Publications by authors named "Michelle Winn"

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Variability in phenotype induced by the podocin variant R229Q plus a single pathogenic mutation.
Paul J Phelan, Gentzon Hall, Delbert Wigfall, John Foreman, Shashi Nagaraj, Michelle P Winn

Clin Kidney J· October 2015

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HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome.
Rasheed A Gbadegesin, Adebowale Adeyemo, Nicholas J A Webb, Larry A Greenbaum, Asiri Abeyagunawardena, Michelle P Winn

J Am Soc Nephrol· July 2015

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Gq signaling causes glomerular injury by activating TRPC6.
Liming Wang, Grant Jirka, Paul B Rosenberg, Anne F Buckley, Jose A Gomez, Michelle P Winn

J Clin Invest· May 2015

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A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.
Gentzon Hall, Rasheed A Gbadegesin, Peter Lavin, Guanghong Wu, Yangfan Liu, Michelle P Winn

J Am Soc Nephrol· April 2015

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Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis.
Andrew F Malone, Paul J Phelan, Gentzon Hall, Umran Cetincelik, Alison Homstad, Michelle P Winn

Kidney Int· December 2014

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Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS.
Rasheed A Gbadegesin, Gentzon Hall, Adebowale Adeyemo, Nils Hanke, Irini Tossidou, Michelle P Winn

J Am Soc Nephrol· September 2014

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Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity.
Gentzon Hall, Janelle Rowell, Federica Farinelli, Rasheed A Gbadegesin, Peter Lavin, Michelle P Winn

Am J Physiol Renal Physiol· June 2014

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TNXB mutations can cause vesicoureteral reflux.
Rasheed A Gbadegesin, Patrick D Brophy, Adebowale Adeyemo, Gentzon Hall, Indra R Gupta, Michelle P Winn

J Am Soc Nephrol· July 2013

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Genetic testing in nephrotic syndrome--challenges and opportunities.
Rasheed A Gbadegesin, Michelle P Winn, William E Smoyer

Nat Rev Nephrol· March 2013

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A hybrid CFHR3-1 gene causes familial C3 glomerulopathy.
Talat H Malik, Peter J Lavin, Elena Goicoechea de Jorge, Katherine A Vernon, Kirsten L Rose, Michelle P Winn

J Am Soc Nephrol· July 2012

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Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis.
Rasheed A Gbadegesin, Peter J Lavin, Gentzon Hall, Bartlomiej Bartkowiak, Alison Homstad, Michelle P Winn

Kidney Int· January 2012

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Hepatorenal correction in murine glycogen storage disease type I with a double-stranded adeno-associated virus vector.
Xiaoyan Luo, Gentzon Hall, Songtao Li, Andrew Bird, Peter J Lavin, Michelle P Winn

Mol Ther· November 2011

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Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis.
Shreeram Akilesh, Hani Suleiman, Haiyang Yu, M Christine Stander, Peter Lavin, Michelle P Winn

J Clin Invest· October 2011

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TORCing up the importance of calcium signaling.
Peter J Lavin, Michelle P Winn

J Am Soc Nephrol· August 2011

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Pathogenesis and therapy of focal segmental glomerulosclerosis: an update.
Rasheed Gbadegesin, Peter Lavin, John Foreman, Michelle Winn

Pediatr Nephrol· July 2011

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TRPC6 enhances angiotensin II-induced albuminuria.
Jason Eckel, Peter J Lavin, Elizabeth A Finch, Nirvan Mukerji, Jarrett Burch, Michelle P Winn

J Am Soc Nephrol· March 2011

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Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.
Therese C Jungraithmayr, Katrin Hofer, Pierre Cochat, Gil Chernin, Gerard Cortina, Michelle P Winn

J Am Soc Nephrol· March 2011

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Modulation of the BP response to diet by genes in the renin-angiotensin system and the adrenergic nervous system.
Laura P Svetkey, Emily L Harris, Eden Martin, William M Vollmer, Gayle T Meltesen, Michelle P Winn

Am J Hypertens· February 2011

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A new locus for familial FSGS on chromosome 2p.
Rasheed Gbadegesin, Peter Lavin, Louis Janssens, Bartlomiej Bartkowiak, Alison Homstad, Michelle P Winn

J Am Soc Nephrol· August 2010

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TRPC1 channels are critical for hypertrophic signaling in the heart.
Malini Seth, Zhu-Shan Zhang, Lan Mao, Victoria Graham, Jarrett Burch, Michelle Winn

Circ Res· November 2009

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Exclusion of homozygous PLCE1 (NPHS3) mutations in 69 families with idiopathic and hereditary FSGS.
Rasheed Gbadegesin, Bartlomiej Bartkowiak, Peter J Lavin, Nirvan Mukerji, Guanghong Wu, Michelle P Winn

Pediatr Nephrol· February 2009

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Therapeutic targets in focal and segmental glomerulosclerosis.
Peter J Lavin, Rasheed Gbadegesin, Tirupapuliyur V Damodaran, Michelle P Winn

Curr Opin Nephrol Hypertens· July 2008

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2007 Young Investigator Award: TRP'ing into a new era for glomerular disease.
Michelle P Winn

J Am Soc Nephrol· June 2008

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TRPC6 and FSGS: the latest TRP channelopathy.
Nirvan Mukerji, Tirupapuliyur V Damodaran, Michelle P Winn

Biochim Biophys Acta· August 2007

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Focal and segmental glomerulosclerosis: varying biologic mechanisms underlie a final histopathologic end point.
Nikki Daskalakis, Michelle P Winn

Semin Nephrol· March 2006

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