Abnormal lecithin:cholesterol acyltransferase activation by a human apolipoprotein A-I variant in which a single lysine residue is deleted.

THE DISTRIBUTION AND CHEMICAL COMPOSITION OF ULTRACENTRIFUGALLY SEPARATED LIPOPROTEINS IN HUMAN SERUM

1955 • 8,846 citations

Use of Helical Wheels to Represent the Structures of Proteins and to Identify Segments with Helical Potential

1967 • 1,178 citations

DNA Repair in Bacteria and Mammalian Cells

1979 • 854 citations

Human E apoprotein heterogeneity. Cysteine-arginine interchanges in the amino acid sequence of the apo-E isoforms.

1981 • 760 citations

A protein cofactor of lecithin:Cholesterol acyltransferase

1972 • 722 citations

The Metabolic Role of Lecithin: Cholesterol Acyltransferase: Perspectives from Pathology

1973 • 480 citations

A-IMilano apoprotein. Decreased high density lipoprotein cholesterol levels with significant lipoprotein modifications and without clinical atherosclerosis in an Italian family.

1980 • 467 citations

Studies of the Proteins in Human Plasma Very Low Density Lipoproteins

1969 • 467 citations

Polymorphism of apolipoprotein E

1979 • 405 citations

The amino acid sequence of human Apoa-I, an apolipoprotein isolated from high density lipoproteins

1978 • 360 citations

Familial hyperlipoproteinemia type III: Deficiency of a specific apolipoprotein (APO E‐III) in the very‐low‐density lipoproteins

1975 • 342 citations

Isoelectric focusing in layers of granulated gels

1973 • 280 citations

Tangier Disease

1961 • 264 citations

Isolation and characterization of the human apolipoprotein A-I gene.

1983 • 243 citations

A-Imilano apoprotein. Isolation and characterization of a cysteine-containing variant of the A-I apoprotein from human high density lipoproteins.

1980 • 217 citations

Human plasma lecithin-cholesterol acyltransferase. Characterization of cofactor-dependent phospholipase activity.

1978 • 180 citations

Proteolytic processing of human preproapolipoprotein A-I. A proposed defect in the conversion of pro A-I to A-I in Tangier's disease.

1983 • 167 citations

Apolipoprotein A-IMilano. Detection of normal A-I in affected subjects and evidence for a cysteine for arginine substitution in the variant A-I.

1983 • 161 citations

Isolation and characterization of cDNA clones for human apolipoprotein A-I.

1982 • 155 citations

Gene structure of human apolipoprotein Al

1983 • 133 citations

Isoproteins of human apolipoprotein A-I demonstrated in plasma and intestinal organ culture.

1980 • 130 citations

Genetic variants of group A apolipoproteins. Rapid methods for screening and characterization without ultracentrifugation.

1982 • 119 citations

The primary structure of human plasma high density apolipoprotein glutamine I (ApoA-I). II. The amino acid sequence and alignment of cyanogen bromide fragments IV, III, and I.

1975 • 118 citations

One-step screening method for the polymorphism of apolipoproteins A-I, A-II, and A-IV

1982 • 111 citations

Abnormal apoprotein A-I isoprotein composition in patients with Tangier disease.

1982 • 93 citations

Nucleotide sequence of cloned cDNA of human apolipoprotein A-l

1983 • 88 citations

PHOSPHOLIPID BINDING STUDIES WITH SYNTHETIC APOLIPOPROTEIN FRAGMENTS *

1980 • 80 citations

Chain length-function correlation of amphiphilic peptides. Synthesis and surface properties of a tetratetracontapeptide segment of apolipoprotein A-I.

1980 • 76 citations

Tangier Disease

1982 • 74 citations

Human apolipoprotein A-I polymorphism. Identification of amino acid substitutions in three electrophoretic variants of the Münster-3 type.

1984 • 67 citations

Studies on the polymorphism of human apolipoprotein A-I

1980 • 65 citations

Causes of more frequent deletions than insertions in mutations and protein evolution

1981 • 60 citations

Tangier disease: a structural defect in apolipoprotein A-I (apoA-I Tangier).

1982 • 45 citations

Relation between the HDL apoproteins and AI isoproteins in subjects with the AIMilano abnormality

1981 • 38 citations

Apolipoprotein AIMarburg: Studies on two kindreds with a mutant of human apolipoprotein AI

1982 • 33 citations

Tangier disease: defective recombination of a specific Tangier apolipoprotein A-I isoform (pro-apo A-i) with high density lipoproteins.

1983 • 30 citations