Loading…
Mitochondrial Replacement, Evolution, and the Clinic
Mitochondrial replacement therapy might bear health risks, especially for males. Mitochondrial diseases [often caused by mutations in mitochondrial DNA (mtDNA)] can manifest in a range of severe symptoms, for which there are currently no cures ( 1 ). The diseases are passed from mothers to offspring...
Saved in:
Published in: | Science (American Association for the Advancement of Science) 2013-09, Vol.341 (6152), p.1345-1346 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c357t-64051dfcb41789eda99c61c280f11cfeb50699eae78210cdbc87122ffe15b87b3 |
---|---|
cites | cdi_FETCH-LOGICAL-c357t-64051dfcb41789eda99c61c280f11cfeb50699eae78210cdbc87122ffe15b87b3 |
container_end_page | 1346 |
container_issue | 6152 |
container_start_page | 1345 |
container_title | Science (American Association for the Advancement of Science) |
container_volume | 341 |
creator | Reinhardt, Klaus Dowling, Damian K. Morrow, Edward H. |
description | Mitochondrial replacement therapy might bear health risks, especially for males.
Mitochondrial diseases [often caused by mutations in mitochondrial DNA (mtDNA)] can manifest in a range of severe symptoms, for which there are currently no cures (
1
). The diseases are passed from mothers to offspring. Intense research efforts have recently focused on a germline therapeutic strategy to prevent the inheritance of disease-causing mitochondria. However, although there has been increased government interest, especially in the United Kingdom, for using this approach to treat patients, there are reasons to believe that it is premature to move this technology into the clinic at this stage. |
doi_str_mv | 10.1126/science.1237146 |
format | article |
fullrecord | <record><control><sourceid>jstor_proqu</sourceid><recordid>TN_cdi_proquest_journals_1434084694</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>42619344</jstor_id><sourcerecordid>42619344</sourcerecordid><originalsourceid>FETCH-LOGICAL-c357t-64051dfcb41789eda99c61c280f11cfeb50699eae78210cdbc87122ffe15b87b3</originalsourceid><addsrcrecordid>eNo9kE1LAzEURYMoWKtrV8KA206bl2QyyVJK_YCKILoOmUxCU6ZJTVLBf-9Ii6u3uOfeBwehW8BzAMIX2XgbjJ0DoS0wfoYmgGVTS4LpOZpgTHktcNtcoquctxiPmaQTxF59iWYTQ5-8Hqp3ux-0sTsbyqxafcfhUHwMs0qHviobWy0HH7y5RhdOD9nenO4UfT6uPpbP9frt6WX5sK4NbdpSc4Yb6J3pGLRC2l5LaTgYIrADMM52DeZSWm1bQQCbvjOiBUKcs9B0ou3oFN0fd_cpfh1sLmobDymMLxUwyrBgXLKRWhwpk2LOyTq1T36n048CrP7UqJMadVIzNu6OjW0uMf3jjHCQlDH6C_Y2YQ4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1434084694</pqid></control><display><type>article</type><title>Mitochondrial Replacement, Evolution, and the Clinic</title><source>American Association for the Advancement of Science</source><source>JSTOR Archival Journals and Primary Sources Collection</source><source>Alma/SFX Local Collection</source><creator>Reinhardt, Klaus ; Dowling, Damian K. ; Morrow, Edward H.</creator><creatorcontrib>Reinhardt, Klaus ; Dowling, Damian K. ; Morrow, Edward H.</creatorcontrib><description>Mitochondrial replacement therapy might bear health risks, especially for males.
