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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)
Hysi, P.* et al.: NOD1 variation, immunoglobulin E and asthma. Hum. Mol. Genet. 14, 935-941 (2005)
Rivera, A.* et al.: Hypoethical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk. Hum. Mol. Genet. 14, 3227-3236 (2005)
Rafalska, I.* et al.: The intranuclear localization and function of YT521-B is regulated by tyrosine phosphorylation. Hum. Mol. Genet. 13, 1535-1549 (2004)
Hörtnagel, K. ; Prokisch, H.* & Meitinger, T.: An isoform of hPANK2, deficient in pantothenate kinase-associated neurodegeneration, localizes to mitochondria. Hum. Mol. Genet. 12, 321-327 (2003)
Duetsch, G. et al.: STAT6 as an asthma candidate gene : Polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair study. Hum. Mol. Genet. 11, 613-621 (2002)
Palmer, L.J.* et al.: Meta-analysis for linkage to asthma and atopy in the chromosome 5q31-33 candidate region. Hum. Mol. Genet. 10, 891-899 (2001)
Grimm, C. et al.: Isolation and embryonic expression of the novel mouse gene Hic1, the homologue of HIC1, a canditate gene for the Miller-Dieker syndrome. Hum. Mol. Genet. 8, 697-710 (1999)
Becker, K.-F. et al.: Exon Skipping in the E-Cadherin Gene Transcript in Metastatic Human Gastric Carcinomas. Hum. Mol. Genet. 2, 803-804 (1993)