| 1 | MAOA, MAOA/BD, MAOB
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| MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus.
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| Saito M, Yamagata T, Matsumoto A, Shiba Y, Nagashima M, Taniguchi S, Jimbo E, Momoi MY.
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| Brain Dev rain Dev. 2013 Feb 13. doi:pii: S0387-7604(13)00020-X. 10.1016/j.braindev.2013.01.004. [Epub ahead of print]
2013
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| 2 | MAOB
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| G/A polymorphism in intronic sequence affects the processing of MAO-B gene in patients with Parkinson disease.
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| Jakubauskiene E, Janaviciute V, Peciuliene I, Söderkvist P, Kanopka A.
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| FEBS Lett 586(20):3698-704. doi: 10.1016/j.febslet.2012.08.028. Epub 2012 Sep 10. Erratum in: FEBS Lett. 2013 Jan 31;587(3):302-3.
2012
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| 3 | MAOB
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| Comparative platelet proteome analysis reveals an increase of monoamine oxidase-B protein expression in Alzheimer's disease but not in non-demented Parkinson's disease patients.
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| Zellner M, Baureder M, Rappold E, Bugert P, Kotzailias N, Babeluk R, Baumgartner R, Attems J, Gerner C, Jellinger K, Roth E, Oehler R, Umlauf E.
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| J Proteomics 75(7):2080-92. doi: 10.1016/j.jprot.2012.01.014. Epub 2012 Jan 17.
2012
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| 4 | DUPXPP, MAOA, MAOB, NDP
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| Duplication of MAOA, MAOB, and NDP in a patient with mental retardation and epilepsy.
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| Klitten LL, Mřller RS, Ravn K, Hjalgrim H, Tommerup N.
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| Eur J Hum Genet 19(1):1-2. Epub 2010 Sep 1. No abstract available. PMID: 20808325 2011
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| 5 | MAOA, MAOB
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| Behavioral outcomes of monoamine oxidase deficiency: preclinical and clinical evidence.
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| Bortolato M, Shih JC.
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| Int Rev Neurobiol 100:13-42. doi: 10.1016/B978-0-12-386467-3.00002-9. Review.
2011
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| 6 | MAOA, MAOB
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| Structural properties of human monoamine oxidases A and B.
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| Binda C, Mattevi A, Edmondson DE.
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| Int Rev Neurobiol 100:1-11. doi: 10.1016/B978-0-12-386467-3.00001-7. Review.
2011
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| 7 | MAOA, MAOB
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| Transcriptional regulation and multiple functions of MAO genes.
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| Shih JC, Wu JB, Chen K.
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| J Neural Transm 118(7):979-86. doi: 10.1007/s00702-010-0562-9. Epub 2011 Feb 27. Review.
2011
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| 8 | MAOA, MAOB, PRKN
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| Parkin degrades estrogen-related receptors to limit the expression of monoamine oxidases.
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| Ren Y, Jiang H, Ma D, Nakaso K, Feng J.
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| Hum Mol Genet 20(6):1074-83. doi: 10.1093/hmg/ddq550. Epub 2010 Dec 21. 2011
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| 9 | DELXP11, MAOA, MAOA/BD, MAOB
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| Deletion of MAOA and MAOB in a male patient causes severe developmental delay, intermittent hypotonia and stereotypical hand movements.
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| Whibley A, Urquhart J, Dore J, Willatt L, Parkin G, Gaunt L, Black G, Donnai D, Raymond FL.
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| Eur J Hum Genet 18(10):1095-9. Epub 2010 May 19.PMID: 20485326 [ 2010
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| 10 | DELXP11, MAOA, MAOB, ND, NDP
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| Co-segregation of Norrie disease and idiopathic pulmonary hypertension in a family with a microdeletion of the NDP region at Xp11.3-p11.4.
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| Staropoli JF, Xin W, Sims KB.
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| J Med Genet 47(11):786-90. Epub 2010 Aug 2.PMID: 20679667 2010
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| 11 | MAOA, MAOB
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| Monoamine oxidases regulate telencephalic neural progenitors in late embryonic and early postnatal development.
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| Cheng A, Scott AL, Ladenheim B, Chen K, Ouyang X, Lathia JD, Mughal M, Cadet JL, Mattson MP, Shih JC.
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| J Neurosci 30(32):10752-62. doi: 10.1523/JNEUROSCI.2037-10.2010.
2010
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| 12 | MAOA, MAOB
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| Platelet monoamine oxidase activity in children with attention-deficit/hyperactivity disorder.
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| Nedic G, Pivac N, Hercigonja DK, Jovancevic M, Curkovic KD, Muck-Seler D.
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| Psychiatry Res 175(3):252-5. doi: 10.1016/j.psychres.2009.08.013.
2010
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| 13 | MAOB
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| Recent adaptive selection at MAOB and ancestral susceptibility to schizophrenia.
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| Carrera N, Sanjuán J, Moltó MD, Carracedo A, Costas J.
