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Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis

Nature genetics, 2004-01, Vol.36 (1), p.77-82

2004

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A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro

The Journal of clinical investigation, 1997-04, Vol.99 (7), p.1786-1797

1997

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High-level lipoprotein [a] expression in transgenic mice: evidence for oxidized phospholipids in lipoprotein [a] but not in low density lipoproteins

Journal of lipid research, 2005-04, Vol.46 (4), p.769-778

2005

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Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics

The American journal of cardiology, 1993-07, Vol.72 (2), p.171-176

1993

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Hypervariability in a minisatellite 3' of the apolipoprotein B gene in patients with coronary heart disease compared with normal controls

Journal of lipid research, 1990-04, Vol.31 (4), p.659-665

1990

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DGAT1 promoter polymorphism associated with alterations in body mass index, high density lipoprotein levels and blood pressure in Turkish women

Clinical genetics, 2002-07, Vol.62 (1), p.68-73

2002

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Association between a Specific Apolipoprotein B Mutation and Familial Defective Apolipoprotein B-100

Proceedings of the National Academy of Sciences - PNAS, 1989-01, Vol.86 (2), p.587-591

1989

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Human polymorphism of P-selectin glycoprotein ligand 1 attributable to variable numbers of tandem decameric repeats in the mucinlike region

Blood, 2001-05, Vol.97 (10), p.3306-3307

2001

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Polymorphism of human glycoprotein Ib alpha results from a variable number of tandem repeats of a 13-amino acid sequence in the mucin-like macroglycopeptide region. Structure/function implications

The Journal of biological chemistry, 1992-05, Vol.267 (14), p.10055-10061

1992

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High-resolution analysis of a hypervariable region in the human apolipoprotein B gene

American journal of human genetics, 1989-09, Vol.45 (3), p.458-464

1989

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Associations of candidate loci angiotensinogen and angiotensin-converting enzyme with severe hypertension: The NHLBI family heart study

Annals of epidemiology, 1997, Vol.7 (1), p.13-21

1997

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Haplotype analysis of the human apolipoprotein B mutation associated with familial defective apolipoprotein B100

American journal of human genetics, 1990-10, Vol.47 (4), p.712-720

1990

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Association of genetic variations in apolipoprotein B with hypercholesterolemia, coronary artery disease, and receptor binding of low density lipoproteins

Journal of lipid research, 1997-07, Vol.38 (7), p.1361-1373

1997

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Angiotensinogen and angiotensin converting enzyme genotypes and carotid atherosclerosis: The atherosclerosis risk in communities and the NHLBI family heart studies

Atherosclerosis, 1998-05, Vol.138 (1), p.111-116

1998

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Associations between candidate loci angiotensin-converting enzyme and angiotensinogen with coronary heart disease and myocardial infarction: The NHLBI family heart study

Annals of epidemiology, 1997, Vol.7 (1), p.3-12

1997

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Analysis of two different tandem repetitive elements within the human apolipoprotein B gene

Journal of lipid research, 1991-02, Vol.32 (2), p.374-379

1991

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Angiotensin-converting enzyme genotypes and risk for myocardial infarction in women

Journal of the American College of Cardiology, 1998-03, Vol.31 (4), p.790-796

1998

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Genetic Basis of Familial Dyslipidemia and Hypertension: 15-Year Results From Utah

American journal of hypertension, 1993-11, Vol.6 (11-Pt-2), p.319S-327S

1993

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A polymorphism in a region with enhancer activity in the second intron of the human apolipoprotein B gene

Journal of lipid research, 1991-01, Vol.32 (1), p.137-145

1991

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DNA sequence of the human apolipoprotein B gene

DNA (New York, N.Y.), 1987-08, Vol.6 (4), p.363-372

1987

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Comparative analysis of sequences at the 5' end of the human and mouse apolipoprotein B genes

DNA and cell biology, 1991-06, Vol.10 (5), p.329-338

1991

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Effects of 4-nitroestrone 3-methyl ether on dimethylbenz(a)anthracene-induced mammary tumors

Cancer research (Chicago, Ill.), 1983-06, Vol.43 (6), p.2611

1983

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Effect of cortisone on activation of lysosomal enzymes resulting from mengovirus infection of L-929 cells

Biochemical and biophysical research communications, 1966-01, Vol.22 (2), p.181-186

1966

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A cytocidal system in normal human serum active against Ehrlich Lettré ascites tumor cells. I. Identification of the components of the system and site of attachment

Cancer research (Chicago, Ill.), 1967-01, Vol.27 (1), p.181-184

1967

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Cellular changes attending mengovirus-induced cytolysis of mouse L-cells

Biochimica et biophysica acta, 1971-08, Vol.244 (2), p.466-477

1971

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Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis

A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro

High-level lipoprotein [a] expression in transgenic mice: evidence for oxidized phospholipids in lipoprotein [a] but not in low density lipoproteins

Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics

Hypervariability in a minisatellite 3' of the apolipoprotein B gene in patients with coronary heart disease compared with normal controls

DGAT1 promoter polymorphism associated with alterations in body mass index, high density lipoprotein levels and blood pressure in Turkish women

Association between a Specific Apolipoprotein B Mutation and Familial Defective Apolipoprotein B-100

Human polymorphism of P-selectin glycoprotein ligand 1 attributable to variable numbers of tandem decameric repeats in the mucinlike region

Polymorphism of human glycoprotein Ib alpha results from a variable number of tandem repeats of a 13-amino acid sequence in the mucin-like macroglycopeptide region. Structure/function implications

High-resolution analysis of a hypervariable region in the human apolipoprotein B gene

Associations of candidate loci angiotensinogen and angiotensin-converting enzyme with severe hypertension: The NHLBI family heart study

Haplotype analysis of the human apolipoprotein B mutation associated with familial defective apolipoprotein B100

Association of genetic variations in apolipoprotein B with hypercholesterolemia, coronary artery disease, and receptor binding of low density lipoproteins

Angiotensinogen and angiotensin converting enzyme genotypes and carotid atherosclerosis: The atherosclerosis risk in communities and the NHLBI family heart studies

Associations between candidate loci angiotensin-converting enzyme and angiotensinogen with coronary heart disease and myocardial infarction: The NHLBI family heart study

Analysis of two different tandem repetitive elements within the human apolipoprotein B gene

Angiotensin-converting enzyme genotypes and risk for myocardial infarction in women

Genetic Basis of Familial Dyslipidemia and Hypertension: 15-Year Results From Utah

A polymorphism in a region with enhancer activity in the second intron of the human apolipoprotein B gene

DNA sequence of the human apolipoprotein B gene

Comparative analysis of sequences at the 5' end of the human and mouse apolipoprotein B genes

Effects of 4-nitroestrone 3-methyl ether on dimethylbenz(a)anthracene-induced mammary tumors

Effect of cortisone on activation of lysosomal enzymes resulting from mengovirus infection of L-929 cells

A cytocidal system in normal human serum active against Ehrlich Lettré ascites tumor cells. I. Identification of the components of the system and site of attachment

Cellular changes attending mengovirus-induced cytolysis of mouse L-cells

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