Rolf Wibom

Stockholm, AB 17176, Sweden

Last Updated: 09/26/2026

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Found 42 publications

Loss of the mitochondrial SAM transporter reveals a lipoylation-dependent metabolic vulnerability in the postnatal heart.

Loss of the mitochondrial SAM transporter reveals a lipoylation-dependent metabolic vulnerability in the postnatal heart.

Journal: Science advances
Published: August 26, 2026

MitoSAM-dependent lipoylation controls postnatal heart development via metabolic remodeling.

MitoSAM-dependent lipoylation controls postnatal heart development via metabolic remodeling.

Journal: bioRxiv : the preprint server for biology
Published: May 04, 2026

MRPS22 variants alter mitochondrial ribosome assembly in patients with leukodystrophy, movement disorder and intellectual impairment.

MRPS22 variants alter mitochondrial ribosome assembly in patients with leukodystrophy, movement disorder and intellectual impairment.

Journal: Human molecular genetics
Published: December 09, 2025

Advancing a sensitive method for measuring mitochondrial ATP production in small muscle biopsy samples.

Advancing a sensitive method for measuring mitochondrial ATP production in small muscle biopsy samples.

Journal: Analytical biochemistry
Published: September 03, 2025

The mitochondrial protein TMEM177 fine-tunes mammalian cytochrome c oxidase assembly.

The mitochondrial protein TMEM177 fine-tunes mammalian cytochrome c oxidase assembly.

Journal: Mitochondrion
Published: August 11, 2025

Tissue-specific responses to TFAM and mtDNA copy number manipulation in prematurely ageing mice.

Tissue-specific responses to TFAM and mtDNA copy number manipulation in prematurely ageing mice.

Journal: eLife
Published: June 30, 2025

Quantitative proteomics of patient fibroblasts reveal biomarkers and diagnostic signatures of mitochondrial disease.

Quantitative proteomics of patient fibroblasts reveal biomarkers and diagnostic signatures of mitochondrial disease.

Journal: JCI insight
Published: December 19, 2023

Novel Synonymous and Deep Intronic Variants Causing Primary and Secondary Pyruvate Dehydrogenase Complex Deficiency.

Novel Synonymous and Deep Intronic Variants Causing Primary and Secondary Pyruvate Dehydrogenase Complex Deficiency.

Journal: Human mutation
Published: October 20, 2023

PARKIN is not required to sustain OXPHOS function in adult mammalian tissues.

PARKIN is not required to sustain OXPHOS function in adult mammalian tissues.

Journal: NPJ Parkinson's disease
Published: September 12, 2023

Ataxia Syndrome With Hearing Loss and Nephronophthisis Associated With a Novel Homozygous Variant in XPNPEP3.

Ataxia Syndrome With Hearing Loss and Nephronophthisis Associated With a Novel Homozygous Variant in XPNPEP3.

Journal: Neurology. Genetics
Published: June 07, 2023

Inhibition of mammalian mtDNA transcription acts paradoxically to reverse diet-induced hepatosteatosis and obesity.

Inhibition of mammalian mtDNA transcription acts paradoxically to reverse diet-induced hepatosteatosis and obesity.

Journal: Nature metabolism
Published: November 03, 2022

Human mitochondria require mtRF1 for translation termination at non-canonical stop codons.

Human mitochondria require mtRF1 for translation termination at non-canonical stop codons.

Journal: Nature communications
Published: June 17, 2022
Showing 1-12 of 42

Last Updated: 09/26/2026