Mesh : Adult Animals Cell Membrane / chemistry Gene Expression Gestational Age Humans Kidney / chemistry embryology growth & development Kidney Diseases, Cystic / metabolism Mice Mice, Knockout Proteins / analysis genetics TRPP Cation Channels

来  源:   DOI:10.1159/000020670   PDF(Sci-hub)

Abstract:
PKD1, the major gene mutated in autosomal dominant polycystic kidney disease, was identified in 1994, and fully sequenced in 1995. The protein which it encodes, polycystin-1, is the first member of a new family of proteins, whose functions presently remain unclear. This review seeks to highlight the difficulties researchers studying polycystin-1 have faced and to summarize the current areas of consensus and controversy between different groups, particularly with regard to the expression pattern, subcellular location and biochemical characterization of polycystin-1. Where relevant, more recent data regarding polycystin-2, the protein encoded by PKD2, will also be discussed.
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