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Human Genetics|June 1, 1992
Genetic and biochemical heterogeneity in patients with the rhizomelic form of chondrodysplasia punctata--a complementation studyJ C Heikoop, R J Wanders, A Strijland, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1994
Measurement of short-chain acyl-CoA dehydrogenase (SCAD) in cultured skin fibroblasts with hexanoyl-CoA as a competitive inhibitor to eliminate the contribution of medium-chain acyl-CoA dehydrogenaseK E Niezen-Koning, R J Wanders, G T Nagel, et al.Archives of Disease in Childhood. Fetal and Neonatal Edition|July 1, 1994
A new peroxisomal disorder with fetal and neonatal adrenal insufficiencyC Vanhole, F de Zegher, P Casaer, et al.Biochemical and Biophysical Research Communications|March 14, 2002
A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndromeNobuyuki Shimozawa, Tomoko Nagase, Yasuhiko Takemoto, et al.Journal of Immunological Methods|July 6, 1992
Production and characterisation of monoclonal antibodies against native and disassembled human catalaseE A Wiemer, R Ofman, E Middelkoop, et al.The Journal of Nutritional Biochemistry|November 26, 2022
Berry consumption mitigates the hypertensive effects of a high-fat, high-sucrose diet via attenuation of renal and aortic AT1R expression resulting in improved endothelium-derived NO bioavailabilityMaureen L Meister, Rami S Najjar, Jessica P Danh, et al.Frontiers in Cell and Developmental Biology|January 28, 2021
Peroxisomal Metabolite and Cofactor Transport in HumansSerhii Chornyi, Lodewijk IJlst, Carlo W T van Roermund, et al.Journal of Inherited Metabolic Disease|May 22, 2010
The enzymology of mitochondrial fatty acid beta-oxidation and its application to follow-up analysis of positive neonatal screening resultsRonald J A Wanders, Jos P N Ruiter, Lodewijk IJLst, et al.Journal of Affective Disorders|March 21, 2017
Using a hybrid subtyping model to capture patterns and dimensionality of depressive and anxiety symptomatology in the general populationKlaas J Wardenaar, Rob B K Wanders, Margreet Ten Have, et al.Archives of Disease in Childhood. Fetal and Neonatal Edition|January 9, 2004
Novel genotype of mevalonic aciduria with fatalities in premature siblingsP Raupp, E Varady, M Duran, et al.Pageof 132