Pepys MB - Search Results

1

Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesis.

Booth DR, Sunde M, Bellotti V, Robinson CV, Hutchinson WL, Fraser PE, Hawkins PN, Dobson CM, Radford SE, Blake CC, Pepys MB. Booth DR, et al. Among authors: pepys mb. Nature. 1997 Feb 27;385(6619):787-93. doi: 10.1038/385787a0. Nature. 1997. PMID: 9039909

2

Treatment of amyloidosis.

Tan SY, Pepys MB, Hawkins PN. Tan SY, et al. Among authors: pepys mb. Am J Kidney Dis. 1995 Aug;26(2):267-85. doi: 10.1016/0272-6386(95)90647-9. Am J Kidney Dis. 1995. PMID: 7645531 Review.

3

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. Nature. 1993 Apr 8;362(6420):553-7. doi: 10.1038/362553a0. Nature. 1993. PMID: 8464497

4

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. Ciba Found Symp. 1996;199:73-81; discussion 81-9. doi: 10.1002/9780470514924.ch6. Ciba Found Symp. 1996. PMID: 8915605

5

Amyloid and the gut.

Lovat LB, Pepys MB, Hawkins PN. Lovat LB, et al. Among authors: pepys mb. Dig Dis. 1997 May-Jun;15(3):155-71. doi: 10.1159/000171596. Dig Dis. 1997. PMID: 9158925 Review.

6

Amyloid deposition is delayed in mice with targeted deletion of the serum amyloid P component gene.

Botto M, Hawkins PN, Bickerstaff MC, Herbert J, Bygrave AE, McBride A, Hutchinson WL, Tennent GA, Walport MJ, Pepys MB. Botto M, et al. Among authors: pepys mb. Nat Med. 1997 Aug;3(8):855-9. doi: 10.1038/nm0897-855. Nat Med. 1997. PMID: 9256275

7

Amyloidosis: a review of recent diagnostic and therapeutic developments.

Gillmore JD, Hawkins PN, Pepys MB. Gillmore JD, et al. Among authors: pepys mb. Br J Haematol. 1997 Nov;99(2):245-56. doi: 10.1046/j.1365-2141.1997.303194.x. Br J Haematol. 1997. PMID: 9375734 Free article. Review.

8

Hereditary renal amyloidosis associated with variant lysozyme in a large English family.

Gillmore JD, Booth DR, Madhoo S, Pepys MB, Hawkins PN. Gillmore JD, et al. Among authors: pepys mb. Nephrol Dial Transplant. 1999 Nov;14(11):2639-44. doi: 10.1093/ndt/14.11.2639. Nephrol Dial Transplant. 1999. PMID: 10534505

9

Targeted pharmacological depletion of serum amyloid P component for treatment of human amyloidosis.

Pepys MB, Herbert J, Hutchinson WL, Tennent GA, Lachmann HJ, Gallimore JR, Lovat LB, Bartfai T, Alanine A, Hertel C, Hoffmann T, Jakob-Roetne R, Norcross RD, Kemp JA, Yamamura K, Suzuki M, Taylor GW, Murray S, Thompson D, Purvis A, Kolstoe S, Wood SP, Hawkins PN. Pepys MB, et al. Nature. 2002 May 16;417(6886):254-9. doi: 10.1038/417254a. Nature. 2002. PMID: 12015594

10

Specific localization and imaging of amyloid deposits in vivo using 123I-labeled serum amyloid P component.

Hawkins PN, Myers MJ, Epenetos AA, Caspi D, Pepys MB. Hawkins PN, et al. Among authors: pepys mb. J Exp Med. 1988 Mar 1;167(3):903-13. doi: 10.1084/jem.167.3.903. J Exp Med. 1988. PMID: 3351437 Free PMC article.

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