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2009
Mark The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjects
Choquet, Helene ; Cavalcanti-Proenca, Christine ; Lecoeur, Cecile ; Dina, Christian ; Cauchi, Stephane ; Vaxillaire, Martine ; Hadjadj, Samy ; Horber, Fritz ; Potoczna, Natasha and Charpentier, Guillaume , et al. (2009) In Human Molecular Genetics 18(13). p.2495-2501
- Contribution to journal › Article
Mark The P446L variant in GCKR associated with fasting plasma glucose and triglyceride levels exerts its effect through increased glucokinase activity in liver
Beer, Nicola L. ; Tribble, Nicholas D. ; McCulloch, Laura J. ; Roos, Charlotta ^LU ; Johnson, Paul R. V. ; Orho-Melander, Marju ^LU and Gloyn, Anna L. (2009) In Human Molecular Genetics 18(21). p.4081-4088
- Contribution to journal › Article
Mark Mutant huntingtin interacts with {beta}-tubulin and disrupts vesicular transport and insulin secretion.
Smith, Ruben ^LU ; Bacos, Karl ^LU ; Fedele, Valentina ^LU ; Soulet, Denis ^LU ; Jones, Helena ^LU ; Obermüller, Stefanie ^LU ; Lindqvist, Anders ^LU ; Björkqvist, Maria ^LU ; Klein, Pontus ^LU and Önnerfjord, Patrik ^LU , et al. (2009) In Human Molecular Genetics 18(20). p.3942-3954
- Contribution to journal › Article
Mark Genetic variation in GPR133 is associated with height: genome wide association study in the self-contained population of Sorbs
Toenjes, Anke ; Koriath, Moritz ; Schleinitz, Dorit ; Dietrich, Kerstin ; Boettcher, Yvonne ; Rayner, Nigel W. ; Almgren, Peter ^LU ; Enigk, Beate ; Richter, Olaf and Rohm, Silvio , et al. (2009) In Human Molecular Genetics 18(23). p.4662-4668
- Contribution to journal › Article
Mark The STAT4 gene influences the genetic predisposition to systemic sclerosis phenotype
Rueda, B. ; Broen, J. ; Simeon, C. ; Hesselstrand, Roger ^LU ; Diaz, B. ; Suarez, H. ; Ortego-Centeno, N. ; Riemekasten, G. ; Fonollosa, V. and Vonk, M. C. , et al. (2009) In Human Molecular Genetics 18(11). p.2071-2077
- Contribution to journal › Article
Mark No evidence for activation of the unfolded protein response in neuronopathic models of Gaucher disease
Farfel-Becker, Tamar ; Vitner, Einat ; Dekel, Hani ; Leshem, Noa ; Berglin-Enquist, Ida ^LU ; Karlsson, Stefan ^LU and Futerman, Anthony H. (2009) In Human Molecular Genetics 18(8). p.1482-1488
- Contribution to journal › Article
Mark The DNA methylome of pediatric acute lymphoblastic leukemia.
Davidsson, Josef ^LU ; Lilljebjörn, Henrik ^LU ; Andersson, Anna ^LU ; Veerla, Srinivas ^LU ; Heldrup, Jesper ^LU ; Behrendtz, Mikael ; Fioretos, Thoas ^LU and Johansson, Bertil ^LU (2009) In Human Molecular Genetics Aug 13. p.4054-4065
- Contribution to journal › Article
Mark Tissue-specific alternative splicing of TCF7L2
Prokunina-Olsson, Ludmila ; Welch, Cullan ; Hansson, Ola ^LU ; Adhikari, Neeta ; Scott, Laura J. ; Usher, Nicolle ; Tong, Maurine ; Sprau, Andrew ; Swift, Amy and Bonnycastle, Lori L. , et al. (2009) In Human Molecular Genetics 18(20). p.3795-3804
- Contribution to journal › Article
2008
Mark Sex differences in a transgenic rat model of Huntington's disease: decreased 17 beta-estradiol levels correlate with reduced numbers of DARPP32(+) neurons in males
Bode, Felix J. ; Stephan, Michael ; Suhling, Hendrik ; Pabst, Reinhard ; Straub, Rainer H. ; Raber, Kerstin A. ; Bonin, Michael ; Nguyen, Huu Phuc ; Riess, Olaf and Bauer, Andreas , et al. (2008) In Human Molecular Genetics 17(17). p.2595-2609
- Contribution to journal › Article
Mark Comprehensive evaluation of the genetic variants of interferon regulatory factor 5 (IRF5) reveals a novel 5 bp length polymorphism as strong risk factor for systemic lupus erythematosus
Sigurdsson, Snaevar ; Goering, Harald H H ; Kristjansdottir, Gudlaug ; Milani, Lili ; Nordmark, Gunnel ; Sandling, Johanna K ; Eloranta, Maija-Leena ; Feng, Di ; Sangster-Guity, Niquiche and Gunnarsson, Iva , et al. (2008) In Human Molecular Genetics 17(6). p.872-881
- Contribution to journal › Article

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