Hasil Pencarian - Harriet Feilotter

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  1. 1
    A single institution study evaluating outcomes of PD-L1 high KRAS-mutant advanced non-small cell lung cancer (NSCLC) patients treated with first line immune checkpoint inhibitors

    A single institution study evaluating outcomes of PD-L1 high KRAS-mutant advanced non-small cell lung cancer (NSCLC) patients treated with first line immune checkpoint inhibitors oleh Adi Kartolo, Harriet Feilotter, Wilma Hopman, Andrea S. Fung, Andrew Robinson

    Diterbitkan 2021-01-01
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  2. 2
    The microRNA-200 family is upregulated in endometrial carcinoma.

    The microRNA-200 family is upregulated in endometrial carcinoma. oleh Jaime Snowdon, Xiao Zhang, Tim Childs, Victor A Tron, Harriet Feilotter

    Diterbitkan 2011-01-01
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  3. 3
    Clinical Utility of Multigene Profiling Assays in Early-Stage Invasive Breast Cancer: An Ontario Health (Cancer Care Ontario) Clinical Practice Guideline

    Clinical Utility of Multigene Profiling Assays in Early-Stage Invasive Breast Cancer: An Ontario Health (Cancer Care Ontario) Clinical Practice Guideline oleh Phillip Blanchette, Duvaraga Sivajohanathan, John Bartlett, Andrea Eisen, Harriet Feilotter, Rossanna Pezo, Gulisa Turashvili, Phillip Williams

    Diterbitkan 2022-04-01
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  4. 4
    Precision Oncology in Canada: Converting Vision to Reality with Lessons from International Programs

    Precision Oncology in Canada: Converting Vision to Reality with Lessons from International Programs oleh Geoffrey Liu, Winson Y. Cheung, Harriet Feilotter, Jackie Manthorne, Tracy Stockley, ManTek Yeung, Daniel J. Renouf

    Diterbitkan 2022-09-01
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  5. 5
    Future Role of Health Technology Assessment for Genomic Medicine in Oncology: A Canadian Laboratory Perspective

    Future Role of Health Technology Assessment for Genomic Medicine in Oncology: A Canadian Laboratory Perspective oleh Don Husereau, Yvonne Bombard, Tracy Stockley, Michael Carter, Scott Davey, Diana Lemaire, Erik Nohr, Paul Park, Alan Spatz, Christine Williams, Aaron Pollett, Bryan Lo, Stephen Yip, Soufiane El Hallani, Harriet Feilotter

    Diterbitkan 2023-10-01
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  6. 6
    Multisite verification of the accuracy of a multi-gene next generation sequencing panel for detection of mutations and copy number alterations in solid tumours.

    Multisite verification of the accuracy of a multi-gene next generation sequencing panel for detection of mutations and copy number alterations in solid tumours. oleh John Bartlett, Yutaka Amemiya, Heleen Arts, Jane Bayani, Barry Eng, Daria Grafodatskaya, Suzanne Kamel Reid, Mathieu Lariviere, Bryan Lo, Rebecca McClure, Vinay Mittal, Bekim Sadikovic, Seth Sadis, Arun Seth, Jeff Smith, Xiao Zhang, Harriet Feilotter

    Diterbitkan 2021-01-01
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  7. 7
    Canadian Consensus for Biomarker Testing and Treatment of TRK Fusion Cancer in Adults

    Canadian Consensus for Biomarker Testing and Treatment of TRK Fusion Cancer in Adults oleh D. Gwyn Bebb, Shantanu Banerji, Normand Blais, Patrice Desmeules, Sharlene Gill, Andrea Grin, Harriet Feilotter, Aaron R. Hansen, Martin Hyrcza, Monika Krzyzanowska, Barbara Melosky, Jonathan Noujaim, Bibiana Purgina, Dean Ruether, Christine E. Simmons, Denis Soulieres, Emina Emilia Torlakovic, Ming-Sound Tsao

    Diterbitkan 2021-01-01
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  8. 8
    P862: How to conduct equitable genetics research to include underserved populations: A systematic review of best practices