Mitochondrial diseases [often caused by mutations in mitochondrial DNA (mtDNA)] can manifest in a range of severe symptoms, for which there are currently no cures (
1
). The diseases are passed from mothers to offspring. Intense research efforts have recently focused on a germline therapeutic strategy to prevent the inheritance of disease-causing mitochondria. However, although there has been increased government interest, especially in the United Kingdom, for using this approach to treat patients, there are reasons to believe that it is premature to move this technology into the clinic at this stage.</description><identifier>ISSN: 0036-8075</identifier><identifier>EISSN: 1095-9203</identifier><identifier>DOI: 10.1126/science.1237146</identifier><identifier>CODEN: SCIEAS</identifier><language>eng</language><publisher>Washington: American Association for the Advancement of Science</publisher><subject>Deoxyribonucleic acid ; Disease risks ; Diseases ; DNA ; Evolution ; Genetic mutation ; Health outcomes ; Mitochondria ; Mitochondrial diseases ; Mitochondrial DNA ; Mutation ; Oocytes ; POLICY FORUM ; Species ; Therapy</subject><ispartof>Science (American Association for the Advancement of Science), 2013-09, Vol.341 (6152), p.1345-1346</ispartof><rights>Copyright © 2013 American Association for the Advancement of Science</rights><rights>Copyright © 2013, American Association for the Advancement of Science</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-64051dfcb41789eda99c61c280f11cfeb50699eae78210cdbc87122ffe15b87b3</citedby><cites>FETCH-LOGICAL-c357t-64051dfcb41789eda99c61c280f11cfeb50699eae78210cdbc87122ffe15b87b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/42619344$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/42619344$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,2884,2885,27924,27925,58238,58471</link.rule.ids></links><search><creatorcontrib>Reinhardt, Klaus</creatorcontrib><creatorcontrib>Dowling, Damian K.</creatorcontrib><creatorcontrib>Morrow, Edward H.</creatorcontrib><title>Mitochondrial Replacement, Evolution, and the Clinic</title><title>Science (American Association for the Advancement of Science)</title><description>Mitochondrial replacement therapy might bear health risks, especially for males.
Mitochondrial diseases [often caused by mutations in mitochondrial DNA (mtDNA)] can manifest in a range of severe symptoms, for which there are currently no cures (
1
). The diseases are passed from mothers to offspring. Intense research efforts have recently focused on a germline therapeutic strategy to prevent the inheritance of disease-causing mitochondria. However, although there has been increased government interest, especially in the United Kingdom, for using this approach to treat patients, there are reasons to believe that it is premature to move this technology into the clinic at this stage.</description><subject>Deoxyribonucleic acid</subject><subject>Disease risks</subject><subject>Diseases</subject><subject>DNA</subject><subject>Evolution</subject><subject>Genetic mutation</subject><subject>Health outcomes</subject><subject>Mitochondria</subject><subject>Mitochondrial diseases</subject><subject>Mitochondrial DNA</subject><subject>Mutation</subject><subject>Oocytes</subject><subject>POLICY FORUM</subject><subject>Species</subject><subject>Therapy</subject><issn>0036-8075</issn><issn>1095-9203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNo9kE1LAzEURYMoWKtrV8KA206bl2QyyVJK_YCKILoOmUxCU6ZJTVLBf-9Ii6u3uOfeBwehW8BzAMIX2XgbjJ0DoS0wfoYmgGVTS4LpOZpgTHktcNtcoquctxiPmaQTxF59iWYTQ5-8Hqp3ux-0sTsbyqxafcfhUHwMs0qHviobWy0HH7y5RhdOD9nenO4UfT6uPpbP9frt6WX5sK4NbdpSc4Yb6J3pGLRC2l5LaTgYIrADMM52DeZSWm1bQQCbvjOiBUKcs9B0ou3oFN0fd_cpfh1sLmobDymMLxUwyrBgXLKRWhwpk2LOyTq1T36n048CrP7UqJMadVIzNu6OjW0uMf3jjHCQlDH6C_Y2YQ4</recordid><startdate>20130920</startdate><enddate>20130920</enddate><creator>Reinhardt, Klaus</creator><creator>Dowling, Damian K.</creator><creator>Morrow, Edward H.