Adenoviruses have long been identified as good candidates for use as viral vectors in gene therapy and as vaccines. These viruses can infect multiple cell types, while in division or in quiescence, and are relatively easy to manipulate so that parts of their genome can be replaced with exogenous genes. Progressive safety improvements in replication-deficient adenoviral vectors have been achieved with the second and third generation, and ending with the gutless adenoviral vectors. Adenoviral vectors are immunogenic and can act as adjuvants. Nonetheless, the potency of human recombinant adenoviral vaccines was below expectations in clinical trials mainly because of the pre-existing adenoviral immunity found in the general population. This dra...
Adenoviruses have been extensively researched for use as vectors for both gene therapy and vaccinati...
Adenoviruses are efficient gene delivery vectors based on their ability to transduce a wide variety ...
The goal of this research was to examine the feasibility of designing gene delivery vectors based on...
Adenoviruses have long been identified as good candidates for use as viral vectors in gene therapy a...
Adenoviruses have long been identified as good candidates for use as viral vectors in gene therapy a...
Adenoviruses are one of the most genetically diverse DNA viruses and cause non-life-threatening infe...
Adenoviruses are among the most studied and at the same time most mysterious of viruses. In this boo...
Background: Engineered adenoviruses are being increasingly explored as immunoprophylactic or immunot...
Background: Engineered adenoviruses are being increasingly explored as immunoprophylactic or immunot...
It is hoped that the use of gene transfer technology to treat both monogenetic and acquired diseases...
There are no effective approaches to treatment and prevention of many infectious diseases representi...
Adenoviruses are one of the most widely investigated vectors for gene therapy. Their attributes incl...
Adenoviruses are efficient gene delivery vectors based on their ability to transduce a wide variety ...
Adenoviruses have been extensively researched for use as vectors for both gene therapy and vaccinati...
AbstractNonhuman adenoviruses including bovine adenovirus serotype 3 (BAd3) and porcine adenovirus s...
Adenoviruses have been extensively researched for use as vectors for both gene therapy and vaccinati...
Adenoviruses are efficient gene delivery vectors based on their ability to transduce a wide variety ...
The goal of this research was to examine the feasibility of designing gene delivery vectors based on...
Adenoviruses have long been identified as good candidates for use as viral vectors in gene therapy a...
Adenoviruses have long been identified as good candidates for use as viral vectors in gene therapy a...
Adenoviruses are one of the most genetically diverse DNA viruses and cause non-life-threatening infe...
Adenoviruses are among the most studied and at the same time most mysterious of viruses. In this boo...
Background: Engineered adenoviruses are being increasingly explored as immunoprophylactic or immunot...
Background: Engineered adenoviruses are being increasingly explored as immunoprophylactic or immunot...
It is hoped that the use of gene transfer technology to treat both monogenetic and acquired diseases...
There are no effective approaches to treatment and prevention of many infectious diseases representi...
Adenoviruses are one of the most widely investigated vectors for gene therapy. Their attributes incl...
Adenoviruses are efficient gene delivery vectors based on their ability to transduce a wide variety ...
Adenoviruses have been extensively researched for use as vectors for both gene therapy and vaccinati...
AbstractNonhuman adenoviruses including bovine adenovirus serotype 3 (BAd3) and porcine adenovirus s...
Adenoviruses have been extensively researched for use as vectors for both gene therapy and vaccinati...
Adenoviruses are efficient gene delivery vectors based on their ability to transduce a wide variety ...
The goal of this research was to examine the feasibility of designing gene delivery vectors based on...