Literature DB >> 20362096

Polycystic kidney disease, cilia, and planar polarity.

Luis F Menezes1, Gregory G Germino.   

Abstract

Cystic kidney diseases are characterized by dilated or cystic kidney tubular segments. Changes in planar cell polarity, flow sensing, and/or proliferation have been proposed to explain these disorders. Over the last few years, several groups have suggested that ciliary dysfunction is a central component of cyst formation. We review evidence for and against each of these models, stressing some of the inconsistencies that should be resolved if an accurate understanding of cyst formation is to be achieved. We also comment on data supporting a model in which ciliary function could play different roles at different developmental stages and on the relevance of dissecting potential differences between pathways required for tubule formation and/or maintenance. 2009 Elsevier Inc. All rights reserved.

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Year:  2009        PMID: 20362096     DOI: 10.1016/S0091-679X(08)94014-0

Source DB:  PubMed          Journal:  Methods Cell Biol        ISSN: 0091-679X            Impact factor:   1.441


  18 in total

Review 1.  Axonemal positioning and orientation in three-dimensional space for primary cilia: what is known, what is assumed, and what needs clarification.

Authors:  Cornelia E Farnum; Norman J Wilsman
Journal:  Dev Dyn       Date:  2011-11       Impact factor: 3.780

Review 2.  Systems biology of polycystic kidney disease: a critical review.

Authors:  Luis Fernando Menezes; Gregory G Germino
Journal:  Wiley Interdiscip Rev Syst Biol Med       Date:  2015-02-02

Review 3.  Developmental signaling: does it bridge the gap between cilia dysfunction and renal cystogenesis?

Authors:  Pamela V Tran; Madhulika Sharma; Xiaogang Li; James P Calvet
Journal:  Birth Defects Res C Embryo Today       Date:  2014-05-26

Review 4.  Gli-similar proteins: their mechanisms of action, physiological functions, and roles in disease.

Authors:  Kristin Lichti-Kaiser; Gary ZeRuth; Hong Soon Kang; Shivakumar Vasanth; Anton M Jetten
Journal:  Vitam Horm       Date:  2012       Impact factor: 3.421

Review 5.  Autosomal recessive polycystic kidney disease: a hepatorenal fibrocystic disorder with pleiotropic effects.

Authors:  Erum A Hartung; Lisa M Guay-Woodford
Journal:  Pediatrics       Date:  2014-08-11       Impact factor: 7.124

6.  A genetic interaction network of five genes for human polycystic kidney and liver diseases defines polycystin-1 as the central determinant of cyst formation.

Authors:  Sorin V Fedeles; Xin Tian; Anna-Rachel Gallagher; Michihiro Mitobe; Saori Nishio; Seung Hun Lee; Yiqiang Cai; Lin Geng; Craig M Crews; Stefan Somlo
Journal:  Nat Genet       Date:  2011-06-19       Impact factor: 38.330

Review 7.  The role of the cilium in normal and abnormal cell cycles: emphasis on renal cystic pathologies.

Authors:  Junmin Pan; Tamina Seeger-Nukpezah; Erica A Golemis
Journal:  Cell Mol Life Sci       Date:  2012-07-11       Impact factor: 9.261

8.  Controlling the direction of division.

Authors:  Peter Satir
Journal:  Stem Cell Res Ther       Date:  2010-07-23       Impact factor: 6.832

9.  Murine Models of Polycystic Kidney Disease.

Authors:  Luis Fernando Menezes; Gregory George Germino
Journal:  Drug Discov Today Dis Mech       Date:  2013-12-01

10.  Cdc42 deficiency causes ciliary abnormalities and cystic kidneys.

Authors:  Soo Young Choi; Maria F Chacon-Heszele; Liwei Huang; Sarah McKenna; F Perry Wilson; Xiaofeng Zuo; Joshua H Lipschutz
Journal:  J Am Soc Nephrol       Date:  2013-06-13       Impact factor: 10.121

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