Risultati della ricerca - Michael C. Quinn

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  1. 1
    Derivation and characterization of matched cell lines from primary and recurrent serous ovarian cancer

    Derivation and characterization of matched cell lines from primary and recurrent serous ovarian cancer di Isabelle J. Létourneau, Michael C. Quinn, Lu-Lin Wang, Lise Portelance, Katia Caceres, Louis Cyr, Nathalie Delvoye, Liliane Meunier, Manon de Ladurantaye, Zhen Shen, Suzanna L. Arcand, Patricia N. Tonin, Diane Provencher, Anne‐Marie Mes‐Masson

    Pubblicazione 2012
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  2. 2
    Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services

    Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services di Stephanie Best, Zoe Fehlberg, C. Richards, Michael C. Quinn, Sebastian Lunke, Amanda B. Spurdle, Karin S. Kassahn, Chirag Patel, Danya F. Vears, Ilias Goranitis, Fiona Lynch, Alan J. Robertson, Emma Tudini, John Christodoulou, Hamish S. Scott, Julie McGaughran, Zornitza Stark

    Pubblicazione 2024
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  3. 3
    Methotrexate-related central neurotoxicity: clinical characteristics, risk factors and genome-wide association study in children treated for acute lymphoblastic leukemia

    Methotrexate-related central neurotoxicity: clinical characteristics, risk factors and genome-wide association study in children treated for acute lymphoblastic leukemia di Marion K. Mateos, Glenn M. Marshall, Pasquale Barbaro, Michael C. Quinn, Carly George, Chelsea Mayoh, Rosemary Sutton, Tamás Révész, Jodie E. Giles, Draga Barbaric, Frank Alvaro, Françoise Méchinaud, Daniel Catchpoole, John A. Lawson, Georgia Chenevix‐Trench, Stuart MacGregor, Rishi S. Kotecha, Luciano Dalla‐Pozza, Toby N. Trahair

    Pubblicazione 2021
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  4. 4
    Enhancing diagnostic outcomes in kidney genetic disorders: the KidGen national kidney genomics study protocol

    Enhancing diagnostic outcomes in kidney genetic disorders: the KidGen national kidney genomics study protocol di Amali Mallawaarachchi, Hugh J. McCarthy, Thomas Forbes, Kushani Jayasinghe, Chirag Patel, Stephen I. Alexander, Tiffany Boughtwood, Jeffrey Braithwaite, Aron Chakera, Sam Crafter, Ira W. Deveson, Randall Faull, Trudie Harris, Lilian Johnstone, Matthew Jose, A Leaver, Melissa H. Little, Daniel G. MacArthur, Tessa Mattiske, Christine Mincham, Kathy Nicholls, Catherine Quinlan, Michael C. Quinn, Gopala K. Rangan, Jessica Ryan, Cas Simons, Ian Smyth, Madhivanan Sundaram, Peter Trnka, Laura Wedd, Erik Biroš, Zornitza Stark, Andrew Mallett

    Pubblicazione 2025
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  5. 5
    Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis

    Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis di Kátia Nones, Nicola Waddell, Nicci Wayte, Ann‐Marie Patch, Peter J. Bailey, Felicity Newell, Oliver Holmes, J. Lynn Fink, Michael C. Quinn, Yue Tang, Guy Lampe, Kelly Quek, Kelly A. Loffler, Suzanne Manning, Senel Idrisoglu, David S. Miller, Qinying Xu, Nick M. Waddell, Peter J. Wilson, Timothy J. C. Bruxner, Angelika N. Christ, Ivon Harliwong, Craig Nourse, Ehsan Nourbakhsh, Matthew J. Anderson, Stephen H. Kazakoff, Conrad Leonard, Scott Wood, Peter T. Simpson, Lynne Reid, Lutz Krause, Damian J. Hussey, David I. Watson, Reginald V. Lord, Derek J. Nancarrow, Wayne A. Phillips, D. C. Gotley, B. Mark Smithers, David C. Whiteman, Nicholas K. Hayward, Peter J. Campbell, John V. Pearson, Sean M. Grimmond, Andrew P. Barbour

