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Publication : A genetically determined murine model of infantile polycystic kidney disease.

First Author  Fry JL Jr Year  1985
Journal  J Urol Volume  134
Issue  4 Pages  828-33
PubMed ID  4032601 Mgi Jnum  J:99620
Mgi Id  MGI:3583334 Doi  10.1016/s0022-5347(17)47448-9
Citation  Fry JL Jr, et al. (1985) A genetically determined murine model of infantile polycystic kidney disease. J Urol 134(4):828-33
abstractText  We have evaluated a congenic strain of mice with congenital polycystic kidney disease in which the disease process appears to closely resemble human infantile polycystic kidney disease. Cysts formed first in the proximal tubules of the nephron and appeared, by light microscopy, to be preceded by vacuolization of the cells. These spaces, as seen by electron microscopy, occurred between adjacent cells. The pancreas was severely involved with reduction of both exocrine and endocrine elements. Cyst formation in the liver was minimal. Serum samples evaluated for urea nitrogen and creatinine were significantly elevated in affected mice. Serum glucose was within normal limits.
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