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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

Data up to Jan 2025

Published1990
Citations62
References19

Total Citations Per Year

Abstract

References (19)

Plasma and cytoplasmic gelsolins are encoded by a single gene and contain a duplicated actin-binding domain

1986 • 477 citations

Identification of amyloid prealbumin variant in familial amyloidotic polyneuropathy (Japanese type)

1983 • 367 citations

Variant apolipoprotein AI as a major constituent of a human hereditary amyloid

1988 • 229 citations

Structure and biosynthesis of cytoplasmic and secreted variants of gelsolin.

1984 • 215 citations

Expression of human plasma gelsolin in Escherichia coli and dissection of actin binding sites by segmental deletion mutagenesis.

1989 • 195 citations

Identification of critical functional and regulatory domains in gelsolin.

1989 • 194 citations

Genomic organization and biosynthesis of secreted and cytoplasmic forms of gelsolin

1988 • 165 citations

Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosis.

1986 • 160 citations

Gelsolin has three actin-binding sites.

1988 • 156 citations

Identification of a polyphosphoinositide-modulated domain in gelsolin which binds to the sides of actin filaments.

1988 • 148 citations

Characterization of a transthyretin (prealbumin) variant associated with familial amyloidotic polyneuropathy type II (Indiana/Swiss).

1986 • 133 citations

Finnish hereditary amyloidosis

1990 • 119 citations

Revised analysis of amino acid replacement in a prealbumin variant (SKO-III) associated with familial amyloidotic polyneuropathy of jewish origin

1984 • 100 citations

Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding protein

1990 • 94 citations

Hereditary amyloidosis

1970 • 73 citations

Identification of a new hereditary amyloidosis prealbumin variant, Tyr-77, and detection of the gene by DNA analysis.

1988 • 72 citations

Amyloid in familial amyloidosis, Finnish type, is antigenically and structurally related to gelsolin.

1990 • 71 citations

Hereditary amyloidosis: description of a new american kindred with late onset cardiomyopathy

1987 • 66 citations

Family Studies of the Genetic Abnormality in Transthyretin (Prealbumin) in Portuguese Patients with Familial Amyloidotic Poly neuropathya

1984 • 58 citations

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Isolation and characterization of cardiac amyloid in familial amyloid polyneuropathy type… (1990) – Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease | Metascience Observatory Explorer