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Journal Abstract Search

220 related items for PubMed ID: 26272340

  • 1. Polymorphism in COMT is associated with IgG3 subclass level and susceptibility to infection in patients with chronic fatigue syndrome.
    Löbel M, Mooslechner AA, Bauer S, Günther S, Letsch A, Hanitsch LG, Grabowski P, Meisel C, Volk HD, Scheibenbogen C.
    J Transl Med; 2015 Aug 14; 13():264. PubMed ID: 26272340
    [Abstract] [Full Text] [Related]

  • 2. Genetic and epigenetic regulation of Catechol-O-methyltransferase in relation to inflammation in chronic fatigue syndrome and Fibromyalgia.
    Polli A, Hendrix J, Ickmans K, Bakusic J, Ghosh M, Monteyne D, Velkeniers B, Bekaert B, Nijs J, Godderis L.
    J Transl Med; 2022 Oct 25; 20(1):487. PubMed ID: 36284330
    [Abstract] [Full Text] [Related]

  • 3. Genetic variation in catechol-O-methyltransferase modifies effects of clonidine treatment in chronic fatigue syndrome.
    Hall KT, Kossowsky J, Oberlander TF, Kaptchuk TJ, Saul JP, Wyller VB, Fagermoen E, Sulheim D, Gjerstad J, Winger A, Mukamal KJ.
    Pharmacogenomics J; 2016 Oct 25; 16(5):454-60. PubMed ID: 27457818
    [Abstract] [Full Text] [Related]

  • 4. Moderate exercise increases expression for sensory, adrenergic, and immune genes in chronic fatigue syndrome patients but not in normal subjects.
    Light AR, White AT, Hughen RW, Light KC.
    J Pain; 2009 Oct 25; 10(10):1099-112. PubMed ID: 19647494
    [Abstract] [Full Text] [Related]

  • 5. Frequent IgG subclass and mannose binding lectin deficiency in patients with chronic fatigue syndrome.
    Guenther S, Loebel M, Mooslechner AA, Knops M, Hanitsch LG, Grabowski P, Wittke K, Meisel C, Unterwalder N, Volk HD, Scheibenbogen C.
    Hum Immunol; 2015 Oct 25; 76(10):729-35. PubMed ID: 26429318
    [Abstract] [Full Text] [Related]

  • 6. Combinations of single nucleotide polymorphisms in neuroendocrine effector and receptor genes predict chronic fatigue syndrome.
    Goertzel BN, Pennachin C, de Souza Coelho L, Gurbaxani B, Maloney EM, Jones JF.
    Pharmacogenomics; 2006 Apr 25; 7(3):475-83. PubMed ID: 16610957
    [Abstract] [Full Text] [Related]

  • 7. Genetic association of FKBP5 and CRHR1 with cortisol response to acute psychosocial stress in healthy adults.
    Mahon PB, Zandi PP, Potash JB, Nestadt G, Wand GS.
    Psychopharmacology (Berl); 2013 May 25; 227(2):231-41. PubMed ID: 23274505
    [Abstract] [Full Text] [Related]

  • 8. 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; 25(4):218-27. PubMed ID: 20531207
    [Abstract] [Full Text] [Related]

  • 9. 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 25; 14(12):1558-1565. PubMed ID: 29198511
    [Abstract] [Full Text] [Related]

  • 10. Catechol-O-methyltransferase gene Val158Met polymorphism and obsessive compulsive disorder susceptibility: a meta-analysis.
    Kumar P, Rai V.
    Metab Brain Dis; 2020 Feb 25; 35(2):241-251. PubMed ID: 31879835
    [Abstract] [Full Text] [Related]

  • 11. Interactive effects of DAOA (G72) and catechol-O-methyltransferase on neurophysiology in prefrontal cortex.
    Nixon DC, Prust MJ, Sambataro F, Tan HY, Mattay VS, Weinberger DR, Callicott JH.
    Biol Psychiatry; 2011 May 15; 69(10):1006-8. PubMed ID: 21215384
    [Abstract] [Full Text] [Related]

  • 12. Association between Val158Met functional polymorphism in the COMT gene and risk of preeclampsia in a Chinese population.
    Liang S, Liu X, Fan P, Liu R, Zhang J, He G, Liu Y, Bai H.
    Arch Med Res; 2012 Feb 15; 43(2):154-8. PubMed ID: 22475780
    [Abstract] [Full Text] [Related]

  • 13. Glucocorticoid receptor polymorphisms and haplotypes associated with chronic fatigue syndrome.
    Rajeevan MS, Smith AK, Dimulescu I, Unger ER, Vernon SD, Heim C, Reeves WC.
    Genes Brain Behav; 2007 Mar 15; 6(2):167-76. PubMed ID: 16740143
    [Abstract] [Full Text] [Related]

  • 14. Meta-Analysis of the COMT Val158Met Polymorphism in Major Depressive Disorder: Effect of Ethnicity.
    Wang M, Ma Y, Yuan W, Su K, Li MD.
    J Neuroimmune Pharmacol; 2016 Sep 15; 11(3):434-45. PubMed ID: 26803486
    [Abstract] [Full Text] [Related]

  • 15. Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia.
    Handoko HY, Nyholt DR, Hayward NK, Nertney DA, Hannah DE, Windus LC, McCormack CM, Smith HJ, Filippich C, James MR, Mowry BJ.
    Mol Psychiatry; 2005 Jun 15; 10(6):589-97. PubMed ID: 15505638
    [Abstract] [Full Text] [Related]

  • 16. Association between catechol-O-methyl transferase gene polymorphisms and fibromyalgia in a Korean population: A case-control study.
    Park DJ, Kim SH, Nah SS, Lee JH, Kim SK, Lee YA, Hong SJ, Kim HS, Lee HS, Kim HA, Joung CI, Kim SH, Lee SS.
    Eur J Pain; 2016 Aug 15; 20(7):1131-9. PubMed ID: 26849490
    [Abstract] [Full Text] [Related]

  • 17. Lack of association between COMT Val158Met polymorphism and late-onset Alzheimer's disease in Han Chinese.
    Zhou J, Li XM, Jiang T, Liu Y, Chi S, Yu JT, Tan L.
    Neurosci Lett; 2013 Oct 25; 554():162-6. PubMed ID: 24035893
    [Abstract] [Full Text] [Related]

  • 18. Interaction between cytochrome P450 2A6 and Catechol-O-Methyltransferase genes and their association with smoking risk in young men.
    Ou WC, Huang YC, Huang CL, Lin MH, Chen YC, Chen YJ, Liu CN, Chen MC, Huang CS, Chen PL.
    Behav Brain Funct; 2017 May 04; 13(1):8. PubMed ID: 28472995
    [Abstract] [Full Text] [Related]

  • 19. Catechol-O-methyltransferase Val158Met polymorphism: modulation of wearing-off susceptibility in a Chinese cohort of Parkinson's disease.
    Wu H, Dong F, Wang Y, Xiao Q, Yang Q, Zhao J, Quinn TJ, Chen SD, Liu J.
    Parkinsonism Relat Disord; 2014 Oct 04; 20(10):1094-6. PubMed ID: 25108642
    [Abstract] [Full Text] [Related]

  • 20. Catechol-O-methyltransferase (COMT) gene variants and pain in chronic pancreatitis.
    van Esch AA, de Vries E, Te Morsche RH, van Oijen MG, Jansen JB, Drenth JP.
    Neth J Med; 2011 Oct 04; 69(7):330-4. PubMed ID: 21934178
    [Abstract] [Full Text] [Related]

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