List of works - Rolf Wibom

A switch in metabolism precedes increased mitochondrial biogenesis in respiratory chain-deficient mouse hearts

scholarly article

Altered dopamine metabolism and increased vulnerability to MPTP in mice with partial deficiency of mitochondrial complex I in dopamine neurons

scientific article published on 16 November 2011

Complete Deletion of a POLG1 Allele in a Patient with Alpers Syndrome

scientific article published on 20 October 2011

Defects of mitochondrial RNA turnover lead to the accumulation of double-stranded RNA in vivo

scientific article published on 31 July 2019

Impaired mitochondrial transport and Parkin-independent degeneration of respiratory chain-deficient dopamine neurons in vivo

scientific article

Increased mitochondrial mass in mitochondrial myopathy mice

scientific article

LRPPRC is necessary for polyadenylation and coordination of translation of mitochondrial mRNAs

scientific article

MTERF1 binds mtDNA to prevent transcriptional interference at the light-strand promoter but is dispensable for rRNA gene transcription regulation

scientific journal article

MTERF3 is a negative regulator of mammalian mtDNA transcription

scientific article

MTERF3 regulates mitochondrial ribosome biogenesis in invertebrates and mammals

scientific article

MTERF4 regulates translation by targeting the methyltransferase NSUN4 to the mammalian mitochondrial ribosome

scientific article

Maintenance of respiratory chain function in mouse hearts with severely impaired mtDNA transcription

scientific article published on 20 June 2010

Methylation of 12S rRNA is necessary for in vivo stability of the small subunit of the mammalian mitochondrial ribosome

scientific article

MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome

scientific article

Mutations in the mitochondrial tRNA Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy.

scientific article

Mutations in the mitochondrial tRNASer(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy

scientific article published on 19 July 2012

Respiratory chain dysfunction in skeletal muscle does not cause insulin resistance

scientific article

SOD2 overexpression: enhanced mitochondrial tolerance but absence of effect on UCP activity

scientific article published on 10 November 2005

Secondary metabolic effects in complex I deficiency

scientific article published in October 2005

Sensory ataxic neuropathy in golden retriever dogs is caused by a deletion in the mitochondrial tRNATyr gene

scientific article

Somatic mtDNA mutations cause aging phenotypes without affecting reactive oxygen species production

scientific article

TEFM regulates both transcription elongation and RNA processing in mitochondria.

scientific article

The bicoid stability factor controls polyadenylation and expression of specific mitochondrial mRNAs in Drosophila melanogaster

scientific article

Two novel mutations in thymidine kinase-2 cause early onset fatal encephalomyopathy and severe mtDNA depletion

scientific article published on 18 January 2010

List of works by Rolf Wibom

A switch in metabolism precedes increased mitochondrial biogenesis in respiratory chain-deficient mouse hearts

Altered dopamine metabolism and increased vulnerability to MPTP in mice with partial deficiency of mitochondrial complex I in dopamine neurons

Complete Deletion of a POLG1 Allele in a Patient with Alpers Syndrome

Defects of mitochondrial RNA turnover lead to the accumulation of double-stranded RNA in vivo

Impaired mitochondrial transport and Parkin-independent degeneration of respiratory chain-deficient dopamine neurons in vivo

Increased mitochondrial mass in mitochondrial myopathy mice

LRPPRC is necessary for polyadenylation and coordination of translation of mitochondrial mRNAs

MTERF1 binds mtDNA to prevent transcriptional interference at the light-strand promoter but is dispensable for rRNA gene transcription regulation

MTERF3 is a negative regulator of mammalian mtDNA transcription

MTERF3 regulates mitochondrial ribosome biogenesis in invertebrates and mammals

MTERF4 regulates translation by targeting the methyltransferase NSUN4 to the mammalian mitochondrial ribosome

Maintenance of respiratory chain function in mouse hearts with severely impaired mtDNA transcription

Methylation of 12S rRNA is necessary for in vivo stability of the small subunit of the mammalian mitochondrial ribosome

MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome

Mutations in the mitochondrial tRNA Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy.

Mutations in the mitochondrial tRNASer(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy

Respiratory chain dysfunction in skeletal muscle does not cause insulin resistance

SOD2 overexpression: enhanced mitochondrial tolerance but absence of effect on UCP activity

Secondary metabolic effects in complex I deficiency

Sensory ataxic neuropathy in golden retriever dogs is caused by a deletion in the mitochondrial tRNATyr gene

Somatic mtDNA mutations cause aging phenotypes without affecting reactive oxygen species production

TEFM regulates both transcription elongation and RNA processing in mitochondria.

The bicoid stability factor controls polyadenylation and expression of specific mitochondrial mRNAs in Drosophila melanogaster

Two novel mutations in thymidine kinase-2 cause early onset fatal encephalomyopathy and severe mtDNA depletion