease (Q33537438) (← links)
- Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome (Q33608693) (← links)
- Linkage study of catechol-O-methyltransferase and attention-deficit hyperactivity disorder. (Q33784470) (← links)
- Catechol-O-methyltransferase (COMT) gene variants: possible association of the Val158Met variant with opiate addiction in Hispanic women (Q34016279) (← links)
- Genetics of psychosis in Alzheimer's disease: a review (Q34098861) (← links)
- Genetic contribution of catechol-O-methyltransferase variants in treatment outcome of low back pain: a prospective genetic association study (Q34276193) (← links)
- A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children (Q34334067) (← links)
- Race moderates the association of Catechol-O-methyltransferase genotype and posttraumatic stress disorder in preschool children. (Q34369985) (← links)
- Association of COMT Val158Met polymorphism and breast cancer risk: an updated meta-analysis (Q34435081) (← links)
- Functionally gene-linked polymorphic regions and genetically controlled neurotransmitters metabolism (Q34435115) (← links)
- Polymorphism of the catechol-O-methyltransferase gene in Han Chinese patients with psoriasis vulgaris (Q34548462) (← links)
- Catechol-O-methyltransferase and its inhibitors in Parkinson's disease (Q34693019) (← links)
- Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome (Q34735834) (← links)
- Review and meta-analysis of antidepressant pharmacogenetic findings in major depressive disorder (Q34871885) (← links)
- Separation methods for catechol O-methyltransferase activity assay: physiological and pathophysiological relevance (Q35008832) (← links)
- Catechol O-methyltransferase pharmacogenomics and selective serotonin reuptake inhibitor response (Q35040545) (← links)
- Dopamine genes and attention-deficit hyperactivity disorder: a review (Q35066854) (← links)
- Detection and management of comorbidity in patients with schizophrenia (Q35102472) (← links)
- The role of catechol-O-methyltransferase in the inactivation of catecholestrogen (Q35162226) (← links)
- Molecular epidemiology of sporadic breast cancer. The role of polymorphic genes involved in oestrogen biosynthesis and metabolism (Q35187748) (← links)
- Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases (Q35195236) (← links)
- Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders. (Q35238706) (← links)
- Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients (Q35249478) (← links)
- Differential regulation of catechol-O-methyltransferase expression in a mouse model of aggression. (Q35421990) (← links)
- A Genetic Variant (COMT) Coding Dopaminergic Activity Predicts Personality Traits in Healthy Elderly (Q35575569) (← links)
- From molecular biology to pharmacogenetics: a review of the literature on antidepressant treatment and suggestions of possible candidate genes (Q35680883) (← links)
- Genetic Variation in the Catechol-O-Methyl Transferase Val108/158Met Is Linked to the Caudate and Posterior Cingulate Cortex Volume in Healthy Subjects: Voxel-Based Morphometry Analysis of Brain Magnetic Resonance Imaging (Q35840931) (← links)
- Estrogen metabolism and breast cancer (Q35861660) (← links)
- No association between Val158Met of the COMT gene and susceptibility to schizophrenia in the Syrian population (Q35913466) (← links)
- Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder (Q36139662) (← links)
- Association between the COMT Val158Met polymorphism and risk of cancer: evidence from 99 case-control studies (Q36142309) (← links)
- Pharmacogenetic tools for the development of target-oriented cognitive-enhancing drugs (Q36401912) (← links)
- The Role of the Catechol-o-Methyltransferase (COMT) GeneVal158Met in Aggressive Behavior, a Review of Genetic Studies (Q36863953) (← links)
- Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene (Q36694090) (← links)
- Breast cancer risk reduction and membrane-bound catechol O-methyltransferase genetic polymorphisms (Q36841465) (← links)