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PUBMED FOR HANDHELDS

Journal Abstract Search


290 related items for PubMed ID: 28729419

  • 1. The exocyst is required for photoreceptor ciliogenesis and retinal development.
    Lobo GP, Fulmer D, Guo L, Zuo X, Dang Y, Kim SH, Su Y, George K, Obert E, Fogelgren B, Nihalani D, Norris RA, Rohrer B, Lipschutz JH.
    J Biol Chem; 2017 Sep 08; 292(36):14814-14826. PubMed ID: 28729419
    [Abstract] [Full Text] [Related]

  • 2. Conditional Loss of the Exocyst Component Exoc5 in Retinal Pigment Epithelium (RPE) Results in RPE Dysfunction, Photoreceptor Cell Degeneration, and Decreased Visual Function.
    Rohrer B, Biswal MR, Obert E, Dang Y, Su Y, Zuo X, Fogelgren B, Kondkar AA, Lobo GP, Lipschutz JH.
    Int J Mol Sci; 2021 May 11; 22(10):. PubMed ID: 34064901
    [Abstract] [Full Text] [Related]

  • 3. The exocyst acting through the primary cilium is necessary for renal ciliogenesis, cystogenesis, and tubulogenesis.
    Zuo X, Lobo G, Fulmer D, Guo L, Dang Y, Su Y, Ilatovskaya DV, Nihalani D, Rohrer B, Body SC, Norris RA, Lipschutz JH.
    J Biol Chem; 2019 Apr 26; 294(17):6710-6718. PubMed ID: 30824539
    [Abstract] [Full Text] [Related]

  • 4. Primary cilia and the exocyst are linked to urinary extracellular vesicle production and content.
    Zuo X, Kwon SH, Janech MG, Dang Y, Lauzon SD, Fogelgren B, Polgar N, Lipschutz JH.
    J Biol Chem; 2019 Dec 13; 294(50):19099-19110. PubMed ID: 31694916
    [Abstract] [Full Text] [Related]

  • 5. Cilia-deficient renal tubule cells are primed for injury with mitochondrial defects and aberrant tryptophan metabolism.
    Zuo X, Winkler B, Lerner K, Ilatovskaya DV, Zamaro AS, Dang Y, Su Y, Deng P, Fitzgibbon W, Hartman J, Park KM, Lipschutz JH.
    Am J Physiol Renal Physiol; 2024 Jul 01; 327(1):F61-F76. PubMed ID: 38721661
    [Abstract] [Full Text] [Related]

  • 6. Disruption of the exocyst induces podocyte loss and dysfunction.
    Nihalani D, Solanki AK, Arif E, Srivastava P, Rahman B, Zuo X, Dang Y, Fogelgren B, Fermin D, Gillies CE, Sampson MG, Lipschutz JH.
    J Biol Chem; 2019 Jun 28; 294(26):10104-10119. PubMed ID: 31073028
    [Abstract] [Full Text] [Related]

  • 7. Exocyst Complex Member EXOC5 Is Required for Survival of Hair Cells and Spiral Ganglion Neurons and Maintenance of Hearing.
    Lee B, Baek JI, Min H, Bae SH, Moon K, Kim MA, Kim YR, Fogelgren B, Lipschutz JH, Lee KY, Bok J, Kim UK.
    Mol Neurobiol; 2018 Aug 28; 55(8):6518-6532. PubMed ID: 29327200
    [Abstract] [Full Text] [Related]

  • 8. Photoreceptor cell development requires prostaglandin signaling in the zebrafish retina.
    Li W, Jin D, Zhong TP.
    Biochem Biophys Res Commun; 2019 Mar 05; 510(2):230-235. PubMed ID: 30685088
    [Abstract] [Full Text] [Related]

  • 9. Disrupted glucose homeostasis and skeletal-muscle-specific glucose uptake in an exocyst knockout mouse model.
    Fujimoto BA, Young M, Nakamura N, Ha H, Carter L, Pitts MW, Torres D, Noh HL, Suk S, Kim JK, Polgar N.
    J Biol Chem; 2021 Mar 05; 296():100482. PubMed ID: 33647317
    [Abstract] [Full Text] [Related]

