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Extra info for Amyloidosis - Mechanisms and Prospects for Therapy
New England Journal of Medicine, Vol. 356, No. 23, (June 2007), pp. , Solomon, A. & Westermark, P. (2002). Transmissibility of systemic amyloidosis by a prion-like mechanism. Proceedings of National Academy of Sciences (USA), Vol. 99, No. 10, (May 2002), pp. , Olsén, A. & Westermark, P. (2005). Protein fibrils in nature can enhance amyloid protein A amyloidosis in mice: cross-seeding as a disease mechanism. Proceedings of National Academy of Sciences (USA), Vol. 102, No. 17, (April 2005), pp. J.
For a period, it was debated whether or not amyloid deposits were fatty or carbohydrate deposits until it was finally found that they were, in fact, deposits of proteinaceous mass. The underlying molecular abnormalities may be either acquired or hereditary and more than 20 different proteins can form clinically or pathologically significant amyloid fibrils in vivo. Current nomenclature lists of amyloid fibril protein have been provided from the nomenclature committee of the International Society of Amyloidosis.
L. (2007). Structural characterization of the partially folded intermediates of an immunoglobulin light chain leading to amyloid fibrillation and amorphous aggregation. Biochemistry 46,11: 3521-31. , Sagara, Y. and Kimura, H. (1995). Amyloid peptides are toxic via a common oxidative mechanism. Proc Natl Acad Sci U S A 92,6: 1989-93. , Brenner, D. , Ward, J. , Connors, L. , Sawyer, D. , Semigran, M. , Macgillivray, T. , Seldin, D. , Falk, R. and Liao, R. (2010). Amyloidogenic light chains induce cardiomyocyte contractile dysfunction and apoptosis via a non-canonical p38alpha MAPK pathway.