Resultados de procura - Bradley K. Yoder

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  1. 1
    Role of Primary Cilia in the Pathogenesis of Polycystic Kidney Disease

    Role of Primary Cilia in the Pathogenesis of Polycystic Kidney Disease por Bradley K. Yoder

    Publicado 2007
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  2. 2
    Normal Ciliogenesis Requires Synergy between the Cystic Kidney Disease Genes MKS-3 and NPHP-4

    Normal Ciliogenesis Requires Synergy between the Cystic Kidney Disease Genes MKS-3 and NPHP-4 por Corey Williams, Svetlana V. Masyukova, Bradley K. Yoder

    Publicado 2010
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  3. 3
    The Polycystic Kidney Disease Proteins, Polycystin-1, Polycystin-2, Polaris, and Cystin, Are Co-Localized in Renal Cilia

    The Polycystic Kidney Disease Proteins, Polycystin-1, Polycystin-2, Polaris, and Cystin, Are Co-Localized in Renal Cilia por Bradley K. Yoder, Xiaoying Hou, Lisa M. Guay‐Woodford

    Publicado 2002
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  4. 4
    An Essential Role for Dermal Primary Cilia in Hair Follicle Morphogenesis

    An Essential Role for Dermal Primary Cilia in Hair Follicle Morphogenesis por Jonathan M. Lehman, Essam Laag, Edward J. Michaud, Bradley K. Yoder

    Publicado 2008
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  5. 5
    Inflammation and Fibrosis in Polycystic Kidney Disease

    Inflammation and Fibrosis in Polycystic Kidney Disease por Cheng Song, Kurt A. Zimmerman, Scott J. Henke, Bradley K. Yoder

    Publicado 2017
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  6. 6
    High-Throughput Genome Editing and Phenotyping Facilitated by High Resolution Melting Curve Analysis

    High-Throughput Genome Editing and Phenotyping Facilitated by High Resolution Melting Curve Analysis por Holly R. Thomas, Stefanie M. Percival, Bradley K. Yoder, John M. Parant

    Publicado 2014
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  7. 7
    Polaris, a Protein Involved in Left-Right Axis Patterning, Localizes to Basal Bodies and Cilia

    Polaris, a Protein Involved in Left-Right Axis Patterning, Localizes to Basal Bodies and Cilia por Patrick D. Taulman, Courtney J. Haycraft, Daniel F. Balkovetz, Bradley K. Yoder

    Publicado 2001
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  8. 8
    Primary Cilia and Signaling Pathways in Mammalian Development, Health and Disease

    Primary Cilia and Signaling Pathways in Mammalian Development, Health and Disease por Iben R. Veland, A. Awan, Lotte B. Pedersen, Bradley K. Yoder, Søren T. Christensen

    Publicado 2009
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  9. 9
    Development of the post-natal growth plate requires intraflagellar transport proteins

    Development of the post-natal growth plate requires intraflagellar transport proteins por Buer Song, Courtney J. Haycraft, Hwa‐seon Seo, Bradley K. Yoder, Rosa Serra

    Publicado 2007
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  10. 10
    Functional Redundancy of the B9 Proteins and Nephrocystins in<i>Caenorhabditis elegans</i>Ciliogenesis

    Functional Redundancy of the B9 Proteins and Nephrocystins in<i>Caenorhabditis elegans</i>Ciliogenesis por Corey Williams, Marlene E. Winkelbauer, Jenny Schäfer, Edward J. Michaud, Bradley K. Yoder

    Publicado 2008
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  11. 11
    XBX-1 Encodes a Dynein Light Intermediate Chain Required for Retrograde Intraflagellar Transport and Cilia Assembly in<i>Caenorhabditis elegans</i>

    XBX-1 Encodes a Dynein Light Intermediate Chain Required for Retrograde Intraflagellar Transport and Cilia Assembly in<i>Caenorhabditis elegans</i> por Jenny Schäfer, Courtney J. Haycraft, James H. Thomas, Bradley K. Yoder, Peter Swoboda

    Publicado 2003
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  12. 12
    The Primary Cilium as a Complex Signaling Center

    The Primary Cilium as a Complex Signaling Center por Nicolas F. Berbari, Amber K. O’Connor, Courtney J. Haycraft, Bradley K. Yoder

    Publicado 2009
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  13. 13
    Soluble levels of cytosolic tubulin regulate ciliary length control

    Soluble levels of cytosolic tubulin regulate ciliary length control por Neeraj Sharma, Zachary A. Kosan, Jannese E. Stallworth, Nicolas F. Berbari, Bradley K. Yoder

    Publicado 2011
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  14. 14
    Disruption of IFT results in both exocrine and endocrine abnormalities in the pancreas of Tg737 mutant mice

    Disruption of IFT results in both exocrine and endocrine abnormalities in the pancreas of Tg737 mutant mice por Qihong Zhang, James R. A. Davenport, Mandy J. Croyle, Courtney J. Haycraft, Bradley K. Yoder

    Publicado 2004
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  15. 15
    Gli2 and Gli3 Localize to Cilia and Require the Intraflagellar Transport Protein Polaris for Processing and Function

    Gli2 and Gli3 Localize to Cilia and Require the Intraflagellar Transport Protein Polaris for Processing and Function por Courtney J. Haycraft, Boglárka Banizs, Yeşim Aydın Son, Qihong Zhang, Edward J. Michaud, Bradley K. Yoder

    Publicado 2005
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  16. 16
    A Novel Dynein Light Intermediate Chain Colocalizes with the Retrograde Motor for Intraflagellar Transport at Sites of Axoneme Assembly in<i>Chlamydomonas</i>and Mammalian Cells

    A Novel Dynein Light Intermediate Chain Colocalizes with the Retrograde Motor for Intraflagellar Transport at Sites of Axoneme Assembly in<i>Chlamydomonas</i>and Mammalian Cells por Catherine A. Perrone, Douglas Tritschler, Patrick D. Taulman, Raqual Bower, Bradley K. Yoder, Mary E. Porter

    Publicado 2003
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  17. 17
    The <i>Oak Ridge Polycystic Kidney</i> (<i>orpk</i>) disease gene is required for left-right axis determination

    The <i>Oak Ridge Polycystic Kidney</i> (<i>orpk</i>) disease gene is required for left-right axis determination por Noel Murcia, William G. Richards, Bradley K. Yoder, Michael L. Mucenski, John R. Dunlap, Richard P. Woychik

    Publicado 2000
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  18. 18
    Intraflagellar transport is essential for endochondral bone formation

    Intraflagellar transport is essential for endochondral bone formation por Courtney J. Haycraft, Qihong Zhang, Buer Song, Walker S. Jackson, Peter J. Detloff, Rosa Serra, Bradley K. Yoder

    Publicado 2006
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  19. 19
    Cilia-driven fluid flow in the zebrafish pronephros, brain and Kupffer's vesicle is required for normal organogenesis

    Cilia-driven fluid flow in the zebrafish pronephros, brain and Kupffer's vesicle is required for normal organogenesis por Albrecht Kramer-Zucker, Felix Olale, Courtney J. Haycraft, Bradley K. Yoder, Alexander F. Schier, Iain A. Drummond

    Publicado 2005
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  20. 20
    Mutations in Traf3ip1 reveal defects in ciliogenesis, embryonic development, and altered cell size regulation

    Mutations in Traf3ip1 reveal defects in ciliogenesis, embryonic development, and altered cell size regulation por Nicolas F. Berbari, Nicholas W. Kin, Neeraj Sharma, Edward J. Michaud, Robert A. Kesterson, Bradley K. Yoder

    Publicado 2011
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