207 related articles for article (PubMed ID: 32236879)
1. In Silico Prediction of the Effects of Nonsynonymous Single Nucleotide Polymorphisms in the Human Catechol-O-Methyltransferase (COMT) Gene.
Yilmaz A; Çetin İ
Cell Biochem Biophys; 2020 Jun; 78(2):227-239. PubMed ID: 32236879
[TBL] [Abstract][Full Text] [Related]
2. Preliminary Evidence for an Association Between Variants of the Catechol-O-Methyltransferase (COMT) Gene and Premature Ejaculation.
Jern P; Johansson A; Strohmaier J; Treutlein J; Piha J; Rietschel M
J Sex Med; 2017 Dec; 14(12):1558-1565. PubMed ID: 29198511
[TBL] [Abstract][Full Text] [Related]
3. Computational analysis of deleterious single nucleotide polymorphisms in catechol O-Methyltransferase conferring risk to post-traumatic stress disorder.
Chitrala KN; Nagarkatti P; Nagarkatti M
J Psychiatr Res; 2021 Jun; 138():207-218. PubMed ID: 33865170
[TBL] [Abstract][Full Text] [Related]
4. Low enzymatic activity haplotypes of the human catechol-O-methyltransferase gene: enrichment for marker SNPs.
Nackley AG; Shabalina SA; Lambert JE; Conrad MS; Gibson DG; Spiridonov AN; Satterfield SK; Diatchenko L
PLoS One; 2009; 4(4):e5237. PubMed ID: 19365560
[TBL] [Abstract][Full Text] [Related]
5. Catechol O-methyltransferase pharmacogenomics: human liver genotype-phenotype correlation and proximal promoter studies.
Zhang J; Ji Y; Moon I; Pelleymounter LL; Ezequel Salavaggione O; Wu Y; Jenkins GD; Batzler AJ; Schaid DJ; Weinshilboum RM
Pharmacogenet Genomics; 2009 Aug; 19(8):577-87. PubMed ID: 19641441
[TBL] [Abstract][Full Text] [Related]
6. In silico analysis and high-risk pathogenic phenotype predictions of non-synonymous single nucleotide polymorphisms in human Crystallin beta A4 gene associated with congenital cataract.
Wang Z; Huang C; Lv H; Zhang M; Li X
PLoS One; 2020; 15(1):e0227859. PubMed ID: 31935276
[TBL] [Abstract][Full Text] [Related]
7. Analysis of catechol-O-methyltransferase gene mutation and identification of new pathogenic gene for paroxysmal kinesigenic dyskinesia.
Gu C; Li J; Zhu L; Lu Z; Huang H
Neurol Sci; 2016 Mar; 37(3):377-83. PubMed ID: 26650803
[TBL] [Abstract][Full Text] [Related]
8. The Val158Met polymorphism in COMT gene and cancer risk: role of endogenous and exogenous catechols.
Sak K
Drug Metab Rev; 2017 Feb; 49(1):56-83. PubMed ID: 27826992
[TBL] [Abstract][Full Text] [Related]
9. The impact of catechol-O-methyltransferase SNPs and haplotypes on treatment response phenotypes in major depressive disorder: a case-control association study.
Kocabas NA; Faghel C; Barreto M; Kasper S; Linotte S; Mendlewicz J; Noro M; Oswald P; Souery D; Zohar J; Massat I
Int Clin Psychopharmacol; 2010 Jul; 25(4):218-27. PubMed ID: 20531207
[TBL] [Abstract][Full Text] [Related]
10. A bioinformatics approach for the phenotype prediction of nonsynonymous single nucleotide polymorphisms in human cytochromes P450.
Wang LL; Li Y; Zhou SF
Drug Metab Dispos; 2009 May; 37(5):977-91. PubMed ID: 19204079
[TBL] [Abstract][Full Text] [Related]
11. Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain.
Chen J; Lipska BK; Halim N; Ma QD; Matsumoto M; Melhem S; Kolachana BS; Hyde TM; Herman MM; Apud J; Egan MF; Kleinman JE; Weinberger DR
Am J Hum Genet; 2004 Nov; 75(5):807-21. PubMed ID: 15457404
[TBL] [Abstract][Full Text] [Related]
12. Phenotype prediction of deleterious nonsynonymous single nucleotide polymorphisms in human alcohol metabolism-related genes: a bioinformatics study.
Wang LL; Yang AK; Li Y; Liu JP; Zhou SF
Alcohol; 2010 Aug; 44(5):425-38. PubMed ID: 20804942
[TBL] [Abstract][Full Text] [Related]
13. Association of Ala72Ser polymorphism with COMT enzyme activity and the risk of schizophrenia in Koreans.
Lee SG; Joo Y; Kim B; Chung S; Kim HL; Lee I; Choi B; Kim C; Song K
Hum Genet; 2005 Mar; 116(4):319-28. PubMed ID: 15645182
[TBL] [Abstract][Full Text] [Related]
14. Catechol-O-methyltransferase: effects of the val108met polymorphism on protein turnover in human cells.
Doyle AE; Yager JD
Biochim Biophys Acta; 2008 Jan; 1780(1):27-33. PubMed ID: 17980711
[TBL] [Abstract][Full Text] [Related]
15. Polymorphisms in catechol-O-methyltransferase modify treatment effects of aspirin on risk of cardiovascular disease.
Hall KT; Nelson CP; Davis RB; Buring JE; Kirsch I; Mittleman MA; Loscalzo J; Samani NJ; Ridker PM; Kaptchuk TJ; Chasman DI
Arterioscler Thromb Vasc Biol; 2014 Sep; 34(9):2160-7. PubMed ID: 25035343
[TBL] [Abstract][Full Text] [Related]
16. In silico analysis of nonsynonymous single-nucleotide polymorphisms (nsSNPs) of the SMPX gene.
Arifuzzaman M; Mitra S; Das R; Hamza A; Absar N; Dash R
Ann Hum Genet; 2020 Jan; 84(1):54-71. PubMed ID: 31583691
[TBL] [Abstract][Full Text] [Related]
17. Systematic exploration of predicted destabilizing nonsynonymous single nucleotide polymorphisms (nsSNPs) of human aldehyde oxidase: A Bio-informatics study.
Coelho C; Muthukumaran J; Santos-Silva T; João Romão M
Pharmacol Res Perspect; 2019 Dec; 7(6):e00538. PubMed ID: 31768259
[TBL] [Abstract][Full Text] [Related]
18. Predicting the Most Deleterious Missense Nonsynonymous Single-Nucleotide Polymorphisms of Hennekam Syndrome-Causing CCBE1 Gene, In Silico Analysis.
Shinwari K; Guojun L; Deryabina SS; Bolkov MA; Tuzankina IA; Chereshnev VA
ScientificWorldJournal; 2021; 2021():6642626. PubMed ID: 34234628
[TBL] [Abstract][Full Text] [Related]
19. The enzymatic activities of brain catechol-O-methyltransferase (COMT) and methionine sulphoxide reductase are correlated in a COMT Val/Met allele-dependent fashion.
Moskovitz J; Walss-Bass C; Cruz DA; Thompson PM; Hairston J; Bortolato M
Neuropathol Appl Neurobiol; 2015 Dec; 41(7):941-51. PubMed ID: 25640985
[TBL] [Abstract][Full Text] [Related]
20. Identification of most damaging nsSNPs in human CCR6 gene: In silico analyses.
Akhtar M; Jamal T; Jamal H; Din JU; Jamal M; Arif M; Arshad M; Jalil F
Int J Immunogenet; 2019 Dec; 46(6):459-471. PubMed ID: 31364806
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]