L. Ijlst

发表

Subcellular localization and physiological role of alpha-methylacyl-CoA racemase.

S. Ferdinandusse, S. Denis, L. Ijlst, 2000, Journal of lipid research.

The Saccharomyces cerevisiae ABC subfamily D transporter Pxa1/Pxa2p co‐imports CoASH into the peroxisome

L. Ijlst, H. Waterham, R. Wanders, 2020, FEBS letters.

Spontaneous pregnancy in a patient with classical galactosaemia

P. Vreken, L. Ijlst, R. Wanders, 1999, Journal of Inherited Metabolic Disease.

Fatty acid metabolism in Saccharomyces cerevisiae

L. Ijlst, H. Waterham, R. Wanders, 2003, Cellular and Molecular Life Sciences CMLS.

Reinvestigation of peroxisomal 3-ketoacyl-CoA thiolase deficiency: identification of the true defect at the level of d-bifunctional protein.

S. Ferdinandusse, S. Denis, L. Ijlst, 2002, American journal of human genetics.

Molecular cloning and expression of human carnitine octanoyltransferase: evidence for its role in the peroxisomal beta-oxidation of branched-chain fatty acids.

S. Ferdinandusse, S. Denis, L. Ijlst, 1999, Biochemical and biophysical research communications.

Octanoate and palmitateβ-oxidation in human leukocytes: Implications for the rapid diagnosis of fatty acidβ-oxidation disorders

L. Ijlst, R. Wanders, H. Przyrembel, 1991, Journal of Inherited Metabolic Disease.

Apparatus for Continuous Dielectric-medium Separation of Mineral Grains

L. Ijlst, R. Verschure, L. IJlst, 1966, Nature.

Primary plasmalemmal carnitine transporter defect manifested with dicarboxylic aciduria and impaired fatty acid oxidation

L. Ijlst, R. Wanders, N. M. Hjelm, 1998, Journal of Inherited Metabolic Disease.

Identificationn of a Peroxisomal ATP Carrier Required for Medium-Chainn Fatty Acid p-Oxidation and Normal Peroxisome Proliferationn in Saccharomyces cerevisiae

H. Tabak, L. Ijlst, H. Waterham, 2007 .