A Bolhuis - JoVE Visualize

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Biochimica Et Biophysica Acta|May 23, 1979

Isolation and partial characterization of human factor VP A Bolhuis, T B Hakvoort, K Breederveld, et al.

Biochimica Et Biophysica Acta|September 8, 1993

Molecular basis of an adult form of Sandhoff disease: substitution of glutamine for arginine at position 505 of the beta-chain of beta-hexosaminidase results in a labile enzymeP A Bolhuis, N J Ponne, H Bikker, et al.

Human Genetics|April 1, 1989

Eco RI RFLP in the human thyroid peroxidase (TPO) gene on chromosome 2H Bikker, P A Bolhuis, G Vassart, et al.

Clinical Chemistry|August 1, 1988

Rapid determination of the hypoxanthine increase in ischemic exercise testsP A Bolhuis, R Zwart, P R Bär, et al.

Blood|January 1, 1984

Adhesion of platelets to human artery subendothelium: effect of factor VIII-von Willebrand factor of various multimeric compositionJ J Sixma, K S Sakariassen, N H Beeser-Visser, et al.

Journal of Medical Genetics|April 1, 1994

Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcomeR J Oostra, P A Bolhuis, F A Wijburg, et al.

Applied and Environmental Microbiology|December 3, 1998

Cloning, expression, and chromosomal stabilization of the Propionibacterium shermanii proline iminopeptidase gene (pip) for food-grade application in Lactococcus lactisK Leenhouts, A Bolhuis, J Boot, et al.

Annals of Neurology|February 1, 1995

Concentrations of amyloid beta protein in cerebrospinal fluid of patients with Alzheimer's diseaseW A van Gool, M A Kuiper, G J Walstra, et al.

Biochimica Et Biophysica Acta|June 9, 1992

Steady-state transcript levels of cytochrome c oxidase genes during human myogenesis indicate subunit switching of subunit VIa and co-expression of subunit VIIa isoformsJ W Taanman, N H Herzberg, H De Vries, et al.

Journal of the Neurological Sciences|August 1, 1996

Evidence against increased oxidative stress in fibroblasts from patients with non-superoxide-dismutase-1 mutant familial amyotrophic lateral sclerosisG A Jansen, R J Wanders, G J Jöbsis, et al.

Pageof 14

Showing results (41-50 of 131) with videos related to

Sort By:

Pageof 14

Biochimica Et Biophysica Acta|May 23, 1979

Isolation and partial characterization of human factor VP A Bolhuis, T B Hakvoort, K Breederveld, et al.

Biochimica Et Biophysica Acta|September 8, 1993

Molecular basis of an adult form of Sandhoff disease: substitution of glutamine for arginine at position 505 of the beta-chain of beta-hexosaminidase results in a labile enzymeP A Bolhuis, N J Ponne, H Bikker, et al.

Human Genetics|April 1, 1989

Eco RI RFLP in the human thyroid peroxidase (TPO) gene on chromosome 2H Bikker, P A Bolhuis, G Vassart, et al.

Clinical Chemistry|August 1, 1988

Rapid determination of the hypoxanthine increase in ischemic exercise testsP A Bolhuis, R Zwart, P R Bär, et al.

Blood|January 1, 1984

Adhesion of platelets to human artery subendothelium: effect of factor VIII-von Willebrand factor of various multimeric compositionJ J Sixma, K S Sakariassen, N H Beeser-Visser, et al.

Journal of Medical Genetics|April 1, 1994

Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcomeR J Oostra, P A Bolhuis, F A Wijburg, et al.

Applied and Environmental Microbiology|December 3, 1998

Cloning, expression, and chromosomal stabilization of the Propionibacterium shermanii proline iminopeptidase gene (pip) for food-grade application in Lactococcus lactisK Leenhouts, A Bolhuis, J Boot, et al.

Annals of Neurology|February 1, 1995

Concentrations of amyloid beta protein in cerebrospinal fluid of patients with Alzheimer's diseaseW A van Gool, M A Kuiper, G J Walstra, et al.

Biochimica Et Biophysica Acta|June 9, 1992

Steady-state transcript levels of cytochrome c oxidase genes during human myogenesis indicate subunit switching of subunit VIa and co-expression of subunit VIIa isoformsJ W Taanman, N H Herzberg, H De Vries, et al.

Journal of the Neurological Sciences|August 1, 1996

Evidence against increased oxidative stress in fibroblasts from patients with non-superoxide-dismutase-1 mutant familial amyotrophic lateral sclerosisG A Jansen, R J Wanders, G J Jöbsis, et al.

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