Ciliary function of polycystins: A new model for cystogenesis

Nephrology Dialysis Transplantation

Volumn 18, Issue 9, 2003, Pages 1689-1692

  Joly, Dominique ^a   Hummel, Aurélie ^a   Ruello, Antonella ^a   Knebelmann, Bertrand ^a  

^a INSERM   (France)

Author keywords

Autosomal dominant polycystic kidney disease; Polycystins cation channels; Primary cilia

Indexed keywords

BETA CATENIN; CALCIUM; GUANINE NUCLEOTIDE BINDING PROTEIN; POLYCYSTIN; PROTEIN P21; RYANODINE RECEPTOR; STAT1 PROTEIN; TAXANE DERIVATIVE; WNT PROTEIN;

ANIMAL CELL; CALCIUM CELL LEVEL; CELL DIFFERENTIATION; CELL ORGANELLE; CELL PROLIFERATION; CELL STRUCTURE; CENTRIOLE; CILIARY MOTILITY; EDITORIAL; ENDOPLASMIC RETICULUM; EXTRACELLULAR MATRIX; GENE MUTATION; GENETIC CODE; GENETIC DISORDER; GENETIC TRANSDUCTION; GLOMERULUS FILTRATION; KIDNEY ANOMALY; KIDNEY CELL; KIDNEY EPITHELIUM; KIDNEY POLYCYSTIC DISEASE; MECHANORECEPTOR; MICROTUBULE ASSEMBLY; MOLECULAR MODEL; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; TREATMENT PLANNING;

ANIMALS; CILIA; HUMANS; KIDNEY; MEMBRANE PROTEINS; MICE; MUTATION; POLYCYSTIC KIDNEY, AUTOSOMAL DOMINANT; PROTEINS; TRPP CATION CHANNELS; URINE;

EID: 0042385071     PISSN: 09310509     EISSN: None     Source Type: Journal    
DOI: 10.1093/ndt/gfg256     Document Type: Editorial

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