2023 - Research.com Genetics in Sweden Leader Award
2007 - Member of Academia Europaea
Member of the European Molecular Biology Organization (EMBO)
His scientific interests lie mostly in Mitochondrial DNA, Genetics, Mitochondrion, Respiratory chain and Mutation. His studies deal with areas such as Molecular biology and Regulation of gene expression as well as Mitochondrial DNA. His Mitochondrion research is classified as research in Cell biology.
His Respiratory chain research includes themes of Electron transport chain, Electron Transport Chain Complex Proteins, Computational biology and Neurodegeneration. His study in Mutation is interdisciplinary in nature, drawing from both Oxidative stress, Free-radical theory of aging, Ageing and Somatic cell. Nils-Göran Larsson interconnects Knockout mouse, Mitochondrial myopathy and Skeletal muscle in the investigation of issues within TFAM.
Nils-Göran Larsson mostly deals with Mitochondrial DNA, Mitochondrion, Genetics, Cell biology and Molecular biology. His Mitochondrial DNA research is multidisciplinary, incorporating elements of Mutation and Point mutation. His work deals with themes such as Oxidative stress and Somatic cell, which intersect with Mutation.
His Mitochondrion research includes elements of Oxidative phosphorylation and Transcription. His research in Cell biology intersects with topics in mitochondrial fusion, Knockout mouse, RNA and Gene knockout. His TFAM research incorporates elements of Endocrinology, Internal medicine and DNA-binding protein.
His primary areas of study are Mitochondrial DNA, Cell biology, Mitochondrion, Mitochondrial disease and Oxidative phosphorylation. The Mitochondrial DNA portion of his research involves studies in Genetics and Gene. His work on Mitochondrial nucleoid as part of general Cell biology research is often related to Snapshot, thus linking different fields of science.
The various areas that he examines in his Mitochondrion study include Nucleotide, Mitochondrial ribosome, Transcription and Mitochondrial translation. In his research, Sequence alignment, Computational biology and DNA sequencing is intimately related to Genome, which falls under the overarching field of Mitochondrial disease. His Oxidative phosphorylation study integrates concerns from other disciplines, such as Human disease, Respiratory chain and Pharmacology.
Nils-Göran Larsson mainly investigates Mitochondrial DNA, Mitochondrion, Mitochondrial disease, Genetics and Cell biology. His Mitochondrial DNA study combines topics in areas such as Mutation, Point mutation and Heart metabolism. He has researched Mutation in several fields, including Phenotype and Molecular biology.
His work in the fields of Mitochondrion, such as Inner mitochondrial membrane, intersects with other areas such as Lipid bilayer fusion. His Mitochondrial disease research incorporates themes from Chronic progressive external ophthalmoplegia, Topoisomerase, TOP3A and DNA replication. His Cell biology research is multidisciplinary, incorporating perspectives in Ribosome biogenesis, Biogenesis, Mitochondrial ribosome assembly and Pentatricopeptide repeat.
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Premature ageing in mice expressing defective mitochondrial DNA polymerase
Aleksandra Trifunovic;Anna Wredenberg;Maria Falkenberg;Johannes N. Spelbrink.
Nature (2004)
Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice
Nils-Göran Larsson;Jianming Wang;Hans Wilhelmsson;Anders Oldfors.
Nature Genetics (1998)
The role of mitochondria in aging
Ana Bratic;Nils-Göran Larsson.
Journal of Clinical Investigation (2013)
Mitochondrial transcription factor A regulates mtDNA copy number in mammals
Mats I. Ekstrand;Maria Falkenberg;Anja Rantanen;Chan Bae Park.
Human Molecular Genetics (2004)
DNA Replication and Transcription in Mammalian Mitochondria
Maria Falkenberg;Nils-Göran Larsson;Claes M. Gustafsson.
Annual Review of Biochemistry (2007)
Unraveling the biological roles of reactive oxygen species.
Michael P. Murphy;Arne Holmgren;Nils Göran Larsson;Barry Halliwell.
Cell Metabolism (2011)
Mitochondrial transcription factors B1 and B2 activate transcription of human mtDNA
Maria Falkenberg;Martina Gaspari;Anja Rantanen;Aleksandra Trifunovic.
Nature Genetics (2002)
Molecular Genetic Aspects of Human Mitochondrial Disorders
Nils-Göran Larsson;David A. Clayton.
Annual Review of Genetics (1995)
Somatic mitochondrial DNA mutations in mammalian aging.
Nils-Göran Larsson.
Annual Review of Biochemistry (2010)
Progressive parkinsonism in mice with respiratory-chain-deficient dopamine neurons.
Mats I. Ekstrand;Mügen Terzioglu;Dagmar Galter;Shunwei Zhu.
Proceedings of the National Academy of Sciences of the United States of America (2007)
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