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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Early exploration of two candidate breast cancer susceptibility genes identified by whole-exome sequencing</title><author><name sortKey="Blanc, R" sort="Blanc, R" uniqKey="Blanc R" first="R" last="Blanc">R. Blanc</name><affiliation><nlm:aff id="I1">Genetic Epidemiology Laboratory, The University of Melbourne, Melbourne, VIC, Australia</nlm:aff></affiliation><affiliation><nlm:aff id="I2">Universite Catholique de Lyon, Lyon, France</nlm:aff></affiliation></author><author><name sortKey="Jammot, A" sort="Jammot, A" uniqKey="Jammot A" first="A" last="Jammot">A. Jammot</name><affiliation><nlm:aff id="I1">Genetic Epidemiology Laboratory, The University of Melbourne, Melbourne, VIC, Australia</nlm:aff></affiliation><affiliation><nlm:aff id="I2">Universite Catholique de Lyon, Lyon, France</nlm:aff></affiliation></author><author><name sortKey="Nguyen Dumont, T" sort="Nguyen Dumont, T" uniqKey="Nguyen Dumont T" first="T" last="Nguyen-Dumont">T. Nguyen-Dumont</name><affiliation><nlm:aff id="I1">Genetic Epidemiology Laboratory, The University of Melbourne, Melbourne, VIC, Australia</nlm:aff></affiliation></author><author><name sortKey="Teo, Zl" sort="Teo, Zl" uniqKey="Teo Z" first="Zl" last="Teo">Zl Teo</name><affiliation><nlm:aff id="I1">Genetic Epidemiology Laboratory, The University of Melbourne, Melbourne, VIC, Australia</nlm:aff></affiliation></author><author><name sortKey="Odefrey, Fa" sort="Odefrey, Fa" uniqKey="Odefrey F" first="Fa" last="Odefrey">Fa Odefrey</name><affiliation><nlm:aff id="I1">Genetic Epidemiology Laboratory, The University of Melbourne, Melbourne, VIC, Australia</nlm:aff></affiliation></author><author><name sortKey="Hammet, F" sort="Hammet, F" uniqKey="Hammet F" first="F" last="Hammet">F. Hammet</name><affiliation><nlm:aff id="I1">Genetic Epidemiology Laboratory, The University of Melbourne, Melbourne, VIC, Australia</nlm:aff></affiliation></author><author><name sortKey="Goldgar, De" sort="Goldgar, De" uniqKey="Goldgar D" first="De" last="Goldgar">De Goldgar</name><affiliation><nlm:aff id="I3">Department of Dermatology, University of Utah School of Medicine, Salt Lake City, Utah, USA</nlm:aff></affiliation></author><author><name sortKey="Park, Dj" sort="Park, Dj" uniqKey="Park D" first="Dj" last="Park">Dj Park</name><affiliation><nlm:aff id="I1">Genetic Epidemiology Laboratory, The University of Melbourne, Melbourne, VIC, Australia</nlm:aff></affiliation></author><author><name sortKey="Southey, Mc" sort="Southey, Mc" uniqKey="Southey M" first="Mc" last="Southey">Mc Southey</name><affiliation><nlm:aff id="I1">Genetic Epidemiology Laboratory, The University of Melbourne, Melbourne, VIC, Australia</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmc">3327170</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3327170</idno><idno type="RBID">PMC:3327170</idno><idno type="doi">10.1186/1897-4287-10-S2-A91</idno><idno type="pmid">NONE</idno><date when="2012">2012</date><idno type="wicri:Area/Pmc/Corpus">001156</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001156</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Early exploration of two candidate breast cancer susceptibility genes identified by whole-exome sequencing</title><author><name sortKey="Blanc, R" sort="Blanc, R" uniqKey="Blanc R" first="R" last="Blanc">R. Blanc</name><affiliation><nlm:aff id="I1">Genetic Epidemiology Laboratory, The University of Melbourne, Melbourne, VIC, Australia</nlm:aff></affiliation><affiliation><nlm:aff id="I2">Universite Catholique de Lyon, Lyon, France</nlm:aff></affiliation></author><author><name sortKey="Jammot, A" sort="Jammot, A" uniqKey="Jammot A" first="A" last="Jammot">A. Jammot</name><affiliation><nlm:aff id="I1">Genetic Epidemiology Laboratory, The University of Melbourne, Melbourne, VIC, Australia</nlm:aff></affiliation><affiliation><nlm:aff id="I2">Universite Catholique de Lyon, Lyon, France</nlm:aff></affiliation></author><author><name sortKey="Nguyen Dumont, T" sort="Nguyen Dumont, T" uniqKey="Nguyen Dumont T" first="T" last="Nguyen-Dumont">T. Nguyen-Dumont</name><affiliation><nlm:aff