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| Am J Med Genet B Neuropsychiatr Genet 150B(3):369-74. doi: 10.1002/ajmg.b.30823.
2009
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| 14 | FGF20, MAOB
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| Gene-gene interaction between FGF20 and MAOB in Parkinson disease.
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| Gao X, Scott WK, Wang G, Mayhew G, Li YJ, Vance JM, Martin ER.
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| Ann Hum Genet 72(Pt 2):157-62. Epub 2008 Jan 20.PMID: 18205889 2008
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| 15 | DELXP11, EFHC2, MAOA, MAOB, ND, NDP
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| Contiguous deletion of the NDP, MAOA, MAOB, and EFHC2 genes in a patient with Norrie disease, severe psychomotor retardation and myoclonic epilepsy.
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| Rodriguez-Revenga L, Madrigal I, Alkhalidi LS, Armengol L, González E, Badenas C, Estivill X, Milŕ M.
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| Am J Med Genet A 143A(9):916-20.PMID: 17431911 2007
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| 16 | MAOA, MAOB
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| Association of variations in monoamine oxidases A and B with Parkinson's disease subgroups.
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| Parsian A, Racette B, Zhang ZH, Rundle M, Perlmutter JS.
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| Genomics 83(3):454-60. 2004
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| 17 | EGR1, MAOB
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| Activation of human monoamine oxidase B gene expression by a protein kinase C MAPK signal transduction pathway involves c-Jun and Egr-1.
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| Wong WK, Ou XM, Chen K, Shih JC.
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| J Biol Chem 277(25):22222-30. 2002
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| 18 | MAOB
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| Association of monoamine oxidase B alleles with age at onset in amyotrophic lateral sclerosis.
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| Orru S, Mascia V, Casula M, Giuressi E, Loizedda A, Carcassi C, Giagheddu M, Contu L.
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| Neuromuscul Disord 9(8):593-7. 1999
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| 19 | MAOB
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| Screening the monoamine oxidase B gene in 100 male patients with schizophrenia : a cluster of polymorphisms in African-Americans but lack of functionally significant sequence changes.
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| Sobell JL, et al.
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| Am J Med Genet 74 : 44-49. 1997
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| 20 | MAOA, MAOB, MRIB
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| Specific genetic deficiencies of the A and B isoenzymes of monoamine oxidase are characterized by distinct neurochemical and clinical phenotypes.
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| Lenders JWM, et al.
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| J Clin Invest 97 : 1010-1019. 1996
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| 21 | MAOA, MAOB
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| Linkage analysis of the monoamine A and B genes using newly-defined polymorphisms.
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| Harris BD, et al.
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| Cytogenet Cell Genet 62 : 236-237. 1993
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| 22 | MAOB
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| Dinucleotide repeat (TG)23 polymorphism in the MAOB gene.
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| Grimsby J, et al.
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| Nucleic Acids Res 20 : 924. 1992
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| 23 | MAOB
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| Highly polymorphic (GT)n repeat sequence in intron II of the human MAOB gene.
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| Konradi C, et al.
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| Genomics 12 : 176-177. 1992
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| 24 | DELXP11, MAOA, MAOB, ND, NDP
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| Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes.
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| Collins FA, Murphy DL, Reiss AL, Sims KB, Lewis JG, Freund L, Karoum F, Zhu D, Maumenee IH, Antonarakis SE.
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| Am J Med Genet 42(1):127-34.PMID: 1308352 [ 1992
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| 25 | MAOA, MAOB
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| Long range physical mapping and organisation of the region including the genes for monoamine oxidase A and B, (MAOA & MAOB).
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| Chen ZY, et al.
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| (HGM11) Cytogenet Cell Genet 58 : 2059. 1991
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| 26 | DXS7, MAOA, MAOB
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| Characterisation of a 650 kb yeast artificial chromosome (YAC) containing DXS7, MAOA and MAOB loci implications for the isolation of the Norrie disease locus.
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| Chen ZY, et al.
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| (HGM11) Cytogenet Cell Genet 58 : 2060. 1991
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| 27 | MAOA, MAOB, ND, NDP
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| Human monoamine oxidase A and B genes map to Xp11.23 and are deleted in a patient with Norrie disease.
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| Lan NC, Heinzmann C, Gal A, Klisak I, Orth U, Lai E, Grimsby J, Sparkes RS, Mohandas T, Shih JC.
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| Genomics 4 : 552-559. 1989
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| 28 | MAOA, MAOB
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| cDNA cloning of human liver monoamine oxidase A and B: Molecular basis of differences in enzymatic properties.
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| Bach AWJ, et al.
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| Proc Natl Acad Sci U S A 85 : 4934-4938. 1988
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| 29 | MAOA, MAOB
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| X-linked monoamine oxidase deficiency in humans.
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| Breakefield XO, et al.
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| Am J Hum Genet 43 : A178. 1988
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| 30 | MAOB
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| Assignment of genes for human monoamine oxidases A and B to the X chromosome.
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| Kochersperger LM, et al.
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| J Neurosci Res 16 : 601-616. 1986
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