Literature DB >> 18039103

Cystic disease of the kidney.

Patricia D Wilson1, Beatrice Goilav.   

Abstract

This review focuses on the mechanisms that underlie the development of human renal cystic diseases. A pathological, clinical, and pathophysiological overview is given. Initial analysis of the cell biology of inappropriate hyperproliferation accompanied by fluid secretion of cyst-lining epithelia has been followed by the elucidation of fundamental defects in epithelial polarity, cell-matrix and cell-cell interactions, and apoptosis, all of which are discussed. Identification of the genes and proteins responsible for several renal cystic diseases has led to a more complete understanding of defects in renal developmental programming, differentiation, and morphogenesis, all of which underlie cystic diseases of the kidney.

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Year:  2007        PMID: 18039103     DOI: 10.1146/annurev.pathol.2.010506.091850

Source DB:  PubMed          Journal:  Annu Rev Pathol        ISSN: 1553-4006            Impact factor:   23.472


  38 in total

1.  2-Hydroxyestradiol slows progression of experimental polycystic kidney disease.

Authors:  Sharon Anderson; Terry T Oyama; Jessie N Lindsley; William E Schutzer; Douglas R Beard; Vincent H Gattone; Radko Komers
Journal:  Am J Physiol Renal Physiol       Date:  2011-12-07

Review 2.  Tubulogenesis.

Authors:  M Luisa Iruela-Arispe; Greg J Beitel
Journal:  Development       Date:  2013-07       Impact factor: 6.868

3.  Induced pluripotent stem cells from polycystic kidney disease patients: a novel tool to model the pathogenesis of cystic kidney disease.

Authors:  Alexis Hofherr; Michael Köttgen
Journal:  J Am Soc Nephrol       Date:  2013-09-05       Impact factor: 10.121

Review 4.  Extending the knowledge in histochemistry and cell biology.

Authors:  Wolfgang-Moritz Heupel; Detlev Drenckhahn
Journal:  Histochem Cell Biol       Date:  2009-11-28       Impact factor: 4.304

Review 5.  Regulation of transport in the connecting tubule and cortical collecting duct.

Authors:  Alexander Staruschenko
Journal:  Compr Physiol       Date:  2012-04       Impact factor: 9.090

6.  Determination of urinary lithogenic parameters in murine models orthologous to autosomal dominant polycystic kidney disease.

Authors:  Renato Ribeiro Nogueira Ferraz; Jonathan Mackowiak Fonseca; Gregory George Germino; Luiz Fernando Onuchic; Ita Pfeferman Heilberg
Journal:  Urolithiasis       Date:  2014-05-10       Impact factor: 3.436

7.  Inactivation of Pkd1 in principal cells causes a more severe cystic kidney disease than in intercalated cells.

Authors:  Kalani L Raphael; Kevin A Strait; Peter K Stricklett; R Lance Miller; Raoul D Nelson; Klaus B Piontek; Gregory G Germino; Donald E Kohan
Journal:  Kidney Int       Date:  2009-01-14       Impact factor: 10.612

8.  Carboxy terminal tail of polycystin-1 regulates localization of TSC2 to repress mTOR.

Authors:  Ruhee Dere; Patricia D Wilson; Richard N Sandford; Cheryl Lyn Walker
Journal:  PLoS One       Date:  2010-02-16       Impact factor: 3.240

9.  Conditional mutation of Pkd2 causes cystogenesis and upregulates beta-catenin.

Authors:  Ingyu Kim; Tianbing Ding; Yulong Fu; Cunxi Li; Lan Cui; Ao Li; Peiwen Lian; Dan Liang; Dao W Wang; Caiying Guo; Jie Ma; Ping Zhao; Robert J Coffey; Qimin Zhan; Guanqing Wu
Journal:  J Am Soc Nephrol       Date:  2009-11-25       Impact factor: 10.121

10.  Abnormalities in focal adhesion complex formation, regulation, and function in human autosomal recessive polycystic kidney disease epithelial cells.

Authors:  Sharon Israeli; Kurt Amsler; Nadezhda Zheleznova; Patricia D Wilson
Journal:  Am J Physiol Cell Physiol       Date:  2009-11-18       Impact factor: 4.249

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