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Charles E. Alpers

Researcher at University of Washington

Publications -  418
Citations -  35650

Charles E. Alpers is an academic researcher from University of Washington. The author has contributed to research in topics: Renal pathology & Glomerulonephritis. The author has an hindex of 89, co-authored 409 publications receiving 32440 citations. Previous affiliations of Charles E. Alpers include New York Medical College & University of Washington Medical Center.

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Lung cancer induced in mice by the envelope protein of jaagsiekte sheep retrovirus (JSRV) closely resembles lung cancer in sheep infected with JSRV

TL;DR: Lung cancers induced by J SRV infection in sheep and by JSRV Env expression in mice have similar histologic features and are primarily characterized by adenomatous proliferation of peripheral lung epithelial cells, so it is unnecessary to invoke a role for insertional mutagenesis, gene activation, viral replication, or expression of other viral gene products in sheep lung tumorigenesis.
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A new function for parietal epithelial cells: a second glomerular barrier

TL;DR: It is proposed that together with its underlying Bowman's basement membrane, the TJ of PECs serve as a second barrier to protein when disturbed following PEC injury, and the increase in permeability of this layer to filtered protein is a mechanism underlying periglomerular inflammation characteristic of anti-GBM disease.
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Exogenous PDGF-D Is a Potent Mesangial Cell Mitogen and Causes a Severe Mesangial Proliferative Glomerulopathy

TL;DR: It is demonstrated that PDGF-D is a major mediator of mesangial cell proliferation and the importance of engagement of PDGF receptor-beta in transducing mesangia proliferative glomerulopathy is emphasized.
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Serum amyloid A and inflammation in diabetic kidney disease and podocytes

TL;DR: It is concluded that SAA is increased in the blood and produced in the kidneys of people with DKD and corresponding diabetic mouse models and is a compelling candidate for DKD therapeutic and biomarker discovery.
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Replication in a Superficial Epithelial Cell Niche Explains the Lack of Pathogenicity of Primate Foamy Virus Infections

TL;DR: It is shown that superficial differentiated epithelial cells of the oral mucosa are the major cell type in which SFV replicates, which can explain the innocuous nature of SFV infection and the highly efficient transmission of FVs among NHPs.