These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

268 related items for PubMed ID: 24821012

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Water permeability of C-terminally truncated aquaporin 0 (AQP0 1-243) observed in the aging human lens.
    Ball LE, Little M, Nowak MW, Garland DL, Crouch RK, Schey KL.
    Invest Ophthalmol Vis Sci; 2003 Nov; 44(11):4820-8. PubMed ID: 14578404
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Deletion of beaded filament proteins or the C-terminal end of Aquaporin 0 causes analogous abnormal distortion aberrations in mouse lens.
    Varadaraj K, FitzGerald PG, Kumari SS.
    Exp Eye Res; 2021 Aug; 209():108645. PubMed ID: 34087204
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Regulation of aquaporin water permeability in the lens.
    Varadaraj K, Kumari S, Shiels A, Mathias RT.
    Invest Ophthalmol Vis Sci; 2005 Apr; 46(4):1393-402. PubMed ID: 15790907
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Functional characterization of a human aquaporin 0 mutation that leads to a congenital dominant lens cataract.
    Varadaraj K, Kumari SS, Patil R, Wax MB, Mathias RT.
    Exp Eye Res; 2008 Jul; 87(1):9-21. PubMed ID: 18501347
    [Abstract] [Full Text] [Related]

  • 14. Structural function of MIP/aquaporin 0 in the eye lens; genetic defects lead to congenital inherited cataracts.
    Chepelinsky AB.
    Handb Exp Pharmacol; 2009 Jul; (190):265-97. PubMed ID: 19096783
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. AQP0-LTR of the Cat Fr mouse alters water permeability and calcium regulation of wild type AQP0.
    Kalman K, Németh-Cahalan KL, Froger A, Hall JE.
    Biochim Biophys Acta; 2006 Aug; 1758(8):1094-9. PubMed ID: 16515771
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Spatial distributions of AQP5 and AQP0 in embryonic and postnatal mouse lens development.
    Petrova RS, Schey KL, Donaldson PJ, Grey AC.
    Exp Eye Res; 2015 Mar; 132():124-35. PubMed ID: 25595964
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.