Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

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Publikationen

Suchbegriffe: POLYMORPHISM, GENETIC - , . Treffer: 80

2015

Mangge, H; Baumgartner, BG; Zelzer, S; Prüller, F; Schnedl, WJ; Reininghaus, EZ; Haybaeck, J; Lackner, C; Stauber, R; Aigner, E; Weghuber, D Patatin-like phospholipase 3 (rs738409) gene polymorphism is associated with increased liver enzymes in obese adolescents and metabolic syndrome in all ages.
Aliment Pharmacol Ther. 2015; 42(1):99-105 [OPEN ACCESS]
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Wagner, B; Melzer, H; Freymüller, G; Stumvoll, S; Rendi-Wagner, P; Paulke-Korinek, M; Repa, A; Mooi, FR; Kollaritsch, H; Mittermayer, H; Kessler, HH; Stanek, G; Steinborn, R; Duchêne, M; Wiedermann, U Genetic Variation of Bordetella pertussis in Austria.
PLoS One. 2015; 10(7):e0132623-e0132623 [OPEN ACCESS]
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2014

Benhaim, L; Gerger, A; Bohanes, P; Paez, D; Wakatsuki, T; Yang, D; Labonte, MJ; Ning, Y; El-Khoueiry, R; Loupakis, F; Zhang, W; Laurent-Puig, P; Lenz, HJ Gender-specific profiling in SCN1A polymorphisms and time-to-recurrence in patients with stage II/III colorectal cancer treated with adjuvant 5-fluoruracil chemotherapy.
Pharmacogenomics J. 2014; 14(2):135-141
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Scharnagl, H; Kleber, ME; Genser, B; Kickmaier, S; Renner, W; Weihrauch, G; Grammer, T; Rossmann, C; Winkelmann, BR; Boehm, BO; Sattler, W; März, W; Malle, E Association of myeloperoxidase with total and cardiovascular mortality in individuals undergoing coronary angiography--the LURIC study.
Int J Cardiol. 2014; 174(1):96-105 [OPEN ACCESS]
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Sunakawa, Y; Wakatsuki, T; Yang, D; Zhang, W; Ning, Y; Stintzing, S; Stremitzer, S; Yamauchi, S; Sebio, A; El-khoueiry, R; Iqbal, S; Barzi, A; Gerger, A; Stotz, M; Azuma, M; Watanabe, M; Koizumi, W; Lenz, HJ Prognostic impact of the c-MET polymorphism on the clinical outcome in locoregional gastric cancer patients.
Pharmacogenet Genomics. 2014; 24(12):588-596 [OPEN ACCESS]
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2013

Friedrich, K; Rupp, C; Hov, JR; Steinebrunner, N; Weiss, KH; Stiehl, A; Brune, M; Schaefer, PK; Schemmer, P; Sauer, P; Schirmacher, P; Runz, H; Karlsen, TH; Stremmel, W; Gotthardt, DN A frequent PNPLA3 variant is a sex specific disease modifier in PSC patients with bile duct stenosis.
PLoS One. 2013; 8(3):e58734-e58734 [OPEN ACCESS]
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Lenk, J; Bornhauser, M; Kramer, M; Hölig, K; Poppe-Thiede, K; Schmidt, H; Wiesneth, M; Schaefer-Eckart, K; Schlenke, P; Punzel, M; Martin, S; Kroschinsky, F; Schmidt, AH; Ehninger, G; Thiede, C Sex and body mass index but not CXCL12 801 G/A polymorphism determine the efficacy of hematopoietic cell mobilization: a study in healthy volunteer donors.
Biol Blood Marrow Transplant. 2013; 19(10):1517-1521 [OPEN ACCESS]
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Lindner, E; Steinwender, G; Plainer, S; Poeschl, EM; Weger, M; Ardjomand, N; Renner, W; El-Shabrawi, Y Role of IL-10 gene polymorphisms in intermediate and HLA-B27-associated uveitis.
Acta Ophthalmol. 2013; 91(5):e415-e417 [OPEN ACCESS]
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Ouchari, M; Polin, H; Romdhane, H; Abdelkefi, S; Houissa, B; Chakroun, T; Gabriel, C; Hmida, S; Jemni Yacoub, S RHD*weak partial 4.0 is associated with an altered RHCE*ce(48C, 105T, 733G, 744C, 1025T) allele in the Tunisian population.
Transfus Med. 2013; 23(4): 245-249.
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Told, R; Palkovits, S; Haslacher, H; Frantal, S; Schmidl, D; Boltz, A; Lasta, M; Kaya, S; Werkmeister, RM; Garhöfer, G; Schmetterer, L Alterations of choroidal blood flow regulation in young healthy subjects with complement factor H polymorphism.
PLoS One. 2013; 8(4):e60424-e60424 [OPEN ACCESS]
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2012

