Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1→q11.2
- 30 April 1992
- journal article
- research article
- Published by Elsevier BV in Genomics
- Vol. 12 (4), 822-825
- https://doi.org/10.1016/0888-7543(92)90316-k
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- The Inheritance of human erythrocyte catechol-O-methyltransferase activityClinical Genetics, 2008
- Electrophoretic analysis of low and high activity forms of catechol-O-methyltransferase in human erythrocytesLife Sciences, 1992
- Cloning and Characterization of Human Placental Catechol--Methyltransferase cDNADNA and Cell Biology, 1991
- Human differentiation-stimulating factor (leukemia inhibitory factor, human interleukin DA) gene maps distal to the Ewing sarcoma breakpoint on 22qCytogenetic and Genome Research, 1989
- Assignment of the catechol-O-methyltransferase gene to human chromosome 22 in somatic cell hybridsHuman Genetics, 1986
- Purification and Kinetic Mechanism of Human Brain Soluble Catechol-O-MethyltransferaseJournal of Neurochemistry, 1985
- Soluble and Particulate Forms of Rat Catechol‐O‐Methyltransferase Distinguished by Gel Electrophoresis and Immune FixationJournal of Neurochemistry, 1985
- Characterization of Membrane‐Bound and Soluble Catechol‐O‐Methyltransferase from Human Frontal CortexJournal of Neurochemistry, 1984
- Platelet phenol sulfotransferase and erythrocyte catechol-O-methytransferase activities: Correlation with methyldopa metabolismClinical Pharmacology & Therapeutics, 1984
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityAnalytical Biochemistry, 1983