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Rune R Frants

Showing results (71-80 of 104) with videos related to

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European Journal of Human Genetics : EJHG|November 27, 2008
The expression of type III hyperlipoproteinemia: involvement of lipolysis genesPeter Henneman, Femke van der Sman-de Beer, Payman Hanifi Moghaddam, et al.
Proteomics|April 15, 2010
Quantitative cortical synapse proteomics of a transgenic migraine mouse model with mutated Ca(V)2.1 calcium channelsOleg I Klychnikov, Ka Wan Li, Igor A Sidorov, et al.
Human Mutation|April 3, 2007
The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. OnlineKaate R J Vanmolkot, Elena Babini, Boukje de Vries, et al.
Neuron|March 9, 2004
A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depressionArn M J M van den Maagdenberg, Daniela Pietrobon, Tommaso Pizzorusso, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 5, 2008
Increased risk of cancer other than melanoma in CDKN2A founder mutation (p16-Leiden)-positive melanoma familiesFemke A de Snoo, D Timothy Bishop, Wilma Bergman, et al.
Twin Research : the Official Journal of the International Society for Twin Studies|September 27, 2003
Two-locus linkage analysis applied to putative quantitative trait loci for lipoprotein(a) levelsMarian Beekman, Bastiaan T Heijmans, Nicholas G Martin, et al.
Journal of Human Genetics|October 24, 2007
Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraineMaria-José Castro, Anine H Stam, Carolina Lemos, et al.
Diabetes Care|March 29, 2005
Metabolic syndrome and risk of restenosis in patients undergoing percutaneous coronary interventionJamal S Rana, Pascalle S Monraats, Aeilko H Zwinderman, et al.
Molecular Endocrinology (Baltimore, Md.)|April 26, 2007
The cholesterol-raising factor from coffee beans, cafestol, as an agonist ligand for the farnesoid and pregnane X receptorsMarie-Louise Ricketts, Mark V Boekschoten, Arja J Kreeft, et al.
European Journal of Human Genetics : EJHG|October 23, 2003
Evidence for a QTL on chromosome 19 influencing LDL cholesterol levels in the general populationMarian Beekman, Bastiaan T Heijmans, Nicholas G Martin, et al.
Pageof 11

Showing results (71-80 of 104) with videos related to

Sort By:
Pageof 11
European Journal of Human Genetics : EJHG|November 27, 2008
The expression of type III hyperlipoproteinemia: involvement of lipolysis genesPeter Henneman, Femke van der Sman-de Beer, Payman Hanifi Moghaddam, et al.
Proteomics|April 15, 2010
Quantitative cortical synapse proteomics of a transgenic migraine mouse model with mutated Ca(V)2.1 calcium channelsOleg I Klychnikov, Ka Wan Li, Igor A Sidorov, et al.
Human Mutation|April 3, 2007
The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. OnlineKaate R J Vanmolkot, Elena Babini, Boukje de Vries, et al.
Neuron|March 9, 2004
A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depressionArn M J M van den Maagdenberg, Daniela Pietrobon, Tommaso Pizzorusso, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 5, 2008
Increased risk of cancer other than melanoma in CDKN2A founder mutation (p16-Leiden)-positive melanoma familiesFemke A de Snoo, D Timothy Bishop, Wilma Bergman, et al.
Twin Research : the Official Journal of the International Society for Twin Studies|September 27, 2003
Two-locus linkage analysis applied to putative quantitative trait loci for lipoprotein(a) levelsMarian Beekman, Bastiaan T Heijmans, Nicholas G Martin, et al.
Journal of Human Genetics|October 24, 2007
Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraineMaria-José Castro, Anine H Stam, Carolina Lemos, et al.
Diabetes Care|March 29, 2005
Metabolic syndrome and risk of restenosis in patients undergoing percutaneous coronary interventionJamal S Rana, Pascalle S Monraats, Aeilko H Zwinderman, et al.
Molecular Endocrinology (Baltimore, Md.)|April 26, 2007
The cholesterol-raising factor from coffee beans, cafestol, as an agonist ligand for the farnesoid and pregnane X receptorsMarie-Louise Ricketts, Mark V Boekschoten, Arja J Kreeft, et al.
European Journal of Human Genetics : EJHG|October 23, 2003
Evidence for a QTL on chromosome 19 influencing LDL cholesterol levels in the general populationMarian Beekman, Bastiaan T Heijmans, Nicholas G Martin, et al.
Pageof 11