Kraus, JP; Spector, E; Venezia, S; Estes, P; Chiang, PW; Creadon-Swindell, G; Müllerleile, S; de Silva, L; Barth, M; Walter, M; Walter, K; Meissner, T; Lindner, M; Ensenauer, R; Santer, R; Bodamer, OA; Baumgartner, MR; Brunner-Krainz, M; Karall, D; Haase, C; Knerr, I; Marquardt, T; Hennermann, JB; Steinfeld, R; Beblo, S; Koch, HG; Konstantopoulou, V; Scholl-Bürgi, S; van Teeffelen-Heithoff, A; Suormala, T; Ugarte, M; Sperl, W; Superti-Furga, A; Schwab, KO; Grünert, SC; Sass, JO Mutation analysis in 54 propionic acidemia patients.
J INHERIT METAB DIS. 2012; 35(1): 51-63.
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Kumari, M; Schoiswohl, G; Chitraju, C; Paar, M; Cornaciu, I; Rangrez, AY; Wongsiriroj, N; Nagy, HM; Ivanova, PT; Scott, SA; Knittelfelder, O; Rechberger, GN; Birner-Gruenberger, R; Eder, S; Brown, HA; Haemmerle, G; Oberer, M; Lass, A; Kershaw, EE; Zimmermann, R; Zechner, R Adiponutrin functions as a nutritionally regulated lysophosphatidic acid acyltransferase.
Cell Metab. 2012; 15(5):691-702 [OPEN ACCESS]
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Szkandera, J; Absenger, G; Dandachi, N; Regitnig, P; Lax, S; Stotz, M; Samonigg, H; Renner, W; Gerger, A Analysis of functional germline polymorphisms for prediction of response to anthracycline-based neoadjuvant chemotherapy in breast cancer.
Mol Genet Genomics. 2012; 287(9):755-764
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Szkandera, J; Absenger, G; Stotz, M; Weissmueller, M; Winder, T; Langsenlehner, T; Samonigg, H; Renner, W; Schippinger, W; Gerger, A The Functional Polymorphism of Erythropoietin Gene rs1617640 G>T Is Not Associated with Susceptibility and Clinical Outcome of Early-stage Breast Cancer.
Anticancer Res. 2012; 32(8):3473-3478
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Tarner, IH; Erkal, MZ; Obermayer-Pietsch, BM; Hofbauer, LC; Bergmann, S; Goettsch, C; Madlener, K; Müller-Ladner, U; Lange, U Osteometabolic and osteogenetic pattern of Turkish immigrants in Germany.
Exp Clin Endocrinol Diabetes. 2012; 120(9):517-523 [OPEN ACCESS]
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2011

