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Lipoprotein(a): resurrected by genetics

Journal of internal medicine, 2013-01, Vol.273 (1), p.6-30

2013

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Switch from antagonist to agonist of the androgen receptor blocker bicalutamide is associated with prostate tumour progression in a new model system

British Journal of Cancer, 1999-09, Vol.81 (2), p.242-251

1999

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Chromosomal microaberrations in patients with epilepsy, intellectual disability, and congenital anomalies

Clinical genetics, 2014-10, Vol.86 (4), p.361-366

2014

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Lipoprotein(a) in renal disease

American Journal of Kidney Diseases, 1996, Vol.27 (1), p.1-25

1996

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Lipoprotein(a) in homozygous familial hypercholesterolemia

Arteriosclerosis, thrombosis, and vascular biology, 2000-02, Vol.20 (2), p.522-528

2000

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Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations

Journal of medical genetics, 2008-04, Vol.45 (4), p.200-209

2008

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Apolipoprotein(a) kringle IV repeat number predicts risk for coronary heart disease

Arteriosclerosis, thrombosis, and vascular biology, 1996-06, Vol.16 (6), p.713-719

1996

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Mutational Spectrum in the Δ7-Sterol Reductase Gene and Genotype-Phenotype Correlation in 84 Patients with Smith-Lemli-Opitz Syndrome

American journal of human genetics, 2000, Vol.66 (2), p.402-412

2000

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Maternal apo E genotype is a modifier of the Smith-Lemli-Opitz syndrome

Journal of medical genetics, 2004-08, Vol.41 (8), p.577-584

2004

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Protein kinase C-theta isoenzyme selective stimulation of the transcription factor complex AP-1 in T lymphocytes

Molecular and Cellular Biology, 1996-04, Vol.16 (4), p.1842-1850

1996

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Lipoproteinstoffwechsel und koronare Herzkrankheit

Medizinische Genetik, 2011-03, Vol.23 (1), p.7-14

Utermann, G.

2011

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Lipoproteinstoffwechsel und koronare Herzkrankheit: Modellsysteme für komplexe Erkrankungen

Medizinische Genetik, 2011-03, Vol.23 (1), p.7-14

Utermann, G.

2011

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Whole Genome Amplification from Microdissected Chromosomes

Cytogenetic and genome research, 2009-01, Vol.125 (2), p.98-102

2009

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Parental Origin of de novo Cytogenetically Balanced Reciprocal Non-Robertsonian Translocations

Cytogenetic and genome research, 2012-06, Vol.136 (4), p.242-245

2012

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Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysis

Clinical genetics, 2010-12, Vol.78 (6), p.548-553

2010

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Uniparental paternal disomy in a genetic cancer-predisposing syndrome

Nature (London), 1991-06, Vol.351 (6328), p.665-667

1991

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The apolipoprotein (a) gene : a transcribed hypervariable locus controlling plasma lipoprotein (a) concentration

Human genetics, 1992-11, Vol.90 (3), p.220-230

1992

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Apo(a) isoforms predict risk for coronary heart disease. A study in six populations

Arteriosclerosis and thrombosis, 1992-10, Vol.12 (10), p.1214-1226

1992

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Lp(a) glycoprotein phenotypes: inheritance and relation to Lp(a)-lipoprotein concentrations in plasma

The Journal of clinical investigation, 1987-08, Vol.80 (2), p.458-465

1987

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Effect of sample storage on the measurement of lipoprotein[a], apolipoproteins B and A-IV, total and high density lipoprotein cholesterol and triglycerides

Journal of lipid research, 1994-07, Vol.35 (7), p.1318-1328

1994

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Effects of the apolipoprotein(a) size polymorphism on the lipoprotein(a) concentration in 7 ethnic groups

Human genetics, 1991-04, Vol.86 (6), p.607-614

1991

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Apolipoprotein(a) phenotypes, Lp(a) concentration and plasma lipid levels in relation to coronary heart disease in a Chinese population : evidence for the role of the apo(a) gene in coronary heart disease

The Journal of clinical investigation, 1992-03, Vol.89 (3), p.1040-1046

1992

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Simultaneous effects of the apolipoprotein E polymorphism on apolipoprotein E, apolipoprotein B, and cholesterol metabolism

American journal of human genetics, 1988, Vol.42 (1), p.104-112

1988

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Identification of 14 novel mutations in DHCR7 causing the Smith-Lemli-Opitz syndrome and delineation of the DHCR7 mutational spectra in Spain and Italy

Human mutation, 2005-04, Vol.25 (4), p.412-412

2005

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Renovascular arteriovenous differences in Lp[a] plasma concentrations suggest removal of Lp[a] from the renal circulation

Journal of lipid research, 1997-09, Vol.38 (9), p.1755-1763

1997

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Lipoprotein(a): resurrected by genetics

Switch from antagonist to agonist of the androgen receptor blocker bicalutamide is associated with prostate tumour progression in a new model system

Chromosomal microaberrations in patients with epilepsy, intellectual disability, and congenital anomalies

Lipoprotein(a) in renal disease

Lipoprotein(a) in homozygous familial hypercholesterolemia

Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations

Apolipoprotein(a) kringle IV repeat number predicts risk for coronary heart disease

Mutational Spectrum in the Δ7-Sterol Reductase Gene and Genotype-Phenotype Correlation in 84 Patients with Smith-Lemli-Opitz Syndrome

Maternal apo E genotype is a modifier of the Smith-Lemli-Opitz syndrome

Protein kinase C-theta isoenzyme selective stimulation of the transcription factor complex AP-1 in T lymphocytes

Lipoproteinstoffwechsel und koronare Herzkrankheit

Lipoproteinstoffwechsel und koronare Herzkrankheit: Modellsysteme für komplexe Erkrankungen

Whole Genome Amplification from Microdissected Chromosomes

Parental Origin of de novo Cytogenetically Balanced Reciprocal Non-Robertsonian Translocations

Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysis

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

The apolipoprotein (a) gene : a transcribed hypervariable locus controlling plasma lipoprotein (a) concentration

Apo(a) isoforms predict risk for coronary heart disease. A study in six populations

Lp(a) glycoprotein phenotypes: inheritance and relation to Lp(a)-lipoprotein concentrations in plasma

Effect of sample storage on the measurement of lipoprotein[a], apolipoproteins B and A-IV, total and high density lipoprotein cholesterol and triglycerides

Effects of the apolipoprotein(a) size polymorphism on the lipoprotein(a) concentration in 7 ethnic groups

Apolipoprotein(a) phenotypes, Lp(a) concentration and plasma lipid levels in relation to coronary heart disease in a Chinese population : evidence for the role of the apo(a) gene in coronary heart disease

Simultaneous effects of the apolipoprotein E polymorphism on apolipoprotein E, apolipoprotein B, and cholesterol metabolism

Identification of 14 novel mutations in DHCR7 causing the Smith-Lemli-Opitz syndrome and delineation of the DHCR7 mutational spectra in Spain and Italy

Renovascular arteriovenous differences in Lp[a] plasma concentrations suggest removal of Lp[a] from the renal circulation

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