Hasil Pencarian - Gregory J Pazour

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  1. 1
    Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes

    Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes oleh George C. Gabriel, Gregory J. Pazour, Cecilia W. Lo

    Diterbitkan 2018-06-01
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  2. 2
    c-Jun N-terminal kinase (JNK) signaling contributes to cystic burden in polycystic kidney disease.

    c-Jun N-terminal kinase (JNK) signaling contributes to cystic burden in polycystic kidney disease. oleh Abigail O Smith, Julie A Jonassen, Kenley M Preval, Roger J Davis, Gregory J Pazour

    Diterbitkan 2021-12-01
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  3. 3
    The Golgin GMAP210/TRIP11 anchors IFT20 to the Golgi complex.

    The Golgin GMAP210/TRIP11 anchors IFT20 to the Golgi complex. oleh John A Follit, Jovenal T San Agustin, Fenghui Xu, Julie A Jonassen, Rajeev Samtani, Cecilia W Lo, Gregory J Pazour

    Diterbitkan 2008-12-01
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  4. 4
    Arf4 is required for Mammalian development but dispensable for ciliary assembly.

    Arf4 is required for Mammalian development but dispensable for ciliary assembly. oleh John A Follit, Jovenal T San Agustin, Julie A Jonassen, Tingting Huang, Jaime A Rivera-Perez, Kimberly D Tremblay, Gregory J Pazour

    Diterbitkan 2014-02-01
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  5. 5
    Loss of Primary Cilia Protein IFT20 Dysregulates Lymphatic Vessel Patterning in Development and Inflammation

    Loss of Primary Cilia Protein IFT20 Dysregulates Lymphatic Vessel Patterning in Development and Inflammation oleh Delayna Paulson, Delayna Paulson, Rebecca Harms, Rebecca Harms, Cody Ward, Cody Ward, Mackenzie Latterell, Mackenzie Latterell, Gregory J. Pazour, Darci M. Fink, Darci M. Fink

    Diterbitkan 2021-05-01
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  6. 6
    Erratum: Genetic link between renal birth defects and congenital heart disease

    Erratum: Genetic link between renal birth defects and congenital heart disease oleh Jovenal T. San Agustin, Nikolai Klena, Kristi Granath, Ashok Panigrahy, Eileen Stewart, William Devine, Lara Strittmatter, Julie A. Jonassen, Xiaoqin Liu, Cecilia W. Lo, Gregory J. Pazour

    Diterbitkan 2016-06-01
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  7. 7
    Genetic link between renal birth defects and congenital heart disease

    Genetic link between renal birth defects and congenital heart disease oleh Jovenal T. San Agustin, Nikolai Klena, Kristi Granath, Ashok Panigrahy, Eileen Stewart, William Devine, Lara Strittmatter, Julie A. Jonassen, Xiaoqin Liu, Cecilia W. Lo, Gregory J. Pazour

    Diterbitkan 2016-03-01
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  8. 8
    Autonomous and non-cell autonomous role of cilia in structural birth defects in mice.

    Autonomous and non-cell autonomous role of cilia in structural birth defects in mice. oleh Richard J B Francis, Jovenal T San Agustin, Heather L Szabo Rogers, Cheng Cui, Julie A Jonassen, Thibaut Eguether, John A Follit, Cecilia W Lo, Gregory J Pazour

    Diterbitkan 2023-12-01
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  9. 9
    Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome

    Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome oleh Cheng Cui, Bishwanath Chatterjee, Deanne Francis, Qing Yu, Jovenal T. SanAgustin, Richard Francis, Terry Tansey, Charisse Henry, Baolin Wang, Bethan Lemley, Gregory J. Pazour, Cecilia W. Lo

    Diterbitkan 2011-01-01
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  10. 10
    Ror2 signaling regulates Golgi structure and transport through IFT20 for tumor invasiveness

    Ror2 signaling regulates Golgi structure and transport through IFT20 for tumor invasiveness oleh Michiru Nishita, Seung-Yeol Park, Tadashi Nishio, Koki Kamizaki, ZhiChao Wang, Kota Tamada, Toru Takumi, Ryuju Hashimoto, Hiroki Otani, Gregory J. Pazour, Victor W. Hsu, Yasuhiro Minami

