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.
3. Mechanism of insolubilization by a single-point mutation in alphaA-crystallin linked with hereditary human cataracts. Andley UP, Hamilton PD, Ravi N. Biochemistry; 2008 Sep 09; 47(36):9697-706. PubMed ID: 18700785 [Abstract] [Full Text] [Related]
4. AlphaA-crystallin R49Cneo mutation influences the architecture of lens fiber cell membranes and causes posterior and nuclear cataracts in mice. Andley UP. BMC Ophthalmol; 2009 Jul 20; 9():4. PubMed ID: 19619312 [Abstract] [Full Text] [Related]
6. In vivo substrates of the lens molecular chaperones αA-crystallin and αB-crystallin. Andley UP, Malone JP, Townsend RR. PLoS One; 2014 Jul 20; 9(4):e95507. PubMed ID: 24760011 [Abstract] [Full Text] [Related]
7. Probing the changes in gene expression due to α-crystallin mutations in mouse models of hereditary human cataract. Andley UP, Tycksen E, McGlasson-Naumann BN, Hamilton PD. PLoS One; 2018 Jul 20; 13(1):e0190817. PubMed ID: 29338044 [Abstract] [Full Text] [Related]
8. Activation of the unfolded protein response by a cataract-associated αA-crystallin mutation. Watson GW, Andley UP. Biochem Biophys Res Commun; 2010 Oct 15; 401(2):192-6. PubMed ID: 20833134 [Abstract] [Full Text] [Related]
10. The common modification in alphaA-crystallin in the lens, N101D, is associated with increased opacity in a mouse model. Gupta R, Asomugha CO, Srivastava OP. J Biol Chem; 2011 Apr 01; 286(13):11579-92. PubMed ID: 21245144 [Abstract] [Full Text] [Related]
11. An alphaA-crystallin gene mutation, Arg12Cys, causing inherited cataract-microcornea exhibits an altered heat-shock response. Zhang LY, Yam GH, Tam PO, Lai RY, Lam DS, Pang CP, Fan DS. Mol Vis; 2009 Jun 04; 15():1127-38. PubMed ID: 19503744 [Abstract] [Full Text] [Related]
13. Alpha-crystallin mutations alter lens metabolites in mouse models of human cataracts. Frankfater C, Bozeman SL, Hsu FF, Andley UP. PLoS One; 2020 Jun 04; 15(8):e0238081. PubMed ID: 32833997 [Abstract] [Full Text] [Related]
14. sHSP in the eye lens: crystallin mutations, cataract and proteostasis. Clark AR, Lubsen NH, Slingsby C. Int J Biochem Cell Biol; 2012 Oct 04; 44(10):1687-97. PubMed ID: 22405853 [Abstract] [Full Text] [Related]
15. Cell death triggered by a novel mutation in the alphaA-crystallin gene underlies autosomal dominant cataract linked to chromosome 21q. Mackay DS, Andley UP, Shiels A. Eur J Hum Genet; 2003 Oct 04; 11(10):784-93. PubMed ID: 14512969 [Abstract] [Full Text] [Related]
16. Loss of αBa-crystallin, but not αA-crystallin, increases age-related cataract in the zebrafish lens. Posner M, Garver T, Kaye T, Brdicka S, Suttle M, Patterson B, Farnsworth DR. Exp Eye Res; 2024 Jul 04; 244():109918. PubMed ID: 38705506 [Abstract] [Full Text] [Related]
17. Nucleosomal association and altered interactome underlie the mechanism of cataract caused by the R54C mutation of αA-crystallin. Ahsan SM, Bakthisaran R, Tangirala R, Rao CM. Biochim Biophys Acta Gen Subj; 2021 May 04; 1865(5):129846. PubMed ID: 33444727 [Abstract] [Full Text] [Related]
18. A novel mutation in the CRYAA gene associated with congenital cataract and microphthalmia in a Chinese family. Song Z, Si N, Xiao W. BMC Med Genet; 2018 Oct 19; 19(1):190. PubMed ID: 30340470 [Abstract] [Full Text] [Related]
19. Altered chaperone-like activity of alpha-crystallins promotes cataractogenesis. Cheng C, Xia CH, Huang Q, Ding L, Horwitz J, Gong X. J Biol Chem; 2010 Dec 24; 285(52):41187-93. PubMed ID: 20959464 [Abstract] [Full Text] [Related]