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A C Havelaar

Showing results (1-10 of 10) with videos related to

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Human Molecular Genetics|December 1, 1992
PCR detection of a dinucleotide repeat in the human histidine-rich glycoprotein (HRG) geneB C Hennis, A C Havelaar, C Kluft
Journal of Inherited Metabolic Disease|June 23, 2000
Lysosomal transport disordersG M Mancini, A C Havelaar, F W Verheijen
FEBS Letters|April 1, 1999
Transport of organic anions by the lysosomal sialic acid transporter: a functional approach towards the gene for sialic acid storage diseaseA C Havelaar, C E Beerens, G M Mancini, et al.
The Journal of Biological Chemistry|December 16, 1998
Purification of the lysosomal sialic acid transporter. Functional characteristics of a monocarboxylate transporterA C Havelaar, G M Mancini, C E Beerens, et al.
Journal of Medical Genetics|October 23, 1998
Fibroblast silver loading for the diagnosis of Menkes diseaseF W Verheijen, C E Beerens, A C Havelaar, et al.
FEBS Letters|October 22, 1998
Characterization of a heavy metal ion transporter in the lysosomal membraneA C Havelaar, I L de Gast, S Snijders, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
NPT4, a new microsomal phosphate transporter: mutation analysis in glycogen storage disease type IcD Melis, A C Havelaar, E Verbeek, et al.
Biochimica Et Biophysica Acta|June 30, 1992
A role for the transient increase of cytoplasmic free calcium in cell rescue after photodynamic treatmentL C Penning, M H Rasch, E Ben-Hur, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 1, 1996
Interindividual and intraindividual variability in plasma fibrinogen, TPA antigen, PAI activity, and CRP in healthy, young volunteers and patients with angina pectorisM P de Maat, A C de Bart, B C Hennis, et al.
Nature Genetics|December 2, 1999
A new gene, encoding an anion transporter, is mutated in sialic acid storage diseasesF W Verheijen, E Verbeek, N Aula, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Human Molecular Genetics|December 1, 1992
PCR detection of a dinucleotide repeat in the human histidine-rich glycoprotein (HRG) geneB C Hennis, A C Havelaar, C Kluft
Journal of Inherited Metabolic Disease|June 23, 2000
Lysosomal transport disordersG M Mancini, A C Havelaar, F W Verheijen
FEBS Letters|April 1, 1999
Transport of organic anions by the lysosomal sialic acid transporter: a functional approach towards the gene for sialic acid storage diseaseA C Havelaar, C E Beerens, G M Mancini, et al.
The Journal of Biological Chemistry|December 16, 1998
Purification of the lysosomal sialic acid transporter. Functional characteristics of a monocarboxylate transporterA C Havelaar, G M Mancini, C E Beerens, et al.
Journal of Medical Genetics|October 23, 1998
Fibroblast silver loading for the diagnosis of Menkes diseaseF W Verheijen, C E Beerens, A C Havelaar, et al.
FEBS Letters|October 22, 1998
Characterization of a heavy metal ion transporter in the lysosomal membraneA C Havelaar, I L de Gast, S Snijders, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
NPT4, a new microsomal phosphate transporter: mutation analysis in glycogen storage disease type IcD Melis, A C Havelaar, E Verbeek, et al.
Biochimica Et Biophysica Acta|June 30, 1992
A role for the transient increase of cytoplasmic free calcium in cell rescue after photodynamic treatmentL C Penning, M H Rasch, E Ben-Hur, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 1, 1996
Interindividual and intraindividual variability in plasma fibrinogen, TPA antigen, PAI activity, and CRP in healthy, young volunteers and patients with angina pectorisM P de Maat, A C de Bart, B C Hennis, et al.
Nature Genetics|December 2, 1999
A new gene, encoding an anion transporter, is mutated in sialic acid storage diseasesF W Verheijen, E Verbeek, N Aula, et al.
Pageof 1