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Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 16, 2020
A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypesHeike Kollmus, Helmut Fuchs, Christoph Lengger, et al.
The Journal of Clinical Investigation|July 19, 2013
Rapamycin extends murine lifespan but has limited effects on agingFrauke Neff, Diana Flores-Dominguez, Devon P Ryan, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 26, 2012
Cytochrome c oxidase subunit 4 isoform 2-knockout mice show reduced enzyme activity, airway hyporeactivity, and lung pathologyMaik Hüttemann, Icksoo Lee, Xiufeng Gao, et al.
American Journal of Ophthalmology|June 17, 2026
SEARCHING FOR NEW GENES THAT CAUSE USHER SYNDROMEAla Moshiri, Niusha Kasiri, Michael Shea, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 7, 2009
Systemic first-line phenotypingValérie Gailus-Durner, Helmut Fuchs, Thure Adler, 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.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 18, 2018
A mouse model for intellectual disability caused by mutations in the X-linked 2'‑O‑methyltransferase Ftsj1 geneLars R Jensen, Lillian Garrett, Sabine M Hölter, et al.
Nature|November 5, 2020
Inhibition of LTβR signalling activates WNT-induced regeneration in lungThomas M Conlon, Gerrit John-Schuster, Danijela Heide, et al.
EMBO Molecular Medicine|November 9, 2021
Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypesSilvia Vidali, Raffaele Gerlini, Kyle Thompson, et al.
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