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M B Pepys

Showing results (231-240 of 241) with videos related to

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The Journal of Pathology|October 24, 2007
Disease-associated prion protein is not detectable in human systemic amyloid depositsG A Tennent, M W Head, M Bishop, et al.
Circulation|December 1, 1998
Enhanced inflammatory response to coronary angioplasty in patients with severe unstable anginaG Liuzzo, A Buffon, L M Biasucci, et al.
Kidney International|July 1, 1996
Long term effect of renal transplantation on dialysis-related amyloid deposits and symptomatologyS Y Tan, A Irish, C G Winearls, et al.
Nature|April 8, 1993
Human lysozyme gene mutations cause hereditary systemic amyloidosisM B Pepys, P N Hawkins, D R Booth, et al.
The Journal of Rheumatology|January 1, 1997
Individual relationship between progression of radiological damage and the acute phase response in early rheumatoid arthritis. Towards development of a decision support systemM A van Leeuwen, M H van Rijswijk, W J Sluiter, et al.
Nature Medicine|June 17, 1999
Serum amyloid P component controls chromatin degradation and prevents antinuclear autoimmunityM C Bickerstaff, M Botto, W L Hutchinson, et al.
Nature|February 27, 1997
Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesisD R Booth, M Sunde, V Bellotti, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|August 24, 2006
Organ transplantation in hereditary apolipoprotein AI amyloidosisJ D Gillmore, A J Stangou, H J Lachmann, et al.
The Journal of Clinical Investigation|June 15, 1996
Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI geneD R Booth, S Y Tan, S E Booth, et al.
Ciba Foundation Symposium|January 1, 1996
Molecular mechanisms of fibrillogenesis and the protective role of amyloid P component: two possible avenues for therapyM B Pepys, G A Tennent, D R Booth, et al.
Pageof 25

Showing results (231-240 of 241) with videos related to

Sort By:
Pageof 25
The Journal of Pathology|October 24, 2007
Disease-associated prion protein is not detectable in human systemic amyloid depositsG A Tennent, M W Head, M Bishop, et al.
Circulation|December 1, 1998
Enhanced inflammatory response to coronary angioplasty in patients with severe unstable anginaG Liuzzo, A Buffon, L M Biasucci, et al.
Kidney International|July 1, 1996
Long term effect of renal transplantation on dialysis-related amyloid deposits and symptomatologyS Y Tan, A Irish, C G Winearls, et al.
Nature|April 8, 1993
Human lysozyme gene mutations cause hereditary systemic amyloidosisM B Pepys, P N Hawkins, D R Booth, et al.
The Journal of Rheumatology|January 1, 1997
Individual relationship between progression of radiological damage and the acute phase response in early rheumatoid arthritis. Towards development of a decision support systemM A van Leeuwen, M H van Rijswijk, W J Sluiter, et al.
Nature Medicine|June 17, 1999
Serum amyloid P component controls chromatin degradation and prevents antinuclear autoimmunityM C Bickerstaff, M Botto, W L Hutchinson, et al.
Nature|February 27, 1997
Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesisD R Booth, M Sunde, V Bellotti, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|August 24, 2006
Organ transplantation in hereditary apolipoprotein AI amyloidosisJ D Gillmore, A J Stangou, H J Lachmann, et al.
The Journal of Clinical Investigation|June 15, 1996
Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI geneD R Booth, S Y Tan, S E Booth, et al.
Ciba Foundation Symposium|January 1, 1996
Molecular mechanisms of fibrillogenesis and the protective role of amyloid P component: two possible avenues for therapyM B Pepys, G A Tennent, D R Booth, et al.
Pageof 25