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Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 9, 2023
Knockout mouse models as a resource for the study of rare diseasesPatricia da Silva-Buttkus, Nadine Spielmann, Tanja Klein-Rodewald, et al.Plos One|March 23, 2016
Generation and Standardized, Systemic Phenotypic Analysis of Pou3f3L423P Mutant MiceSudhir Kumar, Birgit Rathkolb, Elisabeth Kemter, et al.The EMBO Journal|July 27, 2014
Aberrant methylation of tRNAs links cellular stress to neuro-developmental disordersSandra Blanco, Sabine Dietmann, Joana V Flores, et al.Acta Neuropathologica|April 15, 2017
Spinal poly-GA inclusions in a C9orf72 mouse model trigger motor deficits and inflammation without neuron lossMartin H Schludi, Lore Becker, Lillian Garrett, et al.Plos One|November 27, 2013
A broad phenotypic screen identifies novel phenotypes driven by a single mutant allele in Huntington's disease CAG knock-in miceSabine M Hölter, Mary Stromberg, Marina Kovalenko, et al.Science Advances|April 11, 2025
Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenitaAdrián Sanz-Moreno, Lore Becker, Kan Xie, et al.Plos One|December 16, 2014
MTO1-deficient mouse model mirrors the human phenotype showing complex I defect and cardiomyopathyLore Becker, Eva Kling, Evelyn Schiller, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 27, 2021
A comprehensive phenotypic characterization of a whole-body Wdr45 knock-out mouseCaroline A Biagosch, Silvia Vidali, Michael Faerberboeck, et al.The Journal of Biological Chemistry|February 12, 2014
Mitochondrial dysfunction and decrease in body weight of a transgenic knock-in mouse model for TDP-43Carola Stribl, Aladin Samara, Dietrich Trümbach, et al.BMC Developmental Biology|December 24, 2008
Pleiotropic effects in Eya3 knockout miceTorben Söker, Claudia Dalke, Oliver Puk, et al.Pageof 10