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Jonathan Stephens

Showing results (11-20 of 48) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|July 8, 2020
A new pedigree with thrombomodulin-associated coagulopathy in which delayed fibrinolysis is partially attenuated by co-inherited TAFI deficiencySarah K Westbury, Claire S Whyte, Jonathan Stephens, et al.
Journal of Immunological Methods|October 10, 2006
Production of calmodulin-tagged proteins in Drosophila Schneider S2 cells: a novel system for antigen production and phage antibody isolationNicola S Jennings, Peter A Smethurst, C Graham Knight, et al.
Nature Communications|July 24, 2020
Author Correction: Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humansWei Wei, Alistair T Pagnamenta, Nicholas Gleadall, et al.
Blood|December 11, 2007
A nonsynonymous SNP in the ITGB3 gene disrupts the conserved membrane-proximal cytoplasmic salt bridge in the alphaIIbbeta3 integrin and cosegregates dominantly with abnormal proplatelet formation and macrothrombocytopeniaCedric Ghevaert, Alexandre Salsmann, Nicholas A Watkins, et al.
Cell Reports|March 4, 2015
Leukemia-associated somatic mutations drive distinct patterns of age-related clonal hemopoiesisThomas McKerrell, Naomi Park, Thaidy Moreno, et al.
Blood|June 24, 2020
Mutational and phenotypic characterization of hereditary hemorrhagic telangiectasiaClaire L Shovlin, Ilenia Simeoni, Kate Downes, et al.
Transfusion|May 31, 2020
Multiple GYPB gene deletions associated with the U- phenotype in those of African ancestryWilliam J Lane, Nicholas S Gleadall, Judith Aeschlimann, et al.
American Journal of Human Genetics|December 27, 2008
A genome-wide association study identifies three loci associated with mean platelet volumeChrista Meisinger, Holger Prokisch, Christian Gieger, et al.
Nature Genetics|July 19, 2011
Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndromeCornelis A Albers, Ana Cvejic, Rémi Favier, et al.
Thrombosis and Haemostasis|June 28, 2022
Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin DeficiencyBelén de la Morena-Barrio, Jonathan Stephens, María Eugenia de la Morena-Barrio, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Journal of Thrombosis and Haemostasis : JTH|July 8, 2020
A new pedigree with thrombomodulin-associated coagulopathy in which delayed fibrinolysis is partially attenuated by co-inherited TAFI deficiencySarah K Westbury, Claire S Whyte, Jonathan Stephens, et al.
Journal of Immunological Methods|October 10, 2006
Production of calmodulin-tagged proteins in Drosophila Schneider S2 cells: a novel system for antigen production and phage antibody isolationNicola S Jennings, Peter A Smethurst, C Graham Knight, et al.
Nature Communications|July 24, 2020
Author Correction: Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humansWei Wei, Alistair T Pagnamenta, Nicholas Gleadall, et al.
Blood|December 11, 2007
A nonsynonymous SNP in the ITGB3 gene disrupts the conserved membrane-proximal cytoplasmic salt bridge in the alphaIIbbeta3 integrin and cosegregates dominantly with abnormal proplatelet formation and macrothrombocytopeniaCedric Ghevaert, Alexandre Salsmann, Nicholas A Watkins, et al.
Cell Reports|March 4, 2015
Leukemia-associated somatic mutations drive distinct patterns of age-related clonal hemopoiesisThomas McKerrell, Naomi Park, Thaidy Moreno, et al.
Blood|June 24, 2020
Mutational and phenotypic characterization of hereditary hemorrhagic telangiectasiaClaire L Shovlin, Ilenia Simeoni, Kate Downes, et al.
Transfusion|May 31, 2020
Multiple GYPB gene deletions associated with the U- phenotype in those of African ancestryWilliam J Lane, Nicholas S Gleadall, Judith Aeschlimann, et al.
American Journal of Human Genetics|December 27, 2008
A genome-wide association study identifies three loci associated with mean platelet volumeChrista Meisinger, Holger Prokisch, Christian Gieger, et al.
Nature Genetics|July 19, 2011
Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndromeCornelis A Albers, Ana Cvejic, Rémi Favier, et al.
Thrombosis and Haemostasis|June 28, 2022
Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin DeficiencyBelén de la Morena-Barrio, Jonathan Stephens, María Eugenia de la Morena-Barrio, et al.
Pageof 5