Volkmar Gieselmann
Bonn, NW 53127, Germany
Last Updated: 09/26/2026
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Found 40 publications
Beta arrestin 1 is a key regulator of pulmonary vascular tone.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: February 09, 2026
Publisher Correction: Starvation-induced metabolic rewiring affects mTORC1 composition in vivo.
Journal: Scientific reports
Published: January 29, 2025
ARSA Variants Associated With Cognitive Decline and Long-Term Preservation of Motor Function in Metachromatic Leukodystrophy.
Journal: Journal of inherited metabolic disease
Published: January 20, 2025
Starvation-induced metabolic rewiring affects mTORC1 composition in vivo.
Journal: Scientific reports
Published: July 23, 2024
Engineered arylsulfatase A with increased activity, stability and brain delivery for therapy of metachromatic leukodystrophy.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: June 06, 2023
Proteomic investigation of neural stem cell to oligodendrocyte precursor cell differentiation reveals phosphorylation-dependent Dclk1 processing.
Journal: Cellular and molecular life sciences : CMLS
Published: April 21, 2023
Cross-linking of the endolysosomal system reveals potential flotillin structures and cargo.
Journal: Nature communications
Published: February 11, 2022
Extremely low arylsulfatase A enzyme activity does not necessarily cause symptoms: A long-term follow-up and review of the literature.
Journal: JIMD reports
Published: February 02, 2022
CLN6 deficiency causes selective changes in the lysosomal protein composition.
Journal: Proteomics
Published: February 18, 2021
Deletion of fatty acid amide hydrolase reduces lyso-sulfatide levels but exacerbates metachromatic leukodystrophy in mice.
Journal: The Journal of biological chemistry
Published: January 28, 2021
Brain cell type-specific endocytosis of arylsulfatase A identifies limitations of enzyme-based therapies for metachromatic leukodystrophy.
Journal: Human molecular genetics
Published: November 09, 2020
Decreased turnover of the CNS myelin protein Opalin in a mouse model of hereditary spastic paraplegia 35.
Journal: Human molecular genetics
Published: October 20, 2020
Last Updated: 09/26/2026