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A common 936 C/T mutation in the gene for vascular endothelial growth factor is associated with vascular endothelial growth factor plasma levels.
Renner W, Kotschan S, Hoffmann C, Obermayer-Pietsch B, Pilger E. Renner W, et al. J Vasc Res. 2000 Nov-Dec;37(6):443-8. doi: 10.1159/000054076. J Vasc Res. 2000. PMID: 11146397
Association of vascular endothelial growth factor--a gene polymorphisms and haplotypes with breast cancer metastases.
Langsenlehner U, Hofmann G, Renner W, Gerger A, Krenn-Pilko S, Thurner EM, Krippl P, Langsenlehner T. Langsenlehner U, et al. Among authors: renner w. Acta Oncol. 2015 Mar;54(3):368-76. doi: 10.3109/0284186X.2014.948056. Epub 2014 Aug 25. Acta Oncol. 2015. PMID: 25152223
Association between polymorphism of the vitamin D metabolism gene CYP27B1 and HLA-B27-associated uveitis. Is a state of relative immunodeficiency pathogenic in HLA B27-positive uveitis?
Steinwender G, Lindner E, Weger M, Plainer S, Renner W, Ardjomand N, El-Shabrawi Y. Steinwender G, et al. Among authors: renner w. PLoS One. 2013 Apr 17;8(4):e62244. doi: 10.1371/journal.pone.0062244. Print 2013. PLoS One. 2013. PMID: 23614044 Free PMC article.
Role of inflammation-related gene polymorphisms in patients with central retinal vein occlusion.
Maier R, Steinbrugger I, Haas A, Selimovic M, Renner W, El-Shabrawi Y, Werner C, Wedrich A, Schmut O, Weger M. Maier R, et al. Among authors: renner w. Ophthalmology. 2011 Jun;118(6):1125-9. doi: 10.1016/j.ophtha.2010.10.014. Epub 2011 Jan 26. Ophthalmology. 2011. PMID: 21269700
The fibrinogen gamma (FGG) 10034C>T polymorphism is associated with venous thrombosis.
Grünbacher G, Weger W, Marx-Neuhold E, Pilger E, Köppel H, Wascher T, März W, Renner W. Grünbacher G, et al. Among authors: renner w. Thromb Res. 2007;121(1):33-6. doi: 10.1016/j.thromres.2007.03.007. Epub 2007 Apr 19. Thromb Res. 2007. PMID: 17445871
Polymorphisms of the hypoxia-inducible factor 1 gene and peripheral artery disease.
Bahadori B, Uitz E, Mayer A, Harauer J, Dam K, Truschnig-Wilders M, Pilger E, Renner W. Bahadori B, et al. Among authors: renner w. Vasc Med. 2010 Oct;15(5):371-4. doi: 10.1177/1358863X10379674. Vasc Med. 2010. PMID: 20926496
Single nucleotide polymorphisms in the hypoxia-inducible factor-1 gene and colorectal cancer risk.
Knechtel G, Szkandera J, Stotz M, Hofmann G, Langsenlehner U, Krippl P, Samonigg H, Renner W, Langner C, Dehchamani D, Gerger A. Knechtel G, et al. Among authors: renner w. Mol Carcinog. 2010 Sep;49(9):805-9. doi: 10.1002/mc.20655. Mol Carcinog. 2010. PMID: 20572162
The angiotensin-converting-enzyme insertion/deletion polymorphism is not related to venous thrombosis.
Köppel H, Renner W, Gugl A, Cichocki L, Gasser R, Wascher TC, Pilger E. Köppel H, et al. Among authors: renner w. Thromb Haemost. 2004 Jan;91(1):76-9. doi: 10.1160/TH03-05-0266. Thromb Haemost. 2004. PMID: 14691571
Association of angiotensinogen haplotypes with angiotensinogen levels but not with blood pressure or coronary artery disease: the Ludwigshafen Risk and Cardiovascular Health Study.
Renner W, Nauck M, Winkelmann BR, Hoffmann MM, Scharnagl H, Mayer V, Boehm BO, März W; LURIC Study team. Renner W, et al. J Mol Med (Berl). 2005 Mar;83(3):235-9. doi: 10.1007/s00109-004-0618-0. Epub 2004 Dec 15. J Mol Med (Berl). 2005. PMID: 15599691
Role of the vitamin K epoxide reductase complex subunit 1 (VKORC1) -1639G>A gene polymorphism in patients with retinal vein occlusion.
Weger M, Steinbrugger I, Renner W, Pöschl EM, Brockmann T, Rabensteiner DF, El-Shabrawi Y, Haas A. Weger M, et al. Among authors: renner w. Curr Eye Res. 2013 Dec;38(12):1278-82. doi: 10.3109/02713683.2013.820329. Epub 2013 Aug 23. Curr Eye Res. 2013. PMID: 23972066
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