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Treatment of polycystic kidney disease with a novel tyrosine kinase inhibitor

Kidney international, 2000-01, Vol.57 (1), p.33-40

2000

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

The Journal of clinical investigation, 1998-03, Vol.101 (5), p.935-939

1998

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Epidermal growth factor receptor expression is abnormal in murine polycystic kidney

Kidney international, 1995-02, Vol.47 (2), p.490-499

1995

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New insights into the molecular pathophysiology of polycystic kidney disease

Kidney international, 1999-04, Vol.55 (4), p.1187-1197

1999

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Candidate Gene Associated with a Mutation Causing Recessive Polycystic Kidney Disease in Mice

Science (American Association for the Advancement of Science), 1994-05, Vol.264 (5163), p.1329-1333

1994

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The severe perinatal form of autosomal recessive polycystic kidney disease maps to chromosome 6p21.1-p12 : implications for genetic counseling

American journal of human genetics, 1995-05, Vol.56 (5), p.1101-1107

1995

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In vitro modulation of cyst formation by a novel tyrosine kinase inhibitor

Kidney international, 1999-08, Vol.56 (2), p.406-413

1999

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Abnormal Sodium Pump Distribution During Renal Tubulogenesis in Congenital Murine Polycystic Kidney Disease

Proceedings of the National Academy of Sciences - PNAS, 1992-08, Vol.89 (16), p.7447-7451

1992

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Childhood ADPKD: Answers and more questions

Kidney international, 2001-05, Vol.59 (5), p.1979-1980

Avner, Ellis D.

2001

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Differential rescue of the renal and hepatic disease in an autosomal recessive polycystic kidney disease mouse mutant. A new model to study the liver lesion

The American journal of pathology, 1997-06, Vol.150 (6), p.2231-2241

1997

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Safety and efficacy of erythropoietin in children with chronic renal failure

Pediatric nephrology (Berlin, West), 1999-02, Vol.13 (2), p.143-147

1999

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Glomerulosclerosis and hypoplasia—A common theme?

Kidney international, 1999-11, Vol.56 (5), p.1962-1963

Avner, Ellis D.

1999

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Renal dysfunction but not cystic change is ameliorated by neonatal epidermal growth factor in bpk mice

Pediatric nephrology (Berlin, West), 2001, Vol.16 (1), p.45-50

2001

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Renal transplantation and chronic dialysis in children and adolescents: the 1993 annual report of the North American Pediatric Renal Transplant Cooperative Study

Pediatric nephrology (Berlin, West), 1995-02, Vol.9 (1), p.61-73

1995

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Tyrosine kinase activity of the EGF receptor in murine metanephric organ culture

Kidney international, 1995-03, Vol.47 (3), p.774-781

1995

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PKD and CF: An interesting family provides insight into the molecular pathophysiology of polycystic kidney disease

American journal of kidney diseases, 1998-12, Vol.32 (6), p.1081-1083

1998

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A novel inhibitor of tumor necrosis factor-α converting enzyme ameliorates polycystic kidney disease

Kidney international, 2001-10, Vol.60 (4), p.1240-1248

2001

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Epithelial polarity and differentiation in polycystic kidney disease

Journal of cell science, 1993-01, Vol.1993 (Supplement_17), p.217-222

Avner, Ellis D.

1993

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Functional activity of epidermal growth factor receptors in autosomal recessive polycystic kidney disease

American journal of physiology. Renal physiology, 1998-09, Vol.275 (3), p.F387-F394

1998

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The molecular biology of polycystic kidney disease

Pediatric nephrology (Berlin, West), 1998-11, Vol.12 (9), p.721-726

1998

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Expression of the orpk disease gene during kidney development and maturation

Pediatric nephrology (Berlin, West), 2001-03, Vol.16 (3), p.219-226

2001

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Biliary epithelial cells from mice with congenital polycystic kidney disease are hyperresponsive to epidermal growth factor

Pediatric research, 1995-06, Vol.37 (6), p.755-763

1995

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Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelic

Kidney international, 1996-10, Vol.50 (4), p.1158-1165

1996

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Functional correction of renal defects in a mouse model for ARPKD through expression of the cloned wild-type Tg737 cDNA

Kidney international, 1996-10, Vol.50 (4), p.1240-1248

1996

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Hypercalciuria and Nephrocalcinosis in the Oculocerebrorenal syndrome

The Journal of urology, 1995-04, Vol.153 (4), p.1244-1246

1995

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Treatment of polycystic kidney disease with a novel tyrosine kinase inhibitor

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

Epidermal growth factor receptor expression is abnormal in murine polycystic kidney

New insights into the molecular pathophysiology of polycystic kidney disease

Candidate Gene Associated with a Mutation Causing Recessive Polycystic Kidney Disease in Mice

The severe perinatal form of autosomal recessive polycystic kidney disease maps to chromosome 6p21.1-p12 : implications for genetic counseling

In vitro modulation of cyst formation by a novel tyrosine kinase inhibitor

Abnormal Sodium Pump Distribution During Renal Tubulogenesis in Congenital Murine Polycystic Kidney Disease

Childhood ADPKD: Answers and more questions

Differential rescue of the renal and hepatic disease in an autosomal recessive polycystic kidney disease mouse mutant. A new model to study the liver lesion

Safety and efficacy of erythropoietin in children with chronic renal failure

Glomerulosclerosis and hypoplasia—A common theme?

Renal dysfunction but not cystic change is ameliorated by neonatal epidermal growth factor in bpk mice

Renal transplantation and chronic dialysis in children and adolescents: the 1993 annual report of the North American Pediatric Renal Transplant Cooperative Study

Tyrosine kinase activity of the EGF receptor in murine metanephric organ culture

PKD and CF: An interesting family provides insight into the molecular pathophysiology of polycystic kidney disease

A novel inhibitor of tumor necrosis factor-α converting enzyme ameliorates polycystic kidney disease

Epithelial polarity and differentiation in polycystic kidney disease

Functional activity of epidermal growth factor receptors in autosomal recessive polycystic kidney disease

The molecular biology of polycystic kidney disease

Expression of the orpk disease gene during kidney development and maturation

Biliary epithelial cells from mice with congenital polycystic kidney disease are hyperresponsive to epidermal growth factor

Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelic

Functional correction of renal defects in a mouse model for ARPKD through expression of the cloned wild-type Tg737 cDNA

Hypercalciuria and Nephrocalcinosis in the Oculocerebrorenal syndrome

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