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11 in total

1. Recombinant human growth hormone therapy in autosomal recessive polycystic kidney disease.

Authors: Marusia Lilova; Bernard S Kaplan; Kevin E C Meyers
Journal: Pediatr Nephrol Date: 2002-11-26 Impact factor: 3.714

Review 2. Transient receptor potential channelopathies.

Authors: Bernd Nilius; Grzegorz Owsianik
Journal: Pflugers Arch Date: 2010-02-04 Impact factor: 3.657

3. Epidermal growth factor receptor activity mediates renal cyst formation in polycystic kidney disease.

Authors: W G Richards; W E Sweeney; B K Yoder; J E Wilkinson; R P Woychik; E D Avner
Journal: J Clin Invest Date: 1998-03-01 Impact factor: 14.808

4. Polycystin 1 is required for the structural integrity of blood vessels.

Authors: K Kim; I Drummond; O Ibraghimov-Beskrovnaya; K Klinger; M A Arnaout
Journal: Proc Natl Acad Sci U S A Date: 2000-02-15 Impact factor: 11.205

5. Isolation and characterization of liver epithelial cell lines from wild-type and mutant TgN737Rpw mice.

Authors: W G Richards; B K Yoder; R J Isfort; P G Detilleux; C Foster; N Neilsen; R P Woychik; J E Wilkinson
Journal: Am J Pathol Date: 1997-04 Impact factor: 4.307

6. Characterization and cell distribution of polycystin, the product of autosomal dominant polycystic kidney disease gene 1.

Authors: R Palsson; C P Sharma; K Kim; M McLaughlin; D Brown; M A Arnaout
Journal: Mol Med Date: 1996-11 Impact factor: 6.354

Polycystic kidney disease: hereditary and acquired.

1. Recombinant human growth hormone therapy in autosomal recessive polycystic kidney disease.

Review 2. Transient receptor potential channelopathies.

3. Epidermal growth factor receptor activity mediates renal cyst formation in polycystic kidney disease.

4. Polycystin 1 is required for the structural integrity of blood vessels.

5. Isolation and characterization of liver epithelial cell lines from wild-type and mutant TgN737Rpw mice.

6. Characterization and cell distribution of polycystin, the product of autosomal dominant polycystic kidney disease gene 1.

7. Oval cell proliferation associated with the murine insertional mutation TgN737Rpw.

8. Polycystic kidney disease as a result of loss of the tuberous sclerosis 2 tumor suppressor gene during development.

Review 9. The transient receptor potential family of ion channels.

10. Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment.