Modifications of transthyretin in amyloid fibrils: analysis of amyloid from homozygous and heterozygous individuals with the Met30 mutation.

Antibodies, a laboratory manual

1989 • 12,929 citations

Sequence from picomole quantities of proteins electroblotted onto polyvinylidene difluoride membranes.

1987 • 5,066 citations

Amyloid deposition as the central event in the aetiology of Alzheimer's disease

1991 • 2,375 citations

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

1991 • 871 citations

Structure of prealbumin: Secondary, tertiary and quaternary interactions determined by Fourier refinement at 1.8 Å

1978 • 784 citations

Fibril in senile systemic amyloidosis is derived from normal transthyretin.

1990 • 683 citations

Frequency and distribution of senile cardiovascular amyloid

1983 • 452 citations

Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin).

1984 • 427 citations

Amyloid fibril protein related to prealbumin in familial amyloidotic polyneuropathy.

1978 • 426 citations

The Amino Acid Sequence of Human Plasma Prealbumin

1974 • 368 citations

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

1983 • 367 citations

Physical change in cytoplasmic messenger ribonucleoproteins in cells treated with inhibitors of mRNA transcription.

1984 • 334 citations

Senile Systemic Amyloidosis

1986 • 229 citations

Evidence that the amyloid fibril protein in senile systemic amyloidosis is derived from normal prealbumin

1988 • 166 citations

Mutation in gelsolin gene in Finnish hereditary amyloidosis.

1990 • 161 citations

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

1986 • 160 citations

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

1986 • 133 citations

Primary structure of an amyloid prealbumin variant in familial polyneuropathy of Jewish origin.

1983 • 118 citations

Localization of the human prealbumin gene to chromosome 18

1985 • 115 citations

Physical Change in Cytoplasmic Messenger Ribonucleoproteins in Cells Treated with Inhibitors of mRNA Transcription

1984 • 110 citations

Intermediates in the refolding of reduced pancreatic trypsin inhibitor

1974 • 97 citations

Homozygosity for the transthyretin‐met³⁰‐gene in two Swedish sibs with familial amyloidotic polyneuropathy

1988 • 80 citations

Vitreous involvement in familial amyloidotic neuropathy: a genealogical and genetic study

1991 • 41 citations

Prealbumin in Swedish Patients with Senile Systemic Amyloidosis and Familial Amyloidotic Polyneuropathy

1985 • 41 citations

Homozygosity for the met30 transthyretin gene in a Turkish kindred with familial amyloidotic polyneuropathy

1990 • 40 citations

Vitreous Amyloidosis Associated With Homozygosity for the Transthyretin Methionine-30 Gene

1990 • 38 citations

Methods in Protein Sequence Analysis · 1986

1987 • 37 citations

Different types of microheterogeneity of human thyroxine-binding prealbumin

1987 • 35 citations

The transmissible amyloidoses: Genetical control of spontaneous generation of infectious amyloid proteins by nucleation of configurational change in host precursors: Kuru-CJD-GSS-Scrapie-BSE

1991 • 30 citations

Linkage of G8 (D4S10) in two Swedish families with Huntington's disease

1987 • 12 citations