Torthaí cuardaigh - David Li‐Kroeger

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  1. 1
    Hox and Senseless Antagonism Functions as a Molecular Switch to Regulate EGF Secretion in the Drosophila PNS

    Hox and Senseless Antagonism Functions as a Molecular Switch to Regulate EGF Secretion in the Drosophila PNS de réir David Li‐Kroeger, Lorraine M. Witt, H. Leighton Grimes, Tiffany Cook, Brian Gebelein

    Foilsithe / Cruthaithe 2008
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  2. 2
    NMNATs, evolutionarily conserved neuronal maintenance factors

    NMNATs, evolutionarily conserved neuronal maintenance factors de réir Yousuf Ali, David Li‐Kroeger, Hugo J. Bellen, R. Grace Zhai, Hui‐Chen Lu

    Foilsithe / Cruthaithe 2013
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  3. 3
    An expanded toolkit for gene tagging based on MiMIC and scarless CRISPR tagging in Drosophila

    An expanded toolkit for gene tagging based on MiMIC and scarless CRISPR tagging in Drosophila de réir David Li‐Kroeger, Oguz Kanca, Pei-Tseng Lee, Sierra Cowan, Michael T Lee, Manish Jaiswal, Jose L. Salazar, Yuchun He, Zhongyuan Zuo, Hugo J. Bellen

    Foilsithe / Cruthaithe 2018
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  4. 4
    Lysosomal Degradation Is Required for Sustained Phagocytosis of Bacteria by Macrophages

    Lysosomal Degradation Is Required for Sustained Phagocytosis of Bacteria by Macrophages de réir Ching‐On Wong, Steven R. Gregory, Hongxiang Hu, Yufang Chao, Victoria E. Sepúlveda, Yuchun He, David Li‐Kroeger, William E. Goldman, Hugo J. Bellen, Kartik Venkatachalam

    Foilsithe / Cruthaithe 2017
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  5. 5
    Retromer subunit, VPS29, regulates synaptic transmission and is required for endolysosomal function in the aging brain

    Retromer subunit, VPS29, regulates synaptic transmission and is required for endolysosomal function in the aging brain de réir Hui Ye, Shamsideen A. Ojelade, David Li‐Kroeger, Zhongyuan Zuo, Liping Wang, Yarong Li, Jessica Gu, Ulrich Tepaß, Avital A. Rodal, Hugo J. Bellen, Joshua M. Shulman

    Foilsithe / Cruthaithe 2020
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  6. 6
    Dietary restriction and the transcription factor clock delay eye aging to extend lifespan in Drosophila Melanogaster

    Dietary restriction and the transcription factor clock delay eye aging to extend lifespan in Drosophila Melanogaster de réir Brian A. Hodge, Geoffrey T. Meyerhof, Subhash D. Katewa, Ting Lian, Charles Lau, Sudipta Bar, Nicole Y. Leung, Menglin Li, David Li‐Kroeger, Simon Melov, Birgit Schilling, Craig Montell, Pankaj Kapahi

    Foilsithe / Cruthaithe 2022
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  7. 7
    NMNAT2:HSP90 Complex Mediates Proteostasis in Proteinopathies

    NMNAT2:HSP90 Complex Mediates Proteostasis in Proteinopathies de réir Yousuf Ali, Hunter M. Allen, Lei Yu, David Li‐Kroeger, Dena Bakhshizadehmahmoudi, Asante Hatcher, Cristin McCabe, Jishu Xu, Nicole L. Bjorklund, Giulio Taglialatela, David A. Bennett, Philip L. De Jager, Joshua Shulman, Hugo J. Bellen, Hui‐Chen Lu

    Foilsithe / Cruthaithe 2016
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  8. 8
    A gene-specific T2A-GAL4 library for Drosophila