    P862: How to conduct equitable genetics research to include underserved populations: A systematic review of best practices oleh Vernie Aguda, Sonya Grewal, Arielle Nsenga, Daena Hirjikaka, Saumeh Saeedi, Emma Reble, Marc Clausen, Charles Law, Francine Holness, Kristal John, Tracy Reece, Aaron Pollett, Aisha Lofters, Ambreen Sayani, Andrea Eisen, David Lightfoot, Harriet Feilotter, Jordan Lerner-Ellis, Melyssa Aronson, Nav Persaud, Yvonne Bombard

    Diterbitkan 2024-01-01
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  9. 9
    Consensus Recommendations to Optimize the Detection and Reporting of <i>NTRK</i> Gene Fusions by RNA-Based Next-Generation Sequencing

    Consensus Recommendations to Optimize the Detection and Reporting of <i>NTRK</i> Gene Fusions by RNA-Based Next-Generation Sequencing oleh Tracy L. Stockley, Bryan Lo, Adrian Box, Andrea Gomez Corredor, John DeCoteau, Patrice Desmeules, Harriet Feilotter, Daria Grafodatskaya, Cynthia Hawkins, Weei Yuarn Huang, Iyare Izevbaye, Guylaine Lepine, Andreas I. Papadakis, Paul C. Park, Brandon S. Sheffield, Danh Tran-Thanh, Stephen Yip, Ming Sound Tsao

    Diterbitkan 2023-03-01
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  10. 10
    P054: Creation of the Ontario Hereditary Cancer Research Network (OHCRN)

    P054: Creation of the Ontario Hereditary Cancer Research Network (OHCRN) oleh Lauren Hughes, Kirsten Farncombe, Michelle Brazas, Melyssa Aronson, Kathleen Bell, Brandon Chan, Andrea Eisen, Harriet Feilotter, Bailey Gallinger, Jordan Lerner-Ellis, David Malkin, Ellen MacDougall, Steven Narod, Karen Panabaker, Trevor Pugh, Sarah Sawyer, Alison Rusnak, Andrea Vaags, Laszlo Radvanyi, Lincoln Stein, Raymond Kim

    Diterbitkan 2023-01-01
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  11. 11
    Optimizing the number of variants tracked to follow disease burden with circulating tumor DNA assays in metastatic colorectal cancer

    Optimizing the number of variants tracked to follow disease burden with circulating tumor DNA assays in metastatic colorectal cancer oleh Mélina Boutin, James T. Topham, Harriet Feilotter, Hagen F. Kennecke, Félix Couture, Mohammed Harb, Peter Kavan, Scott Berry, Howard J. Lim, John R. Goffin, Chaudhary Ahmad, Anthony Lott, Daniel J. Renouf, Derek J. Jonker, Dongsheng Tu, Chris J. O’Callaghan, Eric X. Chen, Jonathan M. Loree

    Diterbitkan 2023-06-01
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  12. 12
    P541: Development of a provincial genetics program in Ontario

    P541: Development of a provincial genetics program in Ontario oleh Kathleen Bell, Raymond Kim, Aaron Pollett, Wilson Yu, Syed Ahmed, Muna Aden, Rae Brager, June Carroll, Melissa Carter, Dervla Connaughton, James Dowling, Angela Du, Hanna Faghfoury, Harriet Feilotter, Elaine Goh, Andrea Guerin, Jennifer Hart, Ivy Haw, Rachel Healey, Richard Kim, Goran Klaric, Kaitlyn Lemay, Jerom Nguyen, Luis Peña, Erin Redwood, Julie Richer, Mary Schmitz, Julia Su, Frank Telfer

    Diterbitkan 2024-01-01
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  13. 13
    Programmed Cell Death Protein 1 Inhibitors and MET Targeted Therapies in NSCLC With MET Exon 14 Skipping Mutations: Efficacy and Toxicity as Sequential Therapies

