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Biochemical and Biophysical Research Communications|August 14, 2018
The heterozygous R155C VCP mutation: Toxic in humans! Harmless in mice?Christoph S Clemen, Lilli Winter, Karl-Heinz Strucksberg, 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.
Molecular and Cellular Biology|March 2, 2006
Generation and characterization of dickkopf3 mutant miceIvan del Barco Barrantes, Ana Montero-Pedrazuela, Ana Guadaño-Ferraz, 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.
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.
Scientific Reports|April 15, 2018
Defective immuno- and thymoproteasome assembly causes severe immunodeficiencyIrina Treise, Eva M Huber, Tanja Klein-Rodewald, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 14, 2015
MFAP4 Promotes Vascular Smooth Muscle Migration, Proliferation and Accelerates Neointima FormationAnders Schlosser, Bartosz Pilecki, Line E Hemstra, et al.
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