  • 10. Cdc42 deficiency causes ciliary abnormalities and cystic kidneys.
    Choi SY, Chacon-Heszele MF, Huang L, McKenna S, Wilson FP, Zuo X, Lipschutz JH.
    J Am Soc Nephrol; 2013 Sep 05; 24(9):1435-50. PubMed ID: 23766535
    [Abstract] [Full Text] [Related]

  • 11. The ciliopathy gene cc2d2a controls zebrafish photoreceptor outer segment development through a role in Rab8-dependent vesicle trafficking.
    Bachmann-Gagescu R, Phelps IG, Stearns G, Link BA, Brockerhoff SE, Moens CB, Doherty D.
    Hum Mol Genet; 2011 Oct 15; 20(20):4041-55. PubMed ID: 21816947
    [Abstract] [Full Text] [Related]

  • 12. Defects in the Exocyst-Cilia Machinery Cause Bicuspid Aortic Valve Disease and Aortic Stenosis.
    Fulmer D, Toomer K, Guo L, Moore K, Glover J, Moore R, Stairley R, Lobo G, Zuo X, Dang Y, Su Y, Fogelgren B, Gerard P, Chung D, Heydarpour M, Mukherjee R, Body SC, Norris RA, Lipschutz JH.
    Circulation; 2019 Oct 15; 140(16):1331-1341. PubMed ID: 31387361
    [Abstract] [Full Text] [Related]

  • 13. Loss of Ift74 Leads to Slow Photoreceptor Degeneration and Ciliogenesis Defects in Zebrafish.
    Zhu P, Xu J, Wang Y, Zhao C.
    Int J Mol Sci; 2021 Aug 28; 22(17):. PubMed ID: 34502236
    [Abstract] [Full Text] [Related]

  • 14. Arl13b and the exocyst interact synergistically in ciliogenesis.
    Seixas C, Choi SY, Polgar N, Umberger NL, East MP, Zuo X, Moreiras H, Ghossoub R, Benmerah A, Kahn RA, Fogelgren B, Caspary T, Lipschutz JH, Barral DC.
    Mol Biol Cell; 2016 Jan 15; 27(2):308-20. PubMed ID: 26582389
    [Abstract] [Full Text] [Related]

  • 15. Male germ cell-associated kinase is required for axoneme formation during ciliogenesis in zebrafish photoreceptors.
    Chiang HJ, Nishiwaki Y, Chiang WC, Masai I.
    Dis Model Mech; 2024 Jul 01; 17(7):. PubMed ID: 38813692
    [Abstract] [Full Text] [Related]

  • 16. Cluap1 is essential for ciliogenesis and photoreceptor maintenance in the vertebrate eye.
    Lee C, Wallingford JB, Gross JM.
    Invest Ophthalmol Vis Sci; 2014 Jun 26; 55(7):4585-92. PubMed ID: 24970261
    [Abstract] [Full Text] [Related]

  • 17. ARL13B, a Joubert Syndrome-Associated Protein, Is Critical for Retinogenesis and Elaboration of Mouse Photoreceptor Outer Segments.
    Dilan TL, Moye AR, Salido EM, Saravanan T, Kolandaivelu S, Goldberg AFX, Ramamurthy V.
    J Neurosci; 2019 Feb 20; 39(8):1347-1364. PubMed ID: 30573647
    [Abstract] [Full Text] [Related]

  • 18. Knockdown of poc1b causes abnormal photoreceptor sensory cilium and vision impairment in zebrafish.
    Zhang C, Zhang Q, Wang F, Liu Q.
    Biochem Biophys Res Commun; 2015 Oct 02; 465(4):651-7. PubMed ID: 26188096
    [Abstract] [Full Text] [Related]

  • 19. The role of the exocyst in renal ciliogenesis, cystogenesis, tubulogenesis, and development.
    Lipschutz JH.
    Kidney Res Clin Pract; 2019 Sep 30; 38(3):260-266. PubMed ID: 31284362
    [Abstract] [Full Text] [Related]

  • 20. Loss of ift122, a Retrograde Intraflagellar Transport (IFT) Complex Component, Leads to Slow, Progressive Photoreceptor Degeneration Due to Inefficient Opsin Transport.
    Boubakri M, Chaya T, Hirata H, Kajimura N, Kuwahara R, Ueno A, Malicki J, Furukawa T, Omori Y.
    J Biol Chem; 2016 Nov 18; 291(47):24465-24474. PubMed ID: 27681595
    [Abstract] [Full Text] [Related]


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