References analysis of the Wikipedia article "モノアミン酸化酵素B" in the Japanese version

doi.org

“Redefining differential roles of MAO-A in dopamine degradation and MAO-B in tonic GABA synthesis”. Experimental & Molecular Medicine 53 (7): 1148–1158. (July 2021). doi:10.1038/s12276-021-00646-3. PMC 8333267. PMID 34244591.

“Structural insights into the mechanism of amine oxidation by monoamine oxidases A and B”. Arch. Biochem. Biophys. 464 (2): 269–76. (August 2007). doi:10.1016/j.abb.2007.05.006. PMC 1993809. PMID 17573034.

“Crystal structures of monoamine oxidase B in complex with four inhibitors of the N-propargylaminoindan class”. J. Med. Chem. 47 (7): 1767–74. (March 2004). doi:10.1021/jm031087c. PMID 15027868.

“Structure-function relationships in flavoenzyme-dependent amine oxidations: A comparison of polyamine oxidase and monoamine oxidase”. Journal of Biological Chemistry 277 (27): 23973–23976. (July 5, 2002). doi:10.1074/jbc.R200005200. PMID 12015330.

“Therapeutic applications of selective and non-selective inhibitors of monoamine oxidase A and B that do not cause significant tyramine potentiation”. Neurotoxicology 25 (1–2): 243–50. (January 2004). doi:10.1016/S0161-813X(03)00103-7. PMID 14697899.

“MAO-inhibitors in Parkinson's Disease”. Exp Neurobiol 20 (1): 1–17. (March 2011). doi:10.5607/en.2011.20.1.1. PMC 3213739. PMID 22110357.

“Increased monoamine oxidase B activity in plaque-associated astrocytes of Alzheimer brains revealed by quantitative enzyme radioautography”. Neuroscience 62 (1): 15–30. (September 1994). doi:10.1016/0306-4522(94)90311-5. PMID 7816197.

“Metabolic control analysis in a cellular model of elevated MAO-B: relevance to Parkinson's disease”. Neurotox Res 16 (3): 186–93. (October 2009). doi:10.1007/s12640-009-9032-2. PMC 2727365. PMID 19526285.

“Molecular mechanism of the relation of monoamine oxidase B and its inhibitors to Parkinson's disease: Possible implications of glial cells”. Oxidative Stress and Neuroprotection. Journal of Neural Transmission. Supplementa. 71. (2006). 53–65. doi:10.1007/978-3-211-33328-0_7. ISBN 978-3-211-33327-3. PMID 17447416

“Perspectives on MAO-B in aging and neurological disease: where do we go from here?”. Mol. Neurobiol. 30 (1): 77–89. (August 2004). doi:10.1385/MN:30:1:077. PMID 15247489.

“Negative emotionality: monoamine oxidase B gene variants modulate personality traits in healthy humans”. J Neural Transm 116 (10): 1323–34. (October 2009). doi:10.1007/s00702-009-0281-2. PMC 3653168. PMID 19657584.

“Monoamine oxidases (MAO) in the pathogenesis of heart failure and ischemia/reperfusion injury”. Biochim. Biophys. Acta 1813 (7): 1323–32. (July 2011). doi:10.1016/j.bbamcr.2010.09.010. PMC 3030628. PMID 20869994.

“Monoamine oxidase B prompts mitochondrial and cardiac dysfunction in pressure overloaded hearts”. Antioxid. Redox Signal. 20 (2): 267–80. (January 2014). doi:10.1089/ars.2012.4616. PMC 3887464. PMID 23581564.

“Monoamine oxidase B is elevated in Alzheimer disease neurons, is associated with γ-secretase and regulates neuronal amyloid β-peptide levels”. Alzheimer's Research & Therapy 9 (1): 57. (August 2017). doi:10.1186/s13195-017-0279-1. PMC 5540560. PMID 28764767.

“Monoamine oxidase inhibitors: promising therapeutic agents for Alzheimer's disease (Review)”. Molecular Medicine Reports 9 (5): 1533–41. (May 2014). doi:10.3892/mmr.2014.2040. PMID 24626484.

“Increased stress response and beta-phenylethylamine in MAOB-deficient mice.”. Nature Genetics 17 (2): 206–10. (October 1997). doi:10.1038/ng1097-206. PMID 9326944.

“Monoamine oxidase: from genes to behavior.”. Annual Review of Neuroscience 22: 197–217. (1999). doi:10.1146/annurev.neuro.22.1.197. PMC 2844879. PMID 10202537.

“Cloning, after cloning, knock-out mice, and physiological functions of MAO A and B.”. Neurotoxicology 25 (1–2): 21–30. (January 2004). doi:10.1016/s0161-813x(03)00112-8. PMID 14697877.

