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Disease Models & Mechanisms|December 29, 2021
Post-synaptic scaffold protein TANC2 in psychiatric and somatic disease riskLillian Garrett, Patricia Da Silva-Buttkus, Birgit Rathkolb, et al.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.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.Biochimica Et Biophysica Acta. Molecular Basis of Disease|May 25, 2023
AOX delays the onset of the lethal phenotype in a mouse model of Uqcrh (complex III) diseaseHoward T Jacobs, Marten Szibor, Birgit Rathkolb, et al.Nature Communications|December 5, 2024
X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomesTim P Hasenbein, Sarah Hoelzl, Zachary D Smith, et al.Genes & Development|March 29, 2020
The rRNA m6A methyltransferase METTL5 is involved in pluripotency and developmental programsValentina V Ignatova, Paul Stolz, Steffen Kaiser, et al.Behavioural Brain Research|October 3, 2017
Understanding gene functions and disease mechanisms: Phenotyping pipelines in the German Mouse ClinicHelmut Fuchs, Juan Antonio Aguilar-Pimentel, Oana V Amarie, et al.Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.Kidney International|December 28, 2023
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.Cell|December 5, 2025
A fin-loop-like structure in GPX4 underlies neuroprotection from ferroptosisSvenja M Lorenz, Adam Wahida, Mark J Bostock, et al.Pageof 2