    Pubblicazione 2014
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  6. 6
    Integrated genomic and transcriptomic analysis of human brain metastases identifies alterations of potential clinical significance

    Integrated genomic and transcriptomic analysis of human brain metastases identifies alterations of potential clinical significance di Jodi M. Saunus, Michael C. Quinn, Ann‐Marie Patch, John V. Pearson, Peter J. Bailey, Kátia Nones, Amy E. McCart Reed, David S. Miller, Peter J. Wilson, Fares Al‐Ejeh, Mythily Mariasegaram, Queenie Lau, Teresa Withers, Rosalind L. Jeffree, Lynne Reid, Leonard Da Silva, Admire Matsika, Colleen Niland, Margaret C. Cummings, Timothy J. C. Bruxner, Angelika N. Christ, Ivon Harliwong, Senel Idrisoglu, Suzanne Manning, Craig Nourse, Ehsan Nourbakhsh, Shivangi Wani, Matthew Anderson, J. Lynn Fink, Oliver Holmes, Stephen H. Kazakoff, Conrad Leonard, Felicity Newell, Darrin F. Taylor, Nick M. Waddell, Scott Wood, Qinying Xu, Karin S. Kassahn, Vairavan Narayanan, Nur Aishah Mohd Taib, Soo‐Hwang Teo, Yock Ping Chow, kConFab, Parmjit Jat, Sebastian Brandner, Adrienne M. Flanagan, Kum Kum Khanna, Georgia Chenevix‐Trench, Sean M. Grimmond, Peter T. Simpson, Nicola Waddell, Sunil R. Lakhani

    Pubblicazione 2015
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  7. 7
    Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare

    Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare di Zornitza Stark, Tiffany Boughtwood, Matilda Haas, Jeffrey Braithwaite, Clara Gaff, Ilias Goranitis, Amanda B. Spurdle, David Hansen, Oliver Hofmann, Nigel G. Laing, Sylvia A. Metcalfe, Ainsley J. Newson, Hamish S. Scott, Natalie Thorne, Robyn L. Ward, Marcel E. Dinger, Stephanie Best, Janet C. Long, Sean M. Grimmond, John V. Pearson, Nicola Waddell, Christopher Barnett, Matthew Cook, Michael Field, David Fielding, Stephen B. Fox, Jozef Gécz, Adam Jaffé, Richard J. Leventer, Paul J. Lockhart, Sebastian Lunke, Andrew Mallett, Julie McGaughran, Linda Mileshkin, Kátia Nones, Tony Roscioli, Ingrid E. Scheffer, Christopher Semsarian, Cas Simons, David M. Thomas, David R. Thorburn, Richard W. Tothill, Deborah White, Sally L. Dunwoodie, Peter T. Simpson, Peta Phillips, Marie‐Jo Brion, Keri Finlay, Michael C. Quinn, Tessa Mattiske, Emma Tudini, Kirsten Boggs, Seán Murray, Kathy Wells, John Cannings, Andrew Sinclair, John Christodoulou, Kathryn N. North

    Pubblicazione 2023
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  8. 8
    Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System

    Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System di Sebastian Lunke, Stefanie Eggers, Meredith Wilson, Chirag Patel, Christopher Barnett, Jason Pinner, Sarah A. Sandaradura, Michael F. Buckley, Emma Krzesinski, M. De Silva, Gemma R. Brett, Kirsten Boggs, David Mowat, Edwin P. Kirk, Lesley C. Adès, Lauren Akesson, David J. Amor, Samantha Ayres, Anne Baxendale, Sarah Borrie, Alessandra Bray, Natasha J. Brown, Cheng Yee Chan, Belinda Chong, Corrina Cliffe, Martin B. Delatycki, Matthew Edwards, George Elakis, Michael Fahey, Andrew Fennell, Lindsay Fowles, Lyndon Gallacher, Megan Higgins, Katherine B. Howell, L. Hunt, Matthew F. Hunter, Kristi Jones, Sarah King, Smitha Kumble, Sarah Lang, Maelle Le Moing, Alan Ma, Dean Phelan, Michael C. Quinn, A. Mark Richards, Christopher M. Richmond, Jessica R. Riseley, Jonathan Rodgers, Rani Sachdev, Simon Sadedin, Luregn J. Schlapbach, Janine Smith, Amanda Springer, Natalie B. Tan, Tiong Yang Tan, Suzanna L. Temple, Christiane Theda, Anand Vasudevan, Susan M. White, Alison Yeung, Ying Zhu, Melissa Martyn, Stephanie Best, Tony Roscioli, John Christodoulou, Zornitza Stark

