Christopher B. Jackson Department of Biochemistry and Developmental Biology, Faculty of Medicine University of Helsinki Biography Publications Institution JoVE Articles Christopher B. Jackson has not added a biography. If you are Christopher B. Jackson and would like to personalize this page please email our Author Liaison for assistance. Publications The Roles of Assembly Factors in Mammalian Mitoribosome Biogenesis Mitochondrion. Sep, 2021 | Pubmed ID: 34339868 In-frame Deletion in Canine PITRM1 is Associated with a Severe Early-onset Epilepsy, Mitochondrial Dysfunction and Neurodegeneration Human Genetics. Nov, 2021 | Pubmed ID: 33835239 Progressive Myoclonus Epilepsies-Residual Unsolved Cases Have Marked Genetic Heterogeneity Including Dolichol-dependent Protein Glycosylation Pathway Genes American Journal of Human Genetics. 04, 2021 | Pubmed ID: 33798445 SUCLA2 Mutations Cause Global Protein Succinylation Contributing to the Pathomechanism of a Hereditary Mitochondrial Disease Nature Communications. 11, 2020 | Pubmed ID: 33230181 Therapeutic Manipulation of MtDNA Heteroplasmy: A Shifting Perspective Trends in Molecular Medicine. 07, 2020 | Pubmed ID: 32589937 3D Co-culture of HiPSC-Derived Cardiomyocytes With Cardiac Fibroblasts Improves Tissue-Like Features of Cardiac Spheroids Frontiers in Molecular Biosciences. 2020 | Pubmed ID: 32118040 Fibroblast Growth Factor 21 Drives Dynamics of Local and Systemic Stress Responses in Mitochondrial Myopathy with MtDNA Deletions Cell Metabolism. 12, 2019 | Pubmed ID: 31523008 Novel Synonymous and Missense Variants in FGFR1 Causing Hartsfield Syndrome American Journal of Medical Genetics. Part A. 12, 2019 | Pubmed ID: 31512363 A Variant in MRPS14 (uS14m) Causes Perinatal Hypertrophic Cardiomyopathy with Neonatal Lactic Acidosis, Growth Retardation, Dysmorphic Features and Neurological Involvement Human Molecular Genetics. 02, 2019 | Pubmed ID: 30358850 Neutrophil Extracellular Trap Formation Requires OPA1-dependent Glycolytic ATP Production Nature Communications. 07, 2018 | Pubmed ID: 30054480 Reply to 'Letter to Editor by Finsterer J and Zarrouk-Mahjoub S: Phenotypic Manifestations of the M.8969G>A Variant' Neurogenetics. 05, 2018 | Pubmed ID: 29480378 Defective Mitochondrial ATPase Due to Rare MtDNA M.8969G>A Mutation-causing Lactic Acidosis, Intellectual Disability, and Poor Growth Neurogenetics. 01, 2018 | Pubmed ID: 29350304 Loss of MtDNA Activates Astrocytes and Leads to Spongiotic Encephalopathy Nature Communications. 01, 2018 | Pubmed ID: 29302033 A Novel Mitochondrial ATP6 Frameshift Mutation Causing Isolated Complex V Deficiency, Ataxia and Encephalomyopathy European Journal of Medical Genetics. Jun, 2017 | Pubmed ID: 28412374 SDHA Mutation with Dominant Transmission Results in Complex II Deficiency with Ocular, Cardiac, and Neurologic Involvement American Journal of Medical Genetics. Part A. Jan, 2017 | Pubmed ID: 27683074 A Novel Mutation in BCS1L Associated with Deafness, Tubulopathy, Growth Retardation and Microcephaly European Journal of Pediatrics. Apr, 2016 | Pubmed ID: 26563427 La respirométrie à haute résolution pour évaluer la bioénergétique dans les cellules et les tissus à l’aide de respiromètres à chambre et à plaques Ryan Awadhpersad1, Christopher B. Jackson1 1Department of Biochemistry and Developmental Biology, Faculty of Medicine, University of Helsinki JoVE 63000 Biology
La respirométrie à haute résolution pour évaluer la bioénergétique dans les cellules et les tissus à l’aide de respiromètres à chambre et à plaques Ryan Awadhpersad1, Christopher B. Jackson1 1Department of Biochemistry and Developmental Biology, Faculty of Medicine, University of Helsinki JoVE 63000 Biology
