Jean-francois Conrotte
Esch-sur-alzette, ES, Luxembourg
Last Updated: 09/26/2026
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Found 8 publications
NAXD Deficiency: Heterogeneous Phenotypes and Positive Response to Niacin Treatment.
Journal: Journal of inherited metabolic disease
Published: March 04, 2026
Molecular mechanisms of transhydrogenase activity and allosteric regulation in eukaryotic type II PHGDH Ser33.
Journal: Nature communications
Published: March 09, 2025
CLYBL averts vitamin B12 depletion by repairing malyl-CoA.
Journal: Nature chemical biology
Published: May 23, 2023
l-Isoaspartyl Methyltransferase Deficiency in Zebrafish Leads to Impaired Calcium Signaling in the Brain.
Journal: Frontiers in genetics
Published: September 30, 2020
3-Phosphoglycerate Transhydrogenation Instead of Dehydrogenation Alleviates the Redox State Dependency of Yeast de Novo l-Serine Synthesis.
Journal: Biochemistry
Published: January 23, 2019
NAD(P)HX dehydratase (NAXD) deficiency: a novel neurodegenerative disorder exacerbated by febrile illnesses.
Journal: Brain : a journal of neurology
Published: June 01, 2018
NAD(P)HX repair deficiency causes central metabolic perturbations in yeast and human cells.
Journal: The FEBS journal
Published: March 13, 2018
Saccharomyces cerevisiae Forms D-2-Hydroxyglutarate and Couples Its Degradation to D-Lactate Formation via a Cytosolic Transhydrogenase.
Journal: The Journal of biological chemistry
Published: November 16, 2015
Showing 1-8 of 8
Last Updated: 09/26/2026