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Publication Name World Journal of Nephrology
Manuscript ID 10321
Country Japan
Received
2014-03-26 14:35
Peer-Review Started
2014-03-26 21:14
To Make the First Decision
2014-04-15 15:18
Return for Revision
2014-04-18 10:30
Revised
2014-05-15 09:03
Second Decision
2014-06-27 17:39
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief
2014-06-27 17:53
Articles in Press
2014-06-27 18:12
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2014-09-30 17:21
Publish the Manuscript Online
2014-10-19 20:47
ISSN 2220-6124 (online)
Open Access
Copyright
Article Reprints For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
Permissions For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Medicine, Research & Experimental
Manuscript Type Minireviews
Article Title Therapeutic target for nephrotic syndrome: Identification of novel slit diaphragm associated molecules
Manuscript Source Invited Manuscript
All Author List Yoshiyasu Fukusumi, Naoko Miyauchi, Taeko Hashimoto, Akira Saito and Hiroshi Kawachi
Funding Agency and Grant Number
Corresponding Author Hiroshi Kawachi, MD, PhD, Department of Cell Biology, Institute of Nephrology, Niigata University Graduate School of Medical and Dental Sciences, 1-757, Asahimachi-Dori, Niigata 951-8510, Japan. kawachi@med.niigata-u.ac.jp
Key Words Podocyte; Slit diaphragm; Synaptic vesicle protein 2B; Ephrin-B1; Neurexin
Core Tip The slit diaphragm located between neighboring foot processes of a glomerular podocyte functions as a final barrier to retain plasma proteins. Recently several molecules such as nephrin and podocin were identified as functional molecules of the slit diaphragm. However, the precise molecular compositions of the slit diaphragm are still unclear and the mechanism regulating its barrier function is not fully understood yet. Recently we have reported that synaptic vesicle protein 2B, ephrin-B1 and neurexin are expressed in podocyte and the decreased function of these molecules participates in the initiation of proteinuria. These molecules could be targets for a novel therapy for proteinuria.
Publish Date 2014-10-19 20:47
Citation Fukusumi Y, Miyauchi N, Hashimoto T, Saito A, Kawachi H. Therapeutic target for nephrotic syndrome: Identification of novel slit diaphragm associated molecules. World J Nephrol 2014; 3(3): 77-84
URL http://www.wjgnet.com/2220-6124/full/v3/i3/77.htm
DOI http://dx.doi.org/10.5527/wjn.v3.i3.77
Full Article (PDF) WJN-3-77.pdf
Full Article (Word) WJN-3-77.doc
Manuscript File 10321-Review.docx
Answering Reviewers 10321-Answering reviewers.pdf
Copyright License Agreement 10321-Copyright assignment.pdf
Peer-review Report 10321-Peer review(s).pdf
Scientific Misconduct Check 10321-CrossCheck.jpg
Scientific Editor Work List 10321-Scientific editor work list.pdf