These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

88 related articles for article (PubMed ID: 3160238)

  • 1. Erythrocyte catechol-O-methyltransferase activity: genetic analysis in nuclear families with one child affected by Down syndrome.
    Brahe C; Serra A; Morton NE
    Am J Med Genet; 1985 Jun; 21(2):373-84. PubMed ID: 3160238
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Segregation analysis of dopamine-beta-hydroxylase (DBH) and catechol-O-methyltransferase (COMT): identification of major locus and polygenic components.
    Goldin LR
    Genet Epidemiol; 1985; 2(3):317-25. PubMed ID: 4054603
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Major gene model for the inheritance of catechol-O-methyltransferase activity in five large families.
    Siervogel RM; Weinshilboum R; Wilson AF; Elston RC
    Am J Med Genet; 1984 Oct; 19(2):315-23. PubMed ID: 6594929
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Linkage relationships between a major gene for catechol-o-methyltransferase activity and 25 polymorphic marker systems.
    Wilson AF; Elston RC; Siervogel RM; Weinshilboum R; Ward LJ
    Am J Med Genet; 1984 Nov; 19(3):525-32. PubMed ID: 6507499
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Catechol-o-methyltransferase activity in erythrocytes in Down's syndrome: family studies.
    Gustavson KH; Flodérus Y; Jagell S; Wetterberg L; Ross SB
    Clin Genet; 1982 Jul; 22(1):22-4. PubMed ID: 6216990
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Exclusion of the catechol-o-methyltransferase gene from genes contributing to salt-sensitive hypertension in dahl salt-sensitive rats.
    Kajimoto K; Hiura Y; Sumiya T; Yasui N; Okuda T; Iwai N
    Hypertens Res; 2007 May; 30(5):459-67. PubMed ID: 17587758
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Catechol-O-methyltransferase gene Val108/158Met polymorphism, and susceptibility to schizophrenia: association is more significant in women.
    Sazci A; Ergul E; Kucukali I; Kilic G; Kaya G; Kara I
    Brain Res Mol Brain Res; 2004 Dec; 132(1):51-6. PubMed ID: 15548428
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Human pharmacogenetics of methyl conjugation.
    Weinshilboum RM
    Fed Proc; 1984 May; 43(8):2303-7. PubMed ID: 6714437
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The increased COMT activity in Down syndrome patients is not a consequence of dosage effect owing to location of the gene on chromosome 21: further evidence.
    Brahe C; Bannetta P; Serra A; Arwert F
    Am J Med Genet; 1986 May; 24(1):203-4. PubMed ID: 2939719
    [No Abstract]   [Full Text] [Related]  

  • 10. Lack of association of catechol-O-methyltransferase gene polymorphism in obsessive-compulsive disorder.
    Erdal ME; Tot S; Yazici K; Yazici A; Herken H; Erdem P; Derici E; Camdeviren H
    Depress Anxiety; 2003; 18(1):41-5. PubMed ID: 12900951
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetics of red cell COMT activity: analysis of thermal stability and family data.
    Spielman RS; Weinshilboum RM
    Am J Med Genet; 1981; 10(3):279-90. PubMed ID: 7304673
    [No Abstract]   [Full Text] [Related]  

  • 12. Variants in the catechol-o-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families.
    Chen X; Wang X; O'Neill AF; Walsh D; Kendler KS
    Mol Psychiatry; 2004 Oct; 9(10):962-7. PubMed ID: 15124004
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Catechol-O-methyltransferase low activity genotype (COMTLL) is associated with low levels of COMT protein in human hepatocytes.
    Doyle AE; Goodman JE; Silber PM; Yager JD
    Cancer Lett; 2004 Oct; 214(2):189-95. PubMed ID: 15363545
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Catechol-O-methyltransferase (COMT) polymorphisms predict treatment response in electroconvulsive therapy.
    Anttila S; Huuhka K; Huuhka M; Illi A; Rontu R; Leinonen E; Lehtimäki T
    Pharmacogenomics J; 2008 Apr; 8(2):113-6. PubMed ID: 17700596
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Catechol-O-methyltransferase polymorphism is not associated with ovarian cancer risk.
    Goodman JE; Lavigne JA; Hengstler JG; Tanner B; Helzlsouer KJ; Yager JD
    Cancer Epidemiol Biomarkers Prev; 2000 Dec; 9(12):1373-6. PubMed ID: 11142424
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Erythrocyte catechol O-methyltransferase activity in schizophrenia: analysis of family data.
    Baron M; Gruen R; Levitt M; Hunter C; Asnis L
    Am J Psychiatry; 1984 Jan; 141(1):29-32. PubMed ID: 6691458
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Erythrocyte catechol-O-methyltransferase activity in a Swedish population.
    Floderus Y; Ross SB; Wetterberg L
    Clin Genet; 1981 May; 19(5):389-92. PubMed ID: 7296928
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic segregation analysis of red blood cell (RBC) histamine N-methyltransferase (HNMT) activity.
    Price RA; Scott MC; Weinshilboum RM
    Genet Epidemiol; 1993; 10(2):123-31. PubMed ID: 8339926
    [TBL] [Abstract][Full Text] [Related]  

  • 19. No associations exist between five functional polymorphisms in the catechol-O-methyltransferase gene and schizophrenia in a Japanese population.
    Nunokawa A; Watanabe Y; Muratake T; Kaneko N; Koizumi M; Someya T
    Neurosci Res; 2007 Jul; 58(3):291-6. PubMed ID: 17482701
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic analysis of cleft lip with or without cleft palate in Danish kindreds.
    Marazita ML; Spence MA; Melnick M
    Am J Med Genet; 1984 Sep; 19(1):9-18. PubMed ID: 6496575
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.