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Blood|September 22, 2025
Alternative AAV gene therapy for hemophilia A using expression of Bi8, a novel single-chain FVIII-mimetic antibodyVincent Muczynski, Olivier D Christophe, Lewis Tanner, et al.
Reproduction (Cambridge, England)|February 6, 2014
Concerns about the widespread use of rodent models for human risk assessments of endocrine disruptorsRené Habert, Vincent Muczynski, Tiphany Grisin, et al.
Scientific Reports|November 29, 2016
Soluble Siglec-5 associates to PSGL-1 and displays anti-inflammatory activityMarion Pepin, Soraya Mezouar, Julie Pegon, et al.
Cardiovascular Research|February 12, 2021
The VWF/LRP4/αVβ3-axis represents a novel pathway regulating proliferation of human vascular smooth muscle cellsJérémy Lagrange, Morel E Worou, Jean-Baptiste Michel, et al.
JCI Insight|October 14, 2016
LIM kinase/cofilin dysregulation promotes macrothrombocytopenia in severe von Willebrand disease-type 2BAlexandre Kauskot, Sonia Poirault-Chassac, Frédéric Adam, et al.
The New England Journal of Medicine|June 11, 2025
Sustained Clinical Benefit of AAV Gene Therapy in Severe Hemophilia BUlrike M Reiss, Andrew M Davidoff, Edward G D Tuddenham, et al.
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