Хайлтын үр дүнгүүд - Andrew Farrell

  • 12-н 1 - 12 үр дүнгүүдийг харуулж байна
Үр дүнг сайжруулах
  1. 1
    Genetic basis for phenotypic differences between different Toxoplasma gondii type I strains

    Genetic basis for phenotypic differences between different Toxoplasma gondii type I strains -н Ninghan Yang, Andrew Farrell, Wendy Niedelman, Mariane B. Melo, Diana Lu, Lindsay Julien, Gábor Marth, Marc‐Jan Gubbels, Jeroen P. J. Saeij

    Хэвлэсэн 2013
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    Artigo
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  2. 2
    A DOC2 Protein Identified by Mutational Profiling Is Essential for Apicomplexan Parasite Exocytosis

    A DOC2 Protein Identified by Mutational Profiling Is Essential for Apicomplexan Parasite Exocytosis -н Andrew Farrell, Sivasakthivel Thirugnanam, Alexander Lorestani, Jeffrey D. Dvorin, Keith P. Eidell, David Ferguson, Brooke R. Anderson‐White, Manoj T. Duraisingh, Gábor Marth, Marc‐Jan Gubbels

    Хэвлэсэн 2012
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    Artigo
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  3. 3
    Forward Genetic Screening Identifies a Small Molecule That Blocks Toxoplasma gondii Growth by Inhibiting Both Host- and Parasite-Encoded Kinases

    Forward Genetic Screening Identifies a Small Molecule That Blocks Toxoplasma gondii Growth by Inhibiting Both Host- and Parasite-Encoded Kinases -н Kevin M. Brown, Elena S. Suvorova, Andrew Farrell, Aaron L. McLain, Ashley Dittmar, Graham B. Wiley, Gábor Marth, Patrick M. Gaffney, Marc‐Jan Gubbels, Michael W. White, Ira J. Blader

    Хэвлэсэн 2014
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    Artigo
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  4. 4
    Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathy

    Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathy -н Betsy Ostrander, Russell J. Butterfield, Brent S. Pedersen, Andrew Farrell, Ryan M. Layer, Alistair Ward, Chase Miller, Tonya DiSera, Francis Filloux, Meghan Candee, Tara Newcomb, Joshua L. Bonkowsky, Gábor Marth, Aaron R. Quinlan

    Хэвлэсэн 2018
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    Artigo
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  5. 5
    Phenotype of CM-AVM2 caused by variants in EPHB4: how much overlap with hereditary hemorrhagic telangiectasia (HHT)?

    Phenotype of CM-AVM2 caused by variants in EPHB4: how much overlap with hereditary hemorrhagic telangiectasia (HHT)? -н Whitney Wooderchak‐Donahue, Gülsen Akay, Kevin J. Whitehead, Eric Briggs, David A. Stevenson, Brendan O’Fallon, Matthew Velinder, Andrew Farrell, Wei Shen, Emma Bedoukian, Cara M. Skrabann, Richard J. Antaya, Kate Henderson, Jeffrey Pollak, James R. Treat, Ronald W. Day, Joseph E. Jacher, Mark C. Hannibal, Kelly Bontempo, Gábor Marth, Pınar Bayrak‐Toydemir, Jamie McDonald

    Хэвлэсэн 2019
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    Artigo
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  6. 6
    Genomic analyses implicate noncoding de novo variants in congenital heart disease

    Genomic analyses implicate noncoding de novo variants in congenital heart disease -н Felix Richter, Sarah U. Morton, Seong Won Kim, Alexander Kitaygorodsky, Lauren K. Wasson, Kathleen Chen, Jian Zhou, Hongjian Qi, Nihir Patel, Steven R. DePalma, Michael Parfenov, Jason Homsy, Joshua M. Gorham, Kathryn B. Manheimer, Matthew Velinder, Andrew Farrell, Gábor Marth, Eric E. Schadt, Jonathan R. Kaltman, Jane W. Newburger, Anna Giardini, Elizabeth Goldmuntz, Martina Brueckner, Richard Kim, George A. Porter, Daniel Bernstein, Wendy K. Chung, Deepak Srivastava, Martin Tristani‐Firouzi, Olga G. Troyanskaya, Diane E. Dickel, Yufeng Shen, Jonathan G. Seidman, Christine E. Seidman, Bruce D. Gelb

    Хэвлэсэн 2020
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    Artigo
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  7. 7
    An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

