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Plos One|June 16, 2012
Large-scale phenotyping of an accurate genetic mouse model of JNCL identifies novel early pathology outside the central nervous systemJohn F Staropoli, Larissa Haliw, Sunita Biswas, 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.Methods (San Diego, Calif.)|August 17, 2010
Mouse phenotypingHelmut Fuchs, Valérie Gailus-Durner, Thure Adler, et al.Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Implication of <i>FOXD2</i> dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.Cell|June 4, 2009
A humanized version of Foxp2 affects cortico-basal ganglia circuits in miceWolfgang Enard, Sabine Gehre, Kurt Hammerschmidt, et al.Nature Communications|November 12, 2022
Deep phenotyping and lifetime trajectories reveal limited effects of longevity regulators on the aging process in C57BL/6J miceKan Xie, Helmut Fuchs, Enzo Scifo, et al.G3 (Bethesda, Md.)|November 6, 2016
The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic AlterationsHelmut Fuchs, Sibylle Sabrautzki, Gerhard K H Przemeck, 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.Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 29, 2012
Innovations in phenotyping of mouse models in the German Mouse ClinicHelmut Fuchs, Valérie Gailus-Durner, Susanne Neschen, et al.Nature Genetics|July 28, 2015
Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinicsMartin Hrabě de Angelis, George Nicholson, Mohammed Selloum, et al.Pageof 7