Papers authored by Nils-Göran Larsson
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Göran Andersson,
E. Gerhart H. Wagner,
E. Gerhart H. Wagner,
Ake Hedhammar,
Åke Hedhammar,
Rolf Wibom,
Leif Andersson
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Rolf Wibom,
Gunilla Malm,
Inger Nennesmo,
Ulrika von Döbeln,
Nils-Göran Larsson
MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome
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Claes M. Gustafsson
MTERF2 is a nucleoid component in mammalian mitochondria
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Structure Casts Light on mtDNA Replication
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Yolanda Camara,
Anna Wredenberg,
Maria Antonietta Calvaruso,
Leo G. J. Nijtmans,
Jan Nedergaard,
Barbara Cannon,
Nils-Göran Larsson ,
Aleksandra Trifunovic
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Introduction: Euromit VII - summarizing 50 years of research on mitochondrial disease
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Pierre Chambon,
Larsson Ng,
Eva Lindqvist,
Nils-Goeran Larsson ,
Lars Olson
and 4 other authors
Nurr1 Is Required for Maintenance of Maturing and Adult Midbrain Dopamine Neurons
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Joseph D. Bruton,
Håkan Westerblad
Increased mitochondrial Ca 2+ and decreased sarcoplasmic reticulum Ca 2+ in mitochondrial myopathy
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Age-associated mosaic respiratory chain deficiency causes trans-neuronal degeneration
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José P. Silva,
Francisco H. Andrade,
Anders J. Dahlstedt,
Shi-Jin Zhang,
Abram Katz,
Nils-Göran Larsson ,
Håkan Westerblad
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Christoph Freyer,
Joanna L. Elson,
Anna Wredenberg,
Zekiye Cansu,
Aleksandra Trifunovic,
Nils-Göran Larsson
Strong Purifying Selection in Transmission of Mammalian Mitochondrial DNA
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Christoph Freyer,
Joanna L. Elson,
Nils-Göran Larsson
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Complex I: A complex gateway to the powerhouse
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Barbara Canlon
Somatic mtDNA mutations cause progressive hearing loss in the mouse
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MTERF3 is a negative regulator of mammalian mtDNA transcription
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Claes M. Gustafsson
DNA Replication and Transcription in Mammalian Mitochondria
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Mitochondrial dysfunction in mammalian ageing
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