Suchergebnisse - David B. Beck

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  1. 1
    Deubiquitylases in developmental ubiquitin signaling and congenital diseases

    Deubiquitylases in developmental ubiquitin signaling and congenital diseases von Mohammed A. Basar, David B. Beck, Achim Werner

    Veröffentlicht 2020
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  2. 2
    PR-Set7 and H4K20me1: at the crossroads of genome integrity, cell cycle, chromosome condensation, and transcription

    PR-Set7 and H4K20me1: at the crossroads of genome integrity, cell cycle, chromosome condensation, and transcription von David B. Beck, Hisanobu Oda, Steven S. Shen, Danny Reinberg

    Veröffentlicht 2012
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  3. 3
    Clonal Hematopoiesis, Inflammation, and Hematologic Malignancy

    Clonal Hematopoiesis, Inflammation, and Hematologic Malignancy von Rashmi Kanagal‐Shamanna, David B. Beck, Katherine R. Calvo

    Veröffentlicht 2023
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  4. 4
    Disorders of ubiquitylation: unchained inflammation

    Disorders of ubiquitylation: unchained inflammation von David B. Beck, Achim Werner, Daniel L. Kastner, Ivona Aksentijevich

    Veröffentlicht 2022
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  5. 5
    The Role of Host Genetic Factors in Coronavirus Susceptibility: Review of Animal and Systematic Review of Human Literature

    The Role of Host Genetic Factors in Coronavirus Susceptibility: Review of Animal and Systematic Review of Human Literature von Marissa LoPresti, David B. Beck, Priya Duggal, Derek A. T. Cummings, Benjamin D. Solomon

    Veröffentlicht 2020
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  6. 6
    The role of PR-Set7 in replication licensing depends on Suv4-20h

    The role of PR-Set7 in replication licensing depends on Suv4-20h von David B. Beck, Adam Burton, Hisanobu Oda, Céline Ziegler-Birling, Maria‐Elena Torres‐Padilla, Danny Reinberg

    Veröffentlicht 2012
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  7. 7
    Regulation of the Histone H4 Monomethylase PR-Set7 by CRL4Cdt2-Mediated PCNA-Dependent Degradation during DNA Damage

    Regulation of the Histone H4 Monomethylase PR-Set7 by CRL4Cdt2-Mediated PCNA-Dependent Degradation during DNA Damage von Hisanobu Oda, Michael R. Hübner, David B. Beck, Michiel Vermeulen, Jerard Hurwitz, David L. Spector, Danny Reinberg

    Veröffentlicht 2010
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  8. 8
    The C-Terminal Domain of RNA Polymerase II Is Modified by Site-Specific Methylation

    The C-Terminal Domain of RNA Polymerase II Is Modified by Site-Specific Methylation von Robert J. Sims, Luis Alejandro Rojas, David B. Beck, Roberto Bonasio, Roland Schüller, William J. Drury, Dirk Eick, Danny Reinberg

    Veröffentlicht 2011
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  9. 9
    Asymmetrically Modified Nucleosomes

    Asymmetrically Modified Nucleosomes von Philipp Voigt, Gary LeRoy, William J. Drury, Barry M. Zee, Jinsook Son, David B. Beck, Nicolas L. Young, Benjamin A. García, Danny Reinberg

    Veröffentlicht 2012
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  10. 10
    Novel Somatic <scp><i>UBA1</i></scp> Variant in a Patient With <scp>VEXAS</scp> Syndrome

    Novel Somatic <scp><i>UBA1</i></scp> Variant in a Patient With <scp>VEXAS</scp> Syndrome von Blanka Stibůrková, Kateřina Pavelcová, Monika Beličková, Samuel J. Magaziner, Jason C. Collins, Achim Werner, David B. Beck, Veronika Balajková, Cyril Šálek, Martin Vostrý, H. Mann, Jiří Vencovský

    Veröffentlicht 2023
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  11. 11
    <scp>VEXAS</scp> Syndrome: A Case Series From a <scp>Single‐Center</scp> Cohort of Italian Patients With Vasculitis

    <scp>VEXAS</scp> Syndrome: A Case Series From a <scp>Single‐Center</scp> Cohort of Italian Patients With Vasculitis von Francesco Muratore, Chiara Marvisi, Paola Castrignanò, Davide Nicoli, Enrico Farnetti, Orsola Bonanno, Rosina Longo, Piera Zaldini, Elena Galli, Nicholas Balanda, David B. Beck, Peter C. Grayson, Nicolò Pipitone, Luigi Boiardi, Carlo Salvarani

    Veröffentlicht 2021
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  12. 12
    Second Case of HOIP Deficiency Expands Clinical Features and Defines Inflammatory Transcriptome Regulated by LUBAC

    Second Case of HOIP Deficiency Expands Clinical Features and Defines Inflammatory Transcriptome Regulated by LUBAC von Hirotsugu Oda, David B. Beck, Hye Sun Kuehn, Natalia Sampaio Moura, Patrycja Hoffmann, Maria Ibarra, Jennifer Stoddard, Wanxia Li Tsai, Gustavo Gutierrez-Cruz, Massimo Gadina, Sergio D. Rosenzweig, Daniel L. Kastner, Luigi D. Notarangelo, Ivona Aksentijevich

    Veröffentlicht 2019
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  13. 13
    The tumor suppressor SirT2 regulates cell cycle progression and genome stability by modulating the mitotic deposition of H4K20 methylation

