Hasil Pencarian - Matthew Might

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  1. 1
    cdev: a ground-truth based measure to evaluate RNA-seq normalization performance

    cdev: a ground-truth based measure to evaluate RNA-seq normalization performance oleh Diem-Trang Tran, Matthew Might

    Diterbitkan 2021-10-01
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  2. 2
    A graph-based algorithm for RNA-seq data normalization.

    A graph-based algorithm for RNA-seq data normalization. oleh Diem-Trang Tran, Aditya Bhaskara, Balagurunathan Kuberan, Matthew Might

    Diterbitkan 2020-01-01
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  3. 3
    Metformin Use Is Associated With Reduced Mortality in a Diverse Population With COVID-19 and Diabetes

    Metformin Use Is Associated With Reduced Mortality in a Diverse Population With COVID-19 and Diabetes oleh Andrew B. Crouse, Tiffany Grimes, Peng Li, Matthew Might, Fernando Ovalle, Anath Shalev

    Diterbitkan 2021-01-01
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  4. 4
    Rare disease patient matchmaking: development and outcomes of an internet case-finding strategy in the Undiagnosed Diseases Network

    Rare disease patient matchmaking: development and outcomes of an internet case-finding strategy in the Undiagnosed Diseases Network oleh Kimberly LeBlanc, Emily Glanton, Anna Nagy, Jorick Bater, Tala Berro, Molly A. McGuinness, Courtney Studwell, Undiagnosed Diseases Network, Matthew Might

    Diterbitkan 2021-05-01
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  5. 5
    An induced pluripotent stem cell line (NCATS-CL9075) from a patient carrying compound heterozygote mutations, p.R390P and p.L318P, in the NGLY1 gene

    An induced pluripotent stem cell line (NCATS-CL9075) from a patient carrying compound heterozygote mutations, p.R390P and p.L318P, in the NGLY1 gene oleh Manisha Pradhan, Atena Farkhondeh, Yu-Shan Cheng, Miao Xu, Jeanette Beers, Jizhong Zou, Chengyu Liu, Matthew Might, Steven Rodems, Karsten Baumgärtel, Wei Zheng

    Diterbitkan 2021-07-01
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  6. 6
    Corrigendum to “Generation of two gene corrected human isogenic iPSC lines (NCATS-CL6104 and NCATS-CL6105) from a patient line (NCATS-CL6103) carrying a homozygous p.R401X mutation in the NGLY1 gene using CRISPR/Cas9” [Stem Cell Res. 56 (2021) 102554]

    Corrigendum to “Generation of two gene corrected human isogenic iPSC lines (NCATS-CL6104 and NCATS-CL6105) from a patient line (NCATS-CL6103) carrying a homozygous p.R401X mutation... oleh Ivan Pavlinov, Atena Farkhondeh, Shu Yang, Miao Xu, Yu-Shan Cheng, Jeanette Beers, Jizhong Zou, Chengyu Liu, Matthew Might, Steven Rodems, Karsten Baumgärtel, Wei Zheng

    Diterbitkan 2021-12-01
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  7. 7
    Generation of an induced pluripotent stem cell line (TRNDi002-B) from a patient carrying compound heterozygous p.Q208X and p.G310G mutations in the NGLY1 gene

    Generation of an induced pluripotent stem cell line (TRNDi002-B) from a patient carrying compound heterozygous p.Q208X and p.G310G mutations in the NGLY1 gene oleh Rong Li, Manisha Pradhan, Miao Xu, Amanda Baskfield, Atena Farkhondeh, Yu-Shan Cheng, Jeanette Beers, Jizhong Zou, Chengyu Liu, Matthew Might, Steven Rodems, Wei Zheng

    Diterbitkan 2019-01-01
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  8. 8
    Generation of two gene corrected human isogenic iPSC lines (NCATS-CL6104 and NCATS-CL6105) from a patient line (NCATS-CL6103) carrying a homozygous p.R401X mutation in the NGLY1 gene using CRISPR/Cas9