“Behavioral disinhibition and reduced anxiety-like behaviors in monoamine oxidase B-deficient mice.”. Neuropsychopharmacology 34 (13): 2746–57. (December 2009). doi:10.1038/npp.2009.118. PMC 2783894. PMID 19710633.

“Monoamine oxidase enzymes and oxidative stress in the rat optic nerve: age-related changes”. International Journal of Experimental Pathology 93 (6): 401–5. (December 2012). doi:10.1111/j.1365-2613.2012.00832.x. PMC 3521895. PMID 23082958.

“Chronic treatment of (-)deprenyl prolongs the life span of male Fischer 344 rats. Further evidence”. Life Sci. 52 (3): 281–8. (1993). doi:10.1016/0024-3205(93)90219-S. PMID 8423709.

“Specific genetic deficiencies of the A and B isoenzymes of monoamine oxidase are characterized by distinct neurochemical and clinical phenotypes”. J. Clin. Invest. 97 (4): 1010–9. (February 1996). doi:10.1172/JCI118492. PMC 507147. PMID 8613523.

“The emerging role of trace amine-associated receptor 1 in the functional regulation of monoamine transporters and dopaminergic activity”. J. Neurochem. 116 (2): 164–176. (January 2011). doi:10.1111/j.1471-4159.2010.07109.x. PMC 3005101. PMID 21073468.

“Antiaging treatments have been legally prescribed for approximately thirty years”. Ann. N. Y. Acad. Sci. 1019 (1): 64–9. (June 2004). Bibcode: 2004NYASA1019...64U. doi:10.1196/annals.1297.014. PMID 15246996.

“Impact of species-dependent differences on screening, design, and development of MAO B inhibitors”. J. Med. Chem. 49 (21): 6264–72. (October 2006). doi:10.1021/jm060441e. PMID 17034132.

“Natural and synthetic geiparvarins are strong and selective MAO-B inhibitors. Synthesis and SAR studies”. Bioorg. Med. Chem. Lett. 12 (24): 3551–5. (December 2002). doi:10.1016/S0960-894X(02)00798-9. PMID 12443774.

“Inhibition of platelet MAO-B by kava pyrone-enriched extract from Piper methysticum Forster (kava-kava)”. Pharmacopsychiatry 31 (5): 187–92. (September 1998). doi:10.1055/s-2007-979325. PMID 9832350.

Hou, Wen-Chi; Lin, Rong-Dih; Chen, Cheng-Tang; Lee, Mei-Hsien (2005-08-22). “Monoamine oxidase B (MAO-B) inhibition by active principles from Uncaria rhynchophylla”. Journal of Ethnopharmacology 100 (1-2): 216–220. doi:10.1016/j.jep.2005.03.017. ISSN 0378-8741. PMID 15890481.

“Evidences for the involvement of monoaminergic and GABAergic systems in antidepressant-like activity of garlic extract in mice”. Indian Journal of Pharmacology 40 (4): 175–179. (August 2008). doi:10.4103/0253-7613.43165. PMC 2792615. PMID 20040952.

“Monoamine oxidase inhibition by Rhodiola rosea L. roots”. Journal of Ethnopharmacology 122 (2): 397–401. (March 2009). doi:10.1016/j.jep.2009.01.007. PMID 19168123.

“Solid-phase synthesis and insights into structure-activity relationships of safinamide analogues as potent and selective inhibitors of type B monoamine oxidase”. Journal of Medicinal Chemistry 50 (20): 4909–16. (October 2007). doi:10.1021/jm070725e. PMID 17824599.

compound #2d, “Synthesis, structural reassignment, and biological activity of type B MAO inhibitors based on the 5H-indeno[1,2-c]pyridazin-5-one core”. J. Med. Chem. 49 (12): 3743–7. (June 2006). doi:10.1021/jm051091j. PMID 16759116.

“Synthesis and monoamine oxidase inhibitory activity of new pyridazine-, pyrimidine- and 1,2,4-triazine-containing tricyclic derivatives”. Journal of Medicinal Chemistry 50 (22): 5364–71. (November 2007). doi:10.1021/jm070728r. PMID 17910428.

“Chalcones: a valid scaffold for monoamine oxidases inhibitors”. J. Med. Chem. 52 (9): 2818–24. (May 2009). doi:10.1021/jm801590u. PMID 19378991.

compound #21, “Simple, potent, and selective pyrrole inhibitors of monoamine oxidase types A and B”. J. Med. Chem. 46 (6): 917–20. (March 2003). doi:10.1021/jm0256124. PMID 12620068.

compound # (R)-8b, “Synthesis, stereochemical separation, and biological evaluation of selective inhibitors of human MAO-B: 1-(4-arylthiazol-2-yl)-2-(3-methylcyclohexylidene)hydrazines”. J. Med. Chem. 53 (17): 6516–20. (September 2010). doi:10.1021/jm100120s. hdl:11573/360702. PMID 20715818.

