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The Journal of Allergy and Clinical Immunology|September 5, 2007
Novel mouse mutants with primary cellular immunodeficiencies generated by genome-wide mutagenesisThilo Jakob, Gabriele V Köllisch, Maike Howaldt, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 18, 2012
The hepatic phosphatidylcholine transporter ABCB4 as modulator of glucose homeostasisKatrin Hochrath, Marcin Krawczyk, Reinhild Goebel, et al.
Scientific Reports|January 20, 2018
Epigallocatechin gallate (EGCG) reduces the intensity of pancreatic amyloid fibrils in human islet amyloid polypeptide (hIAPP) transgenic miceAndras Franko, Diana C Rodriguez Camargo, Annett Böddrich, et al.
Communications Biology|October 31, 2020
PAX6 mutation alters circadian rhythm and β cell function in mice without affecting glucose toleranceNirav Florian Chhabra, Oana Veronica Amarie, Moya Wu, 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.
European Journal of Oral Sciences|July 21, 2012
Does enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse linesHelmut Fuchs, Sibylle Sabrautzki, Hartwig Seedorf, et al.
Plos One|April 18, 2013
Mouse nuclear myosin I knock-out shows interchangeability and redundancy of myosin isoforms in the cell nucleusTomáš Venit, Rastislav Dzijak, Alžběta Kalendová, et al.
Scientific Reports|November 17, 2022
New C3H Kit<sup>N824K/WT</sup> cancer mouse model develops late-onset malignant mammary tumors with high penetranceTanja Klein-Rodewald, Kateryna Micklich, Adrián Sanz-Moreno, 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.
Molecular Metabolism|April 22, 2018
Growth hormone receptor-deficient pigs resemble the pathophysiology of human Laron syndrome and reveal altered activation of signaling cascades in the liverArne Hinrichs, Barbara Kessler, Mayuko Kurome, et al.
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