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1دورية أكاديمية
المؤلفون: Light, NicholasAff1, Aff2, Layeghifard, Mehdi, Attery, Ayush, Subasri, VallijahAff1, Aff4, Aff5, Zatzman, MatthewAff1, Aff6, Anderson, Nathaniel D.Aff1, Aff6, Hatkar, RupalAff1, Aff6, Blay, SashaAff1, Aff6, Chen, David, Novokmet, Ana, Fuligni, Fabio, Tran, JamesAff1, Aff4, de Borja, Richard, Agarwal, Himanshi, Waldman, LarissaAff7, Aff8, Abegglen, Lisa M.Aff9, Aff10, Albertson, Daniel, Finlay, Jonathan L., Hansford, Jordan R.Aff13, Aff14, Aff15, Aff16, Aff17, Aff18, Behjati, SamAff19, Aff20, Villani, AnitaAff21, Aff22, Gerstung, MoritzAff23, Aff24, Alexandrov, Ludmil B., Somers, Gino R.Aff6, Aff26, Schiffman, Joshua D.Aff9, Aff10, Rotter, Varda, Malkin, DavidAff1, Aff4, Aff21, Aff22, IDs4146702235727y_cor27, Shlien, AdamAff1, Aff6, Aff26, IDs4146702235727y_cor28
المصدر: Nature Communications. 14(1)
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2دورية أكاديميةThe clinical utility of integrative genomics in childhood cancer extends beyond targetable mutations
المؤلفون: Villani, AnitaAff1, Aff2, Davidson, ScottAff3, Aff4, Kanwar, Nisha, Lo, Winnie W., Li, Yisu, Cohen-Gogo, Sarah, Fuligni, Fabio, Edward, Lisa-Monique, Light, NicholasAff3, Aff5, Layeghifard, Mehdi, Harripaul, Ricardo, Waldman, LarissaAff6, Aff7, Gallinger, BaileyAff6, Aff8, Aff9, Comitani, Federico, Brunga, Ledia, Hayes, Reid, Anderson, Nathaniel D., Ramani, Arun K.Aff3, Aff10, Yuki, Kyoko E., Blay, Sasha, Johnstone, BrittneyAff6, Aff7, Inglese, CaraAff8, Aff9, Hammad, RawanAff1, Aff11, Goudie, CatherineAff12, Aff13, Shuen, Andrew, Wasserman, Jonathan D.Aff2, Aff14, Venier, Rosemarie E.Aff3, Aff6, Aff8, Eliou, Marianne, Lorenti, Miranda, Ryan, Carol Ann, Braga, Michael, Gloven-Brown, Meagan, Han, Jianan, Montero, Maria, Spatare, Famida, Whitlock, James A.Aff1, Aff2, Scherer, Stephen W.Aff3, Aff6, Aff15, Chun, KathyAff4, Aff16, Somerville, Martin J.Aff4, Aff16, Hawkins, CynthiaAff4, Aff16, Abdelhaleem, MohamedAff4, Aff16, Ramaswamy, VijayAff1, Aff2, Somers, Gino R.Aff4, Aff16, Kyriakopoulou, LiannaAff4, Aff16, Hitzler, JohannAff1, Aff2, Aff17, Shago, MaryAff4, Aff16, Morgenstern, Daniel A.Aff1, Aff2, Tabori, UriAff1, Aff2, Meyn, Stephen, Irwin, Meredith S.Aff1, Aff2, Malkin, DavidAff1, Aff2, Aff3, IDs4301802200474y_cor51, Shlien, AdamAff3, Aff4, IDs4301802200474y_cor52
المصدر: Nature Cancer. 4(2):203-221
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3دورية أكاديمية
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4دورية أكاديمية
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5دورية أكاديمية
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6دورية أكاديمية
Alternate Title: Détection de sous-types à risque élevé du virus du papillome humain grâce à l'hybridation in situ d'ARN sur des tissus fixés au formaldéhyde et inclus en paraffine. (French)
المؤلفون: Turashvili, Gulisa, Blay, Sasha, Conner, James, Dickson, Brendan, Demicco, Elizabeth, MacMillan, Christina
المصدر: Canadian Journal of Pathology; Feb2021, Vol. 13 Issue 1, p11-20, 10p
مصطلحات موضوعية: HUMAN papillomavirus vaccines, IN situ hybridization, PHYSICIANS, PATHOLOGISTS, OROPHARYNGEAL cancer
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7دورية أكاديمية
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المؤلفون: Nicholas Light, Mehdi Layeghifard, Ayush Attery, Vallijah Subasri, Matthew Zatzman, Nathaniel D. Anderson, Rupal Hatkar, Sasha Blay, David Chen, Ana Novokmet, Fabio Fuligni, James Tran, Richard de Borja, Himanshi Agarwal, Larissa Waldman, Lisa M. Abegglen, Daniel Albertson, Jonathan L. Finlay, Jordan R. Hansford, Sam Behjati, Anita Villani, Moritz Gerstung, Ludmil B. Alexandrov, Gino R. Somers, Joshua D. Schiffman, Varda Rotter, David Malkin, Adam Shlien
المساهمون: Layeghifard, Mehdi [0000-0002-6224-3628], Subasri, Vallijah [0000-0002-6584-877X], Anderson, Nathaniel D [0000-0003-4523-6327], Blay, Sasha [0000-0002-5611-2330], Agarwal, Himanshi [0000-0003-1738-4525], Abegglen, Lisa M [0000-0003-3607-3001], Hansford, Jordan R [0000-0001-7733-383X], Behjati, Sam [0000-0002-6600-7665], Gerstung, Moritz [0000-0001-6709-963X], Alexandrov, Ludmil B [0000-0003-3596-4515], Schiffman, Joshua D [0000-0002-6968-7694], Malkin, David [0000-0001-5752-9763], Shlien, Adam [0000-0002-0368-5370], Apollo - University of Cambridge Repository
مصطلحات موضوعية: Multidisciplinary, DNA Copy Number Variations, General Physics and Astronomy, General Chemistry, General Biochemistry, Genetics and Molecular Biology, Li-Fraumeni Syndrome, Phosphatidylinositol 3-Kinases, Neoplastic Syndromes, Hereditary, Mutation, Humans, Genetic Predisposition to Disease, Tumor Suppressor Protein p53, Phylogeny, Germ-Line Mutation
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27dcb1e761678902ce2f1426ce8a0ecc
https://www.repository.cam.ac.uk/handle/1810/346286