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Molecular fingerprinting of the podocyte reveals novel gene and protein regulatory networks

Kidney international, 2013-06, Vol.83 (6), p.1052-1064

2013

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Podocyte-Specific Deletion of Dicer Alters Cytoskeletal Dynamics and Causes Glomerular Disease

Journal of the American Society of Nephrology, 2008-11, Vol.19 (11), p.2150-2158

2008

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Glomerular filtration is normal in the absence of both agrin and perlecan–heparan sulfate from the glomerular basement membrane

Nephrology, dialysis, transplantation, 2009-07, Vol.24 (7), p.2044-2051

2009

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Models for studies of proteoglycans in kidney pathophysiology

Methods in molecular biology (Clifton, N.J.), 2012-01, Vol.836, p.259

Harvey, Scott J

2012

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A hypomorphic mutation in the mouse laminin α5 gene causes polycystic kidney disease

Journal of the American Society of Nephrology, 2006-07, Vol.17 (7), p.1913-1922

2006

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MicroRNAs and the kidney: coming of age

Current opinion in nephrology and hypertension, 2009-07, Vol.18 (4), p.317-323

2009

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Disruption of Glomerular Basement Membrane Charge through Podocyte-Specific Mutation of Agrin Does Not Alter Glomerular Permselectivity

The American journal of pathology, 2007-07, Vol.171 (1), p.139-152

2007

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Revisiting the glomerular charge barrier in the molecular era

Current opinion in nephrology and hypertension, 2008-07, Vol.17 (4), p.393-398

2008

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Discovery of microvascular miRNAs using public gene expression data: miR-145 is expressed in pericytes and is a regulator of Fli1

Genome medicine, 2009-11, Vol.1 (11), p.108-108

2009

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Transfer of the α5(IV) Collagen Chain Gene to Smooth Muscle Restores in Vivo Expression of the α6(IV) Collagen Chain in a Canine Model of Alport Syndrome

The American journal of pathology, 2003-03, Vol.162 (3), p.873-885

2003

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Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndrome

Nature genetics, 2001-02, Vol.27 (2), p.205-208

2001

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DDR1-deficient mice show localized subepithelial GBM thickening with focal loss of slit diaphragms and proteinuria

Kidney international, 2004-07, Vol.66 (1), p.102-111

2004

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Cyclosporine A slows the progressive renal disease of Alport syndrome (X-linked hereditary nephritis): Results from a canine model

Journal of the American Society of Nephrology, 2003-03, Vol.14 (3), p.690-698

2003

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Breaking down the barrier: evidence against a role for heparan sulfate in glomerular permselectivity

Journal of the American Society of Nephrology, 2007-03, Vol.18 (3), p.672-674

2007

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Sequential Expression of Type IV Collagen Networks: Testis as a Model and Relevance to Spermatogenesis

The American journal of pathology, 2006-05, Vol.168 (5), p.1587-1597

2006

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Role of distinct type IV collagen networks in glomerular development and function

Kidney international, 1998-12, Vol.54 (6), p.1857-1866

1998

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The Inner Ear of Dogs with X-Linked Nephritis Provides Clues to the Pathogenesis of Hearing Loss in X-Linked Alport Syndrome

The American journal of pathology, 2001-09, Vol.159 (3), p.1097-1104

2001

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Regulation of collagen type IV genes is organ-specific: Evidence from a canine model of Alport syndrome

Kidney international, 2005-11, Vol.68 (5), p.2121-2130, Article 2121

2005

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A hypomorphic mutation in the mouse laminin alpha5 gene causes polycystic kidney disease

Journal of the American Society of Nephrology, 2006-07, Vol.17 (7), p.1913

2006

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Disruption of glomerular basement membrane charge through podocyte-specific mutation of agrin does not alter glomerular permselectivity. Commentary. Author's reply

The American journal of pathology, 2007, Vol.171 (1)

2007

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Transfer of the alpha 5(IV) collagen chain gene to smooth muscle restores in vivo expression of the alpha 6(IV) collagen chain in a canine model of Alport syndrome

The American journal of pathology, 2003-03, Vol.162 (3), p.873-885

2003

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Type IV collagen: A network for development, differentiation, and disease

Advances in Developmental Biology, 2005, Vol.15, p.1-64

2005

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Transfer of the {alpha}5(IV) Collagen Chain Gene to Smooth Muscle Restores in Vivo Expression of the {alpha}6(IV) Collagen Chain in a Canine Model of Alport Syndrome

The American journal of pathology, 2003-03, Vol.162 (3), p.873

2003

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Burden of depressive disorders by country, sex, age, and year: findings from the global burden of disease study 2010

PLoS medicine, 2013-11, Vol.10 (11), p.e1001547-e1001547

2013

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Global Epidemiology and Burden of Schizophrenia: Findings From the Global Burden of Disease Study 2016

Schizophrenia bulletin, 2018-10, Vol.44 (6), p.1195-1203

2018

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Molecular fingerprinting of the podocyte reveals novel gene and protein regulatory networks

Podocyte-Specific Deletion of Dicer Alters Cytoskeletal Dynamics and Causes Glomerular Disease

Glomerular filtration is normal in the absence of both agrin and perlecan–heparan sulfate from the glomerular basement membrane

Models for studies of proteoglycans in kidney pathophysiology

A hypomorphic mutation in the mouse laminin α5 gene causes polycystic kidney disease

MicroRNAs and the kidney: coming of age

Disruption of Glomerular Basement Membrane Charge through Podocyte-Specific Mutation of Agrin Does Not Alter Glomerular Permselectivity

Revisiting the glomerular charge barrier in the molecular era

Discovery of microvascular miRNAs using public gene expression data: miR-145 is expressed in pericytes and is a regulator of Fli1

Transfer of the α5(IV) Collagen Chain Gene to Smooth Muscle Restores in Vivo Expression of the α6(IV) Collagen Chain in a Canine Model of Alport Syndrome

Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndrome

DDR1-deficient mice show localized subepithelial GBM thickening with focal loss of slit diaphragms and proteinuria

Cyclosporine A slows the progressive renal disease of Alport syndrome (X-linked hereditary nephritis): Results from a canine model

Breaking down the barrier: evidence against a role for heparan sulfate in glomerular permselectivity

Sequential Expression of Type IV Collagen Networks: Testis as a Model and Relevance to Spermatogenesis

Role of distinct type IV collagen networks in glomerular development and function

The Inner Ear of Dogs with X-Linked Nephritis Provides Clues to the Pathogenesis of Hearing Loss in X-Linked Alport Syndrome

Regulation of collagen type IV genes is organ-specific: Evidence from a canine model of Alport syndrome

A hypomorphic mutation in the mouse laminin alpha5 gene causes polycystic kidney disease

Disruption of glomerular basement membrane charge through podocyte-specific mutation of agrin does not alter glomerular permselectivity. Commentary. Author's reply

Transfer of the alpha 5(IV) collagen chain gene to smooth muscle restores in vivo expression of the alpha 6(IV) collagen chain in a canine model of Alport syndrome

Type IV collagen: A network for development, differentiation, and disease

Transfer of the {alpha}5(IV) Collagen Chain Gene to Smooth Muscle Restores in Vivo Expression of the {alpha}6(IV) Collagen Chain in a Canine Model of Alport Syndrome

Burden of depressive disorders by country, sex, age, and year: findings from the global burden of disease study 2010

Global Epidemiology and Burden of Schizophrenia: Findings From the Global Burden of Disease Study 2016

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