</creator><general>American Association for the Advancement of Science</general><general>The American Association for the Advancement of Science</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QQ</scope><scope>7QR</scope><scope>7SC</scope><scope>7SE</scope><scope>7SN</scope><scope>7SP</scope><scope>7SR</scope><scope>7SS</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7TK</scope><scope>7TM</scope><scope>7U5</scope><scope>7U9</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9.</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20130920</creationdate><title>Mitochondrial Replacement, Evolution, and the Clinic</title><author>Reinhardt, Klaus ; Dowling, Damian K. ; Morrow, Edward H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-64051dfcb41789eda99c61c280f11cfeb50699eae78210cdbc87122ffe15b87b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Deoxyribonucleic acid</topic><topic>Disease risks</topic><topic>Diseases</topic><topic>DNA</topic><topic>Evolution</topic><topic>Genetic mutation</topic><topic>Health outcomes</topic><topic>Mitochondria</topic><topic>Mitochondrial diseases</topic><topic>Mitochondrial DNA</topic><topic>Mutation</topic><topic>Oocytes</topic><topic>POLICY FORUM</topic><topic>Species</topic><topic>Therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reinhardt, Klaus</creatorcontrib><creatorcontrib>Dowling, Damian K.</creatorcontrib><creatorcontrib>Morrow, Edward H.</creatorcontrib><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Ecology Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Science (American Association for the Advancement of Science)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reinhardt, Klaus</au><au>Dowling, Damian K.</au><au>Morrow, Edward H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mitochondrial Replacement, Evolution, and the Clinic</atitle><jtitle>Science (American Association for the Advancement of Science)</jtitle><date>2013-09-20</date><risdate>2013</risdate><volume>341</volume><issue>6152</issue><spage>1345</spage><epage>1346</epage><pages>1345-1346</pages><issn>0036-8075</issn><eissn>1095-9203</eissn><coden>SCIEAS</coden><abstract>Mitochondrial replacement therapy might bear health risks, especially for males.
Mitochondrial diseases [often caused by mutations in mitochondrial DNA (mtDNA)] can manifest in a range of severe symptoms, for which there are currently no cures (
1
). The diseases are passed from mothers to offspring. Intense research efforts have recently focused on a germline therapeutic strategy to prevent the inheritance of disease-causing mitochondria. However, although there has been increased government interest, especially in the United Kingdom, for using this approach to treat patients, there are reasons to believe that it is premature to move this technology into the clinic at this stage.</abstract><cop>Washington</cop><pub>American Association for the Advancement of Science</pub><doi>10.1126/science.1237146</doi><tpages>2</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0036-8075 |
ispartof | Science (American Association for the Advancement of Science), 2013-09, Vol.341 (6152), p.1345-1346 |
issn | 0036-8075 1095-9203 |
language | eng |
recordid | cdi_proquest_journals_1434084694 |
source | American Association for the Advancement of Science; JSTOR Archival Journals and Primary Sources Collection; Alma/SFX Local Collection |
subjects | Deoxyribonucleic acid Disease risks Diseases DNA Evolution Genetic mutation Health outcomes Mitochondria Mitochondrial diseases Mitochondrial DNA Mutation Oocytes POLICY FORUM Species Therapy |
title | Mitochondrial Replacement, Evolution, and the Clinic |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T00%3A05%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Mitochondrial%20Replacement,%20Evolution,%20and%20the%20Clinic&rft.jtitle=Science%20(American%20Association%20for%20the%20Advancement%20of%20Science)&rft.au=Reinhardt,%20Klaus&rft.date=2013-09-20&rft.volume=341&rft.issue=6152&rft.spage=1345&rft.epage=1346&rft.pages=1345-1346&rft.issn=0036-8075&rft.eissn=1095-9203&rft.coden=SCIEAS&rft_id=info:doi/10.1126/science.1237146&rft_dat=%3Cjstor_proqu%3E42619344%3C/jstor_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c357t-64051dfcb41789eda99c61c280f11cfeb50699eae78210cdbc87122ffe15b87b3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1434084694&rft_id=info:pmid/&rft_jstor_id=42619344&rfr_iscdi=true |