Do polycystins function as cation channels?

Current Opinion in Nephrology and Hypertension

Volumn 11, Issue 5, 2002, Pages 539-545

  Ikeda, Masahiro ^a   Guggino, William B ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Autosomal dominant polycystic kidney disease; Cation channels; Polycystin 1; Polycystin 2; Protein kinase C

Indexed keywords

AMINO ACID; BETA CATENIN; CALCIUM; CATION CHANNEL; COMPLEMENTARY DNA; COMPLEMENTARY RNA; ETHYLENE GLYCOL 1,2 BIS(2 AMINOPHENYL) ETHER N,N,N',N' TETRAACETIC ACID; GUANINE NUCLEOTIDE BINDING PROTEIN; INOSITOL 1,4,5 TRISPHOSPHATE RECEPTOR; LANTHANUM; MEMBRANE PROTEIN; MESSENGER RNA; NIFLUMIC ACID; POLYCYSTIN; PROTEIN KINASE C; RGS PROTEIN; RYANODINE RECEPTOR; TRANSCRIPTION FACTOR AP 1;

CELL MEMBRANE; ENDOPLASMIC RETICULUM; GENE MUTATION; HUMAN; KIDNEY FAILURE; KIDNEY POLYCYSTIC DISEASE; KIDNEY TUBULE; NONHUMAN; PRIORITY JOURNAL; PROTEIN STRUCTURE; REVIEW;

CALCIUM SIGNALING; CATIONS; HUMANS; ION CHANNELS; MEMBRANE PROTEINS; PROTEIN KINASE C; PROTEIN STRUCTURE, TERTIARY; PROTEINS; SIGNAL TRANSDUCTION; TRPP CATION CHANNELS;

EID: 0036736836     PISSN: 10624821     EISSN: None     Source Type: Journal    
DOI: 10.1097/00041552-200209000-00010     Document Type: Review

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