نتایج جستجو برای: comt

تعداد نتایج: 1925  

Journal: :Psychiatry research 2010
Vandana Shashi Timothy D Howard Matcheri S Keshavan Jessica Kaczorowski Margaret N Berry Kelly Schoch Edward J Spence Thomas R Kwapil

The COMT gene is thought to contribute to the cognitive/psychiatric phenotypes in 22q11.2 deletion syndrome. We measured these manifestations against the Val/Met alleles of the COMT gene, in 40 nonpsychotic 22q11DS children. The Val allele was associated with poor IQ, processing speed, executive function and a higher frequency of anxiety disorders, underscoring the importance of the COMT gene i...

2018
Mehmet Oezkur Attila Magyar Phillip Thomas Andreas Reif Stefan Störk Peter U. Heuschmann Rainer G. Leyh Martin Wagner

BACKGROUND The Catechol-O-methyltransferase (COMT) represents the key enzyme in catecholamine degradation. Recent studies suggest that the COMT rs4680 polymorphism is associated with the response to endogenous and exogenous catecholamines. There are, however, conflicting data regarding the COMT Met/Met phenotype being associated with an increased risk of acute kidney injury (AKI) after cardiac ...

Journal: :Cancer research 2008
Yuan Ji Janet Olson Jianping Zhang Michelle Hildebrandt Liewei Wang James Ingle Zachary Fredericksen Thomas Sellers William Miller J Michael Dixon Hiltrud Brauch Michel Eichelbaum Christina Justenhoven Ute Hamann Yon Ko Thomas Brüning Jenny Chang-Claude Shan Wang-Gohrke Daniel Schaid Richard Weinshilboum

Catechol O-methyltransferase (COMT)-catalyzed methylation of catecholestrogens has been proposed to play a protective role in estrogen-induced genotoxic carcinogenesis. We have taken a comprehensive approach to test the hypothesis that genetic variation in COMT might influence breast cancer risk. Fifteen COMT single nucleotide polymorphisms (SNPs) selected on the basis of in-depth resequencing ...

Journal: :Archives of general psychiatry 2010
Kate Langley Jon Heron Michael C O'Donovan Michael J Owen Anita Thapar

CONTEXT As genes associated with common disorders are increasingly identified, we need to progress from observing associations to identifying risk pathways. The high-activity COMT genotype, in the presence of attention-deficit/hyperactivity disorder (ADHD), has previously been shown to be associated with extreme antisocial behavior. The same genotype has also been implicated in affecting cognit...

Journal: :Carcinogenesis 2008
Leane Lehmann Ling Jiang Jörg Wagner

The tissue concentrations of the female sex hormone 17beta-estradiol (E2) and its reactive catechol metabolites such as 4-hydroxyestradiol (4-HO-E2) play important roles in hormonal carcinogenesis. They are influenced by the activity of local enzymes involved in the metabolic activation and inactivation of E2. In the mammary gland, catechol estrogens are predominately inactivated by catechol-O-...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2011
Zhongjian Chen Meng Chen Hao Pan Siyuan Sun Liping Li Su Zeng Huidi Jiang

Luteolin is mainly metabolized by phase II enzymes in animals and humans with glucuronidation and sulfation as the two known metabolic pathways. Although methylation of luteolin was reported previously, the structure of the methylated metabolites and the enzymes involved in the process have not been clarified. In our study, two methylated metabolites, M1 (chrysoeriol) and M2 (diosmetin), were i...

Journal: :Psychological medicine 2008
T van Amelsvoort J Zinkstok M Figee E Daly R Morris M J Owen K C Murphy L De Haan D H Linszen B Glaser D G M Murphy

BACKGROUND Velo-cardio-facial syndrome (VCFS) is associated with deletions at chromosome 22q11, abnormalities in brain anatomy and function, and schizophrenia-like psychosis. Thus it is assumed that one or more genes within the deleted region are crucial to brain development. However, relatively little is known about how genetic variation at 22q11 affects brain structure and function. One gene ...

Journal: :European heart journal 2004
Anna-Lena Eriksson Stanko Skrtic Anders Niklason Lillemor Mattsson Hultén Olov Wiklund Thomas Hedner Claes Ohlsson

AIM Estrogens regulate several biological processes involved in the pathogenesis of myocardial infarction. Catechol-O-methyltransferase (COMT) is a key enzyme in the degradation of estrogens. There is a functional polymorphism in the COMT gene (Val158Met), affecting the activity of the enzyme. We investigated if the low activity genotype of COMT is associated with an altered risk of myocardial ...

Journal: :Journal of Clinical Neurology (Seoul, Korea) 2007
Jeong Wook Park Kwang Soo Lee Joong Seok Kim Yeong In Kim Hae Eun Shin

BACKGROUND Recent genetic association studies have investigated the possible genetic role of the dopaminergic system in migraine. Catechol-O-methyltransferase (COMT) is an enzyme that plays a crucial role in the metabolism of dopamine and its genetic polymorphism is associated with three- to fourfold variation of enzymatic activity. OBJECTIVES The objective of this study was to elucidate the ...

Journal: :Behavior genetics 2011
Q Kennedy J L Taylor A Noda M Adamson G M Murphy J M Zeitzer J A Yesavage

The polymorphic variation in the val158met position of the catechol-O-methyltransferase (COMT) gene is associated with differences in executive performance, processing speed, and attention. The purpose of this study is: (1) replicate previous COMT val158met findings on cognitive performance; (2) determine whether COMT val158met effects extend to a real-world task, aircraft navigation performanc...

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