A hyperprostaglandin E syndrome mutation in Kir1.1 (renal outer medullary potassium) channels reveals a crucial residue for channel function in Kir1.3 channels

Journal of Biological Chemistry

Volumn 273, Issue 37, 1998, Pages 23884-23891

  Derst, Christian ^a   Wischmeyer, Erhard ^b   Preisig Müller, Regina ^a   Spauschus, Alexander ^b   Konrad, Martin ^a   Hensen, Peter ^a   Jeck, Nikola ^a   Seyberth, Hannsjörg W ^a   Daut, Jürgen ^a   Karschin, Andreas ^b  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

^b MAX PLANCK INSTITUTE FOR BIOPHYSICAL CHEMISTRY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ASPARAGINE; BARIUM ION; DNA; LYSINE; POTASSIUM CHANNEL; PROSTAGLANDIN E; RNA;

ANIMAL CELL; ARTICLE; BARTTER SYNDROME; CASE REPORT; CONTROLLED STUDY; DNA SEQUENCE; GENE MUTATION; GUINEA PIG; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPERPROSTAGLANDIN E SYNDROME; INFANT; KIDNEY DISEASE; KIDNEY MEDULLA; KIDNEY TUBULE ABSORPTION; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; XENOPUS LAEVIS;

AMINO ACID SEQUENCE; ANIMALS; BARTTER SYNDROME; CLONING, MOLECULAR; COS CELLS; FEMALE; HUMANS; KIDNEY MEDULLA; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; OOCYTES; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; POTASSIUM CHANNELS; POTASSIUM CHANNELS, INWARDLY RECTIFYING; PROSTAGLANDINS E; RECOMBINANT PROTEINS; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY, AMINO ACID; SYNDROME; TRANSFECTION; XENOPUS LAEVIS;

EID: 15144353151     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.273.37.23884     Document Type: Article

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