A hyperprostaglandin E syndrome mutation in Kir1.1 (renal outer medullary potassium) channels reveals a crucial residue for channel function in Kir1.3 channels.
Derst, C
A hyperprostaglandin E syndrome mutation in Kir1.1 (renal outer medullary potassium) channels reveals a crucial residue for channel function in Kir1.3 channels. [electronic resource] - The Journal of biological chemistry Sep 1998 - 23884-91 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0021-9258
10.1074/jbc.273.37.23884 doi
Amino Acid Sequence
Animals
Bartter Syndrome--embryology
COS Cells
Cloning, Molecular
Female
Humans
Kidney Medulla--metabolism
Molecular Sequence Data
Mutagenesis, Site-Directed
Oocytes--physiology
Point Mutation
Polymerase Chain Reaction
Polymorphism, Single-Stranded Conformational
Potassium Channels--chemistry
Potassium Channels, Inwardly Rectifying
Prostaglandins E--metabolism
Recombinant Proteins--chemistry
Sequence Alignment
Sequence Homology, Amino Acid
Syndrome
Transfection
Xenopus laevis
Kcnj10 Channel
A hyperprostaglandin E syndrome mutation in Kir1.1 (renal outer medullary potassium) channels reveals a crucial residue for channel function in Kir1.3 channels. [electronic resource] - The Journal of biological chemistry Sep 1998 - 23884-91 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0021-9258
10.1074/jbc.273.37.23884 doi
Amino Acid Sequence
Animals
Bartter Syndrome--embryology
COS Cells
Cloning, Molecular
Female
Humans
Kidney Medulla--metabolism
Molecular Sequence Data
Mutagenesis, Site-Directed
Oocytes--physiology
Point Mutation
Polymerase Chain Reaction
Polymorphism, Single-Stranded Conformational
Potassium Channels--chemistry
Potassium Channels, Inwardly Rectifying
Prostaglandins E--metabolism
Recombinant Proteins--chemistry
Sequence Alignment
Sequence Homology, Amino Acid
Syndrome
Transfection
Xenopus laevis
Kcnj10 Channel