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Journal of Molecular Biology|September 29, 2004
The P23T cataract mutation causes loss of solubility of folded gammaD-crystallinP Evans, K Wyatt, G J Wistow, et al.Experimental Eye Research|September 6, 2003
The stability of human acidic beta-crystallin oligomers and hetero-oligomersO A Bateman, R Sarra, S T van Genesen, et al.Journal of Molecular Biology|August 4, 2009
Crystal structures of alpha-crystallin domain dimers of alphaB-crystallin and Hsp20C Bagnéris, O A Bateman, C E Naylor, et al.Nature Structural Biology|March 1, 1996
The X-ray structures of two mutant crystallin domains shed light on the evolution of multi-domain proteinsB V Norledge, E M Mayr, R Glockshuber, et al.Human Molecular Genetics|March 16, 2004
Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataractM A Reddy, O A Bateman, C Chakarova, et al.Pageof 2