    An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder -н Donna M. Werling, Harrison Brand, Joon‐Yong An, Matthew R. Stone, Lingxue Zhu, Joseph Glessner, Ryan L. Collins, Shan Dong, Ryan M. Layer, Eirene Markenscoff-Papadimitriou, Andrew Farrell, Grace Schwartz, Harold Z. Wang, Benjamin Currall, Xuefang Zhao, Jeanselle Dea, Clif Duhn, Carolyn A. Erdman, Michael C. Gilson, Rachita Yadav, Robert E. Handsaker, Seva Kashin, Lambertus Klei, Jeffrey D. Mandell, Tomasz J. Nowakowski, Yuwen Liu, Sirisha Pochareddy, Louw Smith, Michael F. Walker, Matthew J. Waterman, Xin He, Arnold R. Kriegstein, John L.R. Rubenstein, Nenad Šestan, Steven A. McCarroll, Benjamin M. Neale, Hilary Coon, A. Jeremy Willsey, Joseph D. Buxbaum, Mark J. Daly, Matthew W. State, Aaron R. Quinlan, Gábor Marth, Kathryn Roeder, Bernie Devlin, Michael E. Talkowski, Stephan Sanders

    Хэвлэсэн 2018
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    Artigo
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  8. 8
    Alteplase for Acute Ischemic Stroke

    Alteplase for Acute Ischemic Stroke -н Richard I. Lindley, Joanna M. Wardlaw, William Whiteley, Geoff Cohen, Lisa Blackwell, Gordon Murray, Peter Sandercock, Colin Baigent, David Chadwick, Pippa Tyrrell, Gordon Lowe, Martin Dennis, Karen Innes, Heather Goodare, Andrew Farrall, Rüdiger von Kummer, Lesley Cala, Anders von Heijne, Zoë Morris, Alessandro Adami, André Peeters, Gillian Potter, Nick Brady, Rory Collins, Philip M. Bath, J. van Gijn, Richard Gray, Robert G. Hart, Salim Yusuf, Keith W. Muir, Graeme J. Hankey, Karl Matz, Michael Brainin, André Peters, Gord Gubitz, Stephen Phillips, Stefano Ricci, Antonio Araúz, Eivind Berge, Karsten Bruins Slot, Anna Członkowska, Adam Kobayashi, Manuel Correia, Phillippe Lyrer, Stefan T. Engelter, Veronica Murray, Bo Norrving, Andreas Terént, Per Wester, G.S. Venables, Karen Innes, Alison L. Clark, David Perry, Vera Soosay, Alastair M. Buchan, Sheila A. Grant, Eleni Sakka, Jonathan Drever, Pauli Walker, Indee Herath, Ann Leigh Brown, P. Chmielnik, Chris Armit, Andrea Walton, Mischa Hautvast, Steff Lewis, Graeme Heron, Sylvia Odusanya, Pam Linksted, Ingrid Kane, Robin Sellar, Phil White, Peter Keston, Andrew Farrell, Zoë Morris, Héctor Miranda, Maria Grazia Celani, Enrico Righetti, Silvia Cenciarelli, Tatiana Mazzoli, Teresa Anna Cantisani, Jan Bembenek, Eva Isaakson

    Хэвлэсэн 2015
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    Artigo
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  9. 9
    Multi-platform discovery of haplotype-resolved structural variation in human genomes

    Multi-platform discovery of haplotype-resolved structural variation in human genomes -н Mark Chaisson, Ashley D. Sanders, Xuefang Zhao, Ankit Malhotra, David Porubský, Tobias Rausch, Eugene J. Gardner, Oscar L. Rodriguez, Li Guo, Ryan L. Collins, Xian Fan, Jia Wen, Robert E. Handsaker, Susan Fairley, Zev Kronenberg, Xiangmeng Kong, Fereydoun Hormozdiari, Dillon Lee, Aaron M. Wenger, Alex Hastie, Danny Antaki, Peter A. Audano, Harrison Brand, Stuart Cantsilieris, Han Cao, Eliza Cerveira, Chong Chen, Xintong Chen, Chen-Shan Chin, Zechen Chong, Nelson T. Chuang, Christine Lambert, Deanna M. Church, Laura Clarke, Andrew Farrell, Joey Flores, Timur R. Galeev, David U. Gorkin, Madhusudan Gujral, Victor Guryev, Haynes Heaton, Jonas Korlach, Sushant Kumar, Jee Young Kwon, Jong Eun Lee, Joyce Lee, Wan‐Ping Lee, Sau Peng Lee, Shantao Li, Patrick Marks, Karine A. Viaud‐Martinez, Sascha Meiers, Katherine M. Munson, Fábio C. P. Navarro, Bradley J. Nelson, Conor Nodzak, Amina Noor, Sofia Kyriazopoulou-Panagiotopoulou, Andy Wing Chun Pang, Yunjiang Qiu, Gabriel Rosanio, Xian Mallory, Adrian M. Stütz, Diana C.J. Spierings, Alistair Ward, AnneMarie E. Welch, Ming Xiao, Wei Xu, Chengsheng Zhang, Qihui Zhu, Xiangqun Zheng-Bradley, Ernesto Lowy, Sergei Yakneen, Steven A. McCarroll, Goo Jun, Li Ding, Chong‐Lek Koh, Bing Ren, Paul Flicek, Ken Chen, Mark Gerstein, Pui‐Yan Kwok, Peter M. Lansdorp, Gábor Marth, Jonathan Sebat, Xinghua Shi, Ali Bashir, Kai Ye, Scott E. Devine, Michael E. Talkowski, Ryan E. Mills, Tobias Marschall, Jan O. Korbel, Evan E. Eichler, Charles Lee

