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Steffi Goffart

Showing results (41-50 of 54) with videos related to

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Molecular Biology of the Cell|December 20, 2024
MRE11-independent effects of Mirin on mitochondrial DNA integrity and cellular immune responsesKoit Aasumets, Anu Hangas, Georgios Fragkoulis, et al.
Human Molecular Genetics|September 9, 2008
Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletionAnna H Hakonen, Steffi Goffart, Sanna Marjavaara, et al.
Human Molecular Genetics|January 14, 2011
Sequence-specific stalling of DNA polymerase γ and the effects of mutations causing progressive ophthalmoplegiaNeli Atanassova, Javier Miralles Fusté, Sjoerd Wanrooij, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 16, 2025
The POLγ Y951N patient mutation disrupts the switch between DNA synthesis and proofreading, triggering mitochondrial DNA instabilityJosefin M E Forslund, Tran V H Nguyen, Vimal Parkash, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 27, 2017
PrimPol is required for replication reinitiation after mtDNA damageRubén Torregrosa-Muñumer, Josefin M E Forslund, Steffi Goffart, et al.
The Journal of Biological Chemistry|June 16, 2009
Human heart mitochondrial DNA is organized in complex catenated networks containing abundant four-way junctions and replication forksJaakko L O Pohjoismäki, Steffi Goffart, Henna Tyynismaa, et al.
Nature Metabolism|August 12, 2020
Reply to: Proofreading deficiency in mitochondrial DNA polymerase does not affect total dNTP pools in mouse embryosRiikka H Hämäläinen, Juan C Landoni, Kati J Ahlqvist, et al.
Nature Metabolism|August 12, 2020
Author Correction: Defects in mtDNA replication challenge nuclear genome stability through nucleotide depletion and provide a unifying mechanism for mouse progeriasRiikka H Hämäläinen, Juan C Landoni, Kati J Ahlqvist, et al.
Nature Metabolism|July 23, 2020
Defects in mtDNA replication challenge nuclear genome stability through nucleotide depletion and provide a unifying mechanism for mouse progeriasRiikka H Hämäläinen, Juan C Landoni, Kati J Ahlqvist, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|August 22, 2016
Chemoproteomic, biochemical and pharmacological approaches in the discovery of inhibitors targeting human α/β-hydrolase domain containing 11 (ABHD11)Dina Navia-Paldanius, Jayendra Z Patel, Miriam López Navarro, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Molecular Biology of the Cell|December 20, 2024
MRE11-independent effects of Mirin on mitochondrial DNA integrity and cellular immune responsesKoit Aasumets, Anu Hangas, Georgios Fragkoulis, et al.
Human Molecular Genetics|September 9, 2008
Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletionAnna H Hakonen, Steffi Goffart, Sanna Marjavaara, et al.
Human Molecular Genetics|January 14, 2011
Sequence-specific stalling of DNA polymerase γ and the effects of mutations causing progressive ophthalmoplegiaNeli Atanassova, Javier Miralles Fusté, Sjoerd Wanrooij, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 16, 2025
The POLγ Y951N patient mutation disrupts the switch between DNA synthesis and proofreading, triggering mitochondrial DNA instabilityJosefin M E Forslund, Tran V H Nguyen, Vimal Parkash, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 27, 2017
PrimPol is required for replication reinitiation after mtDNA damageRubén Torregrosa-Muñumer, Josefin M E Forslund, Steffi Goffart, et al.
The Journal of Biological Chemistry|June 16, 2009
Human heart mitochondrial DNA is organized in complex catenated networks containing abundant four-way junctions and replication forksJaakko L O Pohjoismäki, Steffi Goffart, Henna Tyynismaa, et al.
Nature Metabolism|August 12, 2020
Reply to: Proofreading deficiency in mitochondrial DNA polymerase does not affect total dNTP pools in mouse embryosRiikka H Hämäläinen, Juan C Landoni, Kati J Ahlqvist, et al.
Nature Metabolism|August 12, 2020
Author Correction: Defects in mtDNA replication challenge nuclear genome stability through nucleotide depletion and provide a unifying mechanism for mouse progeriasRiikka H Hämäläinen, Juan C Landoni, Kati J Ahlqvist, et al.
Nature Metabolism|July 23, 2020
Defects in mtDNA replication challenge nuclear genome stability through nucleotide depletion and provide a unifying mechanism for mouse progeriasRiikka H Hämäläinen, Juan C Landoni, Kati J Ahlqvist, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|August 22, 2016
Chemoproteomic, biochemical and pharmacological approaches in the discovery of inhibitors targeting human α/β-hydrolase domain containing 11 (ABHD11)Dina Navia-Paldanius, Jayendra Z Patel, Miriam López Navarro, et al.
Pageof 6