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A Wanders

Showing results (141-150 of 480) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|August 23, 2006
[From gene to disease; primary hyperoxaluria type I caused by mutations in the AGXT gene]C S van Woerden, J W Groothof, R J A Wanders, et al.
Journal of Cell Science|January 20, 2004
Mevalonate kinase is a cytosolic enzyme in humansSietske Hogenboom, John J M Tuyp, Marc Espeel, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 25, 2003
Primary hyperoxaluria type 1 in The Netherlands: prevalence and outcomeChristiaan S van Woerden, Jaap W Groothoff, Ronald J A Wanders, et al.
American Journal of Human Genetics|November 16, 2002
3-Methylglutaconic aciduria type I is caused by mutations in AUHLodewijk IJlst, Ference J Loupatty, Jos P N Ruiter, et al.
European Journal of Human Genetics : EJHG|March 14, 2003
Carrier frequency of the V377I (1129G>A) MVK mutation, associated with Hyper-IgD and periodic fever syndrome, in the NetherlandsSander M Houten, Christiaan S van Woerden, Frits A Wijburg, et al.
Molecular Genetics and Metabolism|May 18, 2005
dif-1 and colt, both implicated in early embryonic development, encode carnitine acylcarnitine translocaseNadia A Oey, Lodewijk Ijlst, Carlo W T van Roermund, et al.
The International Journal of Biochemistry & Cell Biology|December 6, 2020
Disorders of flavin adenine dinucleotide metabolism: MADD and related deficienciesMichelle Mereis, Ronald J A Wanders, Maryke Schoonen, et al.
Orphanet Journal of Rare Diseases|August 26, 2018
Profiling of intracellular metabolites produced from galactose and its potential for galactosemia researchMichel van Weeghel, Lindsey Welling, Eileen P Treacy, et al.
Neuroradiology|September 18, 2010
Neurodegeneration in D-bifunctional protein deficiency: diagnostic clues and natural history using serial magnetic resonance imagingAneal Khan, Xing-Chang Wei, Floyd F Snyder, et al.
Methods in Molecular Biology (Clifton, N.J.)|April 15, 2017
Clinical and Laboratory Diagnosis of Peroxisomal DisordersRonald J A Wanders, Femke C C Klouwer, Sacha Ferdinandusse, et al.
Pageof 48

Showing results (141-150 of 480) with videos related to

Sort By:
Pageof 48
Nederlands Tijdschrift Voor Geneeskunde|August 23, 2006
[From gene to disease; primary hyperoxaluria type I caused by mutations in the AGXT gene]C S van Woerden, J W Groothof, R J A Wanders, et al.
Journal of Cell Science|January 20, 2004
Mevalonate kinase is a cytosolic enzyme in humansSietske Hogenboom, John J M Tuyp, Marc Espeel, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 25, 2003
Primary hyperoxaluria type 1 in The Netherlands: prevalence and outcomeChristiaan S van Woerden, Jaap W Groothoff, Ronald J A Wanders, et al.
American Journal of Human Genetics|November 16, 2002
3-Methylglutaconic aciduria type I is caused by mutations in AUHLodewijk IJlst, Ference J Loupatty, Jos P N Ruiter, et al.
European Journal of Human Genetics : EJHG|March 14, 2003
Carrier frequency of the V377I (1129G>A) MVK mutation, associated with Hyper-IgD and periodic fever syndrome, in the NetherlandsSander M Houten, Christiaan S van Woerden, Frits A Wijburg, et al.
Molecular Genetics and Metabolism|May 18, 2005
dif-1 and colt, both implicated in early embryonic development, encode carnitine acylcarnitine translocaseNadia A Oey, Lodewijk Ijlst, Carlo W T van Roermund, et al.
The International Journal of Biochemistry & Cell Biology|December 6, 2020
Disorders of flavin adenine dinucleotide metabolism: MADD and related deficienciesMichelle Mereis, Ronald J A Wanders, Maryke Schoonen, et al.
Orphanet Journal of Rare Diseases|August 26, 2018
Profiling of intracellular metabolites produced from galactose and its potential for galactosemia researchMichel van Weeghel, Lindsey Welling, Eileen P Treacy, et al.
Neuroradiology|September 18, 2010
Neurodegeneration in D-bifunctional protein deficiency: diagnostic clues and natural history using serial magnetic resonance imagingAneal Khan, Xing-Chang Wei, Floyd F Snyder, et al.
Methods in Molecular Biology (Clifton, N.J.)|April 15, 2017
Clinical and Laboratory Diagnosis of Peroxisomal DisordersRonald J A Wanders, Femke C C Klouwer, Sacha Ferdinandusse, et al.
Pageof 48