id="I1">Genetic Epidemiology Laboratory, The University of Melbourne, Melbourne, VIC, Australia</nlm:aff></affiliation></author><author><name sortKey="Teo, Zl" sort="Teo, Zl" uniqKey="Teo Z" first="Zl" last="Teo">Zl Teo</name><affiliation><nlm:aff id="I1">Genetic Epidemiology Laboratory, The University of Melbourne, Melbourne, VIC, Australia</nlm:aff></affiliation></author><author><name sortKey="Odefrey, Fa" sort="Odefrey, Fa" uniqKey="Odefrey F" first="Fa" last="Odefrey">Fa Odefrey</name><affiliation><nlm:aff id="I1">Genetic Epidemiology Laboratory, The University of Melbourne, Melbourne, VIC, Australia</nlm:aff></affiliation></author><author><name sortKey="Hammet, F" sort="Hammet, F" uniqKey="Hammet F" first="F" last="Hammet">F. Hammet</name><affiliation><nlm:aff id="I1">Genetic Epidemiology Laboratory, The University of Melbourne, Melbourne, VIC, Australia</nlm:aff></affiliation></author><author><name sortKey="Goldgar, De" sort="Goldgar, De" uniqKey="Goldgar D" first="De" last="Goldgar">De Goldgar</name><affiliation><nlm:aff id="I3">Department of Dermatology, University of Utah School of Medicine, Salt Lake City, Utah, USA</nlm:aff></affiliation></author><author><name sortKey="Park, Dj" sort="Park, Dj" uniqKey="Park D" first="Dj" last="Park">Dj Park</name><affiliation><nlm:aff id="I1">Genetic Epidemiology Laboratory, The University of Melbourne, Melbourne, VIC, Australia</nlm:aff></affiliation></author><author><name sortKey="Southey, Mc" sort="Southey, Mc" uniqKey="Southey M" first="Mc" last="Southey">Mc Southey</name><affiliation><nlm:aff id="I1">Genetic Epidemiology Laboratory, The University of Melbourne, Melbourne, VIC, Australia</nlm:aff></affiliation></author></analytic><series><title level="j">Hereditary Cancer in Clinical Practice</title><idno type="ISSN">1731-2302</idno><idno type="eISSN">1897-4287</idno><imprint><date when="2012">2012</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader></TEI><pmc article-type="abstract" xml:lang="en"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Hered Cancer Clin Pract</journal-id><journal-id journal-id-type="iso-abbrev">Hered Cancer Clin Pract</journal-id><journal-title-group><journal-title>Hereditary Cancer in Clinical Practice</journal-title></journal-title-group><issn pub-type="ppub">1731-2302</issn><issn pub-type="epub">1897-4287</issn><publisher><publisher-name>BioMed Central</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmc">3327170</article-id><article-id pub-id-type="publisher-id">1897-4287-10-S2-A91</article-id><article-id pub-id-type="doi">10.1186/1897-4287-10-S2-A91</article-id><article-categories><subj-group subj-group-type="heading"><subject>Meeting Abstract</subject></subj-group></article-categories><title-group><article-title>Early exploration of two candidate breast cancer susceptibility genes identified by whole-exome sequencing</article-title></title-group><contrib-group><contrib contrib-type="author" corresp="yes" equal-contrib="yes" id="A1"><name><surname>Blanc</surname><given-names>R</given-names></name><xref ref-type="aff" rid="I1">1</xref><xref ref-type="aff" rid="I2">2</xref></contrib><contrib contrib-type="author" corresp="yes" equal-contrib="yes" id="A2"><name><surname>Jammot</surname><given-names>A</given-names></name><xref ref-type="aff" rid="I1">1</xref><xref ref-type="aff" rid="I2">2</xref></contrib><contrib contrib-type="author" id="A3"><name><surname>Nguyen-Dumont</surname><given-names>T</given-names></name><xref ref-type="aff" rid="I1">1</xref></contrib><contrib contrib-type="author" id="A4"><name><surname>Teo</surname><given-names>ZL</given-names></name><xref ref-type="aff" rid="I1">1</xref></contrib><contrib contrib-type="author" id="A5"><name><surname>Odefrey</surname><given-names>FA</given-names></name><xref ref-type="aff" rid="I1">1</xref></contrib><contrib contrib-type="author" id="A6"><name><surname>Hammet</surname><given-names>F</given-names></name><xref ref-type="aff" rid="I1">1</xref></contrib><on-behalf-of>VLSCI</on-behalf-of><on-behalf-of>BCFR</on-behalf-of><on-behalf-of>MCCS</on-behalf-of><contrib contrib-type="author" id="A10"><name><surname>Goldgar</surname><given-names>DE</given-names></name><xref