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Sirtuin 1 inhibition delays cyst formation in autosomal-dominant polycystic kidney disease

The Journal of clinical investigation, 2013-07, Vol.123 (7), p.3084-3098

2013

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Diagnosis and management of childhood polycystic kidney disease

Pediatric nephrology (Berlin, West), 2011-05, Vol.26 (5), p.675-692

2011

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G-protein signaling modulator 1 deficiency accelerates cystic disease in an orthologous mouse model of autosomal dominant polycystic kidney disease

Proceedings of the National Academy of Sciences - PNAS, 2012-12, Vol.109 (52), p.21462-21467

2012

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Chronic blockade of 20-HETE synthesis reduces polycystic kidney disease in an orthologous rat model of ARPKD

American journal of physiology. Renal physiology, 2009-03, Vol.296 (3), p.F575-F582

2009

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Pathophysiology of childhood polycystic kidney diseases: new insights into disease-specific therapy

Pediatric research, 2014-01, Vol.75 (1-2), p.148-157

2014

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HDAC6 regulates epidermal growth factor receptor (EGFR) endocytic trafficking and degradation in renal epithelial cells

PloS one, 2012-11, Vol.7 (11), p.e49418

2012

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Src Inhibition Ameliorates Polycystic Kidney Disease

Journal of the American Society of Nephrology, 2008-07, Vol.19 (7), p.1331-1341

2008

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Smac-Mimetic―Induced Epithelial Cell Death Reduces the Growth of Renal Cysts

Journal of the American Society of Nephrology, 2013-12, Vol.24 (12), p.2010-2022

2013

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Molecular and cellular pathophysiology of autosomal recessive polycystic kidney disease (ARPKD)

Cell and tissue research, 2006-12, Vol.326 (3), p.671-685

2006

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Loss of activator of G‐protein signaling 3 impairs renal tubular regeneration following acute kidney injury in rodents

The FASEB journal, 2011-06, Vol.25 (6), p.1844-1855

2011

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Activator of G Protein Signaling 3 Promotes Epithelial Cell Proliferation in PKD

Journal of the American Society of Nephrology, 2010-08, Vol.21 (8), p.1275-1280

2010

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EGF receptor tyrosine kinase inhibition attenuates the development of PKD in Han:SPRD rats

Kidney international, 2003-11, Vol.64 (5), p.1573-1579

2003

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Role of genetic modifiers in an orthologous rat model of ARPKD

Physiological genomics, 2012-08, Vol.44 (15), p.741-753

2012

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Unique interstitial miRNA signature drives fibrosis in a murine model of autosomal dominant polycystic kidney disease

World journal of nephrology, 2018-09, Vol.7 (5), p.108-116

2018

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Emerging Therapies for Childhood Polycystic Kidney Disease

Frontiers in pediatrics, 2017-04, Vol.5, p.77-77

2017

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Transport, cilia, and PKD: must we in (cyst) on interrelationships? Focus on “Increased Na + /H + exchanger activity on the apical surface of a cilium-deficient cortical collecting duct principal cell model of polycystic kidney disease”

American Journal of Physiology: Cell Physiology, 2012-05, Vol.302 (10), p.C1434-C1435, Article C1434

2012

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Epidermal growth factor receptor tyrosine kinase inhibition is not protective in PCK rats

Kidney international, 2004-11, Vol.66 (5), p.1766-1773

2004

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Combination treatment of PKD utilizing dual inhibition of EGF-receptor activity and ligand bioavailability

Kidney international, 2003-10, Vol.64 (4), p.1310-1319

2003

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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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EGF-related growth factors in the pathogenesis of murine ARPKD

Kidney international, 2004-06, Vol.65 (6), p.2018-2029

2004

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Renal Cystic Disease: New Insights for the Clinician

The Pediatric clinics of North America, 2006-10, Vol.53 (5), p.889-909

2006

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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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Proximal tubular cysts in fetal human autosomal recessive polycystic kidney disease

Journal of the American Society of Nephrology, 2000-04, Vol.11 (4), p.760-763

2000

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Role of CFTR in autosomal recessive polycystic kidney disease

Journal of the American Society of Nephrology, 2001-04, Vol.12 (4), p.719-725

2001

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Segment-specific c-ErbB2 expression in human autosomal recessive polycystic kidney disease

Journal of the American Society of Nephrology, 2001-02, Vol.12 (2), p.379-384

2001

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Nephrology. Urinary Tract Diseases
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Sirtuin 1 inhibition delays cyst formation in autosomal-dominant polycystic kidney disease

Diagnosis and management of childhood polycystic kidney disease

G-protein signaling modulator 1 deficiency accelerates cystic disease in an orthologous mouse model of autosomal dominant polycystic kidney disease

Chronic blockade of 20-HETE synthesis reduces polycystic kidney disease in an orthologous rat model of ARPKD

Pathophysiology of childhood polycystic kidney diseases: new insights into disease-specific therapy

HDAC6 regulates epidermal growth factor receptor (EGFR) endocytic trafficking and degradation in renal epithelial cells

Src Inhibition Ameliorates Polycystic Kidney Disease

Smac-Mimetic―Induced Epithelial Cell Death Reduces the Growth of Renal Cysts

Molecular and cellular pathophysiology of autosomal recessive polycystic kidney disease (ARPKD)

Loss of activator of G‐protein signaling 3 impairs renal tubular regeneration following acute kidney injury in rodents

Activator of G Protein Signaling 3 Promotes Epithelial Cell Proliferation in PKD

EGF receptor tyrosine kinase inhibition attenuates the development of PKD in Han:SPRD rats

Role of genetic modifiers in an orthologous rat model of ARPKD

Unique interstitial miRNA signature drives fibrosis in a murine model of autosomal dominant polycystic kidney disease

Emerging Therapies for Childhood Polycystic Kidney Disease

Transport, cilia, and PKD: must we in (cyst) on interrelationships? Focus on “Increased Na + /H + exchanger activity on the apical surface of a cilium-deficient cortical collecting duct principal cell model of polycystic kidney disease”

Epidermal growth factor receptor tyrosine kinase inhibition is not protective in PCK rats

Combination treatment of PKD utilizing dual inhibition of EGF-receptor activity and ligand bioavailability

Expression of the orpk disease gene during kidney development and maturation

EGF-related growth factors in the pathogenesis of murine ARPKD

Renal Cystic Disease: New Insights for the Clinician

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

Proximal tubular cysts in fetal human autosomal recessive polycystic kidney disease

Role of CFTR in autosomal recessive polycystic kidney disease

Segment-specific c-ErbB2 expression in human autosomal recessive polycystic kidney disease

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