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Articles Published Processes
5/21/2015 2:15:00 PM | Browse: 957 | Download: 1584
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Received |
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2014-09-30 17:01 |
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Peer-Review Started |
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2014-10-02 10:34 |
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To Make the First Decision |
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2014-10-28 14:35 |
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Return for Revision |
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2014-10-30 18:26 |
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Revised |
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2014-11-12 20:57 |
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Second Decision |
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2015-01-29 09:20 |
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Accepted by Journal Editor-in-Chief |
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2015-01-29 09:28 |
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Accepted by Executive Editor-in-Chief |
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2015-02-09 10:42 |
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Articles in Press |
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2015-02-09 10:42 |
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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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2015-04-22 16:06 |
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Publish the Manuscript Online |
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2015-05-21 14:15 |
ISSN |
2220-315x (online) |
Open Access |
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
Copyright |
© The Author(s) 2015. Published by Baishideng Publishing Group Inc. All rights reserved. |
Article Reprints |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
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Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
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Publisher |
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA |
Website |
http://www.wjgnet.com |
Category |
Medical Laboratory Technology |
Manuscript Type |
Minireviews |
Article Title |
Genetic test in multiple endocrine neoplasia type 1 syndrome: An evolving story
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Manuscript Source |
Invited Manuscript |
All Author List |
Francesca Marini, Francesca Giusti and Maria Luisa Brandi |
Funding Agency and Grant Number |
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Corresponding Author |
Maria Luisa Brandi, MD, PhD, Professor of Endocrinology, Department of Surgery and Translational Medicine, University of Florence, Largo Palagi 1, 50134 Florence, Italy. marialuisa.brandi@unifi.it |
Key Words |
Multiple endocrine neoplasia type 1; Genetic test; Clinical practice; Next-generation sequencing |
Core Tip |
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant inherited tumour syndrome. Mutation analysis of the causative gene, the oncosuppressor MEN1 gene, is today the best approach for the early and differential diagnosis of the disease. The manuscript gives an overview on current genetic testing of MEN1 syndrome, reporting the positive aspects and clinical utility of performing the analysis. Moreover, the paper aims to report the future perspectives for improving the performance of the test and its application in clinical practice. |
Publish Date |
2015-05-21 14:15 |
Citation |
Marini F, Giusti F, Brandi ML. Genetic test in multiple endocrine neoplasia type 1 syndrome: An evolving story. World J Exp Med 2015; 5(2): 124-129 |
URL |
http://www.wjgnet.com/2220-315X/full/v5/i2/124.htm |
DOI |
http://dx.doi.org/10.5493/wjem.v5.i2.124 |
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