Renal cyst enlargement in autosomal dominant polycystic kidney disease (ADPKD) is
characterized by increased epithelial cell proliferation and fluid accumulation. Using …

Human autosomal dominant polycystic kidney disease (ADPKD) epithelia were grown in
primary monolayer cultures and their properties compared with intact kidney epithelial …

Genetic polycystic kidney disease (ADPKD) is an autosomal dominant trait in man, the
phenotypic expression of which is characterized by enormous cystic enlargement of renal …

Impaired tubulogenesis of cyst-derived cells from autosomal dominant polycystic kidneys.
Under appropriate growth factor or hormonal influence, renal epithelial cells cultured in …

Cyst formation and growth in autosomal dominant polycystic kidney disease. Previous
morphologic studies on kidneys from adult patients with autosomal dominant polycystic …

Polycystic kidney disease: Primary extracellular matrix abnormality or defective cellular
differentiation? Polycystic kidney disease (PKD) is inherited as a dominant or recessive trait …

Autosomal dominant polycystic kidney disease (ADPKD) is the most common potentially
lethal hereditary disease. The hall mark of the disease is the development of innumerable …

Autosomal dominant polycystic kidney disease (ADPKD) is characterized by cyst formation
initiated by dedifferentiation and proliferation of renal tubular epithelial cells. Renal tubular …

Autosomal dominant polycystic kidney disease (ADPKD) is characterized by progressive
renal enlargement, culminating in renal insufficiency in over one half of affected individuals …

Proliferation of renal tubular epithelial cells is considered a major factor leading to cyst
formation in human polycystic kidney disease (PKD). The Han: SPRD rat model for inherited …