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Disease Models & Mechanisms|June 3, 2020
Diverse dystonin gene mutations cause distinct patterns of Dst isoform deficiency and phenotypic heterogeneity in Dystonia musculorum miceNozomu Yoshioka, Yudai Kabata, Momona Kuriyama, et al.
Disease Models & Mechanisms|May 20, 2020
Modeling human epigenetic disorders in mice: Beckwith-Wiedemann syndrome and Silver-Russell syndromeSuhee Chang, Marisa S Bartolomei
Disease Models & Mechanisms|August 27, 2021
Activation of innate immunity during development induces unresolved dysbiotic inflammatory gut and shortens lifespanKyoko Yamashita, Ayano Oi, Hina Kosakamoto, et al.
Disease Models & Mechanisms|September 2, 2021
Flow cytometry allows rapid detection of protein aggregates in cellular and zebrafish models of spinocerebellar ataxia 3Katherine J Robinson, Madelaine C Tym, Alison Hogan, et al.
Disease Models & Mechanisms|September 3, 2021
Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypesEva Lana-Elola, Heather Cater, Sheona Watson-Scales, et al.
Disease Models & Mechanisms|July 25, 2015
Lung necrosis and neutrophils reflect common pathways of susceptibility to Mycobacterium tuberculosis in genetically diverse, immune-competent miceMuhammad K K Niazi, Nimit Dhulekar, Diane Schmidt, et al.
Disease Models & Mechanisms|August 26, 2025
Multi-modal comparative phenotyping of knock-in mouse models of frontotemporal dementia/amyotrophic lateral sclerosisSevda Boyanova, Gareth Banks, Tatiana V Lipina, et al.
Disease Models & Mechanisms|August 26, 2025
Uncovering an antifibrotic Prrx1-lineage mesenchymal cell subpopulation in fibrotic lungsMeline Homps-Legrand, Madeleine Jaillet, Lou Deneuville, et al.
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