Regional mapping of human chromosome 19: organization of genes for plasma lipid transport (APOC1, -C2, and -E and LDLR) and the genes C3, PEPD, and GPI.

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1975 • 33,059 citations

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1983 • 26,063 citations

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

1977 • 12,015 citations

Selection of Hybrids from Matings of Fibroblasts in vitro and Their Presumed Recombinants

1964 • 2,108 citations

Plasma lipoproteins: apolipoprotein structure and function.

1984 • 1,130 citations

The isolation and characterization of linked δ- and β-globin genes from a cloned library of human DNA

1978 • 1,055 citations

Improved techniques for the induction of mammalian cell hybridization by polyethylene glycol

1976 • 542 citations

GENETICS OF HUMAN CELL LINES, IV. DNA-MEDIATED HERITABLE TRANSFORMATION OF A BIOCHEMICAL TRAIT

1962 • 493 citations

Human complement component C3: cDNA coding sequence and derived primary structure.

1985 • 410 citations

Domain map of the LDL receptor: Sequence homology with the epidermal growth factor precursor

1984 • 377 citations

Human Red Cell Peptidases

1967 • 294 citations

Inherited variations in human phosphohexose isomerase

1968 • 240 citations

Apolipoprotein E synthesis in human kidney, adrenal gland, and liver.

1983 • 224 citations

A New Method for Purifying Lambda DNA From Phage Lysates

1985 • 178 citations

Linkage of human apolipoproteins A-I and C-III genes

1983 • 174 citations

cDNA cloning of the bovine low density lipoprotein receptor: feedback regulation of a receptor mRNA.

1983 • 168 citations

The locus for apolipoprotein E (apoE) is linked to the complement component C3 (C3) locus on chromosome 19 in man

1982 • 161 citations

Assignment of the human gene for the low density lipoprotein receptor to chromosome 19: synteny of a receptor, a ligand, and a genetic disease.

1984 • 138 citations

Human apolipoprotein A-I--C-III gene complex is located on chromosome 11.

1984 • 109 citations

Isolation and sequence of a human apolipoprotein CII cDNA clone and its use to isolate and map to human chromosome 19 the gene for apolipoprotein CII.

1984 • 103 citations

Identification and DNA sequence of a human apolipoprotein E cDNA clone.

1982 • 101 citations

Comparative analysis of repeated sequences in rat apolipoproteins A-I, A-IV, and E.

1985 • 95 citations

Type III hyperlipoproteinemia: recent insights into the genetic defect of familial dysbetalipoproteinemia.

1984 • 93 citations

Cloning and regulation of messenger RNA for mouse apolipoprotein E.

1984 • 84 citations

Evolution of lipoproteins deduced from protein sequence data

1977 • 83 citations

Localisation of genetic markers and orientation of the linkage group on chromosome 19

1984 • 68 citations

Characterisation of mRNAs encoding the precursor for human apolipoprotein CI

1984 • 58 citations

The gene for apolipoprotein C-II is closely linked to the gene for apolipo-protein E on chromosome 19.

1984 • 57 citations

Human apolipoprotein A-I and C-III genes reside in the p11 → q13 region of chromosome 11

1984 • 56 citations

Highly specific transcription of globin sequences in isolated reticulocyte nuclei

1977 • 56 citations

Chromosomal localization of the human apoprotein ci gene and of a polymorphic apoprotein AII gene

1984 • 55 citations

The isolation of a genomic clone containing the apolipoprotein CII gene and the detection of linkage disequilibrium between two common DNA polymorphisms around the gene

1984 • 53 citations

Ouabain as a selective agent in the isolation of somatic cell hybrids

1975 • 53 citations

Linkage studies in a large kindred with familial hypercholesterolemia.

1974 • 49 citations

Human apolipoprotein B: identification of cDNA clones and characterization of mRNA

1985 • 48 citations

Familial apolipoprotein CII deficiency: A preliminary analysis of the gene defect in two independent families

1984 • 47 citations

Linkage between familial hypercholesterolemia with xanthomatosis and the C3 polymorphism confirmed

1978 • 43 citations

The locus for apolipoprotein CII is closely linked to the apolipoprotein E locus on chromosome 19 in man

1984 • 41 citations

The human apolipoprotein A-II gene is located on chromosome 1

1984 • 39 citations

Assignment of the human gene for galactose-1-phosphate uridyltransferase to chromosome 9: studies with Chinese hamster-human somatic cell hybrids.

1977 • 38 citations

The beta chorionic gonadotropin-beta luteinizing gene cluster maps to human chromosome 19

1984 • 36 citations

The two apolipoprotein loci apoA-I and apoA-IV are closely linked in man

1984 • 36 citations

Genetic linkage between the loci for myotonic dystrophy and peptidase D

1983 • 35 citations

Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19

1985 • 30 citations

Report of the committee on the genetic constitution of chromosomes 18, 19, 20, 21, and 22

1984 • 29 citations

Further regional localization of the genes for human acid alpha glucosidase (GAA), peptidase D (PEPD), and alpha mannosidase B (MANB) by somatic cell hybridization

1985 • 27 citations

The localization of the gene for apolipoprotein C-II to chromosome 19

1984 • 26 citations

The use of polymorphic DNA and protein markers for the third complement component for determining linkage of familial hypercholesterolaemia

1984 • 20 citations

The locus for apolipoprotein E (apoE) is close to the Lutheran (Lu) blood group locus on chromosome 19

1984 • 19 citations

Gene for apolipoprotein CII is on human chromosome 19

1984 • 16 citations