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Frank Baas

Showing results (181-190 of 231) with videos related to

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International Journal of Molecular Sciences|September 23, 2022
Therapeutic Intervention with Anti-Complement Component 5 Antibody Does Not Reduce NASH but Does Attenuate Atherosclerosis and MIF Concentrations in Ldlr-/-.Leiden MiceFlorine Seidel, Robert Kleemann, Wim van Duyvenvoorde, et al.
Human Molecular Genetics|May 22, 2014
Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemiaSander M Houten, Simone Denis, Heleen Te Brinke, et al.
American Journal of Human Genetics|August 22, 2017
Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar HypoplasiaIsaac Marin-Valencia, Andreas Gerondopoulos, Maha S Zaki, et al.
Annals of the Rheumatic Diseases|June 21, 2019
Non-response to rituximab therapy in rheumatoid arthritis is associated with incomplete disruption of the B cell receptor repertoireSabrina Pollastro, Paul L Klarenbeek, Marieke E Doorenspleet, et al.
Blood|December 10, 2008
LAD-1/variant syndrome is caused by mutations in FERMT3Taco W Kuijpers, Edith van de Vijver, Marian A J Weterman, et al.
Circulation|August 12, 2009
p27kip1-838C>A single nucleotide polymorphism is associated with restenosis risk after coronary stenting and modulates p27kip1 promoter activityClaudia M van Tiel, Peter I Bonta, Saskia Z H Rittersma, et al.
Human Molecular Genetics|August 21, 2018
Hypermorphic and hypomorphic AARS alleles in patients with CMT2N expand clinical and molecular heterogeneitiesMarian A J Weterman, Molly Kuo, Susan B Kenter, et al.
The Journal of Infectious Diseases|December 17, 2013
Streptococcus pneumoniae arginine synthesis genes promote growth and virulence in pneumococcal meningitisJurgen R Piet, Madelijn Geldhoff, Barbera D C van Schaik, et al.
Journal of Innate Immunity|May 13, 2022
Development, Characterization, and in vivo Validation of a Humanized C6 Monoclonal Antibody that Inhibits the Membrane Attack ComplexHeidi Gytz Olesen, Iliana Michailidou, Wioleta M Zelek, et al.
Plos One|May 5, 2012
Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspectsCasper Jansen, Piero Parchi, Sabina Capellari, et al.
Pageof 24

Showing results (181-190 of 231) with videos related to

Sort By:
Pageof 24
International Journal of Molecular Sciences|September 23, 2022
Therapeutic Intervention with Anti-Complement Component 5 Antibody Does Not Reduce NASH but Does Attenuate Atherosclerosis and MIF Concentrations in Ldlr-/-.Leiden MiceFlorine Seidel, Robert Kleemann, Wim van Duyvenvoorde, et al.
Human Molecular Genetics|May 22, 2014
Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemiaSander M Houten, Simone Denis, Heleen Te Brinke, et al.
American Journal of Human Genetics|August 22, 2017
Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar HypoplasiaIsaac Marin-Valencia, Andreas Gerondopoulos, Maha S Zaki, et al.
Annals of the Rheumatic Diseases|June 21, 2019
Non-response to rituximab therapy in rheumatoid arthritis is associated with incomplete disruption of the B cell receptor repertoireSabrina Pollastro, Paul L Klarenbeek, Marieke E Doorenspleet, et al.
Blood|December 10, 2008
LAD-1/variant syndrome is caused by mutations in FERMT3Taco W Kuijpers, Edith van de Vijver, Marian A J Weterman, et al.
Circulation|August 12, 2009
p27kip1-838C>A single nucleotide polymorphism is associated with restenosis risk after coronary stenting and modulates p27kip1 promoter activityClaudia M van Tiel, Peter I Bonta, Saskia Z H Rittersma, et al.
Human Molecular Genetics|August 21, 2018
Hypermorphic and hypomorphic AARS alleles in patients with CMT2N expand clinical and molecular heterogeneitiesMarian A J Weterman, Molly Kuo, Susan B Kenter, et al.
The Journal of Infectious Diseases|December 17, 2013
Streptococcus pneumoniae arginine synthesis genes promote growth and virulence in pneumococcal meningitisJurgen R Piet, Madelijn Geldhoff, Barbera D C van Schaik, et al.
Journal of Innate Immunity|May 13, 2022
Development, Characterization, and in vivo Validation of a Humanized C6 Monoclonal Antibody that Inhibits the Membrane Attack ComplexHeidi Gytz Olesen, Iliana Michailidou, Wioleta M Zelek, et al.
Plos One|May 5, 2012
Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspectsCasper Jansen, Piero Parchi, Sabina Capellari, et al.
Pageof 24