M. Walport

发表

Macrophage phagocytosis of aging neutrophils in inflammation. Programmed cell death in the neutrophil leads to its recognition by macrophages.

M. Walport, C. Haslett, A. Wyllie, 1989, The Journal of clinical investigation.

Antibody‐mediated glomerulonephritis in mice: the role of endotoxin, complement and genetic background

M. Robson, H. Cook, C. Pusey, 2003, Clinical and experimental immunology.

Genomic organization of human complement component C3.

M. Botto, M. Walport, A. So, 1990, Genomics.

Hypereosinophilic syndromes: association with vasculitis, fibrosis and autoimmunity

M. Walport, F. Hall, 1993, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

A rare mediastinal tumour presenting with systemic effects due to IL‐6 and tumour necrosis factor (TNF) production

A. Cope, T. Krausz, J. Schofield, 1995, Clinical and experimental immunology.

Inhibitory effect of non-steroidal anti-inflammatory drugs on mucosal cell proliferation associated with gastric ulcer healing

N. Wright, R. Goodlad, M. Walport, 1990, The Lancet.

Molecular basis of hereditary C3 deficiency.

M. Botto, M. Walport, A. So, 1990, The Journal of clinical investigation.

Insulin deficient diabetes

A. Kurtz, J. Nabarro, M. Walport, 2004, Diabetologia.

Immune complex processing in C1q‐deficient mice

P. Taylor, M. Botto, M. Walport, 2001, Clinical and experimental immunology.

Erythroid HLA Class I Expression in 300 Patients with Haematological, Renal and Rheumatological Disorders

M. Ritter, C. Pusey, M. Walport, 1990, Vox sanguinis.

Complement Deficiency and Autoimmunity a

M. Botto, M. Walport, B. J. Morley, 1997, Annals of the New York Academy of Sciences.

A 19‐year‐old man with leucocyte adhesion deficiency. In vitro and in vivo studies of leucocyte function

C. Haslett, N. Hotchin, A. Peters, 1991, Clinical and experimental immunology.

Murine glomerular mesangial cell uptake of apoptotic cells is inefficient and involves serum‐mediated but complement‐independent mechanisms

P. Potter, L. Fossati-Jimack, H. Cook, 2002, Clinical and experimental immunology.

Serum sickness and acute renal failure after streptokinase therapy for myocardial infarction

C. Winearls, A. Rees, K. Davies, 1990, Clinical and experimental immunology.

Effects of nonsteroidal anti-inflammatory drugs and misoprostol on gastroduodenal epithelial proliferation in arthritis.

N. Wright, R. Goodlad, M. Walport, 1992, Gastroenterology.

Diabetes and rhabdomyolysis. A rare complication of a common disease.

Graham M Lord, C. Bulpitt, S. Bloom, 1993, BMJ.

Autoantibodies to the collagenous region of C1q occur in three strains of lupus‐prone mice

M. Walport, B. J. Morley, P. Trinder, 1996, Clinical and experimental immunology.

Homozygous hereditary C3 deficiency due to a partial gene deletion.

M. Botto, M. Walport, B. J. Morley, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Serum amyloid P component controls chromatin degradation and prevents antinuclear autoimmunity

P. Butler, M. Pepys, G. Tennent, 1999, Nature Medicine.

Heterogeneity of binding reactivity to different phospholipids of antibodies from patients with systemic lupus erythematosus (SLE) and with syphilis

M. Walport, C. Mackworth-Young, S. Loizou, 1990, Clinical and experimental immunology.

Proteinuria and thrombolytic agents

K. Davies, M. Callan, M. Walport, 1990, The Lancet.

Immunoglobulin class and IgG subclass distribution of anticardiolipin antibodies in patients with systemic lupus erythematosus and associated disorders

A. Weetman, M. Walport, S. Loizou, 1992, Clinical and experimental immunology.

The Clinical and Immunogenetic Features of Patients with Autoantibodies to the Nucleolar Antigen PM-Scl

M. Walport, R. Bernstein, C. Black, 1992, Medicine.

Factor V Leiden mutation and venous thrombosis

K. Davies, H. Ireland, M. Walport, 1995, The Lancet.

FcγRIIa polymorphism in systemic lupus erythematosus (SLE): no association with disease

D. Isenberg, M. Walport, H. Beynon, 1996 .

Proton magnetic resonance spectroscopy of systemic lupus erythematosus involving the central nervous system

G. Barker, M. Ron, C. Davie, 1995, Journal of Neurology.

The molecular basis of hereditary complement factor I deficiency.

M. Walport, T. Vyse, J. Clin, 1996, The Journal of clinical investigation.

Primary antiphospholipid syndrome: features of patients with raised anticardiolipin antibodies and no other disorder.

M. Walport, M. Walport, C. Mackworth-Young, 1989, Annals of the rheumatic diseases.

Effects of C4 null alleles and homoduplications on quantitative expression of C4A and C4B

A. Hammond, M. Walport, W. Ollier, 1992, Clinical and experimental immunology.

Lupus erythematosus profundus with partial C4 deficiency responding to thalidomide

M. Walport, N. Burrows, A. Hammond, 1991, The British journal of dermatology.

Immune complex processing in patients with systemic lupus erythematosus. In vivo imaging and clearance studies.

M. Walport, H. Beynon, A. Peters, 1992, The Journal of clinical investigation.