Wanders, Ronald J.A.

Contributions of Carnitine Acetyltransferases to Intracellular Acetyl Unit Transport in Candida albicans

Strijbis, K., van Roermund, C. W., van den Burg, J., van den Berg, M., Hardy, G. P. M., Wanders, R. J., & Distel, B. (2010) · Journal of Biological Chemistry

Fungal and yeast genetics researchLipid metabolism and biosynthesis

Cited by 25

Structure-Function Analysis of Peroxisomal ATP-binding Cassette Transporters Using Chimeric Dimers

Geillon, F., Gondcaille, C., Charbonnier, S., Van Roermund, C. W., Lopez, T. E., Dias, A. M. M., Pais de Barros, J.-P., Arnould, C., Wanders, R. J., Trompier, D., et al. (2014) · Journal of Biological Chemistry

Metabolism and Genetic DisordersDrug Transport and Resistance Mechanisms

Cited by 24

A misdiagnosis of X‐linked adrenoleucodystrophy in cultured chorionic villus cells by the measurement of very long chain fatty acids

Gray, R. G. F., Green, A., Cole, T., Davidson, V., Giles, M., Schutgens, R. B. H., & Wanders, R. J. A. (1995) · Prenatal Diagnosis

Metabolism and Genetic DisordersPrenatal Screening and Diagnostics

Cited by 23

Methionine metabolism and phenotypic variability in X-linked adrenoleukodystrophy

Linnebank, M., Kemp, S., Wanders, R. J. A., Kleijer, W. J., van der Sterre, M. L. T., Gärtner, J., Fliessbach, K., Semmler, A., Sokolowski, P., Köhler, W., et al. (2006) · Neurology

Metabolism and Genetic DisordersHereditary Neurological Disorders

Cited by 22

Chondrodysplasia punctata with a mild clinical course

Nuoffer, J. M., Pfammatter, J. P., Spahr, A., Toplak, H., Wanders, R. J. A., Schutgens, R. B. H., & Wiesmann, U. N. (1994) · Journal of Inherited Metabolic Disease

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 20

Molecular Mechanism of a Temperature-Sensitive Phenotype in Peroxisomal Biogenesis Disorder

Hashimoto, K., Kato, Z., Nagase, T., Shimozawa, N., Kuwata, K., Omoya, K., Li, A., Matsukuma, E., Yamamoto, Y., Ohnishi, H., et al. (2005) · Pediatric Research

Metabolism and Genetic DisordersProtein Structure and Dynamics

Cited by 16

X-linked adrenomyeloneuropathy due to a novel missense mutation in the ABCD1 start codon presenting as demyelinating neuropathy

Engelen, M., van der Kooi, A. J., Kemp, S., Wanders, R. J. A., Sistermans, E. A., Waterham, H. R., Koelman, J. T. M., van Geel, B. M., & de Visser, M. (2011) · Journal of the Peripheral Nervous System

Hereditary Neurological DisordersMetabolism and Genetic Disorders

Cited by 12