Chromosomal mapping in the mouse of eight K(+)-channel genes representing the four Shaker-like subfamilies Shaker, Shab, Shaw, and Shal (Q28237187)

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S L Roberds

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M M Tamkun

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M Gronemeier

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A Augustin

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B Albrecht

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O Pongs

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H Jockusch

Bad channel genes and weak muscles

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language of work or name

English

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publication date

December 1993

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published in

Genomics

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volume

18

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issue

3

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page(s)

568-74

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cites work

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Evidence of genetic heterogeneity in the long QT syndrome

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Genetic and cytogenetic localisation of the homeo box containing genes on mouse chromosome 6 and human chromosome 7.

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Simplified gene nomenclature

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Nucleotide sequence of murine triosephosphate isomerase cDNA.

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Molecular cloning, characterization, and genomic localization of a human potassium channel gene

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The human met oncogene is related to the tyrosine kinase oncogenes

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A novel potassium channel with delayed rectifier properties isolated from rat brain by expression cloning

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Molecular mapping of the mouse ob mutation

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Molecular mapping of obesity genes

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The potassium channel gene HK1 maps to human chromosome 11p14.1, close to the FSHB gene

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Genomic organization, nucleotide sequence, and cellular distribution of a Shaw-related potassium channel gene, Kv3.3, and mapping of Kv3.3 and Kv3.4 to human chromosomes 19 and 1

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Cloning and expression of a human voltage-gated potassium channel. A novel member of the RCK potassium channel family

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Genetics of hydroxyacid oxidase isozymes in the mouse: Localisation of Hao-2 on linkage group XVI

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Nucleotide sequence of the mouse muscle nicotinic acetylcholine receptor alpha subunit

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How might the diversity of potassium channels be generated?

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Multiple products of the Drosophila Shaker gene may contribute to potassium channel diversity

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Wobbler, a mutation affecting motoneuron survival and gonadal functions in the mouse, maps to proximal chromosome 11

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Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene

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The skeletal muscle chloride channel in dominant and recessive human myotonia

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Shaw-like rat brain potassium channel cDNA's with divergent 3' ends

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Human Colon Carcinoma Ki-ras2 Oncogene and Its Corresponding Proto-Oncogene

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Molecular genetics and ventricular arrhythmias

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Sudden death and the idiopathic long Q-T syndrome

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Chromosomal localization of the mouse titin gene and its relation to "muscular dystrophy with myositis" and nebulin genes on chromosome 2.

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Cloning of genomic and complementary DNA from Shaker, a putative potassium channel gene from Drosophila

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Assignment of human potassium channel gene KCNA4 (Kv1.4, PCN2) to chromosome 11q13.4-->q14.1

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Molecular biology of voltage-dependent potassium channels

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Characterization of a Shaw-related potassium channel family in rat brain

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Localization of a highly conserved human potassium channel gene (NGK2-KV4; KCNC1) to chromosome 11p15

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Genes for epilepsy mapped in the mouse.

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Molecular biology of the voltage-gated potassium channels of the cardiovascular system

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Diversity and ubiquity of K channels

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Cloning of a human cDNA expressing a high voltage-activating, TEA-sensitive, type-A K+ channel which maps to chromosome 1 band p21

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Glucocorticoid and developmental regulation of amylase mRNAs in mouse liver cells

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Multiple potassium-channel components are produced by alternative splicing at the Shaker locus in Drosophila

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Inactivation of muscle chloride channel by transposon insertion in myotonic mice

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Primary structure and functional expression of a developmentally regulated skeletal muscle chloride channel

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Sequence of a probable potassium channel component encoded at Shaker locus of Drosophila

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Pax: a murine multigene family of paired box-containing genes.

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Analysis of the integrant in MyK-103 transgenic mice in which males fail to transmit the integrant

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ras p21 and GAP inhibit coupling of muscarinic receptors to atrial K+ channels

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