ABSTRACTPolyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary cilium, and cytoplasm.BackgroundPKHD1, the autosomal-recessive polycystic kidney disease (ARPKD) gene, encodes multiple alternatively spliced transcripts predicted to generate membrane-bound and secreted proteins. The longest open reading frame encodes polyductin (fibrocystin), a putative 4074 amino acid protein with a single transmembrane domain and an intracellular C-terminus.MethodsTo characterize the PKHD1 products and their expression profile, we raised polyclonal antibodies against different portions of polyductin and analyzed different organs using various methods.ResultsWestern blot analyses demonstrated specific bands of >440 kD in ...
The most common form of autosomal dominant polycystic kidney disease (PKD) results from mutation of ...
O gene PKHD1, mutado na doença renal policística autossômica recessiva, apresenta um padrão de splic...
O gene PKHD1, mutado na doença renal policística autossômica recessiva, apresenta um padrão de splic...
ABSTRACTPolyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary...
Recent evidence suggests that structural and functional abnormalities of primary cilia in kidney epi...
Autosomal recessive polycystic kidney disease (ARPKD) is an inherited disorder causing renal-related...
Autosomal recessive polycystic kidney disease (ARPKD) is a severe form of polycystic kidney disease ...
Abstract. Recent evidence suggests that structural and func-tional abnormalities of primary cilia in...
The longest open reading frame of PKHD1 (polycystic kidney and hepatic disease 1), the autosomal rec...
The longest open reading frame of PKHD1 (polycystic kidney and hepatic disease 1), the autosomal rec...
Recent evidence suggests that fibrocystin/polyductin (FPC), polycystin-1 (PC1), and polycystin-2 (PC...
Recent evidence suggests that fibrocystin/polyductin (FPC), polycystin-1 (PC1), and polycystin-2 (PC...
Recent evidence suggests that fibrocystin/polyductin (FPC), polycystin-1 (PC1), and polycystin-2 (PC...
Item does not contain fulltextThe most common form of autosomal dominant polycystic kidney disease (...
The most common form of autosomal dominant polycystic kidney disease (PKD) results from mutation of ...
The most common form of autosomal dominant polycystic kidney disease (PKD) results from mutation of ...
O gene PKHD1, mutado na doença renal policística autossômica recessiva, apresenta um padrão de splic...
O gene PKHD1, mutado na doença renal policística autossômica recessiva, apresenta um padrão de splic...
ABSTRACTPolyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary...
Recent evidence suggests that structural and functional abnormalities of primary cilia in kidney epi...
Autosomal recessive polycystic kidney disease (ARPKD) is an inherited disorder causing renal-related...
Autosomal recessive polycystic kidney disease (ARPKD) is a severe form of polycystic kidney disease ...
Abstract. Recent evidence suggests that structural and func-tional abnormalities of primary cilia in...
The longest open reading frame of PKHD1 (polycystic kidney and hepatic disease 1), the autosomal rec...
The longest open reading frame of PKHD1 (polycystic kidney and hepatic disease 1), the autosomal rec...
Recent evidence suggests that fibrocystin/polyductin (FPC), polycystin-1 (PC1), and polycystin-2 (PC...
Recent evidence suggests that fibrocystin/polyductin (FPC), polycystin-1 (PC1), and polycystin-2 (PC...
Recent evidence suggests that fibrocystin/polyductin (FPC), polycystin-1 (PC1), and polycystin-2 (PC...
Item does not contain fulltextThe most common form of autosomal dominant polycystic kidney disease (...
The most common form of autosomal dominant polycystic kidney disease (PKD) results from mutation of ...
The most common form of autosomal dominant polycystic kidney disease (PKD) results from mutation of ...
O gene PKHD1, mutado na doença renal policística autossômica recessiva, apresenta um padrão de splic...
O gene PKHD1, mutado na doença renal policística autossômica recessiva, apresenta um padrão de splic...