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The Journal of Biological Chemistry|July 23, 2013
Cellular localization and characterization of cytosolic binding partners for Gla domain-containing proteins PRRG4 and PRRG2Mustafa N Yazicioglu, Luca Monaldini, Kirk Chu, et al.
AIDS (London, England)|December 13, 2002
Platelet- and megakaryocyte-derived microparticles transfer CXCR4 receptor to CXCR4-null cells and make them susceptible to infection by X4-HIVTomasz Rozmyslowicz, Marcin Majka, Jacek Kijowski, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 25, 2007
Pre-existing AAV capsid-specific CD8+ T cells are unable to eliminate AAV-transduced hepatocytesHua Li, Samuel L Murphy, Wynetta Giles-Davis, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 23, 2008
Undetectable transcription of cap in a clinical AAV vector: implications for preformed capsid in immune responsesBernd Hauck, Samuel L Murphy, Peter H Smith, et al.
JACC. Basic to Translational Science|July 30, 2025
Single Ascending-Dose Study of Selective ErbB4 Agonist JK07 in Heart Failure With Reduced Ejection FractionW H Wilson Tang, Johannes Steiner, Mahwash Kassi, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 9, 2012
Pharmacological modulation of humoral immunity in a nonhuman primate model of AAV gene transfer for hemophilia BFederico Mingozzi, Yifeng Chen, Samuel L Murphy, et al.
The Journal of Clinical Investigation|May 14, 2009
Capsid antigen presentation flags human hepatocytes for destruction after transduction by adeno-associated viral vectorsGary C Pien, Etiena Basner-Tschakarjan, Daniel J Hui, et al.
American Journal of Physiology. Heart and Circulatory Physiology|May 19, 2026
ERBB4 activation prevents microvascular dysfunction in a large animal model of hypertensive heart diseaseMichiel Rl Tubeeckx, Tijs Bringmans, Bo Goovaerts, et al.
Nature Medicine|March 21, 2007
CD8(+) T-cell responses to adeno-associated virus capsid in humansFederico Mingozzi, Marcela V Maus, Daniel J Hui, et al.
Nature|June 28, 2011
In vivo genome editing restores haemostasis in a mouse model of haemophiliaHojun Li, Virginia Haurigot, Yannick Doyon, et al.
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