compound #18, “Selective inhibitory activity against MAO and molecular modeling studies of 2-thiazolylhydrazone derivatives”. J. Med. Chem. 50 (4): 707–12. (February 2007). doi:10.1021/jm060869d. hdl:11573/231039. PMID 17253676.

compound #3g, “Monoamine oxidase isoform-dependent tautomeric influence in the recognition of 3,5-diaryl pyrazole inhibitors”. J. Med. Chem. 50 (3): 425–8. (February 2007). doi:10.1021/jm060868l. PMID 17266193.

compound #(S)-1, “Synthesis, molecular modeling studies, and selective inhibitory activity against monoamine oxidase of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydro-(1H)- pyrazole derivatives”. J. Med. Chem. 48 (23): 7113–22. (November 2005). doi:10.1021/jm040903t. PMID 16279769.

“Development of selective and reversible pyrazoline based MAO-B inhibitors: virtual screening, synthesis and biological evaluation”. Bioorg. Med. Chem. Lett. 21 (7): 1969–73. (April 2011). doi:10.1016/j.bmcl.2011.02.030. PMID 21377879.

compound #41, “Structural insights into monoamine oxidase inhibitory potency and selectivity of 7-substituted coumarins from ligand- and target-based approaches”. Journal of Medicinal Chemistry 49 (16): 4912–25. (2006). doi:10.1021/jm060183l. PMID 16884303.

compound #2, “MAO inhibitory activity modulation: 3-Phenylcoumarins versus 3-benzoylcoumarins”. Bioorg. Med. Chem. Lett. 21 (14): 4224–7. (July 2011). doi:10.1016/j.bmcl.2011.05.074. PMID 21684743.

“New halogenated 3-phenylcoumarins as potent and selective MAO-B inhibitors”. Bioorg. Med. Chem. Lett. 20 (17): 5157–60. (September 2010). doi:10.1016/j.bmcl.2010.07.013. PMID 20659799.

“Synthesis and evaluation of 6-methyl-3-phenylcoumarins as potent and selective MAO-B inhibitors”. Bioorg. Med. Chem. Lett. 19 (17): 5053–5. (September 2009). doi:10.1016/j.bmcl.2009.07.039. PMID 19628387.

“A new series of 3-phenylcoumarins as potent and selective MAO-B inhibitors”. Bioorg. Med. Chem. Lett. 19 (12): 3268–70. (June 2009). doi:10.1016/j.bmcl.2009.04.085. PMID 19423346.

compound #9, #12, “Chromone 3-phenylcarboxamides as potent and selective MAO-B inhibitors”. Bioorg. Med. Chem. Lett. 21 (2): 707–9. (January 2011). doi:10.1016/j.bmcl.2010.11.128. PMID 21194943.

compound #9i, “Inhibition of monoamine oxidase by selected C5- and C6-substituted isatin analogues”. Bioorg. Med. Chem. 19 (1): 261–74. (January 2011). doi:10.1016/j.bmc.2010.11.028. PMID 21134756.

compound #5c, “Inhibition of monoamine oxidase by C5-substituted phthalimide analogues”. Bioorg. Med. Chem. 19 (16): 4829–40. (August 2011). doi:10.1016/j.bmc.2011.06.070. PMID 21778064.

“8-Aryl- and alkyloxycaffeine analogues as inhibitors of monoamine oxidase”. Eur J Med Chem 46 (8): 3474–85. (August 2011). doi:10.1016/j.ejmech.2011.05.014. PMID 21621312.

“Inhibition of monoamine oxidase by 8-benzyloxycaffeine analogues”. Bioorg. Med. Chem. 18 (3): 1018–28. (February 2010). doi:10.1016/j.bmc.2009.12.064. PMID 20093036.

“Inhibition of monoamine oxidase B by analogues of the adenosine A2A receptor antagonist (E)-8-(3-chlorostyryl)caffeine (CSC)”. Bioorg. Med. Chem. 14 (10): 3512–21. (May 2006). doi:10.1016/j.bmc.2006.01.011. PMID 16442801.

“Dual inhibition of monoamine oxidase B and antagonism of the adenosine A(2A) receptor by (E,E)-8-(4-phenylbutadien-1-yl)caffeine analogues”. Bioorganic & Medicinal Chemistry 16 (18): 8676–84. (September 2008). doi:10.1016/j.bmc.2008.07.088. PMID 18723354.

“Indazole- and indole-5-carboxamides: selective and reversible monoamine oxidase B inhibitors with subnanomolar potency”. Journal of Medicinal Chemistry 57 (15): 6679–6703. (August 2014). doi:10.1021/jm500729a. PMID 24955776.

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“Reversible monoamine oxidase-A inhibitors in resistant major depression”. Clin Neuropharmacol 16 (Suppl 2): S69–76. (1993). PMID 8313400.