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Proteomics|July 5, 2007
High Performance Proteomics: 7th HUPO Brain Proteome Project Workshop March 7-9, 2007 Wellcome Trust Conference Centre, Hinxton, UKMichael Hamacher, Christian Stephan, Martin Eisenacher, et al.
Scientific Reports|May 27, 2017
Extensive phenotypic characterization of a new transgenic mouse reveals pleiotropic perturbations in physiology due to mesenchymal hGH minigene expressionAimilios Kaklamanos, Jan Rozman, Manolis Roulis, et al.
Plos One|August 12, 2015
Cox4i2, Ifit2, and Prdm11 Mutant Mice: Effective Selection of Genes Predisposing to an Altered Airway Inflammatory Response from a Large Compendium of Mutant Mouse LinesMarion Horsch, Juan Antonio Aguilar-Pimentel, Clemens Bönisch, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 25, 2016
Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasiaSusanne Diener, Sieglinde Bayer, Sibylle Sabrautzki, et al.
Human Molecular Genetics|May 17, 2012
Cardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanismsFrank Thiele, Christian M Cohrs, Armando Flor, et al.
Plos One|October 28, 2016
Sphingomyelin Synthase 1 Is Essential for Male Fertility in MiceAnke Wittmann, Marcus O W Grimm, Harry Scherthan, et al.
Plos One|November 9, 2013
Standardized, systemic phenotypic analysis of Umod(C93F) and Umod(A227T) mutant miceElisabeth Kemter, Petra Prückl, Birgit Rathkolb, et al.
Journal of Inherited Metabolic Disease|February 3, 2016
Mildly compromised tetrahydrobiopterin cofactor biosynthesis due to Pts variants leads to unusual body fat distribution and abdominal obesity in miceGermaine Korner, Tanja Scherer, Dea Adamsen, et al.
Journal of Biomedical Science|August 19, 2017
Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 <sup>I27N</sup> mutant miceSudhir Kumar, Birgit Rathkolb, Sibylle Sabrautzki, et al.
Iscience|October 27, 2025
Abcb5-deficient mice show a subtle, pleiotropic phenotype indicating a role for this transporter in intermediary metabolismJean-Pierre Gillet, Louise Gerard, Wilfred Vieira, et al.
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