Specific genetic deficiencies of the A and B isoenzymes of monoamine oxidase are characterized by distinct neurochemical and clinical phenotypes - Wikidata - wikimedia - TriplyDB

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

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

http://www.wikidata.org/entity/Q24562650

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The dopamine metabolite 3-methoxytyramine is a neuromodulator Monoamine oxidase A and A/B knockout mice display autistic-like features.Negative emotionality: monoamine oxidase B gene variants modulate personality traits in healthy humans Monoamine oxidases (MAO) in the pathogenesis of heart failure and ischemia/reperfusion injury Behavioral disinhibition and reduced anxiety-like behaviors in monoamine oxidase B-deficient mice Key Targets for Multi-Target Ligands Designed to Combat Neurodegeneration Biochemical, behavioral, physiologic, and neurodevelopmental changes in mice deficient in monoamine oxidase A or B Behavioral outcomes of monoamine oxidase deficiency: preclinical and clinical evidence.De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: a genomics approach to personalized medicine.Cognitive abnormalities and hippocampal alterations in monoamine oxidase A and B knockout mice.Comparative gene expression profiling between human cultured myotubes and skeletal muscle tissue.Monoamine oxidase A-mediated enhanced catabolism of norepinephrine contributes to adverse remodeling and pump failure in hearts with pressure overload.Monoamine oxidase in neuropsychiatry and behavior.Forebrain-specific expression of monoamine oxidase A reduces neurotransmitter levels, restores the brain structure, and rescues aggressive behavior in monoamine oxidase A-deficient mice.Biotransformation of xenobiotics by amine oxidases.Deletion of MAOA and MAOB in a male patient causes severe developmental delay, intermittent hypotonia and stereotypical hand movements Catecholamines 101 Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia.Comparison of Monoamine Oxidase Inhibitors in Decreasing Production of the Autotoxic Dopamine Metabolite 3,4-Dihydroxyphenylacetaldehyde in PC12 Cells.Mutations in monoamine oxidase (MAO) genes in mice lead to hypersensitivity to serotonin-enhancing drugs: implications for drug side effects in humans Early infant exposure to excess multivitamin: a risk factor for autism?Polymorphism in serotonin receptor 3B is associated with pain catastrophizing.Cortical enlargement in autism is associated with a functional VNTR in the monoamine oxidase A gene Screen for MAOA mutations in target human groups Evaluation of heritable determinants of blood and brain serotonin homeostasis using recombinant inbred mice Dopamine and renal function and blood pressure regulation.Monoamine oxidase: radiotracer chemistry and human studies.Monoamine neurotransmitter disorders--clinical advances and future perspectives.New insights into Brunner syndrome and potential for targeted therapy.Pilot study indicate role of preferentially transmitted monoamine oxidase gene variants in behavioral problems of male ADHD probands.Adaptive changes in postsynaptic dopamine receptors despite unaltered dopamine dynamics in mice lacking monoamine oxidase B.Platelet monoamine oxidase type B, MAOB intron 13 and MAOA-uVNTR polymorphism and symptoms of post-traumatic stress disorder.Pathway design using de novo steps through uncharted biochemical spaces.Renalase, a novel soluble FAD-dependent protein, is synthesized in the brain and peripheral nerves.Host-parasite co-metabolic activation of antitrypanosomal aminomethyl-benzoxaboroles.A novel contiguous deletion involving NDP, MAOB and EFHC2 gene in a patient with familial Norrie disease: bilateral blindness and leucocoria without other deficits.

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

http://www.wikidata.org/entity/Q24562650

description

1996 nî lūn-bûn

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1996 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

1996 թվականի փետրվարին հրատարակված գիտական հոդված

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1996年の論文

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1996年論文

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1996年論文

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1996年論文

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1996年論文

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1996年論文

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1996年论文

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Specific genetic deficiencies ...... emical and clinical phenotypes

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Specific genetic deficiencies ...... emical and clinical phenotypes

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Specific genetic deficiencies ...... emical and clinical phenotypes

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Specific genetic deficiencies ...... emical and clinical phenotypes

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Specific genetic deficiencies ...... emical and clinical phenotypes

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Specific genetic deficiencies ...... emical and clinical phenotypes

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Specific genetic deficiencies ...... emical and clinical phenotypes

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Specific genetic deficiencies ...... emical and clinical phenotypes

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Specific genetic deficiencies ...... emical and clinical phenotypes

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P1433

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Journal of Clinical Investigation

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Specific genetic deficiencies ...... emical and clinical phenotypes

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P2093

A H van Gennip

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C H Konings

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D L Murphy

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F Karoum

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G Eisenhofer

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H G Brunner

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I J Kopin

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J W Lenders

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L M Wagemakers

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N G Abeling

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P2860

Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A

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

Aggressive behavior and altered amounts of brain serotonin and norepinephrine in mice lacking MAOA

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

A simple salting out procedure for extracting DNA from human nucleated cells

The deduced amino acid sequences of human platelet and frontal cortex monoamine oxidase B are identical

Assignment of genes for human monoamine oxidases A and B to the X chromosome

Biochemistry and genetics of monoamine oxidase.

The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3.

Isolation of a candidate gene for Norrie disease by positional cloning.

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1010-9

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3950523

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10.1172/JCI118492

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4

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97

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8613523

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507147

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