Early infiltrating macrophage subtype correlates with late-stage phenotypic outcome in a mouse model of hepatorenal fibrocystic disease

Author:

Zimmerman Kurt A.,Song Cheng J.,Aloria Ernald J. G.,Li Zhang,Zhou Juling,Bland Sarah J.,Yashchenko AlexORCID,Crossman David K.ORCID,Mrug Michal,Yoder Bradley K.ORCID

Funder

UAB | School of Medicine, University of Alabama at Birmingham

U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases

U.S. Department of Veterans Affairs

PKD Foundation

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology,Pathology and Forensic Medicine

Reference39 articles.

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2. Yoder BK, Richards WG, Sweeney WE, Wilkinson JE, Avener ED, Woychik RP. Insertional mutagenesis and molecular analysis of a new gene associated with polycystic kidney disease. Proc Assoc Am Phys. 1995;107:314–23.

3. Yoder BK, Richards WG, Sommardahl C, Sweeney WE, Michaud EJ, Wilkinson JE, et al. 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. Am J Pathol. 1997;150:2231–41.

4. Woon C, Bielinski-Bradbury A, O’Reilly K, Robinson P. A systematic review of the predictors of disease progression in patients with autosomal dominant polycystic kidney disease. BMC Nephrol. 2015;16:140.

5. Cnossen WR, te Morsche RH, Hoischen A, Gilissen C, Chrispijn M, Venselaar H, et al. Whole-exome sequencing reveals LRP5 mutations and canonical Wnt signaling associated with hepatic cystogenesis. Proc Natl Acad Sci USA. 2014;111:5343–8.

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