Celine Burer
Zurich, ZH, Switzerland
Last Updated: 09/26/2026
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Found 20 publications
Dynamic inter-domain transformations mediate the allosteric regulation of human 5, 10-methylenetetrahydrofolate reductase.
Journal: Nature communications
Published: September 11, 2023
Insights into energy balance dysregulation from a mouse model of methylmalonic aciduria.
Journal: Human molecular genetics
Published: February 16, 2023
Cellular and computational models reveal environmental and metabolic interactions in MMUT-type methylmalonic aciduria.
Journal: Journal of inherited metabolic disease
Published: August 09, 2022
Integrated multi-omics reveals anaplerotic rewiring in methylmalonyl-CoA mutase deficiency.
Journal: Nature metabolism
Published: April 11, 2022
Shifting landscapes of human MTHFR missense-variant effects.
Journal: American journal of human genetics
Published: January 19, 2021
Identification of small molecule allosteric modulators of 5,10-methylenetetrahydrofolate reductase (MTHFR) by targeting its unique regulatory domain.
Journal: Biochimie
Published: October 08, 2020
Genetic, structural, and functional analysis of pathogenic variations causing methylmalonyl-CoA epimerase deficiency.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: November 15, 2018
Protein destabilization and loss of protein-protein interaction are fundamental mechanisms in cblA-type methylmalonic aciduria.
Journal: Human mutation
Published: February 06, 2017
The value of plasma vitamin B6 profiles in early onset epileptic encephalopathies.
Journal: Journal of inherited metabolic disease
Published: April 25, 2016
Last Updated: 09/26/2026