    Хэвлэсэн 2017
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    Pré-impressão
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  10. 10
    BRCA1 secondary splice-site mutations drive exon-skipping and PARP inhibitor resistance

    BRCA1 secondary splice-site mutations drive exon-skipping and PARP inhibitor resistance -н Ksenija Nešić, John J. Krais, Yifan Wang, Cassandra J. Vandenberg, Pooja Patel, Kathy Q. Cai, Tanya T. Kwan, Elizabeth Lieschke, Gwo‐Yaw Ho, Holly E. Barker, Justin Bedő, Silvia Casadei, Andrew Farrell, Marc R. Radke, Kristy Shield‐Artin, Jocelyn Sietsma Penington, Franziska Geissler, Elizabeth L. Kyran, Robert Betsch, Lijun Xu, Fan Zhang, Alexander Dobrovic, Inger Olesen, Rebecca Kristeleit, Amit M. Oza, Iain A. McNeish, Gayanie Ratnayake, Nadia Traficante, Georgia Chenevix‐Trench, A Green, Penelope M. Webb, Dorota M. Gertig, Sián Fereday, Suzanne Moore, Jillian A. Hung, K.R. Harrap, T. Sadkowsky, Nirmala Pandeya, M. Malt, A. Mellon, R. Paul Robertson, T. Vanden Bergh, Milissa U. Jones, P. Mackenzie, J. Maidens, K. Nattress, Yoke-Eng Chiew, Annie Stenlake, Harold C. Sullivan, Brian M. Alexander, P. Ashover, Stephen M. Brown, T. Corrish, L. Green, L. M. Jackman, Kaltin Ferguson, Karla Martin, A. Martyn, B. Ranieri, J. White, V. Jayde, Pam Mamers, Leanne Bowes, Laura Galletta, Daniel A. Giles, Joy Hendley, Thomas Schmidt, H. Shirley, C. Ball, Christian D. Young, S. Viduka, Hang Tran, Sanela Bilic, Lydia Glavinas, Julia Brooks, R. Stuart‐Harris, Fred Kirsten, J Rutovitz, P. Clingan, Akisha Glasgow, Anthony Proietto, Stephen Braye, Geoffrey Otton, Jenny Shannon, Tony Bonaventura, James Stewart, Stephen Begbie, Michael Friedlander, Debra Bell, Sally Baron‐Hay, A. Ferrier, G. Gard, David Nevell, Nick Pavlakis, Susan Valmadre, Bruce W. Young, C. Camaris, R. Crouch, L. Edwards, Neville F. Hacker

    Хэвлэсэн 2024
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    Carta
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  11. 11
    Multi-platform discovery of haplotype-resolved structural variation in human genomes

