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
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