Hasil Pencarian - Jeremy Leipzig

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  1. 1
    Selection of target sites for mobile DNA integration in the human genome.

    Selection of target sites for mobile DNA integration in the human genome. oleh Charles Berry, Sridhar Hannenhalli, Jeremy Leipzig, Frederic D Bushman

    Diterbitkan 2006-11-01
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  2. 2
    Predicting the pathogenicity of novel variants in mitochondrial tRNA with MitoTIP.

    Predicting the pathogenicity of novel variants in mitochondrial tRNA with MitoTIP. oleh Sanjay Sonney, Jeremy Leipzig, Marie T Lott, Shiping Zhang, Vincent Procaccio, Douglas C Wallace, Neal Sondheimer

    Diterbitkan 2017-12-01
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  3. 3
    HTLV-1 integration into transcriptionally active genomic regions is associated with proviral expression and with HAM/TSP.

    HTLV-1 integration into transcriptionally active genomic regions is associated with proviral expression and with HAM/TSP. oleh Kiran N Meekings, Jeremy Leipzig, Frederic D Bushman, Graham P Taylor, Charles R M Bangham

    Diterbitkan 2008-03-01
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  4. 4
    Peripheral Blood Mitochondrial DNA as a Biomarker of Cerebral Mitochondrial Dysfunction following Traumatic Brain Injury in a Porcine Model.

    Peripheral Blood Mitochondrial DNA as a Biomarker of Cerebral Mitochondrial Dysfunction following Traumatic Brain Injury in a Porcine Model. oleh Todd J Kilbaugh, Maria Lvova, Michael Karlsson, Zhe Zhang, Jeremy Leipzig, Douglas C Wallace, Susan S Margulies

    Diterbitkan 2015-01-01
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  5. 5
    Retroviral DNA integration: viral and cellular determinants of target-site selection.

    Retroviral DNA integration: viral and cellular determinants of target-site selection. oleh Mary K Lewinski, Masahiro Yamashita, Michael Emerman, Angela Ciuffi, Heather Marshall, Gregory Crawford, Francis Collins, Paul Shinn, Jeremy Leipzig, Sridhar Hannenhalli, Charles C Berry, Joseph R Ecker, Frederic D Bushman

    Diterbitkan 2006-06-01
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  6. 6
    P146: BeginNGS, an artificial intelligence-enabled genome sequencing system for newborn screening of 409 childhood genetic disorders*

    P146: BeginNGS, an artificial intelligence-enabled genome sequencing system for newborn screening of 409 childhood genetic disorders* oleh Jennifer Schleit, Meredith Wright, Lauren Olsen, Eric Blincow, Sara Caylor, Christina Chambers, Guillermo del Angel, Katarzyna (Kasia) Ellsworth, Annette Feigenbaum, Erwin Frise, Lucia Guidugli, Kevin Hall, Christian Hansen, Charlotte Hobbs, Mark Kiel, Chad Krilow, Chris Kunard, YongHyun Kwon, Rao Madhavrao, Shyamal Mehtalia, William Mowrey, Jennie Le, Jeremy Leipzig, Yupu Liang, Rebecca Mardach, Danny Oh, Mallory Owen, Liana Protopsaltis, Erica Sanford Kobayashi, Gunter Scharer, Brandon Schultz, Seth Shelnutt, Laurie Smith, Duke Tran, Lucita Van Der Kraan, Kristen Wigby, Mary Willis, Aaron Wolen, Mark Yandell, Thomas Defay, Stephen Kingsmore

    Diterbitkan 2024-01-01
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