The role of ELOVL1 in very long‐chain fatty acid homeostasis and X‐linked adrenoleukodystrophy

Rob Ofman, Inge M. E. Dijkstra, Carlo W.T. van Roermund, +6

EMBO Molecular Medicine

Metabolic SyndromeMolecular PhysiologyOxysterolBiochemistryPhysiology +7

Monocarboxylate Transporter 1 Deficiency and Ketone Utilization

Peter M. van Hasselt, Sacha Ferdinandusse, Glen R. Monroe, +20

New England Journal of Medicine

GeneticsPathologyMolecular GeneticsDisease Gene IdentificationCellular Physiology +16

Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in <i>GLS</i>

André B. P. Kuilenburg, Maja Tarailo‐Graovac, Phillip A. Richmond, +42

New England Journal of Medicine

PPARα-activation results in enhanced carnitine biosynthesis and OCTN2-mediated hepatic carnitine accumulation

Naomi van Vlies, Sacha Ferdinandusse, Marjolein Turkenburg, +2

Biochimica et Biophysica Acta (BBA) - Bioenergetics

Enhanced Carnitine BiosynthesisBiochemistryLiver PhysiologyPhysiologyPparα-activation Results +6

Succinyl-CoA Ligase Deficiency: A Mitochondrial Hepatoencephalomyopathy

Johan L.K. Van Hove, Margarita Sáenz, Janet A. Thomas, +9

Pediatric Research

Succinyl-coa Ligase DeficiencyHepatologyMitochondrial FunctionLiver PhysiologyPathology +2

Stress as a Determinant of Saliva-Mediated Adherence and Coadherence of Oral and Nonoral Microorganisms

Jos A. Bosch, Marjolein Turkenburg, Kamran Nazmi, +3

Psychosomatic Medicine

Unprenylated RhoA Contributes to IL-1β Hypersecretion in Mevalonate Kinase Deficiency Model through Stimulation of Rac1 Activity

Robert van der Burgh, Kalliopi Pervolaraki, Marjolein Turkenburg, +3

Journal of Biological Chemistry

Signal TransductionMolecular PhysiologySignaling PathwayCell RegulationMolecular Regulation +10

Fasting adaptation in idiopathic ketotic hypoglycemia: a mismatch between glucose production and demand

Hidde H. Huidekoper, Marinus Durán, Marjolein Turkenburg, +3

European Journal of Pediatrics

ObesityMetabolic SyndromeNutritionIdiopathic Ketotic HypoglycemiaEnergy Homeostasis +10

Mutated SUCLG1 causes mislocalization of SUCLG2 protein, morphological alterations of mitochondria and an early-onset severe neurometabolic disorder

Christos Chinopoulos, Spyros Batzios, Lambertus P. van den Heuvel, +12

Molecular Genetics and Metabolism

Neurodegenerative DiseasesSuclg2 ProteinMolecular NeuroscienceMitochondrial FunctionMitochondrial Dynamic +9

Manipulation of isoprenoid biosynthesis as a possible therapeutic option in mevalonate kinase deficiency

Marit S. Schneiders, Sander M. Houten, Marjolein Turkenburg, +2

Arthritis & Rheumatism