Search Results

Regional distribution of polymorphisms associated to the disease-causing gene of spinocerebellar ataxia type 3 by Elter, Tim (Author) , Sturm, Daniel (Author) , Santana, Magda M. (Author) , Schaprian, Tamara (Author) , Raposo, Mafalda (Author) , Melo, Ana Rosa Vieira (Author) , Lima, Manuela (Author) , Koyak, Berkan (Author) , Oender, Demet (Author) , Grobe-Einsler, Marcus (Author) , Lopes, Sara (Author) , Silva, Patrick (Author) , de Almeida, Luís Pereira (Author) , Giunti, Paola (Author) , Garcia-Moreno, Hector (Author) , Nethisinhe, Suran (Author) , de Vries, Jeroen (Author) , van de Warrenburg, Bart P. (Author) , van Gaalen, Judith (Author) , Synofzik, Matthis (Author) , Schöls, Ludger (Author) , Reetz, Kathrin (Author) , Erdlenbruch, Friedrich (Author) , Jacobi, Heike (Author) , Infante, Jon (Author) , Rieß, Olaf (Author) , Klockgether, Thomas (Author) , Timmann, Dagmar (Author) , Thieme, Andreas (Author) , Faber, Jennifer (Author) , Hübener-Schmid, Jeannette (Author) ,

• Verlag, kostenfrei, Volltext

Glucosinolate profiles and phylogeny in Barbarea compared to other tribe Cardamineae (Brassicaceae) and Reseda (Resedaceae), based on a library of ion trap HPLC-MS/MS data of refer... by Agerbirk, Niels (Author) , Hansen, Cecilie Cetti (Author) , Olsen, Carl Erik (Author) , Kiefer, Christiane (Author) , Hauser, Thure P. (Author) , Christensen, Stina (Author) , Jensen, Karen R. (Author) , Ørgaard, Marian (Author) , Pattison, David I. (Author) , Lange, Conny Bruun Asmussen (Author) , Cipollini, Don (Author) , Koch, Marcus (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Association of DNA repair gene polymorphisms with colorectal cancer risk and treatment outcomes by Al-Shaheri, Fawaz (Author) , Al-Shami, Kamal M. (Author) , Gamal, Eshrak H. (Author) , Mahasneh, Amjad A. (Author) , Ayoub, Nehad M. (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Genome-wide association analysis for severity of coronary artery disease using the gensini scoring system by Zeller, Tanja (Author) , Kleber, Marcus E. (Author) , März, Winfried (Author) ,

• Verlag, kostenfrei, Volltext
• Verlag, kostenfrei, Volltext

Association of norepinephrine transporter (NET, SLC6A2) genotype with ADHD-related phenotypes: findings of a longitudinal study from birth to adolescence by Hohmann, Sarah (Author) , Schmidt, Martin H. (Author) , Banaschewski, Tobias (Author) , Brandeis, Daniel (Author) , Laucht, Manfred (Author) ,

• Verlag, Volltext
• Verlag, Volltext

Seven novel HLA alleles reflect different mechanisms involved in the evolution of HLA diversity: description of the new alleles and review of the literature by Adamek, Martina Maria (Author) , Klages, Cornelia (Author) , Bauer, Manuela (Author) , Kudlek, Evelina (Author) , Drechsler, Alina (Author) , Leuser, Birte (Author) , Scherer, Sabine (Author) , Opelz, Gerhard (Author) , Tran, Thuong Hien (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Is there a link between the calcium sensing receptor and Hirschsprung's disease?: A mutational analysis by Romero, Philipp (Author) , Niesler, Beate (Author) , Schmitz-Winnenthal, Friedrich Hubertus (Author) , Fitze, Guido (Author) , Holland-Cunz, Stefan (Author) ,

• Verlag, Volltext
• Verlag, Volltext

CD24 Ala57Val polymorphism predicts pathologic complete response to sequential anthracycline- and taxane-based neoadjuvant chemotherapy for primary breast cancer by Marmé, Frederik (Author) , Werft, Wiebke (Author) , Keller, Sascha (Author) , Wang, Xiaoli (Author) , Benner, Axel (Author) , Burwinkel, Barbara (Author) , Sinn, Peter (Author) , Fastner, Sarah (Author) , Sohn, Christof (Author) , Moldenhauer, Gerhard (Author) , Rupp, Christian (Author) , Rupp, Anne-Kathleen (Author) , Lichter, Peter (Author) , Altevogt, Peter (Author) , Schneeweiss, Andreas (Author) ,