    Diterbitkan 2017-01-01
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  11. 11
    Tethering of vesicles to the Golgi by GMAP210 controls LAT delivery to the immune synapse

    Tethering of vesicles to the Golgi by GMAP210 controls LAT delivery to the immune synapse oleh Andres Ernesto Zucchetti, Laurence Bataille, Jean-Marie Carpier, Stéphanie Dogniaux, Mabel San Roman-Jouve, Mathieu Maurin, Michael W. Stuck, Rosa M. Rios, Cosima T. Baldari, Gregory J. Pazour, Claire Hivroz

    Diterbitkan 2019-06-01
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  12. 12
    Loss of the ciliary protein Chibby1 in mice leads to exocrine pancreatic degeneration and pancreatitis

    Loss of the ciliary protein Chibby1 in mice leads to exocrine pancreatic degeneration and pancreatitis oleh Benjamin Cyge, Vera Voronina, Mohammed Hoque, Eunice N. Kim, Jason Hall, Jennifer M. Bailey-Lundberg, Gregory J. Pazour, Howard C. Crawford, Randall T. Moon, Feng-Qian Li, Ken-Ichi Takemaru

    Diterbitkan 2021-08-01
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  13. 13
    Loss of Arf4 causes severe degeneration of the exocrine pancreas but not cystic kidney disease or retinal degeneration.

    Loss of Arf4 causes severe degeneration of the exocrine pancreas but not cystic kidney disease or retinal degeneration. oleh Jillian N Pearring, Jovenal T San Agustin, Ekaterina S Lobanova, Christopher J Gabriel, Eric C Lieu, William J Monis, Michael W Stuck, Lara Strittmatter, Samer M Jaber, Vadim Y Arshavsky, Gregory J Pazour

    Diterbitkan 2017-04-01
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  14. 14
    DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia.

    DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia. oleh You Li, Hisato Yagi, Ezenwa Obi Onuoha, Rama Rao Damerla, Richard Francis, Yoshiyuki Furutani, Muhammad Tariq, Stephen M King, Gregory Hendricks, Cheng Cui, Manush Saydmohammed, Dong Min Lee, Maliha Zahid, Iman Sami, Linda Leatherbury, Gregory J Pazour, Stephanie M Ware, Toshio Nakanishi, Elizabeth Goldmuntz, Michael Tsang, Cecilia W Lo

    Diterbitkan 2016-02-01
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  15. 15
    Wdpcp, a PCP protein required for ciliogenesis, regulates directional cell migration and cell polarity by direct modulation of the actin cytoskeleton.

    Wdpcp, a PCP protein required for ciliogenesis, regulates directional cell migration and cell polarity by direct modulation of the actin cytoskeleton. oleh Cheng Cui, Bishwanath Chatterjee, Thomas P Lozito, Zhen Zhang, Richard J Francis, Hisato Yagi, Lisa M Swanhart, Subramaniam Sanker, Deanne Francis, Qing Yu, Jovenal T San Agustin, Chandrakala Puligilla, Tania Chatterjee, Terry Tansey, Xiaoqin Liu, Matthew W Kelley, Elias T Spiliotis, Adam V Kwiatkowski, Rocky Tuan, Gregory J Pazour, Neil A Hukriede, Cecilia W Lo

    Diterbitkan 2013-11-01
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  16. 16
    IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans.

    IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans. oleh Zeineb Bakey, Oscar A Cabrera, Julia Hoefele, Dinu Antony, Kaman Wu, Michael W Stuck, Dimitra Micha, Thibaut Eguether, Abigail O Smith, Nicole N van der Wel, Matias Wagner, Lara Strittmatter, Philip L Beales, Julie A Jonassen, Isabelle Thiffault, Maxime Cadieux-Dion, Laura Boyes, Saba Sharif, Beyhan Tüysüz, Desiree Dunstheimer, Hans W M Niessen, William Devine, Cecilia W Lo, Hannah M Mitchison, Miriam Schmidts, Gregory J Pazour

    Diterbitkan 2023-06-01
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