Gerger, A; Zhang, W; Yang, D; Bohanes, P; Ning, Y; Winder, T; LaBonte, MJ; Wilson, PM; Benhaim, L; Paez, D; El-Khoueiry, R; El-Khoueiry, A; Kahn, M; Lenz, HJ Common cancer stem cell gene variants predict colon cancer recurrence.
Clin Cancer Res. 2011; 17(21):6934-6943 [OPEN ACCESS]
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Hoffmann, MM; März, W; Genser, B; Drechsler, C; Wanner, C Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and cardiovascular risk and efficacy of atorvastatin among subjects with diabetes on dialysis: the 4D study.
Atherosclerosis. 2011; 219(2):659-662
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Maier, R; Steinbrugger, I; Haas, A; Selimovic, M; Renner, W; El-Shabrawi, Y; Werner, C; Wedrich, A; Schmut, O; Weger, M Role of inflammation-related gene polymorphisms in patients with central retinal vein occlusion.
Ophthalmology. 2011; 118(6): 1125-1129.
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Reiberger, T; Rutter, K; Ferlitsch, A; Payer, BA; Hofer, H; Beinhardt, S; Kundi, M; Ferenci, P; Gangl, A; Trauner, M; Peck-Radosavljevic, M Portal pressure predicts outcome and safety of antiviral therapy in cirrhotic patients with hepatitis C virus infection.
Clin Gastroenterol Hepatol. 2011; 9(7):602-608
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Stabentheiner, S; Danzer, M; Niklas, N; Atzmüller, S; Pröll, J; Hackl, C; Polin, H; Hofer, K; Gabriel, C Overcoming methodical limits of standard RHD genotyping by next-generation sequencing.
Vox Sang. 2011; 100(4): 381-388.
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2010

Bahadori, B; Uitz, E; Mayer, A; Harauer, J; Dam, K; Truschnig-Wilders, M; Pilger, E; Renner, W Polymorphisms of the hypoxia-inducible factor 1 gene and peripheral artery disease.
Vasc Med. 2010; 15(5):371-374 [OPEN ACCESS]
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Danzer, M; Polin, H; Stabentheiner, S; Hartmann, CC; Lennartz, K; Gabriel, C Comprehensive polymorphism analysis of ABO using allele-specific separation by bead technology and subsequent sequencing.
Vox Sang. 2010; 98(3 Pt 2): 451-454.
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Görzer, I; Guelly, C; Trajanoski, S; Puchhammer-Stöckl, E The impact of PCR-generated recombination on diversity estimation of mixed viral populations by deep sequencing.
J Virol Methods. 2010; 169(1): 248-252.
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Gruber, HJ; Bernecker, C; Lechner, A; Weiss, S; Wallner-Blazek, M; Meinitzer, A; Hobarth, G; Renner, W; Fauler, G; Horejsi, R; Fazekas, F; Truschnig-Wilders, M Increased nitric oxide stress is associated with migraine.
CEPHALALGIA. 2010; 30(4): 486-492.
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Knechtel, G; Szkandera, J; Stotz, M; Hofmann, G; Langsenlehner, U; Krippl, P; Samonigg, H; Renner, W; Langner, C; Dehchamani, D; Gerger, A Single nucleotide polymorphisms in the hypoxia-inducible factor-1 gene and colorectal cancer risk.
Mol Carcinog. 2010; 49(9):805-809
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Kozian, DH; Barthel, A; Cousin, E; Brunnhofer, R; Anderka, O; Marz, W; Bohm, B; Winkelmann, B; Bornstein, SR; Schmoll, D Glucokinase-activating GCKR polymorphisms increase plasma levels of triglycerides and free fatty acids, but do not elevate cardiovascular risk in the Ludwigshafen Risk and Cardiovascular Health Study.
HORMONE METAB RES. 2010; 42(7): 502-506.
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Mychaleckyj, JC; Noble, JA; Moonsamy, PV; Carlson, JA; Varney, MD; Post, J; Helmberg, W; Pierce, JJ; Bonella, P; Fear, AL; Lavant, E; Louey, A; Boyle, S; Lane, JA; Sali, P; Kim, S; Rappner, R; Williams, DT; Perdue, LH; Reboussin, DM; Tait, BD; Akolkar, B; Hilner, JE; Steffes, MW; Erlich, HA; T1DGC HLA genotyping in the international Type 1 Diabetes Genetics Consortium.
Clin Trials. 2010; 7(1 Suppl): S75-S87. [OPEN ACCESS]
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Resch, B; Radinger, A; Mannhalter, C; Horvath, B; Binder, A; Zenz, W; Walcher, W; Haas, J; Müller, WD; Pertl, B Maternal interleukin-6 (-174) C/C polymorphism is associated with chorioamnionitis and cystic periventricular leucomalacia of the preterm infant.
J Perinatol. 2010; 30(11): 712-716. [OPEN ACCESS]
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Stingl, JC; Parmar, S; Huber-Wechselberger, A; Kainz, A; Renner, W; Seeringer, A; Brockmöller, J; Langsenlehner, U; Krippl, P; Haschke-Becher, E Impact of CYP2D6*4 genotype on progression free survival in tamoxifen breast cancer treatment.
Curr Med Res Opin. 2010; 26(11):2535-2542
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Trottier, J; El Husseini, D; Perreault, M; Pâquet, S; Caron, P; Bourassa, S; Verreault, M; Inaba, TT; Poirier, GG; Bélanger, A; Guillemette, C; Trauner, M; Barbier, O The human UGT1A3 enzyme conjugates norursodeoxycholic acid into a C23-ester glucuronide in the liver.
J Biol Chem. 2010; 285(2):1113-1121 [OPEN ACCESS]
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Yazdani-Biuki, B; Krippl, P; Brickmann, K; Fuerst, F; Langsenlehner, U; Paulweber, B; Pilger, E; Wascher, TC; Brezinschek, HP; Renner, W The functional promoter polymorphism of the coagulation factor XII gene is not associated with peripheral arterial disease.
Angiology. 2010; 61(2):211-215
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Zhang, W; Azuma, M; Lurje, G; Gordon, MA; Yang, D; Pohl, A; Ning, Y; Bohanes, P; Gerger, A; Winder, T; Hollywood, E; Danenberg, KD; Saltz, L; Lenz, HJ Molecular Predictors of Combination Targeted Therapies (Cetuximab, Bevacizumab) in Irinotecan-Refractory Colorectal Cancer (BOND-2 Study).
Anticancer Res. 2010; 30(10):4209-4217
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2009

