Resultados de procura - Dustin L. Gable

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  1. 1
    Germline Mutations in DNA Repair Genes in Lung Adenocarcinoma

    Germline Mutations in DNA Repair Genes in Lung Adenocarcinoma por Erin M. Parry, Dustin L. Gable, Susan E. Stanley, Sara E. Khalil, Valentin Antonescu, Liliana Florea, Mary Armanios

    Publicado 2017
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  2. 2
    <i>ZCCHC8</i>, the nuclear exosome targeting component, is mutated in familial pulmonary fibrosis and is required for telomerase RNA maturation

    <i>ZCCHC8</i>, the nuclear exosome targeting component, is mutated in familial pulmonary fibrosis and is required for telomerase RNA maturation por Dustin L. Gable, Valeriya Gaysinskaya, Christine C. Atik, C. Conover Talbot, Byunghak Kang, Susan E. Stanley, Elizabeth Pugh, Nuria Amat-Codina, Kara M. Schenk, Murat O. Arcasoy, Cory Brayton, Liliana Florea, Mary Armanios

    Publicado 2019
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  3. 3
    Short telomere syndromes cause a primary T cell immunodeficiency

    Short telomere syndromes cause a primary T cell immunodeficiency por Christa L. Wagner, Vidya Sagar Hanumanthu, C. Conover Talbot, Roshini S. Abraham, David Hamm, Dustin L. Gable, Christopher G. Kanakry, Carolyn Applegate, Janet D. Siliciano, J. Brooks Jackson, Stephen Desiderio, Jonathan K. Alder, Leo Luznik, Mary Armanios

    Publicado 2018
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  4. 4
    T cell immune deficiency rather than chromosome instability predisposes patients with short telomere syndromes to squamous cancers

    T cell immune deficiency rather than chromosome instability predisposes patients with short telomere syndromes to squamous cancers por Kristen E. Schratz, Diane A. Flasch, Christine C. Atik, Zoe L. Cosner, Amanda L. Blackford, Wentao Yang, Dustin L. Gable, Paz J. Vellanki, Zhimin Xiang, Valeriya Gaysinskaya, Robert H. Vonderheide, Lisa Rooper, Jinghui Zhang, Mary Armanios

    Publicado 2023
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  5. 5
    Familial Clonal Hematopoiesis in a Long Telomere Syndrome

    Familial Clonal Hematopoiesis in a Long Telomere Syndrome por Emily A. DeBoy, Michael G. Tassia, Kristen E. Schratz, Stephanie M. Yan, Zoe L. Cosner, E. McNally, Dustin L. Gable, Zhimin Xiang, David B. Lombard, Emmanuel S. Antonarakis, Christopher D. Gocke, Rajiv C. McCoy, Mary Armanios

    Publicado 2023
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  6. 6
    Loss-of-function mutations in the RNA biogenesis factor <i>NAF1</i> predispose to pulmonary fibrosis–emphysema

    Loss-of-function mutations in the RNA biogenesis factor <i>NAF1</i> predispose to pulmonary fibrosis–emphysema por Susan E. Stanley, Dustin L. Gable, Christa L. Wagner, Thomas M. Carlile, Vidya Sagar Hanumanthu, Joshua D. Podlevsky, Sara E. Khalil, Amy E. DeZern, María F. Rojas-Durán, Carolyn Applegate, Jonathan K. Alder, Erin M. Parry, Wendy V. Gilbert, Mary Armanios

    Publicado 2016
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  7. 7
    Mendelian etiologies identified with whole exome sequencing in cerebral palsy

    Mendelian etiologies identified with whole exome sequencing in cerebral palsy por Maya Chopra, Dustin L. Gable, Jamie Love‐Nichols, Alexa Tsao, Shira Rockowitz, Piotr Sliz, Elizabeth Barkoudah, Lucia Bastianelli, David L. Coulter, Emily Davidson, Claudio DeGusmao, David Fogelman, Kathleen Huth, Paige Marshall, Donna Nimec, Jessica Solomon Sanders, Benjamin J. Shore, Brian D. Snyder, Scellig Stone, Ana Ubeda, Colyn J. Watkins, Charles B. Berde, Jeffrey Bolton, Catherine A. Brownstein, Michael Costigan, Darius Ebrahimi‐Fakhari, Abbe Lai, Anne O’Donnell‐Luria, Alex R. Paciorkowski, Anna Maria Pinto, John Pugh, Lance H. Rodan, Eugene Roe, Lindsay C. Swanson, Bo Zhang, Michael C. Kruer, Mustafa Şahin, Annapurna Poduri, Siddharth Srivastava

    Publicado 2022
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