    Pubblicazione 2020
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  9. 9
    Whole genomes redefine the mutational landscape of pancreatic cancer

    Whole genomes redefine the mutational landscape of pancreatic cancer di Nicola Waddell, Marina Pajic, Ann‐Marie Patch, David K. Chang, Karin S. Kassahn, Peter J. Bailey, Amber L. Johns, David S. Miller, Kátia Nones, Kelly Quek, Michael C. Quinn, Alan J. Robertson, Muhammad Zaki Hidayatullah Fadlullah, Timothy J. C. Bruxner, Angelika N. Christ, Ivon Harliwong, Senel Idrisoglu, Suzanne Manning, Craig Nourse, Ehsan Nourbakhsh, Shivangi Wani, Peter J. Wilson, Emma Markham, Nicole Cloonan, Matthew J. Anderson, J. Lynn Fink, Oliver Holmes, Stephen H. Kazakoff, Conrad Leonard, Felicity Newell, Barsha Poudel, Sarah Song, Darrin F. Taylor, Nick M. Waddell, Scott Wood, Qinying Xu, Jianmin Wu, Mark Pinese, Mark J. Cowley, Hong C. Lee, Marc D. Jones, Adnan Nagrial, Jeremy L. Humphris, Lorraine A. Chantrill, Venessa Chin, Angela Steinmann, Amanda Mawson, Emily S. Humphrey, Emily K. Colvin, Angela Chou, Christopher J. Scarlett, Andreia V. Pinho, Marc Giry-Laterrière, Ilse Rooman, Jaswinder S. Samra, James G. Kench, Jessica A. Pettitt, Neil D. Merrett, Christopher W. Toon, Krishna Epari, Nam Q. Nguyen, Andrew P. Barbour, Nikolajs Zeps, Nigel B. Jamieson, Janet Graham, Simone P. Niclou, Rolf Bjerkvig, Robert Grützmann, Daniela E. Aust, Ralph H. Hruban, Anirban Maitra, Christine A. Iacobuzio‐Donahue, Christopher L. Wolfgang, Richard A. Morgan, Rita T. Lawlor, Vincenzo Corbo, Claudio Bassi, Massimo Falconi, Giuseppe Zamboni, Giampaolo Tortora, Margaret A. Tempero, Anthony J. Gill, James R. Eshleman, Christian Pilarsky, Aldo Scarpa, Elizabeth A. Musgrove, John V. Pearson, Andrew V. Biankin, Sean M. Grimmond

    Pubblicazione 2015
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  10. 10
    Hypermutation In Pancreatic Cancer

