UB Paderborn / Katalog / Suche / in CDI

Heterozygosity for a Loss-of-Function Mutation in GALNT2 Improves Plasma Triglyceride Clearance in Man

Cell metabolism, 2011-12, Vol.14 (6), p.811-818

2011

Volltextzugriff (PDF)

Proteome of human plasma very low-density lipoprotein and low-density lipoprotein exhibits a link with coagulation and lipid metabolism

Thrombosis and haemostasis, 2014-03, Vol.111 (3), p.518

2014

Volltextzugriff (PDF)

Lipoprotein distribution and serum concentrations of 7α-hydroxy-4-cholesten-3-one and bile acids: effects of monogenic disturbances in high-density lipoprotein metabolism

Clinical science (1979), 2012-04, Vol.122 (8), p.385

2012

Volltextzugriff (PDF)

Identification of a loss-of-function inducible degrader of the low-density lipoprotein receptor variant in individuals with low circulating low-density lipoprotein

European heart journal, 2013-05, Vol.34 (17), p.1292-1297

2013

Volltextzugriff (PDF)

Plasma levels of 27-hydroxycholesterol in humans and mice with monogenic disturbances of high density lipoprotein metabolism

Atherosclerosis, 2011-02, Vol.214 (2), p.448-455

2011

Volltextzugriff (PDF)

Genetic Variant of the Scavenger Receptor BI in Humans

The New England journal of medicine, 2011-01, Vol.364 (2), p.136-145

2011

Volltextzugriff (PDF)

Plasma levels of sphingosine-1-phosphate and apolipoprotein M in patients with monogenic disorders of HDL metabolism

Atherosclerosis, 2011-12, Vol.219 (2), p.855-863

2011

Volltextzugriff (PDF)

SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly

Human genetics, 2006-02, Vol.118 (6), p.708-715

2006

Volltextzugriff (PDF)

A defect in the lonotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardation

American journal of human genetics, 2007-10, Vol.81 (4), p.792-798

2007

Volltextzugriff (PDF)

Impact of Rare and Common Genetic Variants on Lipoprotein Metabolism

Clinical Lipidology: A Companion to Braunwald's Heart Disease, 2015, p.68-77

Second Edition, 2015

Volltextzugriff (PDF)

Menü

Weitere Dienste

Einstellungen

Heterozygosity for a Loss-of-Function Mutation in GALNT2 Improves Plasma Triglyceride Clearance in Man

Proteome of human plasma very low-density lipoprotein and low-density lipoprotein exhibits a link with coagulation and lipid metabolism

Lipoprotein distribution and serum concentrations of 7α-hydroxy-4-cholesten-3-one and bile acids: effects of monogenic disturbances in high-density lipoprotein metabolism

Identification of a loss-of-function inducible degrader of the low-density lipoprotein receptor variant in individuals with low circulating low-density lipoprotein

Plasma levels of 27-hydroxycholesterol in humans and mice with monogenic disturbances of high density lipoprotein metabolism

Genetic Variant of the Scavenger Receptor BI in Humans

Plasma levels of sphingosine-1-phosphate and apolipoprotein M in patients with monogenic disorders of HDL metabolism

SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly

A defect in the lonotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardation

Impact of Rare and Common Genetic Variants on Lipoprotein Metabolism

Suchergebnisse filtern