    The tumor suppressor SirT2 regulates cell cycle progression and genome stability by modulating the mitotic deposition of H4K20 methylation von Lourdes Serrano, Paloma Martínez‐Redondo, Anna Marazuela-Duque, Berta N. Vázquez, Scott Dooley, Philipp Voigt, David B. Beck, Noriko Kane‐Goldsmith, Qiang Tong, Rosa M. Rabanal, Dolors Fondevila, Purificacı́on Muñoz, Marcus Krüger, Jay A. Tischfield, Alejandro Vaquero

    Veröffentlicht 2013
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  14. 14
    <scp>VEXAS</scp> syndrome: A review of bone marrow aspirate and biopsies reporting myeloid and erythroid precursor vacuolation

    <scp>VEXAS</scp> syndrome: A review of bone marrow aspirate and biopsies reporting myeloid and erythroid precursor vacuolation von Hannah Cherniawsky, Jordan Friedmann, Hamish Nicolson, Natasha Dehghan, Ryan J. Stubbins, Lynda Foltz, Heather A. Leitch, Gayatri Sreenivasan, Kimberley Ambler, Thomas J. Nevill, Eric McGinnis, Lorena Wilson, David B. Beck, Luke Y. C. Chen, Krista Marcon

    Veröffentlicht 2023
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  15. 15
    Novel somatic mutations in UBA1 as a cause of VEXAS syndrome

    Novel somatic mutations in UBA1 as a cause of VEXAS syndrome von James A. Poulter, Jason C. Collins, Catherine Cargo, Ruth M. de Tute, Paul Evans, Daniela Ospina Cardona, David Bowen, Joanna R. Cunnington, Elaine Baguley, Mark Quinn, Michael Green, Dennis McGonagle, David B. Beck, Achim Werner, Sinisa Savic

    Veröffentlicht 2021
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  16. 16
    Estimated Prevalence and Clinical Manifestations of <i>UBA1</i> Variants Associated With VEXAS Syndrome in a Clinical Population

    Estimated Prevalence and Clinical Manifestations of <i>UBA1</i> Variants Associated With VEXAS Syndrome in a Clinical Population von David B. Beck, Dale L. Bodian, Vandan Shah, Uyenlinh L. Mirshahi, Jung Kim, Yi Ding, Samuel J. Magaziner, Natasha T. Strande, Anna Cantor, Jeremy S. Haley, Adam Cook, Wesley Hill, Alan L. Schwartz, Peter C. Grayson, Marcela A. Ferrada, Daniel L. Kastner, David J. Carey, Douglas R. Stewart

    Veröffentlicht 2023
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  17. 17
    Early activation of inflammatory pathways in UBA1-mutated hematopoietic stem and progenitor cells in VEXAS

    Early activation of inflammatory pathways in UBA1-mutated hematopoietic stem and progenitor cells in VEXAS von Zhijie Wu, Shouguo Gao, Qingyan Gao, Bhavisha A. Patel, Emma M. Groarke, Xingmin Feng, Ash Lee Manley, Haoran Li, Daniela Ospina Cardona, Sachiko Kajigaya, Lemlem Alemu, Diego Quinones Raffo, Amanda K. Ombrello, Marcela A. Ferrada, Peter C. Grayson, Katherine R. Calvo, Daniel L. Kastner, David B. Beck, Neal S. Young

    Veröffentlicht 2023
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  18. 18
    Shared and distinct mechanisms of UBA1 inactivation across different diseases

    Shared and distinct mechanisms of UBA1 inactivation across different diseases von Jason C. Collins, Samuel J. Magaziner, Maya English, Bakar A. Hassan, Xiang Chen, Nicholas Balanda, Meghan Anderson, Athena Lam, Sebastian Fernandez‐Pol, Bernice Y. Kwong, Peter L. Greenberg, Benjamin Terrier, Mary E. Likhite, Olivier Kosmider, Yan Wang, N.L. Samara, Kylie J. Walters, David B. Beck, Achim Werner

    Veröffentlicht 2024
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  19. 19
    Benign and malignant hematologic manifestations in patients with VEXAS syndrome due to somatic mutations in <i>UBA1</i>

    Benign and malignant hematologic manifestations in patients with VEXAS syndrome due to somatic mutations in <i>UBA1</i> von Ifeyinwa E. Obiorah, Bhavisha A. Patel, Emma M. Groarke, Weixin Wang, Megan Trick, Amanda K. Ombrello, Marcela A. Ferrada, Zhijie Wu, Fernanda Gutierrez‐Rodrigues, Jennifer Lotter, Lorena Wilson, Patrycja Hoffmann, Daniela Ospina Cardona, Nisha Patel, Alina Dulau‐Florea, Daniel L. Kastner, Peter C. Grayson, David B. Beck, Neal S. Young, Katherine R. Calvo

    Veröffentlicht 2021
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  20. 20
    Deficiency of Adenosine Deaminase 2 (DADA2): Hidden Variants, Reduced Penetrance, and Unusual Inheritance

    Deficiency of Adenosine Deaminase 2 (DADA2): Hidden Variants, Reduced Penetrance, and Unusual Inheritance von Oskar Schnappauf, Qing Zhou, Natalia Sampaio Moura, Amanda K. Ombrello, Drew G. Michael, Natalie Deuitch, Karyl S. Barron, Deborah L. Stone, Patrycja Hoffmann, Michael S. Hershfield, Carolyn Applegate, Hans T. Björnsson, David B. Beck, P. Dane Witmer, Nara Sobreira, Elizabeth Wohler, John A. Chiorini, The American Genome Center, Clifton L. Dalgard, NIH Intramural Sequencing Center, Daniel L. Kastner, Ivona Aksentijevich

    Veröffentlicht 2020
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