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Journal Abstract Search

89 related items for PubMed ID: 9419949

  • 21. Polymorphisms of COMT (c.649G>A), MAO-A (c.1460C>T), NET (c.1287G>A) Genes and the Level of Catecholamines, Serotonin in Patients with Parkinson's Disease.
    Florczak-Wyspianska J, Rozycka A, Wolny L, Lianeri M, Kozubski W, Dorszewska J.
    DNA Cell Biol; 2017 Jun; 36(6):501-512. PubMed ID: 28418735
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  • 22. A genetic polymorphism of MAO-B modifies the association of cigarette smoking and Parkinson's disease.
    Checkoway H, Franklin GM, Costa-Mallen P, Smith-Weller T, Dilley J, Swanson PD, Costa LG.
    Neurology; 1998 May; 50(5):1458-61. PubMed ID: 9596006
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  • 25. Variations in the monoamine oxidase B (MAOB) gene are associated with Parkinson's disease.
    Mellick GD, Buchanan DD, McCann SJ, James KM, Johnson AG, Davis DR, Liyou N, Chan D, Le Couteur DG.
    Mov Disord; 1999 Mar; 14(2):219-24. PubMed ID: 10091612
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  • 27. Genetic polymorphism of dopamine D2 receptors in Parkinson's disease and interactions with cigarette smoking and MAO-B intron 13 polymorphism.
    Costa-Mallen P, Costa LG, Smith-Weller T, Franklin GM, Swanson PD, Checkoway H.
    J Neurol Neurosurg Psychiatry; 2000 Oct; 69(4):535-7. PubMed ID: 10990520
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  • 28. G/A polymorphism in intronic sequence affects the processing of MAO-B gene in patients with Parkinson disease.
    Jakubauskiene E, Janaviciute V, Peciuliene I, Söderkvist P, Kanopka A.
    FEBS Lett; 2012 Oct 19; 586(20):3698-704. PubMed ID: 22974659
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  • 29. The lack of association between monoamine oxidase (MAO) intron 13 polymorphism and platelet MAO-B activity among men.
    Pivac N, Knezevic J, Mustapic M, Dezeljin M, Muck-Seler D, Kozaric-Kovacic D, Balija M, Matijevic T, Pavelic J.
    Life Sci; 2006 May 30; 79(1):45-9. PubMed ID: 16427095
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  • 30. Genotype combinations for monoamine oxidase-B intron 13 polymorphism and dopamine D2 receptor TaqIB polymorphism are associated with ever-smoking status among men.
    Costa-Mallen P, Costa LG, Checkoway H.
    Neurosci Lett; 2005 Sep 09; 385(2):158-62. PubMed ID: 15955630
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  • 32. Monoamine oxidases A and B gene polymorphisms in migraine patients.
    Filic V, Vladic A, Stefulj J, Cicin-Sain L, Balija M, Sucic Z, Jernej B.
    J Neurol Sci; 2005 Feb 15; 228(2):149-53. PubMed ID: 15694196
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  • 35. [Association between cytochrome P-450 enzyme gene polymorphisms and Parkinson's disease].
    Wang J, Liu Z, Chen B.
    Zhonghua Yi Xue Za Zhi; 2000 Aug 15; 80(8):585-7. PubMed ID: 11798822
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  • 36. Association analysis of the functional monoamine oxidase A gene promotor polymorphism in migraine.
    Marziniak M, Mössner R, Benninghoff J, Syagailo YV, Lesch KP, Sommer C.
    J Neural Transm (Vienna); 2004 May 15; 111(5):603-9. PubMed ID: 15088153
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  • 37. Association study between schizophrenia and monoamine oxidase A and B DNA polymorphisms.
    Coron B, Campion D, Thibaut F, Dollfus S, Preterre P, Langlois S, Vasse T, Moreau V, Martin C, Charbonnier F, Laurent C, Mallet J, Petit M, Frebourg T.
    Psychiatry Res; 1996 Jun 01; 62(3):221-6. PubMed ID: 8804132
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  • 38. Characterization of the in vitro transcriptional activity of polymorphic alleles of the human monoamine oxidase-B gene.
    Costa-Mallen P, Kelada SN, Costa LG, Checkoway H.
    Neurosci Lett; 1996 Jun 01; 383(1-2):171-5. PubMed ID: 15936531
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  • 39. The association of monoamine oxidase B functional polymorphism with postoperative pain intensity.
    Serý O, Hrazdilová O, Didden W, Klenerová V, Staif R, Znojil V, Sevcík P.
    Neuro Endocrinol Lett; 2006 Jun 01; 27(3):333-7. PubMed ID: 16807522
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  • 40. Monoamine oxidase A gene polymorphism and the pathogenesis of sudden infant death syndrome.
    Courts C, Grabmüller M, Madea B.
    J Pediatr; 2013 Jul 01; 163(1):89-93. PubMed ID: 23391042
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