PuSH - Publication Server of Helmholtz Zentrum München

245 Records found.
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221.
Schormair, B. et al.: PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. Nat. Genet. 40, 946-948 (2008)
222.
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)
223.
den Hollander, A.I.* et al.: Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis. Nat. Genet. 39, 889-895 (2007)
224.
Horn, C.* et al.: Splinkerette PCR for more efficient characterization of gene trap events. Nat. Genet. 39, 933-935 (2007)
225.
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)
226.
Arking, D.E.* et al.: A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. Nat. Genet. 38, 644-651 (2006)
227.
Consonni, C.* et al.: Conserved requirement for a plant host cell protein in powdery mildew pathogenesis. Nat. Genet. 38, 716-720 (2006)
228.
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)
229.
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)
230.
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)
231.
Austin, C.P.* & Wurst, W.: The Knockout Mouse Project. Nat. Genet. 36, 921-924 (2004)
232.
Auwerx, J.* ; Hrabě de Angelis, M. & Wurst, W.: The European dimension for the mouse genome mutagenesis program. Nat. Genet. 36, 925-927 (2004)
233.
Binder, E.B.* et al.: Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment. Nat. Genet. 36, 1319-1325 (2004)
234.
Cichon, S.* ; Klopp, N. & Illig, T.: Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin. Nat. Genet. 36, 783-785 (2004)
235.
Skarnes, W.C.* et al.: A public gene trap resource for mouse functional genomics. Nat. Genet. 36, 543-544 (2004)
236.
van Raamsdonk, C.D.* ; Fitch, K.R.* ; Fuchs, H. ; Hrabě de Angelis, M. & Barsh, G.S.*: Effects of G-protein mutations on skin color. Nat. Genet. 36, 961-968 (2004)
237.
Vrontou, S.* et al.: Fras1 deficiency results in cryptophthalmos, renal agenesis and blebbed phenotype in mice. Nat. Genet. 34, 209-214 (2003)
238.
Vreugde, S.* et al.: Beethoven, a mouse model for dominant, progressive hearing loss DFNA36. Nat. Genet. 30, 257-258 (2002)
239.
* et al.: Mutations in the gene encoding ε-sarcoglycan cause myoclonus-dystonia syndrome. Nat. Genet. 29, 66-69 (2001)
240.
Werner, T.: The promoter connection. Nat. Genet. 29, 105-106 (2001)