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206 related items for PubMed ID: 22140512
1. Congenital cataract causing mutants of αA-crystallin/sHSP form aggregates and aggresomes degraded through ubiquitin-proteasome pathway. Raju I, Abraham EC. PLoS One; 2011; 6(11):e28085. PubMed ID: 22140512 [Abstract] [Full Text] [Related]
2. Quaternary structural parameters of the congenital cataract causing mutants of αA-crystallin. Kore R, Hedges RA, Oonthonpan L, Santhoshkumar P, Sharma KK, Abraham EC. Mol Cell Biochem; 2012 Mar; 362(1-2):93-102. PubMed ID: 22045060 [Abstract] [Full Text] [Related]
3. Mutations in human αA-crystallin/sHSP affect subunit exchange interaction with αB-crystallin. Raju I, Oonthonpan L, Abraham EC. PLoS One; 2012 Mar; 7(2):e31421. PubMed ID: 22347476 [Abstract] [Full Text] [Related]
4. Comparison of effect of gamma ray irradiation on wild-type and N-terminal mutants of αA-crystallin. Ramkumar S, Fujii N, Fujii N, Thankappan B, Sakaue H, Ingu K, Natarajaseenivasan K, Anbarasu K. Mol Vis; 2014 Mar; 20():1002-16. PubMed ID: 25018622 [Abstract] [Full Text] [Related]
5. Trimethylamine N-oxide alleviates the severe aggregation and ER stress caused by G98R alphaA-crystallin. Gong B, Zhang LY, Pang CP, Lam DS, Yam GH. Mol Vis; 2009 Dec 19; 15():2829-40. PubMed ID: 20029648 [Abstract] [Full Text] [Related]
6. Multiple aggregates and aggresomes of C-terminal truncated human αA-crystallins in mammalian cells and protection by αB-crystallin. Raju I, Kumarasamy A, Abraham EC. PLoS One; 2011 May 12; 6(5):e19876. PubMed ID: 21589881 [Abstract] [Full Text] [Related]
7. Real-time heterogeneous protein-protein interaction between αA-crystallin N-terminal mutants and αB-crystallin using quartz crystal microbalance (QCM). Ramkumar S, Fujii N, Sakaue H, Fujii N, Thankappan B, kumari RP, Natarajaseenivasan K, Anbarasu K. Amino Acids; 2015 May 12; 47(5):1035-43. PubMed ID: 25694240 [Abstract] [Full Text] [Related]
8. Cataract mutation P20S of alphaB-crystallin impairs chaperone activity of alphaA-crystallin and induces apoptosis of human lens epithelial cells. Li H, Li C, Lu Q, Su T, Ke T, Li DW, Yuan M, Liu J, Ren X, Zhang Z, Zeng S, Wang QK, Liu M. Biochim Biophys Acta; 2008 May 12; 1782(5):303-9. PubMed ID: 18343237 [Abstract] [Full Text] [Related]
13. Oligomerization with wt αA- and αB-crystallins reduces proteasome-mediated degradation of C-terminally truncated αA-crystallin. Wu M, Zhang X, Bian Q, Taylor A, Liang JJ, Ding L, Horwitz J, Shang F. Invest Ophthalmol Vis Sci; 2012 May 04; 53(6):2541-50. PubMed ID: 22427585 [Abstract] [Full Text] [Related]
15. Deamidation affects structural and functional properties of human alphaA-crystallin and its oligomerization with alphaB-crystallin. Gupta R, Srivastava OP. J Biol Chem; 2004 Oct 22; 279(43):44258-69. PubMed ID: 15284238 [Abstract] [Full Text] [Related]
16. Protein-protein interactions involving congenital cataract T5P gammaC-crystallin mutant: a confocal fluorescence microscopy study. Liu BF, Song S, Hanson M, Liang JJ. Exp Eye Res; 2008 Dec 22; 87(6):515-20. PubMed ID: 18926820 [Abstract] [Full Text] [Related]
17. The R116C mutation in alpha A-crystallin diminishes its protective ability against stress-induced lens epithelial cell apoptosis. Andley UP, Patel HC, Xi JH. J Biol Chem; 2002 Mar 22; 277(12):10178-86. PubMed ID: 11756414 [Abstract] [Full Text] [Related]
18. A Comparative Study of the Impact of Calcium Ion on Structure, Aggregation and Chaperone Function of Human αA-crystallin and its Cataract- Causing R12C Mutant. Saba S, Ghahramani M, Yousefi R. Protein Pept Lett; 2017 Mar 22; 24(11):1048-1058. PubMed ID: 28782478 [Abstract] [Full Text] [Related]
19. The cataract-causing mutation G98R in human alphaA-crystallin leads to folding defects and loss of chaperone activity. Singh D, Raman B, Ramakrishna T, Rao ChM. Mol Vis; 2006 Nov 15; 12():1372-9. PubMed ID: 17149363 [Abstract] [Full Text] [Related]
20. Structural and functional properties of NH(2)-terminal domain, core domain, and COOH-terminal extension of αA- and αB-crystallins. Asomugha CO, Gupta R, Srivastava OP. Mol Vis; 2011 Nov 15; 17():2356-67. PubMed ID: 21921988 [Abstract] [Full Text] [Related] Page: [Next] [New Search]