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Benjamin J Samelson-Jones

Showing results (21-30 of 51) with videos related to

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Transfusion|April 26, 2025
Hypertension and encephalopathy in a pediatric patient following red blood cell transfusionSaarah Hussain, Grace Linder, Craig A Press, et al.
Pediatric Blood & Cancer|November 23, 2021
Andexanet alfa for reversal of rivaroxaban in a child with intracranial hemorrhageKaoru Takasaki, David Hehir, Leslie Raffini, et al.
Pediatric Blood & Cancer|December 30, 2017
MYH9-macrothrombocytopenia caused by a novel variant (E1421K) initially presenting as apparent neonatal alloimmune thrombocytopeniaBenjamin J Samelson-Jones, Paula M Kramer, Michael Chicka, et al.
Molecular Therapy. Methods & Clinical Development|June 4, 2020
Timing of Intensive Immunosuppression Impacts Risk of Transgene Antibodies after AAV Gene Therapy in Nonhuman PrimatesBenjamin J Samelson-Jones, Jonathan D Finn, Patricia Favaro, et al.
JCI Insight|June 21, 2019
Hyperactivity of factor IX Padua (R338L) depends on factor VIIIa cofactor activityBenjamin J Samelson-Jones, Jonathan D Finn, Lindsey A George, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 29, 2021
Real-world cost estimates of initiating emicizumab in US patients with haemophilia ABenjamin J Samelson-Jones, Christine Guelcher, Jan Kuhn, et al.
Open Veterinary Journal|October 2, 2025
Ancient origin of the furin sequence in the wolf F8 geneJoshua I Siner, Shannon Barber-Meyer, Benjamin J Samelson-Jones, et al.
International Journal of Molecular Sciences|October 16, 2024
A Novel Murine Model Enabling rAAV8-PC Gene Therapy for Severe Protein C DeficiencySarina Levy-Mendelovich, Einat Avishai, Benjamin J Samelson-Jones, et al.
Biorxiv : the Preprint Server for Biology|February 3, 2025
Loss of factor VIII in zebrafish rebalances antithrombin deficiency but has a limited bleeding diathesisCatherine E Richter, Azhwar Raghunath, Megan S Griffin, et al.
Blood Advances|March 4, 2018
Complete correction of hemophilia B phenotype by FIX-Padua skeletal muscle gene therapy in an inhibitor-prone dog modelRobert A French, Benjamin J Samelson-Jones, Glenn P Niemeyer, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
Transfusion|April 26, 2025
Hypertension and encephalopathy in a pediatric patient following red blood cell transfusionSaarah Hussain, Grace Linder, Craig A Press, et al.
Pediatric Blood & Cancer|November 23, 2021
Andexanet alfa for reversal of rivaroxaban in a child with intracranial hemorrhageKaoru Takasaki, David Hehir, Leslie Raffini, et al.
Pediatric Blood & Cancer|December 30, 2017
MYH9-macrothrombocytopenia caused by a novel variant (E1421K) initially presenting as apparent neonatal alloimmune thrombocytopeniaBenjamin J Samelson-Jones, Paula M Kramer, Michael Chicka, et al.
Molecular Therapy. Methods & Clinical Development|June 4, 2020
Timing of Intensive Immunosuppression Impacts Risk of Transgene Antibodies after AAV Gene Therapy in Nonhuman PrimatesBenjamin J Samelson-Jones, Jonathan D Finn, Patricia Favaro, et al.
JCI Insight|June 21, 2019
Hyperactivity of factor IX Padua (R338L) depends on factor VIIIa cofactor activityBenjamin J Samelson-Jones, Jonathan D Finn, Lindsey A George, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 29, 2021
Real-world cost estimates of initiating emicizumab in US patients with haemophilia ABenjamin J Samelson-Jones, Christine Guelcher, Jan Kuhn, et al.
Open Veterinary Journal|October 2, 2025
Ancient origin of the furin sequence in the wolf F8 geneJoshua I Siner, Shannon Barber-Meyer, Benjamin J Samelson-Jones, et al.
International Journal of Molecular Sciences|October 16, 2024
A Novel Murine Model Enabling rAAV8-PC Gene Therapy for Severe Protein C DeficiencySarina Levy-Mendelovich, Einat Avishai, Benjamin J Samelson-Jones, et al.
Biorxiv : the Preprint Server for Biology|February 3, 2025
Loss of factor VIII in zebrafish rebalances antithrombin deficiency but has a limited bleeding diathesisCatherine E Richter, Azhwar Raghunath, Megan S Griffin, et al.
Blood Advances|March 4, 2018
Complete correction of hemophilia B phenotype by FIX-Padua skeletal muscle gene therapy in an inhibitor-prone dog modelRobert A French, Benjamin J Samelson-Jones, Glenn P Niemeyer, et al.
Pageof 6