Oliver Stehling

Robert Koch Str. 6
Marburg An Der Lahn, HE 35033, Germany

Last Updated: 09/26/2026

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Found 28 publications

A novel mutation in FDX2 provides insights into the pathogenesis of MEOAL mitochondrial neuromuscular disease.

A novel mutation in FDX2 provides insights into the pathogenesis of MEOAL mitochondrial neuromuscular disease.

Journal: Cell death & disease

Published: July 22, 2025

Patient-Derived Neurons Exhibit α-Synuclein Pathology and Previously Unrecognized Major Histocompatibility Complex Class I Elevation in Mitochondrial Membrane Protein-Associated Neurodegeneration.

Patient-Derived Neurons Exhibit α-Synuclein Pathology and Previously Unrecognized Major Histocompatibility Complex Class I Elevation in Mitochondrial Membrane Protein-Associated Neurodegeneration.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: July 17, 2025

D-cysteine impairs tumour growth by inhibiting cysteine desulfurase NFS1.

D-cysteine impairs tumour growth by inhibiting cysteine desulfurase NFS1.

Journal: Nature metabolism

Published: March 19, 2025

Crucial role and conservation of the three [2Fe-2S] clusters in the human mitochondrial ribosome.

Crucial role and conservation of the three [2Fe-2S] clusters in the human mitochondrial ribosome.

Journal: The Journal of biological chemistry

Published: October 01, 2024

Requirements for the biogenesis of [2Fe-2S] proteins in the human and yeast cytosol.

Requirements for the biogenesis of [2Fe-2S] proteins in the human and yeast cytosol.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: May 14, 2024

Haptoglobin buffers lipopolysaccharides to delay activation of NFκB.

Haptoglobin buffers lipopolysaccharides to delay activation of NFκB.

Journal: Frontiers in immunology

Published: March 15, 2024

A novel IBA57 variant is associated with mitochondrial iron-sulfur protein deficiency and necrotizing myelopathy in dogs.

A novel IBA57 variant is associated with mitochondrial iron-sulfur protein deficiency and necrotizing myelopathy in dogs.

Journal: Frontiers in genetics

Published: March 20, 2023

Mitochondrial [2Fe-2S] ferredoxins: new functions for old dogs.

Mitochondrial [2Fe-2S] ferredoxins: new functions for old dogs.

Journal: FEBS letters

Published: October 20, 2022

Functional spectrum and specificity of mitochondrial ferredoxins FDX1 and FDX2.

Functional spectrum and specificity of mitochondrial ferredoxins FDX1 and FDX2.

Journal: Nature chemical biology

Published: March 24, 2022

N-terminal tyrosine of ISCU2 triggers [2Fe-2S] cluster synthesis by ISCU2 dimerization.

N-terminal tyrosine of ISCU2 triggers [2Fe-2S] cluster synthesis by ISCU2 dimerization.

Journal: Nature communications

Published: April 12, 2021

Function and crystal structure of the dimeric P-loop ATPase CFD1 coordinating an exposed [4Fe-4S] cluster for transfer to apoproteins.

Function and crystal structure of the dimeric P-loop ATPase CFD1 coordinating an exposed [4Fe-4S] cluster for transfer to apoproteins.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: September 12, 2018

ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe-4S] proteins.

ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe-4S] proteins.

Journal: Human molecular genetics

Published: August 17, 2018

Showing 1-12 of 28

Last Updated: 09/26/2026