A Bartter's syndrome mutation of ROMK1 exerts dominant negative effects on K(+) conductance.

Kunzelmann, K; Hübner, M; Vollmer, M; Ruf, R; Hildebrandt, F; Greger, R; Schreiber, R

Kunzelmann, K; Hübner, M; Vollmer, M; Ruf, R; Hildebrandt, F; Greger, R; Schreiber, R.

Affiliation

Kunzelmann K; Physiologisches Institut, Albert-Ludwigs-Universität Freiburg, Freiburg, Germany. kkunzel@mail.physiol.usyd.edu.au

Cell Physiol Biochem ; 10(3): 117-24, 2000.

Article in En | MEDLINE | ID: mdl-10878442

Subject(s)

Bartter Syndrome/genetics; Mutation; Potassium Channels, Inwardly Rectifying; Potassium Channels/genetics; Potassium/metabolism; Bartter Syndrome/metabolism; Cations, Monovalent/metabolism; Electric Conductivity; Electrophysiology; Gene Expression Regulation; Humans; Potassium Channels/metabolism; Protein Kinases/metabolism

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Collection: 01-internacional Database: MEDLINE Main subject: Potassium / Bartter Syndrome / Potassium Channels / Potassium Channels, Inwardly Rectifying / Mutation Limits: Humans Language: En Journal: Cell Physiol Biochem Journal subject: BIOQUIMICA / FARMACOLOGIA Year: 2000 Document type: Article Affiliation country: Germany Country of publication: Germany

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