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ATP-binding cassette transporter A1: regulation of cholesterol efflux

Biochemical Society transactions, 2004-02, Vol.32 (Pt 1), p.124-127

Knight, B L

2004

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The effect of peroxisome-proliferator-activated receptor-alpha on the activity of the cholesterol 7 alpha-hydroxylase gene

Biochemical journal, 2000-11, Vol.351 Pt 3 (3), p.747-753

2000

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C/T polymorphism in the 5' untranslated region of the apolipoprotein(a) gene introduces an upstream ATG and reduces in vitro translation

Arteriosclerosis, thrombosis, and vascular biology, 1995-01, Vol.15 (1), p.58-64

1995

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Variation in lipoprotein(a) concentration associated with different apolipoprotein(a) alleles

The Journal of clinical investigation, 1994-04, Vol.93 (4), p.1481-1492

1994

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Polymorphisms in the Apolipoprotein(a) Gene and Their Relationship to Allele Size and Plasma Lipoprotein(a) Concentration

Human molecular genetics, 1997-07, Vol.6 (7), p.1099-1107

1997

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Peroxisome-proliferator-activated receptor-alpha (PPARalpha) deficiency leads to dysregulation of hepatic lipid and carbohydrate metabolism by fatty acids and insulin

Biochemical journal, 2002-06, Vol.364 (Pt 2), p.361-368

2002

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Treatment with atorvastatin alters interleukin-12 and -10 gene expression

European journal of clinical investigation, 2003-01, Vol.33 (1), p.88-91

2003

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Postgraduate clinical physiotherapy education in acute hospitals: a cohort study

Physiotherapy theory and practice, 2020-01, Vol.36 (1), p.157-169

2020

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Disturbances in the normal regulation of SREBP-sensitive genes in PPAR alpha-deficient mice

Journal of lipid research, 2001-03, Vol.42 (3), p.328-337

2001

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Gene structure of apolipoprotein(a) and the regulation of its expression

Biochemical Society transactions, 1999-08, Vol.27 (4), p.447-452

Knight, B L

1999

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Methapyrilene Toxicity: Anchorage of Pathologic Observations to Gene Expression Alterations

Toxicologic pathology, 2002-07, Vol.30 (4), p.470-482

2002

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Genetic Variation at a Splicing Branch Point in Intron 9 of the Low Density Lipoprotein (LDL)-Receptor Gene: A Rare Mutation that Disrupts mRNA Splicing in a Patient with Familial Hypercholesterolaemia and a Common Polymorphism

Human molecular genetics, 1996-09, Vol.5 (9), p.1325-1331

1996

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The effect of nicotinic acid and acipimox on lipoprotein(a) concentration and turnover

Atherosclerosis, 1993-06, Vol.101 (1), p.61-68

1993

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Treatment of aggressive testicular tumors in four dogs

The Journal of the American Animal Hospital Association, 1999-07, Vol.35 (4), p.311-318

1999

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Identification of a Point Mutation in Growth Factor Repeat C of the Low Density Lipoprotein-Receptor Gene in a Patient with Homozygous Familial Hypercholesterolemia that Affects Ligand Binding and Intracellular Movement of Receptors

Proceedings of the National Academy of Sciences - PNAS, 1989-06, Vol.86 (11), p.4166-4170

1989

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Relationship between apolipoprotein(a) phenotype, lipoprotein(a) concentration in plasma, and low density lipoprotein receptor function in a large kindred with familial hypercholesterolemia due to the pro664→leu mutation in the LDL receptor gene

The Journal of clinical investigation, 1991-08, Vol.88 (2), p.483-492

1991

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Characterization of a splice-site mutation in the gene for the LDL receptor associated with an unpredictably severe clinical phenotype in English patients with heterozygous FH

Arteriosclerosis, thrombosis, and vascular biology, 1995-02, Vol.15 (2), p.219-227

1995

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Effect of the StuI polymorphism in the LDL receptor gene (Ala 370 to Thr) on lipid levels in healthy individuals

Clinical genetics, 1995-02, Vol.47 (2), p.68-74

1995

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Characterization of mutations in the low density lipoprotein (LDL)-receptor gene in patients with homozygous familial hypercholesterolemia, and frequency of these mutations in FH patients in the United Kingdom

