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Jonathan C Stephens

Showing results (1-10 of 18) with videos related to

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Infection and Immunity|June 23, 2006
Stabilization of a plasmid coding for a heterologous antigen in Salmonella enterica serotype typhi vaccine strain CVD908-htrA by using site-specific recombinationJonathan C Stephens, Michael J Darsley, Arthur K Turner
Clinical and Vaccine Immunology : CVI|October 14, 2011
Generation and characterization of a live attenuated enterotoxigenic Escherichia coli combination vaccine expressing six colonization factors and heat-labile toxin subunit BArthur K Turner, Jonathan C Stephens, Juliet C Beavis, et al.
Infection and Immunity|January 24, 2006
Construction and phase I clinical evaluation of the safety and immunogenicity of a candidate enterotoxigenic Escherichia coli vaccine strain expressing colonization factor antigen CFA/IArthur K Turner, Juliet C Beavis, Jonathan C Stephens, et al.
Clinical Immunology (Orlando, Fla.)|May 1, 2020
ADA2 deficiency complicated by EBV-driven lymphoproliferative diseaseEmily Staples, Ilenia Simeoni, Jonathan C Stephens, et al.
European Journal of Human Genetics : EJHG|November 14, 2013
Common genetic variants do not associate with CAD in familial hypercholesterolemiaErik P A van Iperen, Suthesh Sivapalaratnam, S Matthijs Boekholdt, et al.
Blood Advances|October 4, 2024
The common VTE-protective G haplotype of F5 increases factor V-short, TFPI function, and risk of bleedingMatthew C Sims, Magdalena Gierula, Jonathan C Stephens, et al.
Blood|January 9, 2017
Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopeniaSuthesh Sivapalaratnam, Sarah K Westbury, Jonathan C Stephens, et al.
Blood|June 21, 2019
Germline mutations in the transcription factor IKZF5 cause thrombocytopeniaClaire Lentaigne, Daniel Greene, Suthesh Sivapalaratnam, et al.
Nature Genetics|February 28, 2012
Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndromeCornelis A Albers, Dirk S Paul, Harald Schulze, et al.
Human Mutation|September 29, 2019
Next-generation sequencing for the diagnosis of MYH9-RD: Predicting pathogenic variantsLoredana Bury, Karyn Megy, Jonathan C Stephens, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Infection and Immunity|June 23, 2006
Stabilization of a plasmid coding for a heterologous antigen in Salmonella enterica serotype typhi vaccine strain CVD908-htrA by using site-specific recombinationJonathan C Stephens, Michael J Darsley, Arthur K Turner
Clinical and Vaccine Immunology : CVI|October 14, 2011
Generation and characterization of a live attenuated enterotoxigenic Escherichia coli combination vaccine expressing six colonization factors and heat-labile toxin subunit BArthur K Turner, Jonathan C Stephens, Juliet C Beavis, et al.
Infection and Immunity|January 24, 2006
Construction and phase I clinical evaluation of the safety and immunogenicity of a candidate enterotoxigenic Escherichia coli vaccine strain expressing colonization factor antigen CFA/IArthur K Turner, Juliet C Beavis, Jonathan C Stephens, et al.
Clinical Immunology (Orlando, Fla.)|May 1, 2020
ADA2 deficiency complicated by EBV-driven lymphoproliferative diseaseEmily Staples, Ilenia Simeoni, Jonathan C Stephens, et al.
European Journal of Human Genetics : EJHG|November 14, 2013
Common genetic variants do not associate with CAD in familial hypercholesterolemiaErik P A van Iperen, Suthesh Sivapalaratnam, S Matthijs Boekholdt, et al.
Blood Advances|October 4, 2024
The common VTE-protective G haplotype of F5 increases factor V-short, TFPI function, and risk of bleedingMatthew C Sims, Magdalena Gierula, Jonathan C Stephens, et al.
Blood|January 9, 2017
Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopeniaSuthesh Sivapalaratnam, Sarah K Westbury, Jonathan C Stephens, et al.
Blood|June 21, 2019
Germline mutations in the transcription factor IKZF5 cause thrombocytopeniaClaire Lentaigne, Daniel Greene, Suthesh Sivapalaratnam, et al.
Nature Genetics|February 28, 2012
Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndromeCornelis A Albers, Dirk S Paul, Harald Schulze, et al.
Human Mutation|September 29, 2019
Next-generation sequencing for the diagnosis of MYH9-RD: Predicting pathogenic variantsLoredana Bury, Karyn Megy, Jonathan C Stephens, et al.
Pageof 2