检索结果 - Anil Ganesh

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  1. 1
    The rejoining of double-strand breaks in DNA by human cell extracts

    The rejoining of double-strand breaks in DNA by human cell extracts 由 Phillip North, Anil Ganesh, John Thacker

    出版 1990
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  2. 2
    A mechanism for deletion formation in DNA by human cell extracts: the involvement of short sequence repeats

    A mechanism for deletion formation in DNA by human cell extracts: the involvement of short sequence repeats 由 John Thacker, Jeremy Chalk, Anil Ganesh, Phillip North

    出版 1992
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  3. 3
    Mutator phenotypes in human colorectal carcinoma cell lines.

    Mutator phenotypes in human colorectal carcinoma cell lines. 由 Nitai P. Bhattacharyya, Adonis Skandalis, Anil Ganesh, Joanna Groden, M Meuth

    出版 1994
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  4. 4
    Human Pif1 helicase unwinds synthetic DNA structures resembling stalled DNA replication forks

    Human Pif1 helicase unwinds synthetic DNA structures resembling stalled DNA replication forks 由 Tresa George, Qin Wen, Richard Griffiths, Anil Ganesh, Mark Meuth, Cyril M. Sanders

    出版 2009
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  5. 5
    Human CDK18 promotes replication stress signaling and genome stability

    Human CDK18 promotes replication stress signaling and genome stability 由 Giancarlo Barone, Christopher J. Staples, Anil Ganesh, K. Patterson, Dominic P. Bryne, Katie Myers, Abhijit A. Patil, Claire E. Eyers, Sarah Maslen, Mark Skehel, Patrick A. Eyers, Spencer J. Collis

    出版 2016
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  6. 6
    RECON syndrome is a genome instability disorder caused by mutations in the DNA helicase RECQL1

    RECON syndrome is a genome instability disorder caused by mutations in the DNA helicase RECQL1 由 Bassam Abu‐Libdeh, Satpal S. Jhujh, Srijita Dhar, Joshua A. Sommers, Arindam Datta, Gabriel M. C. Longo, Laura Grange, John J. Reynolds, Sophie Cooke, Gavin S. McNee, Robert M. Hollingworth, Beth Woodward, Anil Ganesh, Stephen J. Smerdon, Claudia M. Nicolae, Karina Durlacher-Betzer, Vered Molho‐Pessach, Abdulsalam Abu‐Libdeh, Vardiella Meiner, George‐Lucian Moldovan, Vassilis Roukos, Tamar Harel, Robert Brosh, Grant S. Stewart

    出版 2022
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  7. 7
    Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy

    Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy 由 Laura Grange, John J. Reynolds, Farid Ullah, Bertrand Isidor, Robert F. Shearer, Xénia Latypova, Ryan M. Baxley, Antony W. Oliver, Anil Ganesh, Sophie Cooke, Satpal S. Jhujh, Gavin S. McNee, Robert M. Hollingworth, Martin R. Higgs, Toyoaki Natsume, Tahir Naeem Khan, Gabriel Ángel Martos‐Moreno, Sharon Chupp, Christopher G. Mathew, David Parry, Michael A. Simpson, Nahid Nahavandi, Zafer Yüksel, Mojgan Drasdo, Anja Kron, Petra Vogt, Annemarie Jonasson, Saad Ahmed Seth, Claudia Gonzaga‐Jauregui, Karlla W. Brigatti, Alexander P.A. Stegmann, Masato T. Kanemaki, Dragana Josifova, Yuri Uchiyama, Yukiko Oh, Akira Morimoto, Hitoshi Osaka, Zineb Ammous, Jesús Argente, Naomichi Matsumoto, Constance T. R. M. Stumpel, A. Malcolm R. Taylor, Andrew P. Jackson, Anja‐Katrin Bielinsky, Niels Mailand, Cédric Le Caignec, Erica E. Davis, Grant S. Stewart

    出版 2022
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