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A Wevers

Showing results (221-230 of 543) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 1983
Immunological measurements on the disappearance of creatine kinase MM from the circulationR A Wevers, A A van Landeghem, M W Mul-Steinbusch, et al.
Molecular Genetics and Metabolism|August 30, 2008
Technical and biochemical factors affecting cerebrospinal fluid 5-MTHF, biopterin and neopterin concentrationsM M Verbeek, A M Blom, R A Wevers, et al.
Analytical Chemistry|June 1, 2023
An <i>In Silico</i> Infrared Spectral Library of Molecular Ions for Metabolite IdentificationKas J Houthuijs, Giel Berden, Udo F H Engelke, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 31, 1985
The concentration of blood components related to fuel metabolism during prolonged fasting in childrenK J Lamers, W H Doesburg, F J Gabreëls, et al.
Neuroscience Letters|March 10, 1995
Gene expression of the nicotinic acetylcholine receptor alpha 4 subunit in the frontal cortex in Parkinson's disease patientsH Schröder, R A de Vos, E N Jansen, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 10, 2004
[Hydrops fetalis as an indication for a systematic investigation into the presence of lysosomal storage diseases]P M W Janssens, A N de Groot, J G de Jong, et al.
Analytica Chimica Acta|November 9, 2015
Regularized MANOVA (rMANOVA) in untargeted metabolomicsJ Engel, L Blanchet, B Bloemen, et al.
Translational Psychiatry|July 9, 2014
Early life adversity and serotonin transporter gene variation interact at the level of the adrenal gland to affect the adult hypothalamo-pituitary-adrenal axisR H A van der Doelen, W Deschamps, C D'Annibale, et al.
Journal of Lipid Research|March 19, 2017
A newborn screening method for cerebrotendinous xanthomatosis using bile alcohol glucuronides and metabolite ratiosFrédéric M Vaz, Albert H Bootsma, Willem Kulik, et al.
Human Genetics|December 1, 1996
Two new mutations in the sterol 27-hydroxylase gene in two families lead to cerebrotendinous xanthomatosisA Verrips, G C Steenbergen-Spanjers, J A Luyten, et al.
Pageof 55

Showing results (221-230 of 543) with videos related to

Sort By:
Pageof 55
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 1983
Immunological measurements on the disappearance of creatine kinase MM from the circulationR A Wevers, A A van Landeghem, M W Mul-Steinbusch, et al.
Molecular Genetics and Metabolism|August 30, 2008
Technical and biochemical factors affecting cerebrospinal fluid 5-MTHF, biopterin and neopterin concentrationsM M Verbeek, A M Blom, R A Wevers, et al.
Analytical Chemistry|June 1, 2023
An <i>In Silico</i> Infrared Spectral Library of Molecular Ions for Metabolite IdentificationKas J Houthuijs, Giel Berden, Udo F H Engelke, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 31, 1985
The concentration of blood components related to fuel metabolism during prolonged fasting in childrenK J Lamers, W H Doesburg, F J Gabreëls, et al.
Neuroscience Letters|March 10, 1995
Gene expression of the nicotinic acetylcholine receptor alpha 4 subunit in the frontal cortex in Parkinson's disease patientsH Schröder, R A de Vos, E N Jansen, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 10, 2004
[Hydrops fetalis as an indication for a systematic investigation into the presence of lysosomal storage diseases]P M W Janssens, A N de Groot, J G de Jong, et al.
Analytica Chimica Acta|November 9, 2015
Regularized MANOVA (rMANOVA) in untargeted metabolomicsJ Engel, L Blanchet, B Bloemen, et al.
Translational Psychiatry|July 9, 2014
Early life adversity and serotonin transporter gene variation interact at the level of the adrenal gland to affect the adult hypothalamo-pituitary-adrenal axisR H A van der Doelen, W Deschamps, C D'Annibale, et al.
Journal of Lipid Research|March 19, 2017
A newborn screening method for cerebrotendinous xanthomatosis using bile alcohol glucuronides and metabolite ratiosFrédéric M Vaz, Albert H Bootsma, Willem Kulik, et al.
Human Genetics|December 1, 1996
Two new mutations in the sterol 27-hydroxylase gene in two families lead to cerebrotendinous xanthomatosisA Verrips, G C Steenbergen-Spanjers, J A Luyten, et al.
Pageof 55