<p>Both telomerase immortalized normal kidney (N) proximal and PKD Q4004X (P) cells were grown to confluence for 3 or 7 days. Extracts were made with buffers containing non-ionic detergent and equivalent amounts of protein (50 µg) were loaded in each lane. Lanes labeled N and P represent lysates made from telomerase immortalized normal kidney proximal tubule and PKD Q4004X cells, respectively. Two bands at molecular weights 120 and 100 kDa are seen and the PKD cells have higher expression levels at both time points. At 7 days only the 100 kDa band is observed.</p
The Institute of Bioengineering and Nanotechnology (IBN) has embarked on research work toward the bu...
Expression of polycystin in mouse metanephros and extra-metanephric tissues. The presence of messeng...
The most common form of autosomal dominant polycystic kidney disease (PKD) results from mutation of ...
Autosomal dominant polycystic kidney disease (ADPKD) is associated with a variety of cellular phenot...
Autosomal dominant polycystic kidney disease (ADPKD) is associated with a variety of cellular phenot...
<p>A: Immune blot of membrane preparations from RPTEC, NHPTK and PKD Q4004X cells. Membranes were is...
Telomere-dependent replicative senescence is one of the mechanisms that limit the number of populati...
<p>A: Population doublings of normal and cystic proximal tubule cell lines. Graphical depiction of p...
Renal proximal tubular epithelium from patients with nephropathic cystinosis: Immortalized cell line...
Mutations in the PKD1 and PKD2 genes account for 85 and 15% of cases of autosomal dominant polycysti...
Mutations in the PKD1 and PKD2 genes account for 85 and 15% of cases of autosomal dominant polycysti...
Mutations in the PKD1 and PKD2 genes account for 85 and 15% of cases of autosomal dominant polycysti...
<p>A: Telomerase activity assay and immune blot analysis of transduced and untransduced cells. Left ...
Autosomal-dominant polycystic kidney disease, one of the most frequent human genetic disorders, is g...
Item does not contain fulltextThe most common form of autosomal dominant polycystic kidney disease (...
The Institute of Bioengineering and Nanotechnology (IBN) has embarked on research work toward the bu...
Expression of polycystin in mouse metanephros and extra-metanephric tissues. The presence of messeng...
The most common form of autosomal dominant polycystic kidney disease (PKD) results from mutation of ...
Autosomal dominant polycystic kidney disease (ADPKD) is associated with a variety of cellular phenot...
Autosomal dominant polycystic kidney disease (ADPKD) is associated with a variety of cellular phenot...
<p>A: Immune blot of membrane preparations from RPTEC, NHPTK and PKD Q4004X cells. Membranes were is...
Telomere-dependent replicative senescence is one of the mechanisms that limit the number of populati...
<p>A: Population doublings of normal and cystic proximal tubule cell lines. Graphical depiction of p...
Renal proximal tubular epithelium from patients with nephropathic cystinosis: Immortalized cell line...
Mutations in the PKD1 and PKD2 genes account for 85 and 15% of cases of autosomal dominant polycysti...
Mutations in the PKD1 and PKD2 genes account for 85 and 15% of cases of autosomal dominant polycysti...
Mutations in the PKD1 and PKD2 genes account for 85 and 15% of cases of autosomal dominant polycysti...
<p>A: Telomerase activity assay and immune blot analysis of transduced and untransduced cells. Left ...
Autosomal-dominant polycystic kidney disease, one of the most frequent human genetic disorders, is g...
Item does not contain fulltextThe most common form of autosomal dominant polycystic kidney disease (...
The Institute of Bioengineering and Nanotechnology (IBN) has embarked on research work toward the bu...
Expression of polycystin in mouse metanephros and extra-metanephric tissues. The presence of messeng...
The most common form of autosomal dominant polycystic kidney disease (PKD) results from mutation of ...