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Genetic and Mitochondrial Metabolic Analyses of an Atypical Form of Leigh Syndrome.
Uittenbogaard M, Sen K, Whitehead M, Brantner CA, Wang Y, Wong LJ, Gropman A, Chiaramello A. Uittenbogaard M, et al. Among authors: brantner ca. Front Cell Dev Biol. 2021 Dec 22;9:767407. doi: 10.3389/fcell.2021.767407. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 35004675 Free PMC article.
Molecular genetic and mitochondrial metabolic analyses confirm the suspected mitochondrial etiology in a pediatric patient with an atypical form of alternating hemiplegia of childhood.
Gropman A, Uittenbogaard M, Brantner CA, Wang Y, Wong LJ, Chiaramello A. Gropman A, et al. Among authors: brantner ca. Mol Genet Metab Rep. 2020 May 28;24:100609. doi: 10.1016/j.ymgmr.2020.100609. eCollection 2020 Sep. Mol Genet Metab Rep. 2020. PMID: 32489883 Free PMC article.
The m.11778 A > G variant associated with the coexistence of Leber's hereditary optic neuropathy and multiple sclerosis-like illness dysregulates the metabolic interplay between mitochondrial oxidative phosphorylation and glycolysis.
Uittenbogaard M, Brantner CA, Fang Z, Wong LJ, Gropman A, Chiaramello A. Uittenbogaard M, et al. Among authors: brantner ca. Mitochondrion. 2019 May;46:187-194. doi: 10.1016/j.mito.2018.06.001. Epub 2018 Jun 8. Mitochondrion. 2019. PMID: 29890302 Free PMC article.
Exosomes originating from infection with the cytoplasmic single-stranded RNA virus Rift Valley fever virus (RVFV) protect recipient cells by inducing RIG-I mediated IFN-B response that leads to activation of autophagy.
Alem F, Olanrewaju AA, Omole S, Hobbs HE, Ahsan N, Matulis G, Brantner CA, Zhou W, Petricoin EF, Liotta LA, Caputi M, Bavari S, Wu Y, Kashanchi F, Hakami RM. Alem F, et al. Among authors: brantner ca. Cell Biosci. 2021 Dec 25;11(1):220. doi: 10.1186/s13578-021-00732-z. Cell Biosci. 2021. PMID: 34953502 Free PMC article.
34 results