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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

Volltextzugriff (PDF)

Is EDRF a specific marker for TSEs?

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

Maury, C.P.J

2001

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Familial amyloidosis, Finnish type: G654 → A mutation of the gelsolin gene in Finnish families and an unrelated American family

Genomics (San Diego, Calif.), 1992-07, Vol.13 (3), p.898-901

1992

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CLINICAL USEFULNESS OF SERUM AMYLOID A AND C-REACTIVE PROTEIN MEASUREMENTS IN INFLAMMATORY DISORDERS: A COMPARATIVE STUDY

Proceedings of the Third Symposium, Lyon, France, June 26-28 1985, 2019, Vol.3, p.153-156

Originally published 1986, 2019

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Finnish hereditary amyloidosis

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

1990

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Fibrillogenesis in gelsolin-related familial amyloidosis

Amyloid, 2003-08, Vol.10 (sup1), p.21-25

2003

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Mechanism of anaemia in rheumatoid arthritis: demonstration of raised interleukin 1 beta concentrations in anaemic patients and of interleukin 1 mediated suppression of normal erythropoiesis and proliferation of human erythroleukaemia (HEL) cells in vitro

Annals of the rheumatic diseases, 1988-12, Vol.47 (12), p.972-978

1988

Volltextzugriff (PDF)

Creation of amyloid fibrils from mutant Asn187 gelsolin peptides

Biochemical and biophysical research communications, 1992-02, Vol.183 (1), p.227-231

1992

Volltextzugriff (PDF)

Alzheimer's Disease-Associated Presenilins 1 and 2: Accelerated Amyloid Fibril Formation of Mutant 410 Cys→Tyr and 141 Asn→Ile Peptides

Biochemical and biophysical research communications, 1997-06, Vol.235 (1), p.249-252

1997

Volltextzugriff (PDF)

Acute-phase proteins during hemodialysis: correlations with serum interleukin-1 beta levels and different dialysis membranes

Nephron (2015), 1991, Vol.57 (3), p.283

1991

Volltextzugriff (PDF)

DEMONSTRATION OF TISSUE 90 kD GLYCOPROTEIN AS ANTIGEN IN CIRCULATING IgG IMMUNE COMPLEXES IN DERMATITIS HERPETIFORMIS AND COELIAC DISEASE

The Lancet (British edition), 1984-10, Vol.324 (8408), p.892-894

1984

Volltextzugriff (PDF)

Carbohydrate patterns of endoscopic mucosal biopsies in cancer of the stomach and chronic gastritis

Clinica chimica acta, 1982-12, Vol.126 (2), p.155-159

Maury, C.P.J.

1982

Volltextzugriff (PDF)

Immunodetection of protein composition in cerebral amyloid extracts in Alzheimer's disease: Enrichment of retinol-binding protein

Journal of the neurological sciences, 1987-09, Vol.80 (2), p.221-228

1987

Volltextzugriff (PDF)

Enrichment of high mannose-type glycans in nervous tissue glycoproteins in neuronal ceroid-lipofuscinosis

Journal of the neurological sciences, 1986, Vol.72 (1), p.1-10

1986

Volltextzugriff (PDF)

Serum prealbumin, transferrm and immunoglobulins in fatty liver, alcoholic cirrhosis and primary biliary cirrhosis

Clinica chimica acta, 1983-04, Vol.129 (3), p.279-286

1983

Volltextzugriff (PDF)

Enzyme immunoassay of antibodies to epithelial glycoprotein: Increased level of antibodies in coeliac disease

Journal of immunological methods, 1984-11, Vol.74 (2), p.327-336

1984

Volltextzugriff (PDF)

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

Is EDRF a specific marker for TSEs?

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

Familial amyloidosis, Finnish type: G654 → A mutation of the gelsolin gene in Finnish families and an unrelated American family

CLINICAL USEFULNESS OF SERUM AMYLOID A AND C-REACTIVE PROTEIN MEASUREMENTS IN INFLAMMATORY DISORDERS: A COMPARATIVE STUDY

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

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

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

Finnish hereditary amyloidosis

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

Fibrillogenesis in gelsolin-related familial amyloidosis

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

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

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

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

Mechanism of anaemia in rheumatoid arthritis: demonstration of raised interleukin 1 beta concentrations in anaemic patients and of interleukin 1 mediated suppression of normal erythropoiesis and proliferation of human erythroleukaemia (HEL) cells in vitro

Creation of amyloid fibrils from mutant Asn187 gelsolin peptides

Alzheimer's Disease-Associated Presenilins 1 and 2: Accelerated Amyloid Fibril Formation of Mutant 410 Cys→Tyr and 141 Asn→Ile Peptides

Acute-phase proteins during hemodialysis: correlations with serum interleukin-1 beta levels and different dialysis membranes

DEMONSTRATION OF TISSUE 90 kD GLYCOPROTEIN AS ANTIGEN IN CIRCULATING IgG IMMUNE COMPLEXES IN DERMATITIS HERPETIFORMIS AND COELIAC DISEASE

Carbohydrate patterns of endoscopic mucosal biopsies in cancer of the stomach and chronic gastritis

Immunodetection of protein composition in cerebral amyloid extracts in Alzheimer's disease: Enrichment of retinol-binding protein

Enrichment of high mannose-type glycans in nervous tissue glycoproteins in neuronal ceroid-lipofuscinosis

Serum prealbumin, transferrm and immunoglobulins in fatty liver, alcoholic cirrhosis and primary biliary cirrhosis

Enzyme immunoassay of antibodies to epithelial glycoprotein: Increased level of antibodies in coeliac disease

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