    Hypermutation In Pancreatic Cancer di Jeremy L. Humphris, Ann‐Marie Patch, Kátia Nones, Peter J. Bailey, Amber L. Johns, Skye McKay, David K. Chang, David K. Miller, Marina Pajic, Karin S. Kassahn, Michael C. Quinn, Timothy J. C. Bruxner, Angelika N. Christ, Ivon Harliwong, Senel Idrisoglu, Suzanne Manning, Craig Nourse, Ehsan Nourbakhsh, Andrew Stone, Peter J. Wilson, Matthew J. Anderson, J. Lynn Fink, Oliver Holmes, Stephen H. Kazakoff, Conrad Leonard, Felicity Newell, Nick M. Waddell, Scott Wood, R. Scott Mead, Qinying Xu, Jianmin Wu, Mark Pinese, Mark J. Cowley, Marc D. Jones, Adnan Nagrial, Venessa Chin, Lorraine A. Chantrill, Amanda Mawson, Angela Chou, Christopher J. Scarlett, Andreia V. Pinho, Ilse Rooman, Marc Giry-Laterrière, Jaswinder S. Samra, James G. Kench, Neil D. Merrett, Christopher W. Toon, Krishna Epari, Nam Q. Nguyen, Andrew P. Barbour, Nikolajs Zeps, Nigel B. Jamieson, Colin J. McKay, C Ross Carter, Euan J. Dickson, Janet Graham, Fraser R. Duthie, Karin A. Oien, Jane Hair, Jennifer P. Morton, Owen J. Sansom, Robert Grützmann, Ralph H. Hruban, Anirban Maitra, Christine A. Iacobuzio‐Donahue, Richard D. Schulick, Christopher L. Wolfgang, Richard A. Morgan, Rita T. Lawlor, Borislav C. Rusev, Vincenzo Corbo, Roberto Salvia, Ivana Cataldo, Giampaolo Tortora, Margaret A. Tempero, Oliver Hofmann, James R. Eshleman, Christian Pilarsky, Aldo Scarpa, Elizabeth A. Musgrove, Anthony J. Gill, John V. Pearson, Sean M. Grimmond, Nicola Waddell, Andrew V. Biankin

    Pubblicazione 2016
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  11. 11
    Whole-genome landscape of pancreatic neuroendocrine tumours

    Whole-genome landscape of pancreatic neuroendocrine tumours di Aldo Scarpa, David K. Chang, Kátia Nones, Vincenzo Corbo, Ann‐Marie Patch, Peter J. Bailey, Rita T. Lawlor, Amber L. Johns, David K. Miller, Andrea Mafficini, Borislav C. Rusev, Maria Scardoni, Davide Antonello, Stefano Barbi, Katarzyna Sikora, Sara Cingarlini, Caterina Vicentini, Skye McKay, Michael C. Quinn, Timothy J. C. Bruxner, Angelika N. Christ, Ivon Harliwong, Senel Idrisoglu, Suzanne McLean, Craig Nourse, Ehsan Nourbakhsh, Peter J. Wilson, Matthew J. Anderson, J. Lynn Fink, Felicity Newell, Nick M. Waddell, Oliver Holmes, Stephen H. Kazakoff, Conrad Leonard, Scott Wood, Qinying Xu, Shivashankar H. Nagaraj, Eliana Amato, Irene Dalai, Samantha Bersani, Ivana Cataldo, Angelo Paolo Dei Tos, Paola Capelli, Maria Vittoria Davì, Luca Landoni, Anna Malpaga, Marco Miotto, Vicki Whitehall, Barbara Leggett, Janelle L. Harris, Jonathan M. Harris, Marc D. Jones, Jeremy L. Humphris, Lorraine A. Chantrill, Venessa Chin, Adnan Nagrial, Marina Pajic, Christopher J. Scarlett, Andreia V. Pinho, Ilse Rooman, Christopher W. Toon, Jianmin Wu, Mark Pinese, Mark J. Cowley, Andrew P. Barbour, Amanda Mawson, Emily S. Humphrey, Emily K. Colvin, Angela Chou, Jessica A. Lovell, Nigel B. Jamieson, Fraser R. Duthie, Marie‐Claude Gingras, William E. Fisher, Rebecca A. Dagg, Loretta M. S. Lau, Michael Lee, Hilda A. Pickett, Roger R. Reddel, Jaswinder S. Samra, James G. Kench, Neil D. Merrett, Krishna Epari, Nam Q. Nguyen, Nikolajs Zeps, Massimo Falconi, Michele Simbolo, Giovanni Butturini, George Van Buren, Stefano Partelli, Matteo Fassan, Kum Kum Khanna, Anthony J. Gill, David A. Wheeler, Richard A. Gibbs, Elizabeth A. Musgrove, Claudio Bassi, Giampaolo Tortora, Paolo Pederzoli, John V. Pearson

    Pubblicazione 2017
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