PortalPublikationenGenetic variation at chromosome 1p13.3 affects sortilin mRNA...

Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease.

Standard

Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease. / Linsel-Nitschke, Patrick; Heeren, Jörg; Aherrahrou, Zouhair; Bruse, Petra; Gieger, Christian; Illig, Thomas; Prokisch, Holger; Heim, Katharina; Doering, Angela; Peters, Annette; Meitinger, Thomas; Wichmann, H-Erich; Hinney, Anke; Reinehr, Thomas; Roth, Christian; Ortlepp, Jan R; Soufi, Mouhidien; Sattler, Alexander M; Schaefer, Jürgen; Stark, Klaus; Hengstenberg, Christian; Schaefer, Arne; Schreiber, Stefan; Kronenberg, Florian; Samani, Nilesh J; Schunkert, Heribert; Erdmann, Jeanette.

in: ATHEROSCLEROSIS, Jahrgang 208, Nr. 1, 1, 2010, S. 183-189.

Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung

Harvard

Linsel-Nitschke, P, Heeren, J, Aherrahrou, Z, Bruse, P, Gieger, C, Illig, T, Prokisch, H, Heim, K, Doering, A, Peters, A, Meitinger, T, Wichmann, H-E, Hinney, A, Reinehr, T, Roth, C, Ortlepp, JR, Soufi, M, Sattler, AM, Schaefer, J, Stark, K, Hengstenberg, C, Schaefer, A, Schreiber, S, Kronenberg, F, Samani, NJ, Schunkert, H & Erdmann, J 2010, 'Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease.', ATHEROSCLEROSIS, Jg. 208, Nr. 1, 1, S. 183-189. <http://www.ncbi.nlm.nih.gov/pubmed/19660754?dopt=Citation>

APA

Linsel-Nitschke, P., Heeren, J., Aherrahrou, Z., Bruse, P., Gieger, C., Illig, T., Prokisch, H., Heim, K., Doering, A., Peters, A., Meitinger, T., Wichmann, H-E., Hinney, A., Reinehr, T., Roth, C., Ortlepp, J. R., Soufi, M., Sattler, A. M., Schaefer, J., ... Erdmann, J. (2010). Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease. ATHEROSCLEROSIS, 208(1), 183-189. [1]. http://www.ncbi.nlm.nih.gov/pubmed/19660754?dopt=Citation

Vancouver

Linsel-Nitschke P, Heeren J, Aherrahrou Z, Bruse P, Gieger C, Illig T et al. Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease. ATHEROSCLEROSIS. 2010;208(1):183-189. 1.

Bibtex

@article{98c0fc61013d4656b6b65021865e77fb,
title = "Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease.",
abstract = "A single nucleotide polymorphism (SNP) rs599839 located at chromosome 1p13.3 has previously been associated with risk of coronary artery disease (CAD) and with serum levels of low-density lipoprotein cholesterol (LDL-C). A functional link explaining the association of SNP rs599839 with LDL-C levels and CAD risk has not yet been elucidated.",
author = "Patrick Linsel-Nitschke and J{\"o}rg Heeren and Zouhair Aherrahrou and Petra Bruse and Christian Gieger and Thomas Illig and Holger Prokisch and Katharina Heim and Angela Doering and Annette Peters and Thomas Meitinger and H-Erich Wichmann and Anke Hinney and Thomas Reinehr and Christian Roth and Ortlepp, {Jan R} and Mouhidien Soufi and Sattler, {Alexander M} and J{\"u}rgen Schaefer and Klaus Stark and Christian Hengstenberg and Arne Schaefer and Stefan Schreiber and Florian Kronenberg and Samani, {Nilesh J} and Heribert Schunkert and Jeanette Erdmann",
year = "2010",
language = "Deutsch",
volume = "208",
pages = "183--189",
journal = "ATHEROSCLEROSIS",
issn = "0021-9150",
publisher = "Elsevier Ireland Ltd",
number = "1",

}

RIS

TY - JOUR

T1 - Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease.

AU - Linsel-Nitschke, Patrick

AU - Heeren, Jörg

AU - Aherrahrou, Zouhair

AU - Bruse, Petra

AU - Gieger, Christian

AU - Illig, Thomas

AU - Prokisch, Holger

AU - Heim, Katharina

AU - Doering, Angela

AU - Peters, Annette

AU - Meitinger, Thomas

AU - Wichmann, H-Erich

AU - Hinney, Anke

AU - Reinehr, Thomas

AU - Roth, Christian

AU - Ortlepp, Jan R

AU - Soufi, Mouhidien

AU - Sattler, Alexander M

AU - Schaefer, Jürgen

AU - Stark, Klaus

AU - Hengstenberg, Christian

AU - Schaefer, Arne

AU - Schreiber, Stefan

AU - Kronenberg, Florian

AU - Samani, Nilesh J

AU - Schunkert, Heribert

AU - Erdmann, Jeanette

PY - 2010

Y1 - 2010

N2 - A single nucleotide polymorphism (SNP) rs599839 located at chromosome 1p13.3 has previously been associated with risk of coronary artery disease (CAD) and with serum levels of low-density lipoprotein cholesterol (LDL-C). A functional link explaining the association of SNP rs599839 with LDL-C levels and CAD risk has not yet been elucidated.

AB - A single nucleotide polymorphism (SNP) rs599839 located at chromosome 1p13.3 has previously been associated with risk of coronary artery disease (CAD) and with serum levels of low-density lipoprotein cholesterol (LDL-C). A functional link explaining the association of SNP rs599839 with LDL-C levels and CAD risk has not yet been elucidated.

M3 - SCORING: Zeitschriftenaufsatz

VL - 208

SP - 183

EP - 189

JO - ATHEROSCLEROSIS

JF - ATHEROSCLEROSIS

SN - 0021-9150

IS - 1

M1 - 1

ER -