Results 201 to 210 of about 70,698 (266)
Unlocking the potential of bacteriophage-based therapeutic gene delivery in hepatocellular carcinoma. [PDF]
Mitra S +7 more
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An Ad5-Based COVID-19 Vaccine Encoding SARS-CoV-2 Spike Glycoprotein Induces Measurable Antibody and Cytokine Responses in Mice. [PDF]
Erendor F, Uzer F, Sanlioglu S.
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Viral Signals in Acute Appendicitis: Direct Tissue Infection, Systemic Triggers, and the Unresolved Biology of Spontaneous Resolution. [PDF]
Berikkhanov Z +10 more
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Adenoviral keratoconjunctivitis
Survey of Ophthalmology, 2015Viral conjunctivitis caused by adenovirus is the most common infectious conjunctivitis. Adenoviruses are highly contagious pathogens. The modes of transmission are mainly through hand to eye contact, ocular secretions, respiratory droplets, and contact with ophthalmic care providers and their medical instruments.
Vishal, Jhanji +4 more
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Biosafety of Adenoviral Vectors
Current Gene Therapy, 2003Adenoviral vectors can efficiently transduce a broad variety of different cell types and have been used extensively in preclinical and clinical studies. However, early generation of adenoviral vectors retained residual adenoviral genes that contribute to inflammatory immune responses and toxicity.
Chuah, Marinee K L +2 more
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Construction of Adenoviral Vectors
Molecular Biotechnology, 2001Recombinant adenovirus vectors have proven to be useful tools in facilitating gene transfer. Construction of such vectors requires a knowledge of the adenovirus genome structure and its life cycle. A commonly used recombinant adenovirus involves deletion of the E1 region; such a recombinant is traditionally produced by overlap recombination after ...
A R, Davis +4 more
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Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression, 2002
Replication-defective vectors based on human adenovirus serotypes 2 and 5 (Ad2 and Ad5) possess a number of attributes which favor their use as gene delivery vehicles in gene therapy applications. However, the widespread distribution of the primary cellular receptor for Ad, the coxsackievirus and adenovirus receptor (CAR), allows Ad vectors to infect a
Brian G, Barnett +2 more
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Replication-defective vectors based on human adenovirus serotypes 2 and 5 (Ad2 and Ad5) possess a number of attributes which favor their use as gene delivery vehicles in gene therapy applications. However, the widespread distribution of the primary cellular receptor for Ad, the coxsackievirus and adenovirus receptor (CAR), allows Ad vectors to infect a
Brian G, Barnett +2 more
openaire +2 more sources
Current Protocols in Human Genetics, 2004
AbstractAdenoviral vectors have been widely used as efficient gene delivery vehicles for gene therapy and vaccine development, as well as gene function studies. The recently developed AdEasy system is a simple and efficient method for rapid generation of recombinant adenoviruses.
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AbstractAdenoviral vectors have been widely used as efficient gene delivery vehicles for gene therapy and vaccine development, as well as gene function studies. The recently developed AdEasy system is a simple and efficient method for rapid generation of recombinant adenoviruses.
openaire +2 more sources