ref-type="aff" rid="I3">3</xref></contrib><contrib contrib-type="author" id="A11"><name><surname>Park</surname><given-names>DJ</given-names></name><xref ref-type="aff" rid="I1">1</xref></contrib><contrib contrib-type="author" id="A12"><name><surname>Southey</surname><given-names>MC</given-names></name><xref ref-type="aff" rid="I1">1</xref></contrib></contrib-group><aff id="I1"><label>1</label>Genetic Epidemiology Laboratory, The University of Melbourne, Melbourne, VIC, Australia</aff><aff id="I2"><label>2</label>Universite Catholique de Lyon, Lyon, France</aff><aff id="I3"><label>3</label>Department of Dermatology, University of Utah School of Medicine, Salt Lake City, Utah, USA</aff><pub-date pub-type="collection"><year>2012</year></pub-date><pub-date pub-type="epub"><day>12</day><month>4</month><year>2012</year></pub-date><volume>10</volume><issue>Suppl 2</issue><supplement><named-content content-type="supplement-title">Familial Aspects of Cancer 2011 Research and Practice</named-content><named-content content-type="supplement-editor">Rodney Scott</named-content></supplement><fpage>A91</fpage><lpage>A91</lpage><permissions><copyright-statement>Copyright ©2012 Blanc et al; licensee BioMed Central Ltd.</copyright-statement><copyright-year>2012</copyright-year><copyright-holder>Blanc et al; licensee BioMed Central Ltd.</copyright-holder><license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/2.0"><license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/2.0">http://creativecommons.org/licenses/by/2.0</ext-link>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p></license></permissions><self-uri xlink:href="http://www.hccpjournal.com/content/10/S2/A91"></self-uri><conference><conf-date>23-26 August 2011</conf-date><conf-name>Familial Aspects of Cancer 2011 Research and Practice: A combined meeting of kConFab, Australian Breast Cancer Family Study, Australian Colorectal Cancer Family Study, Australian Ovarian Cancer Study, Family Cancer Clinics of Australia and New Zealand and kConFab</conf-name><conf-loc>Kingscliff, Australia</conf-loc></conference></article-meta></front><body><sec><title></title><p>Breast cancer (BC) is the most frequently diagnosed cancer in women around the world, and an estimated15-20% of BC cases present with a family history of disease. Genetic variants in known susceptibility genes explain a relatively small proportion of the heritable risk for BC. Genetic variants have been broadly classified into three categories with different levels of risk and prevalence: rare mutations in high-risk genes (e.g. BRCA1, BRCA2); rare mutations in intermediate-risk genes (e.g. CHEK2); and common very modest-risk genetic variants (identified throughout the genome). These categories currently account for 20%, 5% and ~15% of the familial risk, respectively, leaving about 60% of the familial BC risk to be determined.</p><p>We have conducted whole-exome capture followed by massive parallel sequencing (XC-MPS)-based analysis on greater than third degree affected relatives from highly selected multiple-case BC families (at least four cases of invasive breast cancer diagnosed before 50 years) which had previously been screened and found not to carry identifiable BRCA1 or BRCA2 mutations.</p><p>In this presentation, we focus on two candidate BC susceptibility genes identified by this analysis, each playing a key-role in DNA repair. In both cases, one individual from the pair of cousins was found to carry a predicted protein damaging genetic variant at a consensus splice site. The variants were confirmed and extended analysis within the respective pedigrees performed by Sanger sequencing, subject to DNA sample availability. Further characterization of these variants is being pursued by much larger scale case-control genotyping using the TaqMan platform.</p><p>Our work further illustrates the complexities of human genetic variation and the technical and analytical challenges of identifying variation that is associated with inherited predisposition to complex diseases such as breast cancer.</p></sec></body></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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