680 related articles for article (PubMed ID: 19096783)
1. Structural function of MIP/aquaporin 0 in the eye lens; genetic defects lead to congenital inherited cataracts.
Chepelinsky AB
Handb Exp Pharmacol; 2009; (190):265-97. PubMed ID: 19096783
[TBL] [Abstract][Full Text] [Related]
2. Interaction of major intrinsic protein (aquaporin-0) with fiber connexins in lens development.
Yu XS; Jiang JX
J Cell Sci; 2004 Feb; 117(Pt 6):871-80. PubMed ID: 14762116
[TBL] [Abstract][Full Text] [Related]
3. Specific interaction between lens MIP/Aquaporin-0 and two members of the gamma-crystallin family.
Fan J; Fariss RN; Purkiss AG; Slingsby C; Sandilands A; Quinlan R; Wistow G; Chepelinsky AB
Mol Vis; 2005 Jan; 11():76-87. PubMed ID: 15692460
[TBL] [Abstract][Full Text] [Related]
4. 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
[TBL] [Abstract][Full Text] [Related]
5. Aquaporin-0 membrane junctions form upon proteolytic cleavage.
Gonen T; Cheng Y; Kistler J; Walz T
J Mol Biol; 2004 Sep; 342(4):1337-45. PubMed ID: 15351655
[TBL] [Abstract][Full Text] [Related]
6. Post-translational modifications of aquaporin 0 (AQP0) in the normal human lens: spatial and temporal occurrence.
Ball LE; Garland DL; Crouch RK; Schey KL
Biochemistry; 2004 Aug; 43(30):9856-65. PubMed ID: 15274640
[TBL] [Abstract][Full Text] [Related]
7. Mutations in the founder of the MIP gene family underlie cataract development in the mouse.
Shiels A; Bassnett S
Nat Genet; 1996 Feb; 12(2):212-5. PubMed ID: 8563764
[TBL] [Abstract][Full Text] [Related]
8. A 76-bp deletion in the Mip gene causes autosomal dominant cataract in Hfi mice.
Sidjanin DJ; Parker-Wilson DM; Neuhäuser-Klaus A; Pretsch W; Favor J; Deen PM; Ohtaka-Maruyama C; Lu Y; Bragin A; Skach WR; Chepelinsky AB; Grimes PA; Stambolian DE
Genomics; 2001 Jun; 74(3):313-9. PubMed ID: 11414759
[TBL] [Abstract][Full Text] [Related]
9. Functional characterization of an AQP0 missense mutation, R33C, that causes dominant congenital lens cataract, reveals impaired cell-to-cell adhesion.
Kumari SS; Gandhi J; Mustehsan MH; Eren S; Varadaraj K
Exp Eye Res; 2013 Nov; 116():371-85. PubMed ID: 24120416
[TBL] [Abstract][Full Text] [Related]
10. Aquaporin-0 membrane junctions reveal the structure of a closed water pore.
Gonen T; Sliz P; Kistler J; Cheng Y; Walz T
Nature; 2004 May; 429(6988):193-7. PubMed ID: 15141214
[TBL] [Abstract][Full Text] [Related]
11. The C terminus of lens aquaporin 0 interacts with the cytoskeletal proteins filensin and CP49.
Lindsey Rose KM; Gourdie RG; Prescott AR; Quinlan RA; Crouch RK; Schey KL
Invest Ophthalmol Vis Sci; 2006 Apr; 47(4):1562-70. PubMed ID: 16565393
[TBL] [Abstract][Full Text] [Related]
12. Degradation of human aquaporin 0 by m-calpain.
Ma H; Azuma M; Shearer TR
FEBS Lett; 2005 Dec; 579(30):6745-8. PubMed ID: 16310784
[TBL] [Abstract][Full Text] [Related]
13. A predominant form of C-terminally end-cleaved AQP0 functions as an open water channel and an adhesion protein in AQP0
Kumari SS; Varadaraj K
Biochem Biophys Res Commun; 2019 Apr; 511(3):626-630. PubMed ID: 30826060
[TBL] [Abstract][Full Text] [Related]
14. Aquaporin 0-calmodulin interaction and the effect of aquaporin 0 phosphorylation.
Rose KM; Wang Z; Magrath GN; Hazard ES; Hildebrandt JD; Schey KL
Biochemistry; 2008 Jan; 47(1):339-47. PubMed ID: 18081321
[TBL] [Abstract][Full Text] [Related]
15. Functional impairment of lens aquaporin in two families with dominantly inherited cataracts.
Francis P; Chung JJ; Yasui M; Berry V; Moore A; Wyatt MK; Wistow G; Bhattacharya SS; Agre P
Hum Mol Genet; 2000 Sep; 9(15):2329-34. PubMed ID: 11001937
[TBL] [Abstract][Full Text] [Related]
16. The MIP family of integral membrane channel proteins: sequence comparisons, evolutionary relationships, reconstructed pathway of evolution, and proposed functional differentiation of the two repeated halves of the proteins.
Reizer J; Reizer A; Saier MH
Crit Rev Biochem Mol Biol; 1993; 28(3):235-57. PubMed ID: 8325040
[TBL] [Abstract][Full Text] [Related]
17. Missense mutations in MIP underlie autosomal dominant 'polymorphic' and lamellar cataracts linked to 12q.
Berry V; Francis P; Kaushal S; Moore A; Bhattacharya S
Nat Genet; 2000 May; 25(1):15-7. PubMed ID: 10802646
[TBL] [Abstract][Full Text] [Related]
18. Water transport in AQP0 aquaporin: molecular dynamics studies.
Han BG; Guliaev AB; Walian PJ; Jap BK
J Mol Biol; 2006 Jul; 360(2):285-96. PubMed ID: 16756992
[TBL] [Abstract][Full Text] [Related]
19. Transgenic expression of AQP1 in the fiber cells of AQP0 knockout mouse: effects on lens transparency.
Varadaraj K; Kumari SS; Mathias RT
Exp Eye Res; 2010 Sep; 91(3):393-404. PubMed ID: 20599966
[TBL] [Abstract][Full Text] [Related]
20. Quantitative analysis of ascorbic acid permeability of aquaporin 0 in the lens.
Nakazawa Y; Oka M; Mitsuishi A; Bando M; Takehana M
Biochem Biophys Res Commun; 2011 Nov; 415(1):125-30. PubMed ID: 22020074
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
