Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gudrun, Sonderegger"'
Autor:
Axel Muendlein, Christoph H Saely, Simone Geller-Rhomberg, Gudrun Sonderegger, Philipp Rein, Thomas Winder, Stefan Beer, Alexander Vonbank, Heinz Drexel
Publikováno v:
PLoS ONE, Vol 6, Iss 3, p e17978 (2011)
BackgroundCoronary artery disease (CAD) shares common risk factors with type 2 diabetes (T2DM). Variations in the transcription factor 7-like 2 (TCF7L2) gene, particularly rs7903146, increase T2DM risk. Potential links between genetic variants of the
Externí odkaz:
https://doaj.org/article/ea521dcd5ff644ad90f0ac0f3f485a2a
Autor:
Ariane Biebl, Axel Muendlein, Zhyrgal Kazakbaeva, Sigrid Heuberger, Gudrun Sonderegger, Heinz Drexel, Susanne Lau, Renate Nickel, Michael Kabesch, Burkhard Simma
Publikováno v:
PLoS ONE, Vol 4, Iss 10, p e7374 (2009)
BackgroundCarriage of Neisseria meningitidis occurs approximately in 10% of the population, onset of invasive meningococcal disease (IMD) cannot be predicted and differs between ages. It remains unclear, which host factors determine invasion of the b
Externí odkaz:
https://doaj.org/article/a3bd7aab61c9444a82b8eb053e4d576f
Autor:
Heinz Drexel, Thomas Winder, Stefan Beer, Simone Geller-Rhomberg, Axel Muendlein, Philipp Rein, Christoph H. Saely, Alexander Vonbank, Gudrun Sonderegger
Publikováno v:
Atherosclerosis. 206:494-499
Objectives Recently, a significant impact of a new locus on chromosome 1p13.3 on serum LDL (low-density lipoprotein) cholesterol and clinical events of coronary artery disease (CAD) was described. Potential associations between variants on this locus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cb74a587aea60b4058e0f04ec8c8fd9
https://doi.org/10.1016/j.atherosclerosis.2009.02.040
https://doi.org/10.1016/j.atherosclerosis.2009.02.040
Autor:
Philipp Rein, Heinz Drexel, Alexander Vonbank, Stephan Loacker, Christoph H. Saely, Thomas Winder, Stefan Beer, Axel Muendlein, Gudrun Sonderegger, Simone Rhomberg
Publikováno v:
Atherosclerosis. 205:174-180
Objectives The chromosomal loci 9p21.3, 6q25.1, and 2q36.3, represented by their respective leading variants rs1333049, rs6922269 and rs2943634, have been linked with a history of coronary artery disease (CAD) by genome-wide association studies. Wher
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::803df64a70005e3294a496bafd2ea58d
https://doi.org/10.1016/j.atherosclerosis.2008.10.035
https://doi.org/10.1016/j.atherosclerosis.2008.10.035
Autor:
Philipp Rein, Heinz Drexel, Gudrun Sonderegger, Alexander Vonbank, Stefan Aczel, Christoph H. Saely, Axel Muendlein, Lorenz Risch
Publikováno v:
Clinica Chimica Acta. 396:18-22
Background The association of the − 675 4G/5G polymorphism of the plasminogen activator inhibitor-1 ( PAI-1 ) gene with cardiovascular disease in patients with type 2 diabetes (T2DM) is unknown. Methods Genotyping was performed in 672 consecutive C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3443092865574ddf06cd2b8d023b7fc3
https://doi.org/10.1016/j.cca.2008.06.015
https://doi.org/10.1016/j.cca.2008.06.015
Autor:
Andreas, Ritsch, Gudrun, Sonderegger, Gudron, Sonderegger, Anton, Sandhofer, Ursula, Stanzl, Ursala, Stanzl, Ivan, Tancevski, Philipp, Eller, Wilfried, Schgoer, Andreas, Wehinger, Thomas, Mueller, Meinhard, Haltmayer, Josef R, Patsch, Joseph R, Patsch
Publikováno v:
Metabolism. 56:1135-1141
Genetic variations of the scavenger receptor class B type I (SR-BI) have been demonstrated to be associated with plasma lipid parameters, anthropomorphic parameters, and coronary artery disease. We determined the frequency of 3 single-nucleotide poly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba0f14e8f6dc9b3b08eec0d93c5d8b1c
https://doi.org/10.1016/j.metabol.2007.04.009
https://doi.org/10.1016/j.metabol.2007.04.009
Autor:
Alexander Vonbank, Christoph H. Saely, Thomas Winder, Stefan Beer, Gudrun Sonderegger, Axel Muendlein, Simone Geller-Rhomberg, Philipp Rein, Heinz Drexel
Publikováno v:
PLoS ONE, Vol 6, Iss 3, p e17978 (2011)
PLoS ONE
PLoS ONE
BackgroundCoronary artery disease (CAD) shares common risk factors with type 2 diabetes (T2DM). Variations in the transcription factor 7-like 2 (TCF7L2) gene, particularly rs7903146, increase T2DM risk. Potential links between genetic variants of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe1006308570ed287d473be3d2e120a9
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21423583/pdf/?tool=EBI
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21423583/pdf/?tool=EBI
Autor:
Susanne Lau, Burkhard Simma, Sigrid Heuberger, Axel Muendlein, Zhyrgal Kazakbaeva, Renate Nickel, Heinz Drexel, Michael Kabesch, Ariane Biebl, Gudrun Sonderegger
Publikováno v:
PLoS ONE
PLoS ONE, Vol 4, Iss 10, p e7374 (2009)
PLoS ONE, Vol 4, Iss 10, p e7374 (2009)
BackgroundCarriage of Neisseria meningitidis occurs approximately in 10% of the population, onset of invasive meningococcal disease (IMD) cannot be predicted and differs between ages. It remains unclear, which host factors determine invasion of the b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed0d451f3d71a8fda6a2442341154a4a
http://europepmc.org/articles/PMC2753648
http://europepmc.org/articles/PMC2753648