Physiology Cambridge Electronic Design Limited
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Physiology 19: 225-230, 2004; doi:10.1152/physiol.00003.2004
1548-9213/04 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (31)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Zhang, Q.
Right arrow Articles by Yoder, B. K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zhang, Q.
Right arrow Articles by Yoder, B. K.
Physiology, Vol. 19, No. 4, 225-230, August 2004
© 2004 Int. Union Physiol. Sci./Am. Physiol. Soc.

REVIEW

Cystic Kidney Diseases: All Roads Lead to the Cilium

Qihong Zhang, Patrick D. Taulman and Bradley K. Yoder

Department of Cell Biology, University of Alabama at Birmingham, Birmingham, Alabama 35294
byoder{at}uab.edu

Cystic kidney disorders are one of the leading causes of end-stage renal disease. Numerous experimental animal models have been used to understand the disease pathogenesis. Recent advancements in this field have provided a surprising finding: that many of the proteins associated with cystic kidney disease localize to a nearly forgotten organelle, the primary cilium.




This article has been cited by other articles:


Home page
Nephrol Dial TransplantHome page
E. Verghese, R. Weidenfeld, J. F. Bertram, S. D. Ricardo, and J. A. Deane
Renal cilia display length alterations following tubular injury and are present early in epithelial repair
Nephrol. Dial. Transplant., March 1, 2008; 23(3): 834 - 841.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
M. E. Winkelbauer, J. C. Schafer, C. J. Haycraft, P. Swoboda, and B. K. Yoder
The C. elegans homologs of nephrocystin-1 and nephrocystin-4 are cilia transition zone proteins involved in chemosensory perception
J. Cell Sci., December 1, 2005; 118(23): 5575 - 5587.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
M. S. Miller, J. M. Esparza, A. M. Lippa, F. G. Lux III, D. G. Cole, and S. K. Dutcher
Mutant Kinesin-2 Motor Subunits Increase Chromosome Loss
Mol. Biol. Cell, August 1, 2005; 16(8): 3810 - 3820.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. ProteomicsHome page
N. Valkova, R. Yunis, S. K. Mak, K. Kang, and D. Kultz
Nek8 Mutation Causes Overexpression of Galectin-1, Sorcin, and Vimentin and Accumulation of the Major Urinary Protein in Renal Cysts of jck Mice
Mol. Cell. Proteomics, July 1, 2005; 4(7): 1009 - 1018.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2004 by the Int. Union Physiol. Sci./Am. Physiol. Soc.