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Articles Published Processes
9/19/2014 8:46:00 PM | Browse: 895 | Download: 835
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Received |
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2013-12-26 10:09 |
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Peer-Review Started |
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2013-12-26 12:01 |
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To Make the First Decision |
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2014-03-12 17:05 |
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Return for Revision |
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2014-03-21 20:31 |
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Revised |
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Second Decision |
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2014-05-16 17:27 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2014-05-16 17:48 |
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Articles in Press |
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2014-05-23 12:26 |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2014-09-03 17:47 |
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Publish the Manuscript Online |
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2014-09-19 20:46 |
Category |
Gastroenterology & Hepatology |
Manuscript Type |
Review |
Article Title |
Molecular genetics of gastric adenocarcinoma in clinical practice
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Manuscript Source |
Invited Manuscript |
All Author List |
Margaret Cho, Ogechukwu Eze and Ruliang Xu |
Funding Agency and Grant Number |
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Corresponding Author |
Ruliang Xu, MD, PhD, Department of Pathology, New York University Langone Medical Center, 550 First Avenue, New York, NY 10016,
United States. ruliang.xu@nyumc.org
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Key Words |
Molecular genetics; Lauren classification; Intestinal type gastric cancer; Diffuse type gastric cancer; Molecular Biomarker |
Core Tip |
Intestinal and diffuse cell types of gastric carcinoma have a significant difference in clinical outcome with different molecular pathogenetic pathways. Intestinal type gastric carcinoma (GC) is associated with chromosomal and/or microsatellite instability, mutation of tumor suppressor genes, and loss of heterozygosity. Diffuse type GC is commonly associated with mutation of the E-cadherin gene, and a manifestation of the hereditary gastric cancer syndrome. Detection of certain mutations may aid in early diagnosis, screening, and prognostication of GC, and common genetic alterations may offer therapeutic targets for treatment. Furthermore, potential therapeutic biomarkers for GC are under investigation and may hold future promise.
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Publish Date |
2014-09-19 20:46 |
Citation |
Cho M, Eze O, Xu R. Molecular genetics of gastric adenocarcinoma in clinical practice. World J Med Genet 2014; 4(3): 58-68 |
URL |
http://www.wjgnet.com/2220-3184/full/v4/i3/58.htm |
DOI |
http://dx.doi.org/10.5496/wjmg.v4.i3.58 |
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