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Page 1
Human lysozyme gene mutations cause hereditary systemic amyloidosis.
Pepys MB, Hawkins PN, Booth DR, Vigushin DM, Tennent GA, Soutar AK, Totty N, Nguyen O, Blake CC, Terry CJ, et al. Pepys MB, et al. Among authors: blake cc. Nature. 1993 Apr 8;362(6420):553-7. doi: 10.1038/362553a0. Nature. 1993. PMID: 8464497
Molecular mechanisms of fibrillogenesis and the protective role of amyloid P component: two possible avenues for therapy.
Pepys MB, Tennent GA, Booth DR, Bellotti V, Lovat LB, Tan SY, Persey MR, Hutchinson WL, Booth SE, Madhoo S, Soutar AK, Hawkins PN, Van Zyl-Smit R, Campistol JM, Fraser PE, Radford SE, Robinson CV, Sunde M, Serpell LC, Blake CC. Pepys MB, et al. Among authors: blake cc. Ciba Found Symp. 1996;199:73-81; discussion 81-9. doi: 10.1002/9780470514924.ch6. Ciba Found Symp. 1996. PMID: 8915605
A molecular model of the amyloid fibril.
Blake CC, Serpell LC, Sunde M, Sandgren O, Lundgren E. Blake CC, et al. Ciba Found Symp. 1996;199:6-15; discussion 15-21, 40-6. doi: 10.1002/9780470514924.ch2. Ciba Found Symp. 1996. PMID: 8915601
The molecular basis of amyloidosis.
Serpell LC, Sunde M, Blake CC. Serpell LC, et al. Among authors: blake cc. Cell Mol Life Sci. 1997 Dec;53(11-12):871-87. doi: 10.1007/s000180050107. Cell Mol Life Sci. 1997. PMID: 9447239 Free PMC article. Review.
84 results