Human retina-specific amine oxidase (RAO): cDNA cloning, tissue expression, and chromosomal mapping (Q24316466)

electron transfer activity

GOA release 2020-03-11

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GOA release 2020-03-11

author name string

Y Imamura

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R Kubota

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Y Wang

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S Asakawa

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J Kudoh

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Y Mashima

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Y Oguchi

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N Shimizu

Cloning and sequencing of phenylethylamine oxidase from Arthrobacter globiformis and implication of Tyr-382 as the precursor to its covalently bound quinone cofactor

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language of work or name

English

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publication date

1 March 1997

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277-83

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The sequence of human retinal S-antigen reveals similarities with alpha-transducin

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Cloning and sequencing of the peroxisomal amine oxidase gene from Hansenula polymorpha

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Cloning of the CDNA for a novel photoreceptor membrane protein (rom-1) identifies a disk rim protein family implicated in human retinopathies

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Identification of topaquinone and its consensus sequence in copper amine oxidases

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Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)

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Primary structure and functional expression from complementary DNA of the rod photoreceptor cyclic GMP-gated channel

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A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

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Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase

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Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase

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Isolation and nucleotide sequence of the gene encoding human rhodopsin

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Phenol emulsion-enhanced DNA-driven subtractive cDNA cloning: isolation of low-abundance monkey cortex-specific mRNAs

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Facilitation of GABAergic signaling in the retina by receptors stimulating adenylate cyclase

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Mutations in the gene encoding the alpha subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosa

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Copper/topa quinone-containing histamine oxidase from Arthrobacter globiformis. Molecular cloning and sequencing, overproduction of precursor enzyme, and generation of topa quinone cofactor.

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An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17q

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Molecular genetics of retinitis pigmentosa

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Molecular cloning and functional expression of different molecular forms of rat amiloride-binding proteins

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Identification of specific transducin alpha subunits in retinal rod and cone photoreceptors

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Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci

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Binding of diamine oxidase activity to rat and guinea pig microvascular endothelial cells. Comparisons with lipoprotein lipase binding

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Dopamine modulates GABAc receptors mediating inhibition of calcium entry into and transmitter release from bipolar cell terminals in tiger salamander retina.

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