Human FXYD2 G41R mutation responsible for renal hypomagnesemia behaves as an inward-rectifying cation channel

American Journal of Physiology - Renal Physiology

Volumn 295, Issue 1, 2008, Pages

  Sha, Qun ^a   Pearson, Wade ^a   Burcea, Lauren C ^a   Wigfall, Darian A ^a   Schlesinger, Paul H ^a   Nichols, Colin G ^a   Mercer, Robert W ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Inward rectification; Ion currents; Mutant proteins; Na K ATPase

Indexed keywords

ARGININE; BARIUM; CALCIUM; CATION CHANNEL; GLYCINE; MAGNESIUM; POLYPEPTIDE; PROTEIN FXYD2; UNCLASSIFIED DRUG; ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); CALCIUM CHANNEL; FXYD2 PROTEIN, HUMAN;

ANIMAL CELL; ARTICLE; BASOLATERAL MEMBRANE; CONTROLLED STUDY; CORONAVIRUS; EPITHELIUM CELL; GENE EXPRESSION; GENE MUTATION; HYPOMAGNESEMIA; NONHUMAN; OOCYTE; PRIORITY JOURNAL; RENAL HYPOMAGNESEMIA; SITE DIRECTED MUTAGENESIS; XENOPUS LAEVIS; AMINO ACID SUBSTITUTION; ANIMAL; BLOOD; CELL MEMBRANE POTENTIAL; DOG; GENETICS; HUMAN; KIDNEY TUBULE DISORDER; PATHOPHYSIOLOGY; PHYSIOLOGY;

AMINO ACID SUBSTITUTION; ANIMALS; CALCIUM CHANNELS; DOGS; HUMANS; MAGNESIUM; MEMBRANE POTENTIALS; OOCYTES; RENAL TUBULAR TRANSPORT, INBORN ERRORS; SODIUM-POTASSIUM-EXCHANGING ATPASE; XENOPUS LAEVIS;

EID: 49949110312     PISSN: 1931857X     EISSN: 15221466     Source Type: Journal    
DOI: 10.1152/ajprenal.00519.2007     Document Type: Article

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