    Programmed Cell Death Protein 1 Inhibitors and MET Targeted Therapies in NSCLC With MET Exon 14 Skipping Mutations: Efficacy and Toxicity as Sequential Therapies oleh Sally C.M. Lau, MD, MPH, Kirstin Perdrizet, MD, Andrea S. Fung, MD, PhD, Danilo Giffoni M.M. Mata, MD, Jessica Weiss, PhD, Nick Holzapfel, MD, Geoffrey Liu, MD, Penelope A. Bradbury, MD, Frances A. Shepherd, MD, Adrian G. Sacher, MD, MMSc, Harriet Feilotter, MD, Brandon Sheffield, MD, David Hwang, MD, Ming Sound Tsao, MD, Susanna Cheng, MD, Parneet Cheema, MD, Natasha B. Leighl, MD, MMSc

    Diterbitkan 2023-10-01
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  14. 14
    Results of the phase I CCTG IND.231 trial of CX-5461 in patients with advanced solid tumors enriched for DNA-repair deficiencies

    Results of the phase I CCTG IND.231 trial of CX-5461 in patients with advanced solid tumors enriched for DNA-repair deficiencies oleh John Hilton, Karen Gelmon, Philippe L. Bedard, Dongsheng Tu, Hong Xu, Anna V. Tinker, Rachel Goodwin, Scott A. Laurie, Derek Jonker, Aaron R. Hansen, Zachary W. Veitch, Daniel J. Renouf, Linda Hagerman, Hongbo Lui, Bingshu Chen, Deb Kellar, Irene Li, Sung-Eun Lee, Takako Kono, Brian Y. C. Cheng, Damian Yap, Daniel Lai, Sean Beatty, John Soong, Kathleen I. Pritchard, Isabel Soria-Bretones, Eric Chen, Harriet Feilotter, Moira Rushton, Lesley Seymour, Samuel Aparicio, David W. Cescon

    Diterbitkan 2022-06-01
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  15. 15
    A Pan-Canadian Validation Study for the Detection of EGFR T790M Mutation Using Circulating Tumor DNA From Peripheral Blood

    A Pan-Canadian Validation Study for the Detection of EGFR T790M Mutation Using Circulating Tumor DNA From Peripheral Blood oleh Shamini Selvarajah, PhD, Sophie Plante, MSc, Marsha Speevak, PhD, Andrea Vaags, PhD, Darren Hamelinck, MSc, Martin Butcher, MSc, Elizabeth McCready, PhD, Daria Grafodatskaya, PhD, Normand Blais, MD, Danh Tran-Thanh, MD, Xiaoduan Weng, MD, Rami Nassabein, MD, Wenda Greer, PhD, Ryan N. Walton, MPH, Bryan Lo, MD, Doug Demetrick, MD, Stephanie Santos, BSc, Bekim Sadikovic, PhD, Xiao Zhang, BSc, MSc, Tong Zhang, MD, Tara Spence, PhD, Tracy Stockley, PhD, Harriet Feilotter, PhD, Philippe Joubert, MD, PhD

    Diterbitkan 2021-08-01
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  16. 16
    MicroRNAs 146a/b-5 and 425-3p and 24-3p are markers of antidepressant response and regulate MAPK/Wnt-system genes

    MicroRNAs 146a/b-5 and 425-3p and 24-3p are markers of antidepressant response and regulate MAPK/Wnt-system genes oleh Juan Pablo Lopez, Laura M. Fiori, Cristiana Cruceanu, Rixing Lin, Benoit Labonte, Hannah M. Cates, Elizabeth A. Heller, Vincent Vialou, Stacy M. Ku, Christophe Gerald, Ming-Hu Han, Jane Foster, Benicio N. Frey, Claudio N. Soares, Daniel J. Müller, Faranak Farzan, Francesco Leri, Glenda M. MacQueen, Harriet Feilotter, Kathrin Tyryshkin, Kenneth R. Evans, Peter Giacobbe, Pierre Blier, Raymond W. Lam, Roumen Milev, Sagar V. Parikh, Susan Rotzinger, Steven C. Strother, Cathryn M. Lewis, Katherine J. Aitchison, Gayle M. Wittenberg, Naguib Mechawar, Eric J. Nestler, Rudolf Uher, Sidney H. Kennedy, Gustavo Turecki

    Diterbitkan 2017-05-01
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