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261.
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)
262.
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)
263.
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)
264.
Austin, C.P.* & Wurst, W.: The Knockout Mouse Project. Nat. Genet. 36, 921-924 (2004)
265.
Auwerx, J.* ; Hrabě de Angelis, M. & Wurst, W.: The European dimension for the mouse genome mutagenesis program. Nat. Genet. 36, 925-927 (2004)
266.
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)
267.
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)
268.
Skarnes, W.C.* et al.: A public gene trap resource for mouse functional genomics. Nat. Genet. 36, 543-544 (2004)
269.
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)
270.
Vrontou, S.* et al.: Fras1 deficiency results in cryptophthalmos, renal agenesis and blebbed phenotype in mice. Nat. Genet. 34, 209-214 (2003)
271.
Vreugde, S.* et al.: Beethoven, a mouse model for dominant, progressive hearing loss DFNA36. Nat. Genet. 30, 257-258 (2002)
272.
* et al.: Mutations in the gene encoding ε-sarcoglycan cause myoclonus-dystonia syndrome. Nat. Genet. 29, 66-69 (2001)
273.
Werner, T.: The promoter connection. Nat. Genet. 29, 105-106 (2001)
274.
Hrabě de Angelis, M. et al.: Genome-wide, large-scale production of mutant mice by ENU mutagenesis. Nat. Genet. 25, 444-447 (2000)
275.
ADHR Consortium (Lorenz-Depiereux, B. ; Grabowski, M. ; Meitinger, T. ; Strom, T.M.): Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23. Nat. Genet. 26, 345-358 (2000)
276.
Vervoort, R.* et al.: Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa. Nat. Genet. 25, 462-466 (2000)
277.
Wiles, M.V.* et al.: Establishment of a gene-trap sequence tag library to generate mutant mice from embryonic stem cells. Nat. Genet. 24, 13-14 (2000)
278.
Timpl, P.* et al.: Impaired stress response and reduced anxiety in mice lacking a functional corticotropin-releasing hormone receptor 1. Nat. Genet. 19, 162-166 (1998)
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