Abnormalities of crystallins in the lens of the CatFraser mouse
Author:
Publisher
Elsevier BV
Subject
Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology
Reference17 articles.
1. Multiple changes in lens protein composition associated with the CatFraser gene in the mouse;Day;Genet. Res.,1972
2. ‘Shrivelled’: a hereditary degeneration of the lens in the house mouse;Fraser;Genet. Res.,1962
3. A possible cataractogenic factor in the Nakano mouse lens;Fukui;Exp. Eye Res.,1978
4. Comparative two-dimensional electrophoretic analysis of water soluble proteins from bovine and murine lens;Garber;Exp. Eye Res.,1982
5. Morphology of hereditary mouse cataract;Hamai;Exp. Eye Res.,1974
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1. Absence of α3 (Cx46) and α8 (Cx50) connexins leads to cataracts by affecting lens inner fiber cells;Experimental Eye Research;2006-09
2. Identification of mouse crystallins in 2D protein patterns by sequencing and mass spectrometry. Application to cataract mutants;FEBS Letters;1998-09-18
3. Calpain II induced insolubilization of lens β-crystallin polypeptides may induce cataract;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;1992-07
4. Progressive modifications of mouse lens crystallins in cataracts induced by buthionine sulfoximine;Experimental Eye Research;1992-04
5. Analysis of lens protein synthesis in a cataractous mutant mouse: The Cat Fraser;Experimental Eye Research;1990-11
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