Biebl, A; Muendlein, A; Kazakbaeva, Z; Heuberger, S; Sonderegger, G; Drexel, H; Lau, S; Nickel, R; Kabesch, M; Simma, B CD14 C-159T and toll-like receptor 4 Asp299Gly polymorphisms in surviving meningococcal disease patients.
PLoS One. 2009; 4(10):e7374-e7374 [OPEN ACCESS]
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Chang, YY; Greinix, HT; Dickinson, AM; Wolff, D; Jackson, GH; Andreesen, R; Holler, E; Hildebrandt, GC G to C transition at position -173 of MIF gene of the recipient is associated with reduced relapse rates after allogeneic stem cell transplantation.
Cytokine. 2009; 48(3): 218-225.
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Clar, H; Krippl, P; Renner, W; Langsenlehner, T; Clar, V; Windhager, R; Langsenlehner, U Association of polymorphisms of angiogenesis genes with breast cancer.
Breast Cancer Res Treat. 2009; 113(1): 197-198.
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Hoffmann, MM; Winkler, K; Renner, W; Winkelmann, BR; Seelhorst, U; Wellnitz, B; Boehm, BO; März, W Genetic variants and haplotypes of lipoprotein associated phospholipase A2 and their influence on cardiovascular disease (The Ludwigshafen Risk and Cardiovascular Health Study).
J Thromb Haemost. 2009; 7(1):41-48 [OPEN ACCESS]
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Hofmann, G; Langsenlehner, U; Langsenlehner, T; Yazdani-Biuki, B; Clar, H; Gerger, A; Fuerst, F; Samonigg, H; Krippl, P; Renner, W A common hereditary single-nucleotide polymorphism in the gene of FAS and colorectal cancer survival.
J Cell Mol Med. 2009; 13(9B):3699-3702 [OPEN ACCESS]
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Karakas, M; Hoffmann, MM; Vollmert, C; Rothenbacher, D; Meisinger, C; Winkelmann, B; Khuseyinova, N; Böhm, BO; Illig, T; März, W; Koenig, W Genetic variation in Fc gamma receptor IIa and risk of coronary heart disease: negative results from two large independent populations.
BMC Med Genet. 2009; 10(2):46-46 [OPEN ACCESS]
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Ludajic, K; Rosenmayr, A; Faé, I; Fischer, GF; Balavarca, Y; Bickeböller, H; Kalhs, P; Greinix, HT Association of HLA-E polymorphism with the outcome of hematopoietic stem-cell transplantation with unrelated donors.
Transplantation. 2009; 88(10): 1227-1228.
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Müssig, K; Staiger, H; Machicao, F; Kirchhoff, K; Guthoff, M; Schäfer, SA; Kantartzis, K; Silbernagel, G; Stefan, N; Holst, JJ; Gallwitz, B; Häring, HU; Fritsche, A Association of type 2 diabetes candidate polymorphisms in KCNQ1 with incretin and insulin secretion.
Diabetes. 2009; 58(7):1715-1720 [OPEN ACCESS]
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Polin, H; Danzer, M; Gaszner, W; Broda, D; St-Louis, M; Pröll, J; Hofer, K; Gabriel, C Identification of RHD alleles with the potential of anti-D immunization among seemingly D- blood donors in Upper Austria.
Transfusion. 2009; 49(4): 676-681.
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Resch, B; Radinger, A; Mannhalter, C; Binder, A; Haas, J; Müller, WD Interleukin-6 G(--174)C polymorphism is associated with mental retardation in cystic periventricular leucomalacia in preterm infants.
Arch Dis Child Fetal Neonatal Ed. 2009; 94(4): F304-F306.
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Schule, R; Brandt, E; Karle, KN; Tsaousidou, M; Klebe, S; Klimpe, S; Auer-Grumbach, M; Crosby, AH; Hubner, CA; Schols, L; Deufel, T; Beetz, C Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegia.
Neurogenetics. 2009; 10(2):97-104
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2008

