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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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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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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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Treatment strategies for amyloid A amyloidosis

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

2008

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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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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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Radioimmunoassay of tumor necrosis factor in serum

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

1987

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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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Molecular mechanism based on self-replicating protein conformation for the inheritance of acquired information in humans

Medical hypotheses, 2006, Vol.67 (5), p.1164-1169

Maury, C.P.J.

2006

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Comparative study of serum amyloid A protein and C-reactive protein in disease

Clinical science (1979), 1985-02, Vol.68 (2), p.233

Maury, C P

1985

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Correlation of serum cytokine levels with haematological abnormalities in human immunodeficiency virus infection

Journal of internal medicine, 1990-04, Vol.227 (4), p.253-257

1990

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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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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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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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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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Self-Propagating [beta]-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

2009

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Tumor necrosis factor α, its soluble receptor I, and –308 gene promoter polymorphism in patients with rheumatoid arthritis with or without amyloidosis: Implications for the pathogenesis of nephropathy and anemia of chronic disease in reactive amyloidosis

Arthritis and rheumatism, 2003-11, Vol.48 (11), p.3068-3076

2003

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Detection of circulating tumour necrosis factor in systemic histiocytosis

British journal of haematology, 1989-02, Vol.71 (2), p.293-295

1989

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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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Lipoproteins and Acute Phase Response during Acute Infection. Interrelationships between C-reactive Protein and Serum Amyloid-A Protein and Lipoproteins

Annals of medicine (Helsinki), 1990, Vol.22 (6), p.397-401

1990

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Tumour Necrosis Factor—an Overview

Acta Medica Scandinavica, 1986-01, Vol.220 (5), p.387-394

MAURY, C. P. J.

1986

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Variant plasma gelsolin responsible for familial amyloidosis (Finnish type) has defective actin severing activity

FEBS letters, 1993-11, Vol.335 (1), p.119-123

1993

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Demonstration of a Circulating 65K Gelsolin Variant Specific for Familial Amyloidosis, Finnish Type

Biochemical and biophysical research communications, 1993-02, Vol.191 (1), p.41-44

1993

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The emerging concept of functional amyloid

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

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

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

Treatment strategies for amyloid A amyloidosis

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)

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

Radioimmunoassay of tumor necrosis factor in serum

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

Molecular mechanism based on self-replicating protein conformation for the inheritance of acquired information in humans

Comparative study of serum amyloid A protein and C-reactive protein in disease

Correlation of serum cytokine levels with haematological abnormalities in human immunodeficiency virus infection

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

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

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

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

Self-Propagating [beta]-Sheet Polypeptide Structures as Prebiotic Informational Molecular Entities: The Amyloid World

Tumor necrosis factor α, its soluble receptor I, and –308 gene promoter polymorphism in patients with rheumatoid arthritis with or without amyloidosis: Implications for the pathogenesis of nephropathy and anemia of chronic disease in reactive amyloidosis

Detection of circulating tumour necrosis factor in systemic histiocytosis

Raised circulating interleukin-18 levels in reactive AA-amyloidosis

Lipoproteins and Acute Phase Response during Acute Infection. Interrelationships between C-reactive Protein and Serum Amyloid-A Protein and Lipoproteins

Tumour Necrosis Factor—an Overview

Variant plasma gelsolin responsible for familial amyloidosis (Finnish type) has defective actin severing activity

Demonstration of a Circulating 65K Gelsolin Variant Specific for Familial Amyloidosis, Finnish Type

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