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9/28/2014 2:57:00 PM | Browse: 942 | Download: 914
Publication Name World Journal of Stem Cells
Manuscript ID 13241
Country Japan
Received
2014-08-13 16:25
Peer-Review Started
2014-08-13 18:12
To Make the First Decision
2014-08-28 14:55
Return for Revision
2014-09-01 10:49
Revised
2014-09-11 20:10
Second Decision
2014-09-17 14:02
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief
2014-09-17 14:30
Articles in Press
2014-09-17 14:30
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2014-09-22 17:37
Publish the Manuscript Online
2014-09-28 14:56
ISSN 1948-0210 (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 Cell Biology
Manuscript Type Review
Article Title Connexin mutant embryonic stem cells and human diseases
Manuscript Source Invited Manuscript
All Author List Kiyomasa Nishii, Yosaburo Shibata and Yasushi Kobayashi
Funding Agency and Grant Number
Corresponding Author Kiyomasa Nishii, MD, PhD, Department of Anatomy and Neurobiology, National Defense Medical College, 3-2 Namiki, Tokorozawa, Saitama 359-8513, Japan. nishii@ndmc.ac.jp
Key Words Embryonic stem cells; Induced pluripotent stem cells; Gap junction; Human diseases; Genetic models; Differentiation; Chimera
Core Tip Numerous gap junction-encoding connexin (Cx) mutant mice have been established as models of human diseases. Although these analyses have facilitated current understanding of native Cx functions and the pathogenesis of related diseases, care must be taken when extrapolating findings from mice to humans, and vice versa, because there can be striking diversity in tissue organization and Cx expression patterns between these species. Recently, the use of human induced pluripotent stem cells (iPSCs) allowed further direct approaches for studying human diseases. According to the studies using mutant mouse embryonic stem cells, Cx mutant human iPSCs may become a useful model.
Publish Date 2014-09-28 14:56
Citation Nishii K, Shibata Y, Kobayashi Y. Connexin mutant embryonic stem cells and human diseases. World J Stem Cells 2014; 6(5): 571-578
URL http://www.wjgnet.com/1948-0210/full/v6/i5/571.htm
DOI http://dx.doi.org/10.4252/wjsc.v6.i5.571
Full Article (PDF) WJSC-6-571.pdf
Full Article (Word) WJSC-6-571.doc
Manuscript File 13241-Review.docx
Answering Reviewers 13241-Answering reviewers.pdf
Copyright License Agreement 13241-Copyright assignment.pdf
Peer-review Report 13241-Peer review(s).pdf
Scientific Misconduct Check 13241-CrossCheck.jpg
Scientific Editor Work List 13241-Scientific editor work list.pdf