Wolfram S. Kunz

Sigmund Freud Str. 25
Bonn, NW 53127, Germany

Last Updated: 09/26/2026

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Found 110 publications

The pyruvate generator is a common phenomenon in mitochondria from different rat and mouse brain regions.

The pyruvate generator is a common phenomenon in mitochondria from different rat and mouse brain regions.

Journal: FEBS letters

Published: March 09, 2026

Correlation of polygenic risk score and clinical phenotype in patients with genetic generalized epilepsy.

Correlation of polygenic risk score and clinical phenotype in patients with genetic generalized epilepsy.

Journal: Epilepsia

Published: February 25, 2026

Pyruvate dehydrogenase autoantibodies in autoantibody-negative patients with seizures are associated with reduced pyruvate dehydrogenase activity.

Pyruvate dehydrogenase autoantibodies in autoantibody-negative patients with seizures are associated with reduced pyruvate dehydrogenase activity.

Journal: Epilepsia

Published: January 29, 2026

Complexity of Inheritance of Pathogenic Mutations Associated with Epilepsy in Consanguine Families from Pakistan.

Complexity of Inheritance of Pathogenic Mutations Associated with Epilepsy in Consanguine Families from Pakistan.

Journal: Genes

Published: December 29, 2025

Turnover and Quality Control of Mitochondrial DNA.

Turnover and Quality Control of Mitochondrial DNA.

Journal: Biochemistry. Biokhimiia

Published: December 26, 2025

Identification of the adhesion GPCR ADGRL4/ELTD1 as a novel potential prognostic biomarker for cerebral cavernous malformation disease.

Identification of the adhesion GPCR ADGRL4/ELTD1 as a novel potential prognostic biomarker for cerebral cavernous malformation disease.

Journal: Molecular medicine (Cambridge, Mass.)

Published: August 05, 2025

Single-cell multi-omic analysis of mitochondrial mutational mosaicism and dynamics.

Single-cell multi-omic analysis of mitochondrial mutational mosaicism and dynamics.

Journal: Nature communications

Published: May 10, 2025

Myopathy and ataxia related to impaired mitochondrial function in mevalonate kinase deficiency.

Myopathy and ataxia related to impaired mitochondrial function in mevalonate kinase deficiency.

Journal: Orphanet journal of rare diseases

Published: February 28, 2025

Ligase 3 prevents oxidative strand break-induced mitochondrial DNA loss but is not essential for replicative circularization.

Ligase 3 prevents oxidative strand break-induced mitochondrial DNA loss but is not essential for replicative circularization.

Journal: Nucleic acids research

Published: February 05, 2025

Blockage of autophagy causes severe skeletal muscle disruption in a mouse model for myofibrillar myopathy 6.

Blockage of autophagy causes severe skeletal muscle disruption in a mouse model for myofibrillar myopathy 6.

Journal: Nature communications

Published: July 17, 2024

Deciphering the Foundations of Mitochondrial Mutational Spectra: Replication-Driven and Damage-Induced Signatures Across Chordate Classes.

Deciphering the Foundations of Mitochondrial Mutational Spectra: Replication-Driven and Damage-Induced Signatures Across Chordate Classes.

Journal: Molecular biology and evolution

Published: April 05, 2024

Rasmussen's encephalitis: structural, functional, and clinical correlates of contralesional epileptiform activity.

Rasmussen's encephalitis: structural, functional, and clinical correlates of contralesional epileptiform activity.

Journal: Journal of neurology

Published: April 03, 2024

Showing 1-12 of 110

Last Updated: 09/26/2026