GA Tennent

Human lysozyme gene mutations cause hereditary systemic amyloidosis

Mark B. Pepys, Philip N. Hawkins, David R. Booth et al. · Nature · 1993 · 655 citations

Alzheimer's Disease, Mendelian Disorder, Genetic Disorder +6

Serum amyloid P component prevents proteolysis of the amyloid fibrils of Alzheimer disease and systemic amyloidosis.

GA Tennent, Laurence Lovat, M B Pepys · Proceedings of the National Academy of Sciences · 1995 · 435 citations · Full text

Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene.

David R. Booth, Shouyong Tan, S E Booth et al. · Journal of Clinical Investigation · 1996 · 106 citations · Full text

Genetics, Molecular Biology, Pathology +16

THE ACUTE-PHASE RESPONSE IN (NZB X NZW)F1 AND MRL/1 MICE - CONTRASTING PATTERNS RESEMBLING THOSE IN HUMAN SYSTEMIC LUPUS-ERYTHEMATOSUS AND RHEUMATOID-ARTHRITIS, RESPECTIVELY

Christiane Rordorf, H P Schnebli, M L Baltz et al. · UCL Discovery (University College London) · 1982 · 11 citations

Inflammation, Rheumatology, Rheumatoid Disorder +10

Transthyretin Ile73Val is associated with familial amyloidotic polyneuropathy in a Bangladeshi family

D. Booth, JD Gillmore, MR Persey et al. · Human Mutation · 1998 · 10 citations