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The emerging concept of functional amyloid

Journal of internal medicine, 2009-03, Vol.265 (3), p.329-334

Maury, C. P. J.

2009

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Self-Propagating β-Sheet Polypeptide Structures as Prebiotic Informational Molecular Entities: The Amyloid World

Origins of life and evolution of biospheres, 2009-04, Vol.39 (2), p.141-150

Maury, C. P. J

2009

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Isolation and characterization of cardiac amyloid in familial amyloid polyneuropathy type IV (Finnish): relation of the amyloid protein to variant gelsolin

Biochimica et biophysica acta, 1990-11, Vol.1096 (1), p.84-86

Maury, C.P.J.

1990

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Treatment strategies for amyloid A amyloidosis

Expert opinion on pharmacotherapy, 2008-08, Vol.9 (12), p.2117-2128

2008

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Variant mannose‐binding lectin 2 genotype is a risk factor for reactive systemic amyloidosis in rheumatoid arthritis

Journal of internal medicine, 2007-10, Vol.262 (4), p.466-469

2007

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Self-replicating protein conformations and information transfer: The adaptive β-sheet model

Bioscience hypotheses, 2008-01, Vol.1 (2), p.82-89

Maury, C.P.J.

2008

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Anaemia of chronic disease in AA amyloidosis is associated with allele 2 of the interleukin‐1β‐511 promoter gene and raised levels of interleukin‐1β and interleukin‐18

Journal of internal medicine, 2004-08, Vol.256 (2), p.145-152

2004

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Elevated levels of circulating cachectin/tumor necrosis factor in patients with acquired immunodeficiency syndrome

The American journal of medicine, 1988-09, Vol.85 (3), p.289-291

1988

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Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187

Nature genetics, 1992-10, Vol.2 (2), p.157-160

1992

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Molecular pathogenesis of beta-amyloidosis in Alzheimer's disease and other cerebral amyloidoses

Laboratory investigation, 1995-01, Vol.72 (1), p.4

Maury, C P

1995

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Raised serum levels of cachectin/tumor necrosis factor α in renal allograft rejection

The Journal of experimental medicine, 1987-10, Vol.166 (4), p.1132-1137

1987

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Is EDRF a specific marker for TSEs?

Nature medicine, 2001-06, Vol.7 (6), p.641-641

Maury, C.P.J

2001

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Serum amyloid A protein: a sensitive indicator of renal allograft rejection in humans

Transplantation, 1983-01, Vol.36 (5), p.501

1983

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Gelsolin-related amyloidosis : identification of the amyloid protein in finnish hereditary amyloidosis as a fragment of variant gelsolin

The Journal of clinical investigation, 1991-04, Vol.87 (4), p.1195-1199

MAURY, C. P. J

1991

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Circulating Interleukin-1β in Patients with Kawasaki Disease

The New England journal of medicine, 1988-12, Vol.319 (25), p.1670-1671

1988

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Danish type gelsolin related amyloidosis: 654G-T mutation is associated with a disease pathogenetically and clinically similar to that caused by the 654G-A mutation (familial amyloidosis of the Finnish type)

Journal of clinical pathology, 2000-02, Vol.53 (2), p.95-99

2000

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Finnish hereditary amyloidosis: Amino acid sequence homology between the amyloid fibril protein and human plasma gelsoline

FEBS letters, 1990-01, Vol.260 (1), p.85-87

1990

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Circulating tumour necrosis factor‐α (cachectin) in myocardial infarction

Journal of internal medicine, 1989-05, Vol.225 (5), p.333-336

1989

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Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene

FEBS letters, 1990-12, Vol.276 (1), p.75-77

1990

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Amyloid fibril formation in gelsolin-derived amyloidosis. Definition of the amyloidogenic region and evidence of accelerated amyloid formation of mutant Asn-187 and Tyr-187 gelsolin peptides

Laboratory investigation, 1994-04, Vol.70 (4), p.558

1994

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Identification of the circulating amyloid precursor and other gelsolin metabolites in patients with G654A mutation in the gelsolin gene (Finnish familial amyloidosis): pathogenetic and diagnostic implications

Laboratory investigation, 1997-10, Vol.77 (4), p.299

1997

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Raised circulating interleukin-18 levels in reactive AA-amyloidosis

Amyloid, 2002-06, Vol.9 (2), p.141-144

2002

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Tumor necrosis factor in the serum of patients with systemic lupus erythematosus

Arthritis and rheumatism, 1989-02, Vol.32 (2), p.146-150

1989

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Radioimmunoassay of tumor necrosis factor in serum

Clinical chemistry (Baltimore, Md.), 1987-11, Vol.33 (11), p.2024

1987

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Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease

Genomics (San Diego, Calif.), 1992-07, Vol.13 (3), p.902-903

1992

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The emerging concept of functional amyloid

Self-Propagating β-Sheet Polypeptide Structures as Prebiotic Informational Molecular Entities: The Amyloid World

Isolation and characterization of cardiac amyloid in familial amyloid polyneuropathy type IV (Finnish): relation of the amyloid protein to variant gelsolin

Treatment strategies for amyloid A amyloidosis

Variant mannose‐binding lectin 2 genotype is a risk factor for reactive systemic amyloidosis in rheumatoid arthritis

Self-replicating protein conformations and information transfer: The adaptive β-sheet model

Anaemia of chronic disease in AA amyloidosis is associated with allele 2 of the interleukin‐1β‐511 promoter gene and raised levels of interleukin‐1β and interleukin‐18

Elevated levels of circulating cachectin/tumor necrosis factor in patients with acquired immunodeficiency syndrome

Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187

Molecular pathogenesis of beta-amyloidosis in Alzheimer's disease and other cerebral amyloidoses

Raised serum levels of cachectin/tumor necrosis factor α in renal allograft rejection

Is EDRF a specific marker for TSEs?

Serum amyloid A protein: a sensitive indicator of renal allograft rejection in humans

Gelsolin-related amyloidosis : identification of the amyloid protein in finnish hereditary amyloidosis as a fragment of variant gelsolin

Circulating Interleukin-1β in Patients with Kawasaki Disease

Danish type gelsolin related amyloidosis: 654G-T mutation is associated with a disease pathogenetically and clinically similar to that caused by the 654G-A mutation (familial amyloidosis of the Finnish type)

Finnish hereditary amyloidosis: Amino acid sequence homology between the amyloid fibril protein and human plasma gelsoline

Circulating tumour necrosis factor‐α (cachectin) in myocardial infarction

Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene

Amyloid fibril formation in gelsolin-derived amyloidosis. Definition of the amyloidogenic region and evidence of accelerated amyloid formation of mutant Asn-187 and Tyr-187 gelsolin peptides

Identification of the circulating amyloid precursor and other gelsolin metabolites in patients with G654A mutation in the gelsolin gene (Finnish familial amyloidosis): pathogenetic and diagnostic implications

Raised circulating interleukin-18 levels in reactive AA-amyloidosis

Tumor necrosis factor in the serum of patients with systemic lupus erythematosus

Radioimmunoassay of tumor necrosis factor in serum

Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease

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