    Multi-platform discovery of haplotype-resolved structural variation in human genomes -н Mark Chaisson, Ashley D. Sanders, Xuefang Zhao, Ankit Malhotra, David Porubský, Tobias Rausch, Eugene J. Gardner, Oscar L. Rodriguez, Li Guo, Ryan L. Collins, Xian Fan, Jia Wen, Robert E. Handsaker, Susan Fairley, Zev Kronenberg, Xiangmeng Kong, Fereydoun Hormozdiari, Dillon Lee, Aaron M. Wenger, Alex Hastie, Danny Antaki, Thomas Anantharaman, Peter A. Audano, Harrison Brand, Stuart Cantsilieris, Han Cao, Eliza Cerveira, Chong Chen, Xintong Chen, Chen-Shan Chin, Zechen Chong, Nelson T. Chuang, Christine Lambert, Deanna M. Church, Laura Clarke, Andrew Farrell, Joey Flores, Timur R. Galeev, David U. Gorkin, Madhusudan Gujral, Victor Guryev, Haynes Heaton, Jonas Korlach, Sushant Kumar, Jee Young Kwon, Ernest T. Lam, Jong Eun Lee, Joyce Lee, Wan-Ping Lee, Sau Peng Lee, Shantao Li, Patrick Marks, Karine A. Viaud‐Martinez, Sascha Meiers, Katherine M. Munson, Fábio C. P. Navarro, Bradley J. Nelson, Conor Nodzak, Amina Noor, Sofia Kyriazopoulou-Panagiotopoulou, Andy Wing Chun Pang, Yunjiang Qiu, Gabriel Rosanio, Xian Mallory, Adrian M. Stütz, Diana C.J. Spierings, Alistair Ward, AnneMarie E. Welch, Ming Xiao, Wei Xu, Chengsheng Zhang, Qihui Zhu, Xiangqun Zheng-Bradley, Ernesto Lowy, Sergei Yakneen, Steven A. McCarroll, Goo Jun, Li Ding, Chong‐Lek Koh, Bing Ren, Paul Flicek, Ken Chen, Mark Gerstein, Pui‐Yan Kwok, Peter M. Lansdorp, Gábor Marth, Jonathan Sebat, Xinghua Shi, Ali Bashir, Kai Ye, Scott E. Devine, Michael E. Talkowski, Ryan E. Mills, Tobias Marschall, Jan O. Korbel, Evan E. Eichler, Charles Lee

    Хэвлэсэн 2019
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    Artigo
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  12. 12
    Human-specific tandem repeat expansion and differential gene expression during primate evolution

    Human-specific tandem repeat expansion and differential gene expression during primate evolution -н Arvis Sulovari, Ruiyang Li, Peter A. Audano, David Porubský, Mitchell R. Vollger, Glennis A. Logsdon, Wesley C. Warren, Alex A. Pollen, Mark Chaisson, Evan E. Eichler, Mark Chaisson, Ashley D. Sanders, Xuefang Zhao, Ankit Malhotra, David Porubský, Tobias Rausch, Eugene J. Gardner, Oscar L. Rodriguez, Li Guo, Ryan L. Collins, Xian Fan, Jia Wen, Robert E. Handsaker, Susan Fairley, Zev Kronenberg, Xiangmeng Kong, Fereydoun Hormozdiari, Dillon Lee, Aaron M. Wenger, Alex Hastie, Danny Antaki, Thomas Anantharaman, Peter A. Audano, Harrison Brand, Stuart Cantsilieris, Han Cao, Eliza Cerveira, Chong Chen, Xintong Chen, Chen-Shan Chin, Zechen Chong, Nelson T. Chuang, Christine Lambert, Deanna M. Church, Laura Clarke, Andrew Farrell, Joey Flores, Timur Galeey, David U. Gorkin, Madhusudan Gujral, Victor Guryev, Haynes Heaton, Jonas Korlach, Sushant Kumar, Jee Young Kwon, Ernest T. Lam, Jong Eun Lee, Joyce Lee, Wan‐Ping Lee, Sau Peng Lee, Shantao Li, Patrick Marks, Karine A. Viaud-Martinez, Sascha Meiers, Katherine M. Munson, Fábio C. P. Navarro, Bradley J. Nelson, Conor Nodzak, Amina Noor, Sofia Kyriazopoulou-Panagiotopoulou, Andy Wing Chun Pang, Yunjiang Qiu, Gabriel Rosanio, Xian Mallory, Adrian M. Stütz, Diana C.J. Spierings, Alistair Ward, AnneMarie E. Welch, Ming Xiao, Wei Xu, Chengsheng Zhang, Qihui Zhu, Xiangqun Zheng-Bradley, Ernesto Lowy, Sergei Yakneen, Steven A. McCarroll, Goo Jun, Li Ding, Chong‐Lek Koh, Bing Ren, Paul Flicek, Ken Chen, Mark Gerstein, Pui‐Yan Kwok, Peter M. Lansdorp, Gábor Marth, Jonathan Sebat, Xinghua Shi, Ali Bashir, Kai Ye

    Хэвлэсэн 2019
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    Artigo
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