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Pediatric Diabetes|January 20, 2021
Associations between diet, the gut microbiome and short chain fatty acids in youth with islet autoimmunity and type 1 diabetesJessica E Harbison, Rebecca L Thomson, John M Wentworth, et al.
Cell Metabolism|September 17, 2019
Fibroblast Growth Factor 21 Drives Dynamics of Local and Systemic Stress Responses in Mitochondrial Myopathy with mtDNA DeletionsSaara Forsström, Christopher B Jackson, Christopher J Carroll, et al.
The Journal of Clinical Investigation|October 27, 2022
Mitochondrial dysfunction reactivates α-fetoprotein expression that drives copper-dependent immunosuppression in mitochondrial disease modelsKimberly A Jett, Zakery N Baker, Amzad Hossain, et al.
Cell Metabolism|March 1, 2016
Mitochondrial DNA Replication Defects Disturb Cellular dNTP Pools and Remodel One-Carbon MetabolismJoni Nikkanen, Saara Forsström, Liliya Euro, et al.
Nature Metabolism|October 1, 2025
DDHD2 provides a flux of saturated fatty acids for neuronal energy and functionSaber H Saber, Nyakuoy Yak, Xuan Ling Hilary Yong, et al.
Neurobiology of Disease|November 4, 2018
Mice harbouring a SCA28 patient mutation in AFG3L2 develop late-onset ataxia associated with enhanced mitochondrial proteotoxicityCecilia Mancini, Eriola Hoxha, Luisa Iommarini, et al.
EMBO Molecular Medicine|September 12, 2018
OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defectKyle Thompson, Nicole Mai, Monika Oláhová, et al.
Nature Communications|December 4, 2025
Hologenomic analysis of rectal mucus sampling for detection of adenomatous polyps and colorectal cancerAndrew J Tock, Kamrun S Patel, Emma Morales-Walker, et al.
American Journal of Human Genetics|October 29, 2021
Bi-allelic variants in the mitochondrial RNase P subunit PRORP cause mitochondrial tRNA processing defects and pleiotropic multisystem presentationsIrit Hochberg, Leigh A M Demain, Julie Richer, et al.
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