    Generation of two gene corrected human isogenic iPSC lines (NCATS-CL6104 and NCATS-CL6105) from a patient line (NCATS-CL6103) carrying a homozygous p.R401X mutation in the NGLY1 ge... oleh Ivan Pavlinov, Atena Farkhondeh, Shu Yang, Miao Xu, Yu-Shan Cheng, Jeanette Beers, Jizhong Zou, Chengyu Liu, Matthew Might, Steven Rodems, Karsten Baumgärtel, Wei Zheng

    Diterbitkan 2021-10-01
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  9. 9
    Exercise mitigates reductive stress-induced cardiac remodeling in mice

    Exercise mitigates reductive stress-induced cardiac remodeling in mice oleh Arun Jyothidasan, Sini Sunny, Asokan Devarajan, Aniqa Sayed, John Kofi Afortude, Brian Dalley, Vivek Nanda, Steven Pogwizd, Silvio H. Litovsky, Joel D. Trinity, Matthew Might, Namakkal S. Rajasekaran

    Diterbitkan 2024-09-01
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  10. 10
    Generation and characterization of NGLY1 patient-derived midbrain organoids

    Generation and characterization of NGLY1 patient-derived midbrain organoids oleh Joshua Abbott, Mitali Tambe, Ivan Pavlinov, Atena Farkhondeh, Ha Nam Nguyen, Ha Nam Nguyen, Miao Xu, Manisha Pradhan, Tate York, Matthew Might, Karsten Baumgärtel, Steven Rodems, Wei Zheng

    Diterbitkan 2023-02-01
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  11. 11
    P508: Medically-actionable disease risk variants in a diverse population

    P508: Medically-actionable disease risk variants in a diverse population oleh Whitley Kelley, Irene Moss, Irfan Asif, Gregory Cooper, Candice Finnila, Susan Hiatt, Donald Latner, James Lawlor, Kelly East, Thomas May, Mariko Nakano-Okuno, Stephen Sodeke, Gregory Barsh, Nita Limdi, Matthew Might, Bruce Korf

    Diterbitkan 2024-01-01
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  12. 12
    COVID-19 bacteremic co-infection is a major risk factor for mortality, ICU admission, and mechanical ventilation

    COVID-19 bacteremic co-infection is a major risk factor for mortality, ICU admission, and mechanical ventilation oleh Michael John Patton, Carlos J. Orihuela, Kevin S. Harrod, Mohammad A. N. Bhuiyan, Paari Dominic, Christopher G. Kevil, Daniel Fort, Vincent X. Liu, Maha Farhat, Jonathan L. Koff, Charitharth V. Lal, Anuj Gaggar, Robert P. Richter, Nathaniel Erdmann, Matthew Might, Amit Gaggar

    Diterbitkan 2023-01-01
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  13. 13
    An open-label study evaluating the safety, behavioral, and electrophysiological outcomes of low-dose ketamine in children with ADNP syndrome

    An open-label study evaluating the safety, behavioral, and electrophysiological outcomes of low-dose ketamine in children with ADNP syndrome oleh Alexander Kolevzon, Tess Levy, Sarah Barkley, Sandra Bedrosian-Sermone, Matthew Davis, Jennifer Foss-Feig, Danielle Halpern, Katherine Keller, Ana Kostic, Christina Layton, Rebecca Lee, Bonnie Lerman, Matthew Might, Sven Sandin, Paige M. Siper, Laura G. Sloofman, Hannah Walker, Jessica Zweifach, Joseph D. Buxbaum

    Diterbitkan 2022-10-01
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  14. 14
    P392: Genomic medicine and primary care: The Alabama Genomic Health Initiative*

    P392: Genomic medicine and primary care: The Alabama Genomic Health Initiative* oleh Whitley Kelley, Kelly East, Irfan Asif, Lori Bateman, Gregory Cooper, Brittney Davis, Candice Finnila, Blake Goff, Melissa Kelly, Irene Moss, Donald Latner, James Lawlor, Thomas May, Mariko Nakano-Okuno, Tiffany Osborne, Stephen Sodeke, Adriana Stout, Michelle Thompson, Gregory Barsh, Nita Limdi, Matthew Might, Bruce Korf

    Diterbitkan 2023-01-01
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  15. 15
    The precision medicine process for treating rare disease using the artificial intelligence tool mediKanren