• Verlag, Volltext
• Verlag, Volltext

Genetic variation in CYP2D6 impacts neural activation during cognitive tasks in humans by Stingl, Julia (Author) , Esslinger, Christine (Author) , Tost, Heike (Author) , Bilek, Edda (Author) , Kirsch, Peter (Author) , Rietschel, Marcella (Author) , Meyer-Lindenberg, Andreas (Author) ,

• Verlag, FL, Volltext
• Verlag, FL, Volltext

Polymorphisms in the apoptotic pathway gene BCL-2 and survival in small cell lung cancer by Knöfel, Lena Franziska (Author) , Werle-Schneider, Gisela (Author) , Dally, Heike (Author) , Müller, Phillip (Author) , Edler, Lutz (Author) , Bartsch, Helmut (Author) , Tuengerthal, Siegfried (Author) , Heußel, Claus Peter (Author) , Reinmuth, Niels (Author) , Thomas, Michael (Author) , Risch, Angela (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Association of the VEGF 936C>T polymorphism with FDG uptake, clinical, histopathological, and metabolic response in patients with adenocarcinomas of the esophagogastric junction by Lorenzen, Sylvie (Author) , Panzram, Benjamin (Author) , Keller, Gisela (Author) , Lordick, Florian (Author) , Herrmann, Ken (Author) , Becker, Karin (Author) , Langer, Ruppert (Author) , Schwaiger, Markus (Author) , Siewert, Jorg Rudiger (Author) , Ott, Katja (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Receptor for advanced glycation end-products (RAGE) provides a link between genetic susceptibility and environmental factors in type 1 diabetes by Forbes, Josephine M. (Author) , Söderlund, J. (Author) , Yap, F. Y. T. (Author) , Knip, M. (Author) , Andrikopoulos, S. (Author) , Ilonen, J. (Author) , Simell, O. (Author) , Veijola, R. (Author) , Sourris, K. C. (Author) , Coughlan, M. T. (Author) , Forsblom, C. (Author) , Slattery, R. (Author) , Grey, S. T. (Author) , Wessman, M. (Author) , Yamamoto, H. (Author) , Bierhaus, Angelika (Author) , Cooper, M. E. (Author) , Groop, P.-H. (Author) ,

• Verlag, lizenzpflichtig, Volltext

Polymorphisms in the CD28/CTLA4/ICOS genes: role in malignant melanoma susceptibility and prognosis? by Bouwhuis, Marna G. (Author) , Gast, Andreas (Author) , Figl, Adina (Author) , Eggermont, Alexander M. M. (Author) , Hemminki, Kari (Author) , Schadendorf, Dirk (Author) , Kumar, Rajiv (Author) ,

• Verlag, lizenzpflichtig, Volltext

ACE I/D polymorphism is a risk factor of Alzheimer's disease but not of vascular dementia by Kölsch, Heike (Author) , Jessen, F. (Author) , Freymann, N. (Author) , Kreis, Markus (Author) , Hentschel, Frank (Author) , Maier, W. (Author) , Heun, R. (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Genotype relationships in the CYP3A locus in Caucasians by Dally, Heike (Author) , Bartsch, Helmut (Author) , Edler, Lutz (Author) , Schmezer, Peter (Author) , Spiegelhalder, Bertold (Author) , Dienemann, Hendrik (Author) , Drings, Peter (Author) , Kayser, Klaus (Author) , Schulz, Volker (Author) , Risch, Angela (Author) ,

• Verlag, Volltext
• Verlag, Volltext

Promoter polymorphism of the 5-HT transporter and Alzheimer's disease by Hu, Mei (Author) , Retz, Wolfgang (Author) , Baader, Miriam (Author) , Pesold, Brigitte (Author) , Adler, Georg (Author) , Henn, Fritz A. (Author) , Rösler, Michael (Author) , Thome, Johannes (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

TAP polymorphism does not influence transport of peptide variants in mice and humans by Obst, Reinhard (Author) , Armandola, Elena A. (Author) , Nijenhuis, Marga (Author) , Momburg, Frank (Author) , Hämmerling, Günter J. (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext