Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 107

Similar articles for PubMed (Select 20671274)


Two distinct aquaporin 0s required for development and transparency of the zebrafish lens.

Froger A, Clemens D, Kalman K, Németh-Cahalan KL, Schilling TF, Hall JE.

Invest Ophthalmol Vis Sci. 2010 Dec;51(12):6582-92. doi: 10.1167/iovs.10-5626. Epub 2010 Jul 29.


In vivo analysis of aquaporin 0 function in zebrafish: permeability regulation is required for lens transparency.

Clemens DM, Németh-Cahalan KL, Trinh L, Zhang T, Schilling TF, Hall JE.

Invest Ophthalmol Vis Sci. 2013 Jul 30;54(7):5136-43. doi: 10.1167/iovs.13-12337.


The effect of the interaction between aquaporin 0 (AQP0) and the filensin tail region on AQP0 water permeability.

Nakazawa Y, Oka M, Furuki K, Mitsuishi A, Nakashima E, Takehana M.

Mol Vis. 2011;17:3191-9. Epub 2011 Dec 13.


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.


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. Epub 2006 Feb 13.


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.


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. doi: 10.1016/j.exer.2010.06.013. Epub 2010 Jun 22.


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. doi: 10.1016/j.exer.2008.04.001. Epub 2008 Apr 10.


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. doi: 10.1016/j.exer.2013.09.019. Epub 2013 Oct 9.


A 28 kDa sarcolemmal antigen in kidney principal cell basolateral membranes: relationship to orthogonal arrays and MIP26.

Verbavatz JM, Van Hoek AN, Ma T, Sabolic I, Valenti G, Ellisman MH, Ausiello DA, Verkman AS, Brown D.

J Cell Sci. 1994 Apr;107 ( Pt 4):1083-94.


Regulation of AQP0 water permeability is enhanced by cooperativity.

Németh-Cahalan KL, Clemens DM, Hall JE.

J Gen Physiol. 2013 Mar;141(3):287-95. doi: 10.1085/jgp.201210884.


Functional expression of aquaporins in embryonic, postnatal, and adult mouse lenses.

Varadaraj K, Kumari SS, Mathias RT.

Dev Dyn. 2007 May;236(5):1319-28.


Cloning and functional expression of an MIP (AQP0) homolog from killifish (Fundulus heteroclitus) lens.

Virkki LV, Cooper GJ, Boron WF.

Am J Physiol Regul Integr Comp Physiol. 2001 Dec;281(6):R1994-2003.


The zebrafish genome encodes the largest vertebrate repertoire of functional aquaporins with dual paralogy and substrate specificities similar to mammals.

Tingaud-Sequeira A, Calusinska M, Finn RN, Chauvigné F, Lozano J, Cerdà J.

BMC Evol Biol. 2010 Feb 11;10:38. doi: 10.1186/1471-2148-10-38.


MIP/Aquaporin 0 represents a direct transcriptional target of PITX3 in the developing lens.

Sorokina EA, Muheisen S, Mlodik N, Semina EV.

PLoS One. 2011;6(6):e21122. doi: 10.1371/journal.pone.0021122. Epub 2011 Jun 17.


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. doi: 10.1007/978-3-540-79885-9_14. Review.


Cloning and characterization of a zebrafish homologue of human AQP1: a bifunctional water and gas channel.

Chen LM, Zhao J, Musa-Aziz R, Pelletier MF, Drummond IA, Boron WF.

Am J Physiol Regul Integr Comp Physiol. 2010 Nov;299(5):R1163-74. doi: 10.1152/ajpregu.00319.2010. Epub 2010 Aug 25.


An MIP/AQP0 mutation with impaired trafficking and function underlies an autosomal dominant congenital lamellar cataract.

Senthil Kumar G, Kyle JW, Minogue PJ, Dinesh Kumar K, Vasantha K, Berthoud VM, Beyer EC, Santhiya ST.

Exp Eye Res. 2013 May;110:136-41. doi: 10.1016/j.exer.2012.10.010. Epub 2012 Oct 29.

Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk