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Barbalic, M.* et al.: Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. Hum. Mol. Genet. 19, 1863-1872 (2010)
Burbulla, L.F.* et al.: Dissecting the role of the mitochondrial chaperone mortalin in Parkinson's disease: Functional impact of disease-related variants on mitochondrial homeostasis. Hum. Mol. Genet. 19, 4437-4452 (2010)
Eijgelsheim, M.* et al.: Genome-wide association analysis identifies multiple loci related to resting heart rate. Hum. Mol. Genet. 19, 3885-3894 (2010)
Kettunen, J.* et al.: European lactase persistence genotype shows evidence of association with increase in body mass index. Hum. Mol. Genet. 19, 1129-1136 (2010)
Perry, J.R.B.* et al.: Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes. Hum. Mol. Genet. 19, 535-544 (2010)
Qi, L.* et al.: Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes. Hum. Mol. Genet. 19, 2706-2715 (2010)
Chio, A.* et al.: A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. Hum. Mol. Genet. 18, 1524-1532 (2009)
Deplazes, J.* et al.: Rac1 and Rho contribute to the migratory and invasive phenotype associated with somatic E-cadherin mutation. Hum. Mol. Genet. 18, 3632-3644 (2009)
Johansson, A.* et al.: Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis. Hum. Mol. Genet. 18, 373-380 (2009)
Kollerits, B.* et al.: Genetic evidence for a role of adiponutrin in the metabolism of apolipoprotein b-containing lipoproteins. Hum. Mol. Genet. 18, 4669-4676 (2009)
Org, E.* et al.: Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations. Hum. Mol. Genet. 18, 2288-2296 (2009)
Schneider, M.R.* ; Wolf, E.* ; Braun, J.* ; Kolb, H.-J. & Adler, H.: Canine embryo-derived stem cells and models for human diseases. Hum. Mol. Genet. 17, R42-R47 (2008)
Baessler, A.* et al.: Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery disease. Hum. Mol. Genet. 16, 887-899 (2007)
Koch, W.* et al.: Association of variants in the BAT1-NFKBIL1-LTA genomic region with protection against myocardial infarction in Europeans. Hum. Mol. Genet. 16, 1821-1827 (2007)
Perveen, R.* ; Favor, J. ; Jamieson, R.V.* ; Ray, D.W.* & Black, G.C.*: A heterozygous c-Maf transactivation domain mutation causes congenital cataract and enhances target gene activation. Hum. Mol. Genet. 16, 1030-1038 (2007)
Gloeckner, C.J. et al.: The parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity. Hum. Mol. Genet. 15, 223-232 (2006)
Huang, K.M.* et al.: Xcat, a novel mouse model for Nance-Horan syndrome inhibits expression of the cytoplasmic-targeted Nhs1 isoform. Hum. Mol. Genet. 15, 319-327 (2006)
Riemenschneider, M.* et al.: A functional polymorphism within plasminogen activator urokinase (PLAU) is associated with Alzheimer's disease. Hum. Mol. Genet. 15, 2446-2456 (2006)
Schaeffer, L. et al.: Common genetic variants of the FADS1 FADS2 gene cluster and their reconstructed haplotypes are associated with the fatty acid composition in phospholipids Hum. Mol. Genet. 15, 1745-1756 (2006)
Benet-Pagès, A. ; Orlik, P.* ; Strom, T.M. & Lorenz-Depiereux, B.: An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia. Hum. Mol. Genet. 14, 385-390 (2005)