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R R Frants

Showing results (51-60 of 282) with videos related to

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Annals of Human Biology|May 1, 1986
ABH secretion polymorphism in Icelanders, Aland Islanders, Finns, Finnish Lapps, Komi and Greenland Eskimos: a review and new dataA W Eriksson, K Partanen, R R Frants, et al.
Annals of Neurology|October 8, 1999
Hyperekplexia phenotype due to compound heterozygosity for GLRA1 gene mutationsM N Vergouwe, M A Tijssen, A C Peters, et al.
Metabolism: Clinical and Experimental|March 1, 1993
Treatment of E2E2 homozygous familial dysbetalipoproteinemic subjects with gemfibrozil does not enhance the binding of their d < 1.019 lipoprotein fraction to the low-density lipoprotein receptorM Mulder, A H Smelt, S P Zhao, et al.
The Journal of Biological Chemistry|December 15, 1993
Inefficient degradation of triglyceride-rich lipoprotein by HepG2 cells is due to a retarded transport to the lysosomal compartmentP Lombardi, M Mulder, H van der Boom, et al.
Current Opinion in Neurology|June 1, 1997
The quest for migraine genesG M Terwindt, J Haan, R A Ophoff, et al.
Lancet (London, England)|June 22, 1991
Alpha-1-antitrypsin and blood pressureD I Boomsma, J F Orbeleke, N G Martin, et al.
Blood|July 1, 1983
Genetic evidence for fetal origin of transcobalamin II in human cord bloodH J Porck, M Fràter-Schröder, R R Frants, et al.
Human Genetics|January 1, 1982
Evidence of duplication of the human salivary amylase geneJ C Pronk, R R Frants, W Jansen, et al.
Human Genetics|January 1, 1988
Apolipoprotein gene cluster on chromosome 19. Definite localization of the APOC2 gene and the polymorphic Hpa I site associated with type III hyperlipoproteinemiaM Smit, E van der Kooij-Meijs, R R Frants, et al.
Neurologia (Barcelona, Spain)|January 22, 1998
Familial hemiplegic migraine: involvement of a calcium neuronal channelR A Ophoff, G M Terwindt, M N Vergouwe, et al.
Pageof 29

Showing results (51-60 of 282) with videos related to

Sort By:
Pageof 29
Annals of Human Biology|May 1, 1986
ABH secretion polymorphism in Icelanders, Aland Islanders, Finns, Finnish Lapps, Komi and Greenland Eskimos: a review and new dataA W Eriksson, K Partanen, R R Frants, et al.
Annals of Neurology|October 8, 1999
Hyperekplexia phenotype due to compound heterozygosity for GLRA1 gene mutationsM N Vergouwe, M A Tijssen, A C Peters, et al.
Metabolism: Clinical and Experimental|March 1, 1993
Treatment of E2E2 homozygous familial dysbetalipoproteinemic subjects with gemfibrozil does not enhance the binding of their d < 1.019 lipoprotein fraction to the low-density lipoprotein receptorM Mulder, A H Smelt, S P Zhao, et al.
The Journal of Biological Chemistry|December 15, 1993
Inefficient degradation of triglyceride-rich lipoprotein by HepG2 cells is due to a retarded transport to the lysosomal compartmentP Lombardi, M Mulder, H van der Boom, et al.
Current Opinion in Neurology|June 1, 1997
The quest for migraine genesG M Terwindt, J Haan, R A Ophoff, et al.
Lancet (London, England)|June 22, 1991
Alpha-1-antitrypsin and blood pressureD I Boomsma, J F Orbeleke, N G Martin, et al.
Blood|July 1, 1983
Genetic evidence for fetal origin of transcobalamin II in human cord bloodH J Porck, M Fràter-Schröder, R R Frants, et al.
Human Genetics|January 1, 1982
Evidence of duplication of the human salivary amylase geneJ C Pronk, R R Frants, W Jansen, et al.
Human Genetics|January 1, 1988
Apolipoprotein gene cluster on chromosome 19. Definite localization of the APOC2 gene and the polymorphic Hpa I site associated with type III hyperlipoproteinemiaM Smit, E van der Kooij-Meijs, R R Frants, et al.
Neurologia (Barcelona, Spain)|January 22, 1998
Familial hemiplegic migraine: involvement of a calcium neuronal channelR A Ophoff, G M Terwindt, M N Vergouwe, et al.
Pageof 29