    A gene-specific T2A-GAL4 library for Drosophila de réir Pei-Tseng Lee, Jonathan Zirin, Oguz Kanca, Wen‐Wen Lin, Karen L. Schulze, David Li‐Kroeger, Rong Tao, Colby Devereaux, Yanhui Hu, Verena Chung, Yīng Fāng, Yuchun He, Hongling Pan, Ming Ge, Zhongyuan Zuo, Benjamin E. Housden, Stephanie E. Mohr, Shinya Yamamoto, Robert Levis, Allan C. Spradling, Norbert Perrimon, Hugo J. Bellen

    Foilsithe / Cruthaithe 2018
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  9. 9
    Loss of Oxidation Resistance 1, OXR1, Is Associated with an Autosomal-Recessive Neurological Disease with Cerebellar Atrophy and Lysosomal Dysfunction

    Loss of Oxidation Resistance 1, OXR1, Is Associated with an Autosomal-Recessive Neurological Disease with Cerebellar Atrophy and Lysosomal Dysfunction de réir Julia Wang, Justine Rousseau, Emily Kim, Sophie Ehresmann, Yi-Ting Cheng, Lita Duraine, Zhongyuan Zuo, Ye-Jin Park, David Li‐Kroeger, Weimin Bi, Lee-Jun Wong, Jill A. Rosenfeld, Joseph G. Gleeson, Eissa Faqeih, Fowzan S. Alkuraya, Klaas J. Wierenga, Jiani Chen, Alexandra Afenjar, Caroline Nava, Diane Doummar, Boris Keren, Jane Juusola, Markus Grompe, Hugo J. Bellen, Philippe M. Campeau

    Foilsithe / Cruthaithe 2019
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  10. 10
    Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms

    Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms de réir Hyunglok Chung, Michael F. Wangler, Paul C. Marcogliese, Ju-Yeon Jo, Thomas A. Ravenscroft, Zhongyuan Zuo, Lita Duraine, Sina Sadeghzadeh, David Li‐Kroeger, Robert E. Schmidt, Alan Pestronk, Jill A. Rosenfeld, Lindsay C. Burrage, Mitchell J. Herndon, Shan Chen, Amelle Shillington, Marissa Vawter‐Lee, Robert J. Hopkin, Jackeline Rodriguez‐Smith, Michael Henrickson, Brendan Lee, Ann B. Moser, Richard O. Jones, Paul A. Watkins, Taekyeong Yoo, Soe Mar, Murim Choi, Robert C. Bucelli, Shinya Yamamoto, Hyun Kyoung Lee, Carlos E. Prada, Jong‐Hee Chae, Tiphanie P. Vogel, Hugo J. Bellen

    Foilsithe / Cruthaithe 2020
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  11. 11
    Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease

    Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease de réir Jóhanna Jakobsdóttir, Sven J. van der Lee, Joshua C. Bis, Vincent Chouraki, David Li‐Kroeger, Shinya Yamamoto, Megan L. Grove, Adam C. Naj, Maria Vronskaya, Jose L. Salazar, Anita L. DeStefano, Jennifer A. Brody, Albert V. Smith, Najaf Amin, Rebecca Sims, Carla A. Ibrahim‐Verbaas, Seung-Hoan Choi, Claudia L. Satizábal, Oscar L. López, Alexa Beiser, M. Arfan Ikram, Melissa E. Garcia, Caroline Hayward, Tibor V. Varga, Samuli Ripatti, Paul W. Franks, Göran Hallmans, Olov Rolandsson, Jan-Håkon Jansson, David J. Porteous, Veikko Salomaa, Gudny Eiriksdottir, Kenneth Rice, Hugo J. Bellen, Daniel Levy, André G. Uitterlinden, Valur Emilsson, Jerome I. Rotter, Thor Aspelund, Christopher J. O’Donnell, Annette L. Fitzpatrick, Lenore J. Launer, Albert Hofman, Li-San Wang, Julie Williams, Gerard D. Schellenberg, Eric Boerwinkle, Bruce M. Psaty, Sudha Seshadri, Joshua Shulman, Vilmundur Guðnason, Cornelia M. van Duijn

    Foilsithe / Cruthaithe 2016
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