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Acta Paediatrica (Oslo, Norway : 1992)|June 13, 2003
Carnitine-acylcarnitine translocase deficiency: case report and review of the literatureM E Rubio-Gozalbo, P Vos, P Ph Forget, et al.
Cancer Chemotherapy and Pharmacology|August 9, 2003
Assessment of normal and tumor tissue uptake of MAG-CPT, a polymer-bound prodrug of camptothecin, in patients undergoing elective surgery for colorectal carcinomaNenad Sarapa, Margaret R Britto, William Speed, et al.
British Journal of Cancer|January 15, 2009
Hsp90 is expressed and represents a therapeutic target in human oesophageal cancer using the inhibitor 17-allylamino-17-demethoxygeldanamycinX Wu, A Wanders, P Wardega, et al.
Human Mutation|May 18, 2004
Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated geneNobuyuki Shimozawa, Toshiro Tsukamoto, Tomoko Nagase, et al.
The Biochemical Journal|April 12, 2011
Conservation of targeting but divergence in function and quality control of peroxisomal ABC transporters: an analysis using cross-kingdom expressionXuebin Zhang, Carine De Marcos Lousa, Nellie Schutte-Lensink, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 7, 2015
UCP1 is an essential mediator of the effects of methionine restriction on energy balance but not insulin sensitivityDesiree Wanders, David H Burk, Cory C Cortez, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|May 9, 2002
Phase I study of MEN-10755, a new anthracycline in patients with solid tumours: a report from the European Organization for Research and Treatment of Cancer, Early Clinical Studies GroupD Schrijvers, A M E Bos, J Dyck, et al.
Diabetes Care|November 16, 2019
Plasma and Dietary Linoleic Acid and 3-Year Risk of Type 2 Diabetes After Myocardial Infarction: A Prospective Analysis in the Alpha Omega CohortKamalita Pertiwi, Anne J Wanders, Marjolein C Harbers, et al.
Biochimica Et Biophysica Acta|July 26, 1991
Peroxisomes of normal morphology but deficient in 3-oxoacyl-CoA thiolase in rhizomelic chondrodysplasia punctata fibroblastsJ C Heikoop, M Van den Berg, A Strijland, et al.
European Journal of Pediatrics|November 1, 1990
Excessive urinary oxalate excretion after combined renal and hepatic transplantation for correction of hyperoxaluria type 1H Ruder, G Otto, R B Schutgens, et al.
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