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21.
Diener, S. et al.: Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia. Mamm. Genome 27, 111-121 (2016)
22.
Raess, M.* ; de Castro, A.A.* ; Gailus-Durner, V. ; Fessele, S.* & Hrabě de Angelis, M.: INFRAFRONTIER: A European resource for studying the functional basis of human disease. Mamm. Genome 27, 445-450 (2016)
23.
Sabrautzki, S. et al.: Viable EdnraY129F mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation. Mamm. Genome 27, 587-598 (2016)
24.
Bönisch, C. et al.: Dexamethasone treatment alters insulin, leptin, and adiponectin levels in male mice as observed in DIO but does not lead to alterations of metabolic phenotypes in the offspring. Mamm. Genome 27, 17-28 (2015)
25.
Keeney, J.G.* et al.: Generation of mice lacking DUF1220 protein domains: Effects on fecundity and hyperactivity. Mamm. Genome 26, 33-42 (2015)
26.
Maier, H. et al.: Principles and application of LIMS in mouse clinics. Mamm. Genome 26, 467-481 (2015)
27.
Rosen, B.* ; Schick, J. & Wurst, W.: Beyond knockouts: The International Knockout Mouse Consortium delivers modular and evolving tools for investigating mammalian genes. Mamm. Genome 26, 456-466 (2015)
28.
Rozman, J. ; Klingenspor, M. & Hrabě de Angelis, M.: A review of standardized metabolic phenotyping of animal models. Mamm. Genome 25, 497-507 (2014)
29.
Szymczak, W. et al.: Online breath gas analysis in unrestrained mice by hs-PTR-MS. Mamm. Genome 25, 129-140 (2014)
30.
Fuchs, H. ; Gau, C. ; Hans, W. ; Gailus-Durner, V. & Hrabě de Angelis, M.: Long-term experiment to study the development, interaction and influencing factors of DEXA parameters. Mamm. Genome 24, 376-388 (2013)
31.
Puk, O. ; Hrabě de Angelis, M. & Graw, J.: Longitudinal fundus and retinal studies with SD-OCT: A comparison of five mouse inbred strains. Mamm. Genome 24, 198-205 (2013)
32.
Puk, O. ; Hrabě de Angelis, M. & Graw, J.: Lens density tracking in mice by Scheimpflug imaging. Mamm. Genome 24, 295-302 (2013)
33.
Sun, M. et al.: Crybb2 coding for βB2-crystallin affects sensorimotor gating and hippocampal function. Mamm. Genome 24, 333-348 (2013)
34.
Ayadi, A.* et al.: Mouse large-scale phenotyping initiatives: Overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute mouse genetics project. Mamm. Genome 23, 600-610 (2012)
35.
Bradley, A.* et al.: The mammalian gene function resource: The International Knockout Mouse Consortium. Mamm. Genome 23, 580-586 (2012)
36.
Donahue, L. R.* et al.: Centralized mouse repositories. Mamm. Genome 23, 559-571 (2012)
37.
Fuchs, H. et al.: Innovations in phenotyping of mouse models in the German Mouse Clinic. Mamm. Genome 23, 611-622 (2012)
38.
Guan, M.* ; Marschall, S. ; Raspa, M.* ; Pickard, A.R.* & Fray, M.D.*: Overview of new developments in and the future of cryopreservation in the laboratory mouse. Mamm. Genome 23, 572-579 (2012)
39.
Sabrautzki, S. et al.: New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis. Mamm. Genome 23, 416-430 (2012)
40.
Stein, C.* et al.: Clinical chemistry of human FcRn transgenic mice. Mamm. Genome 23, 259-269 (2012)
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