PMC Links for OMIM (Select 309860) - PMC

Select item 29874511.

Deletion of MAOA and MAOB in a male patient causes severe developmental delay, intermittent hypotonia and stereotypical hand movements

Annabel Whibley, Jill Urquhart, Jonathan Dore, Lionel Willatt, Georgina Parkin, Lorraine Gaunt, Graeme Black, Dian Donnai, F Lucy Raymond

Eur J Hum Genet. 2010 Oct; 18(10): 1095–1099. Published online 2010 May 19. doi: 10.1038/ejhg.2010.41

PMCID:: PMC2987451

Abstract Article PDF–416K

Select item 28619022.

A Spontaneous Point Mutation Produces Monoamine Oxidase A/B Knock-out Mice with Greatly Elevated Monoamines and Anxiety-like Behavior

Kevin Chen, Daniel P. Holschneider, Weihua Wu, Igor Rebrin, Jean C. Shih

J Biol Chem. Author manuscript; available in PMC 2010 Apr 30.

Published in final edited form as: J Biol Chem. 2004 Sep 17; 279(38): 39645–39652. Published online 2004 Jul 22. doi: 10.1074/jbc.M405550200

PMCID:: PMC2861902

Abstract Article PDF–710K

Select item 16852933.

Segregation and linkage studies of plasma dopamine-beta-hydroxylase (DBH), erythrocyte catechol-O-methyltransferase (COMT), and platelet monoamine oxidase (MAO): possible linkage between the ABO locus and a gene controlling DBH activity.

L R Goldin, E S Gershon, C R Lake, D L Murphy, M McGinniss, R S Sparkes

Am J Hum Genet. 1982 Mar; 34(2): 250–262.

PMCID:: PMC1685293

Summary Page Browse PDF–1.1M

Select item 16843954.

Platelet monoamine oxidase (MAO) activity: evidence for a single major locus.

J Rice, P McGuffin, L R Goldin, E G Shaskan, E S Gershon

Am J Hum Genet. 1984 Jan; 36(1): 36–43.

PMCID:: PMC1684395

Summary Page Browse PDF–796K

Select item 16822785.

X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolism.

H G Brunner, M R Nelen, P van Zandvoort, N G Abeling, A H van Gennip, E C Wolters, M A Kuiper, H H Ropers, B A van Oost

Am J Hum Genet. 1993 Jun; 52(6): 1032–1039.

PMCID:: PMC1682278

Summary Page Browse PDF–1.0M

Select item 5071476.

Specific genetic deficiencies of the A and B isoenzymes of monoamine oxidase are characterized by distinct neurochemical and clinical phenotypes.

J W Lenders, G Eisenhofer, N G Abeling, W Berger, D L Murphy, C H Konings, L M Wagemakers, I J Kopin, F Karoum, A H van Gennip, H G Brunner

J Clin Invest. 1996 Feb 15; 97(4): 1010–1019. doi: 10.1172/JCI118492

PMCID:: PMC507147

Summary PDF–226K

Select item 2805527.

cDNA cloning of human liver monoamine oxidase A and B: molecular basis of differences in enzymatic properties.

A W Bach, N C Lan, D L Johnson, C W Abell, M E Bembenek, S W Kwan, P H Seeburg, J C Shih

Proc Natl Acad Sci U S A. 1988 Jul; 85(13): 4934–4938. doi: 10.1073/pnas.85.13.4934

PMCID:: PMC280552

Summary Page Browse PDF–1.1M

Select item 515078.

Human monoamine oxidase A and B genes exhibit identical exon-intron organization.

J Grimsby, K Chen, L J Wang, N C Lan, J C Shih

Proc Natl Acad Sci U S A. 1991 May 1; 88(9): 3637–3641. doi: 10.1073/pnas.88.9.3637

PMCID:: PMC51507

Summary Page Browse PDF–877K

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