Journal of lipid research, 1996-02, Vol.37 (2), p.368-381

1996

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Characterization of two new point mutations in the low density lipoprotein receptor genes of an English patient with homozygous familial hypercholesterolemia

Journal of lipid research, 1992-05, Vol.33 (5), p.689-698

1992

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Characterization of the Rodent Genes for Arylacetamide Deacetylase, a Putative Microsomal Lipase, and Evidence for Transcriptional Regulation

The Journal of biological chemistry, 2001-10, Vol.276 (43), p.39522-39532

2001

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Catabolism of lipoprotein(a) in familial hypercholesterolaemic subjects

Atherosclerosis, 1991, Vol.87 (2), p.227-237

1991

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Structure and regulation of the LDL- receptor and its gene

British medical bulletin, 1990-10, Vol.46 (4), p.891-916

1990

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Characterization of a novel cellular defect in patients with phenotypic homozygous familial hypercholesterolemia

The Journal of clinical investigation, 1999-09, Vol.104 (5), p.619-628

1999

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The proton hyperfine interaction in HC60, signature of a potential interstellar fullerene

Chemical physics letters, 1993-03, Vol.204 (5-6), p.481-485

1993

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ATP-binding cassette transporter A1: regulation of cholesterol efflux

The effect of peroxisome-proliferator-activated receptor-alpha on the activity of the cholesterol 7 alpha-hydroxylase gene

C/T polymorphism in the 5' untranslated region of the apolipoprotein(a) gene introduces an upstream ATG and reduces in vitro translation

Variation in lipoprotein(a) concentration associated with different apolipoprotein(a) alleles

Polymorphisms in the Apolipoprotein(a) Gene and Their Relationship to Allele Size and Plasma Lipoprotein(a) Concentration

Peroxisome-proliferator-activated receptor-alpha (PPARalpha) deficiency leads to dysregulation of hepatic lipid and carbohydrate metabolism by fatty acids and insulin

Treatment with atorvastatin alters interleukin-12 and -10 gene expression

Postgraduate clinical physiotherapy education in acute hospitals: a cohort study

Disturbances in the normal regulation of SREBP-sensitive genes in PPAR alpha-deficient mice

Gene structure of apolipoprotein(a) and the regulation of its expression

Methapyrilene Toxicity: Anchorage of Pathologic Observations to Gene Expression Alterations

Genetic Variation at a Splicing Branch Point in Intron 9 of the Low Density Lipoprotein (LDL)-Receptor Gene: A Rare Mutation that Disrupts mRNA Splicing in a Patient with Familial Hypercholesterolaemia and a Common Polymorphism

The effect of nicotinic acid and acipimox on lipoprotein(a) concentration and turnover

Treatment of aggressive testicular tumors in four dogs

Identification of a Point Mutation in Growth Factor Repeat C of the Low Density Lipoprotein-Receptor Gene in a Patient with Homozygous Familial Hypercholesterolemia that Affects Ligand Binding and Intracellular Movement of Receptors

Relationship between apolipoprotein(a) phenotype, lipoprotein(a) concentration in plasma, and low density lipoprotein receptor function in a large kindred with familial hypercholesterolemia due to the pro664→leu mutation in the LDL receptor gene

Characterization of a splice-site mutation in the gene for the LDL receptor associated with an unpredictably severe clinical phenotype in English patients with heterozygous FH

Effect of the StuI polymorphism in the LDL receptor gene (Ala 370 to Thr) on lipid levels in healthy individuals

Characterization of mutations in the low density lipoprotein (LDL)-receptor gene in patients with homozygous familial hypercholesterolemia, and frequency of these mutations in FH patients in the United Kingdom

Characterization of two new point mutations in the low density lipoprotein receptor genes of an English patient with homozygous familial hypercholesterolemia

Characterization of the Rodent Genes for Arylacetamide Deacetylase, a Putative Microsomal Lipase, and Evidence for Transcriptional Regulation

Catabolism of lipoprotein(a) in familial hypercholesterolaemic subjects

Structure and regulation of the LDL- receptor and its gene

Characterization of a novel cellular defect in patients with phenotypic homozygous familial hypercholesterolemia

The proton hyperfine interaction in HC60, signature of a potential interstellar fullerene

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