    The precision medicine process for treating rare disease using the artificial intelligence tool mediKanren oleh Aleksandra Foksinska, Camerron M. Crowder, Camerron M. Crowder, Andrew B. Crouse, Jeff Henrikson, William E. Byrd, Gregory Rosenblatt, Michael J. Patton, Kaiwen He, Thi K. Tran-Nguyen, Marissa Zheng, Stephen A. Ramsey, Nada Amin, John Osborne, UAB Precision Medicine Institute, Matthew Might, Stephen Barnes, William E. Byrd, Mei-Jan Chen, Andrew B. Crouse, Camerron M. Crowder, Mary E. Crumbley, Madeline Eckenrode, Crayton A. Fargason, Nathaniel Fehrmann, Aleksandra Foksinska, Kaiwen He, Forest Huls, Matthew Jarrell, Lindsay Jenkins, Meg McCalley, Matthew Might, Tamsyn Osborn, Michael J. Patton, Elizabeth Pollard, Gregory Rosenblatt, Sienna Rucka, Nicholas T. Southern, Thi K. Tran-Nguyen, Jillian Tinglin, Jordan H. Whitlock

    Diterbitkan 2022-09-01
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  16. 16
    Hormonal intervention for the treatment of veterans with COVID-19 requiring hospitalization (HITCH): a multicenter, phase 2 randomized controlled trial of best supportive care vs best supportive care plus degarelix: study protocol for a randomized controlled trial

    Hormonal intervention for the treatment of veterans with COVID-19 requiring hospitalization (HITCH): a multicenter, phase 2 randomized controlled trial of best supportive care vs b... oleh Nicholas G. Nickols, Matthew B. Goetz, Christopher J. Graber, Debika Bhattacharya, Guy Soo Hoo, Matthew Might, David B. Goldstein, Xinchen Wang, Rachel Ramoni, Kenute Myrie, Samantha Tran, Leila Ghayouri, Sonny Tsai, Michelle Geelhoed, Danil Makarov, Daniel J. Becker, Jun-Chieh Tsay, Melissa Diamond, Asha George, Mohammad Al-Ajam, Pooja Belligund, R. Bruce Montgomery, Elahe A. Mostaghel, Carlie Sulpizio, Zhibao Mi, Ellen Dematt, Joseph Tadalan, Leslie E. Norman, Daniel Briones, Christina E. Clise, Zachary W. Taylor, Jeffrey R. Huminik, Kousick Biswas, Matthew B. Rettig

    Diterbitkan 2021-07-01
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  17. 17
    Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders

    Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders oleh Ilaria Mannucci, Nghi D. P. Dang, Hannes Huber, Jaclyn B. Murry, Jeff Abramson, Thorsten Althoff, Siddharth Banka, Gareth Baynam, David Bearden, Ana Beleza-Meireles, Paul J. Benke, Siren Berland, Tatjana Bierhals, Frederic Bilan, Laurence A. Bindoff, Geir Julius Braathen, Øyvind L. Busk, Jirat Chenbhanich, Jonas Denecke, Luis F. Escobar, Caroline Estes, Julie Fleischer, Daniel Groepper, Charlotte A. Haaxma, Maja Hempel, Yolanda Holler-Managan, Gunnar Houge, Adam Jackson, Laura Kellogg, Boris Keren, Catherine Kiraly-Borri, Cornelia Kraus, Christian Kubisch, Gwenael Le Guyader, Ulf W. Ljungblad, Leslie Manace Brenman, Julian A. Martinez-Agosto, Matthew Might, David T. Miller, Kelly Q. Minks, Billur Moghaddam, Caroline Nava, Stanley F. Nelson, John M. Parant, Trine Prescott, Farrah Rajabi, Hanitra Randrianaivo, Simone F. Reiter, Janneke Schuurs-Hoeijmakers, Perry B. Shieh, Anne Slavotinek, Sarah Smithson, Alexander P. A. Stegmann, Kinga Tomczak, Kristian Tveten, Jun Wang, Jordan H. Whitlock, Christiane Zweier, Kirsty McWalter, Jane Juusola, Fabiola Quintero-Rivera, Utz Fischer, Nan Cher Yeo, Hans-Jürgen Kreienkamp, Davor Lessel

    Diterbitkan 2021-05-01
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