Clar, H; Renner, W; Krippl, P; Leithner, A; Gruber, G; Langsenlehner, T; Hofmann, G; Yazdani-Biuki, B; Clar, V; Windhager, R; Langsenlehner, U The LCT 13910 C/T polymorphism as a risk factor for osteoporosis, has no impact on metastatic bone disease in breast cancer.
Breast Cancer Res Treat. 2008; 112(2): 363-365.
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Förstl, H; Bickel, H; Frölich, L; Gertz, HJ; Kurz, A; Marksteiner, J; Monsch, AU; Pantel, J; Schmidt, R; Schönknecht, P Mild cognitive impairment with predictors of rapid decline
Dtsch Med Wochenschr. 2008; 133(9):431-436
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Klintschar, M; Reichenpfader, B; Saternus, KS A functional polymorphism in the tyrosine hydroxylase gene indicates a role of noradrenalinergic signaling in sudden infant death syndrome.
J Pediatr. 2008; 153(2): 190-193.
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Langsenlehner, U; Wolf, G; Langsenlehner, T; Gerger, A; Hofmann, G; Clar, H; Wascher, TC; Paulweber, B; Samonigg, H; Krippl, P; Renner, W Genetic polymorphisms in the vascular endothelial growth factor gene and breast cancer risk. The Austrian "tumor of breast tissue: incidence, genetics, and environmental risk factors" study.
Breast Cancer Res Treat. 2008; 109(2):297-304
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Ludajic, K; Balavarca, Y; Bickeböller, H; Pohlreich, D; Kouba, M; Dobrovolna, M; Vrana, M; Rosenmayr, A; Fischer, GF; Fae, I; Kalhs, P; Greinix, HT Impact of HLA-DPB1 allelic and single amino acid mismatches on HSCT.
Br J Haematol. 2008; 142(3): 436-443.
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Ugurel, S; Schrama, D; Keller, G; Schadendorf, D; Brocker, EB; Houben, R; Zapatka, M; Fink, W; Kaufman, HL; Becker, JC Impact of the CCR5 gene polymorphism on the survival of metastatic melanoma patients receiving immunotherapy.
Cancer Immunol Immunother. 2008; 57(5):685-691
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2007

Allanore, Y; Borderie, D; Airo, P; Guiducci, S; Czirják, L; Nasonov, EL; Riemekasten, G; Caramaschi, P; Majdan, M; Krasowska, D; Friedl, E; Lemarechal, H; Ananieva, LP; Nievskaya, T; Ekindjian, OG; Matucci-Cerinic, M; Kahan, A Lack of association between three vascular endothelial growth factor gene polymorphisms and systemic sclerosis: results from a multicenter EUSTAR study of European Caucasian patients.
Ann Rheum Dis. 2007; 66(2):257-259 [OPEN ACCESS]
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