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 *

106 related articles for article (PubMed ID: 11700166)

  • 1. Monoamine oxidase deficiency: a cause of flushing and attention-deficit/ hyperactivity disorder?
    Cheung NW; Earl J
    Arch Intern Med; 2001 Nov; 161(20):2503-4. PubMed ID: 11700166
    [No Abstract]   [Full Text] [Related]  

  • 2. Associations of MAOA-VNTR or 5HTT-LPR alleles with attention-deficit hyperactivity disorder symptoms are moderated by platelet monoamine oxidase B activity.
    Wargelius HL; Malmberg K; Larsson JO; Oreland L
    Psychiatr Genet; 2012 Feb; 22(1):42-5. PubMed ID: 21610556
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2A, DDC and MAOB.
    Ribasés M; Ramos-Quiroga JA; Hervás A; Bosch R; Bielsa A; Gastaminza X; Artigas J; Rodriguez-Ben S; Estivill X; Casas M; Cormand B; Bayés M
    Mol Psychiatry; 2009 Jan; 14(1):71-85. PubMed ID: 17938636
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic deficiencies of monoamine oxidase enzymes: a key to understanding the function of the enzymes in humans.
    Lenders JW; Brunner HG; Murphy DL; Eisenhofer G
    Adv Pharmacol; 1998; 42():297-301. PubMed ID: 9327899
    [No Abstract]   [Full Text] [Related]  

  • 5. Association study between the monoamine oxidase A gene and attention deficit hyperactivity disorder in Taiwanese samples.
    Xu X; Brookes K; Chen CK; Huang YS; Wu YY; Asherson P
    BMC Psychiatry; 2007 Feb; 7():10. PubMed ID: 17328795
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Family-based and association studies of monoamine oxidase A and attention deficit hyperactivity disorder (ADHD): preferential transmission of the long promoter-region repeat and its association with impaired performance on a continuous performance test (TOVA).
    Manor I; Tyano S; Mel E; Eisenberg J; Bachner-Melman R; Kotler M; Ebstein RP
    Mol Psychiatry; 2002; 7(6):626-32. PubMed ID: 12140786
    [TBL] [Abstract][Full Text] [Related]  

  • 7. MAOA is associated with methylphenidate improvement of oppositional symptoms in boys with attention deficit hyperactivity disorder.
    Guimarães AP; Zeni C; Polanczyk G; Genro JP; Roman T; Rohde LA; Hutz MH
    Int J Neuropsychopharmacol; 2009 Jun; 12(5):709-14. PubMed ID: 19309535
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Regional cerebral cortical activation in monoamine oxidase A-deficient mice: differential effects of chronic versus acute elevations in serotonin and norepinephrine.
    Holschneider DP; Scremin OU; Huynh L; Chen K; Seif I; Shih JC
    Neuroscience; 2000; 101(4):869-77. PubMed ID: 11113335
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Study of susceptibility loci located within Xp11 in attention deficit hyperactivity disorder].
    Jiang S; Xin R; Qian Y; Lin S; Li F; Wu X; Wang D; Tang G; Jiang K
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Jun; 18(3):169-72. PubMed ID: 11402442
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Urinary monoamine metabolites in children with minimal brain dysfunction.
    Wender PH; Epstein RS; Kopin IJ; Gordon EK
    Am J Psychiatry; 1971 Apr; 127(10):1411-5. PubMed ID: 5549938
    [No Abstract]   [Full Text] [Related]  

  • 11. [Content of serotonin, catecholamines and monoamine oxidase activity of the lung in disease].
    Goncharova VA
    Vopr Med Khim; 1983; 29(6):34-9. PubMed ID: 6422630
    [TBL] [Abstract][Full Text] [Related]  

  • 12. MAO-A dysfunctions and aggressive behaviors in patients with ADHD.
    Angriman M; Cortese S
    Hum Psychopharmacol; 2008 Jul; 23(5):437; author reply 438. PubMed ID: 18566955
    [No Abstract]   [Full Text] [Related]  

  • 13. Association between the polymorphisms of the selected genes encoding dopaminergic system with ADHD and autism.
    Nikolac Perkovic M; Nedic Erjavec G; Stefulj J; Muck-Seler D; Pivac N; Kocijan Hercigonja D; Hranilovic D; Curkovic M; Dodig-Curkovic K
    Psychiatry Res; 2014 Jan; 215(1):260-1. PubMed ID: 24210742
    [No Abstract]   [Full Text] [Related]  

  • 14. Studies on monoamine oxidase of rat heart mitochondria. I. Purification and properties of the enzyme.
    Sen R; Parmar SS; Guha SR
    Acta Biol Med Ger; 1968; 21(1):1-11. PubMed ID: 5724353
    [No Abstract]   [Full Text] [Related]  

  • 15. [Metabolism of several free amino acids, catecholamines and serotonin in the brain under the influence of natural physiologic agents].
    Khachatrian GS; Stepanian LA; Avetisian NG
    Vopr Biokhim Mozga; 1973; 8():221-37. PubMed ID: 4804889
    [No Abstract]   [Full Text] [Related]  

  • 16. [Evaluation of the activity of the adrenergic and serotoninergic systems in chronic renal failure in humans and in rats with experimental uremia].
    Ksiazek A
    Pol Tyg Lek; 1978 Jun; 33(26):1045-6. PubMed ID: 212718
    [No Abstract]   [Full Text] [Related]  

  • 17. Monoamine oxidase A polymorphism moderates stability of attention problems and susceptibility to life stress during adolescence.
    Zohsel K; Bianchi V; Mascheretti S; Hohm E; Schmidt MH; Esser G; Brandeis D; Banaschewski T; Nobile M; Laucht M
    Genes Brain Behav; 2015 Nov; 14(8):565-72. PubMed ID: 26449393
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Histochemistry of monoamine metabolism].
    Shimizu N
    Shinkei Kenkyu No Shimpo; 1968 Dec; 12(4):851-8. PubMed ID: 4898005
    [No Abstract]   [Full Text] [Related]  

  • 19. No allele variation of the MAOA gene promoter in male Chinese subjects with attention deficit hyperactivity disorder.
    Lung FW; Yang P; Cheng TS; Kao WT
    Neuropsychobiology; 2006; 54(3):147-51. PubMed ID: 17230031
    [TBL] [Abstract][Full Text] [Related]  

  • 20. New insights into Brunner syndrome and potential for targeted therapy.
    Palmer EE; Leffler M; Rogers C; Shaw M; Carroll R; Earl J; Cheung NW; Champion B; Hu H; Haas SA; Kalscheuer VM; Gecz J; Field M
    Clin Genet; 2016 Jan; 89(1):120-7. PubMed ID: 25807999
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.