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241.
Simon-Sanchez, J.* et al.: Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat. Genet. 41, 1308-1314 (2009)
242.
Soranzo, N.* et al.: A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. Nat. Genet. 41, 1182-1190 (2009)
243.
Tregouet, D.A.* et al.: Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. Nat. Genet. 41, 283-285 (2009)
244.
van Es, M.A.* et al.: Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. Nat. Genet. 41, 1083-1087 (2009)
245.
Willer, C.J.* et al.: Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nat. Genet. 41, 25-34 (2009)
246.
Döring, A. et al.: SLC2A9 influences uric acid concentrations with pronounced sex-specific effects. Nat. Genet. 40, 430-436 (2008)
247.
Lettre, G.* et al.: Identification of ten loci associated with height highlights new biological pathways in human growth. Nat. Genet. 40, 584-591 (2008)
248.
Loos, R.J.* et al.: Common variants near MC4R are associated with fat mass, weight and risk of obesity. Nat. Genet. 40, 768-775 (2008)
249.
McGowan, K.A. et al.: Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects. Nat. Genet. 40, 963-970 (2008)
250.
Schormair, B. et al.: PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. Nat. Genet. 40, 946-948 (2008)
251.
Zeggini, E.* et al.: Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat. Genet. 40, 638-645 (2008)
252.
den Hollander, A.I.* et al.: Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis. Nat. Genet. 39, 889-895 (2007)
253.
Horn, C.* et al.: Splinkerette PCR for more efficient characterization of gene trap events. Nat. Genet. 39, 933-935 (2007)
254.
Winkelmann, J. et al.: Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. Nat. Genet. 39, 1000-1006 (2007)
255.
Arking, D.E.* et al.: A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. Nat. Genet. 38, 644-651 (2006)
256.
Consonni, C.* et al.: Conserved requirement for a plant host cell protein in powdery mildew pathogenesis. Nat. Genet. 38, 716-720 (2006)
257.
Galy, B.* et al.: Iron homeostasis in the brain : Complete iron regulatory protein 2 deficiency without symptomatic neurodegeneration in the mouse. Nat. Genet. 38, 967-969 (2006)
258.
Lorenz-Depiereux, B. et al.: DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis. Nat. Genet. 38, 1248-1250 (2006)
259.
Eumorphia Consortium (Brown, S.D.M. ; Chambon, P. ; Hrabě de Angelis, M. ; Wurst, W. ; Abe, K. ; Beckers, J. ; Busch, D.H. ; Dalke, C. ; Gailus-Durner, V. ; Elvert, R. ; Franz, T. ; Fuchs, H. ; Graw, J. ; Hölter, S.M. ; Jakob, T. ; Kalaydjiev, S. ; Kallnik, M. ; Klempt, M. ; Klingenspor, M. ; Klopstock, T. ; Lengger, C. ; Quintanilla-Martinez, L. ; Pedersen, V. ; Puk, O. ; Schneider, I. ; Vogt Weisenhorn, D.M. ; Wagner, S. ; Wolf, E.): EMPReSS: Standardized phenotype screens for functional annotation of the mouse genome. Nat. Genet. 37, 1155 (2005)
260.
Austin, C.P.* & Wurst, W.: The Knockout Mouse Project. Nat. Genet. 36, 921-924 (2004)
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