AbstractThe adeno-associated virus (AAV) replication proteins Rep78 and Rep68 regulate viral gene expression and DNA amplification. Their effects on both processes suggest that they play roles in all phases of the virus life cycle. We have investigated Rep protein phosphorylation to determine if this modification might alter Rep function. All four Rep proteins were found to be phosphorylated in AAV and adenovirus co-infected cell cultures, and Rep proteins contained phospho-serine whereas no phospho-threonine or -tyrosine was detected. We also observed that when viral DNA synthesis was inhibited, there was a significant decrease in the level of Rep78/68 phosphorylation. Our results suggest a plausible mechanism whereby AAV Rep78/68 function...
AbstractThe adeno-associated virus (AAV) terminal repeats (TR) are cis required, and the AAV encoded...
Adeno-associated virus (AAV) uses three promoters, p5, p19, and p40, to regulate viral gene expressi...
Recent success achieving long-term in vivo gene transfer without a significant immune response by us...
AbstractThe adeno-associated virus (AAV) replication proteins Rep78 and Rep68 regulate viral gene ex...
AbstractRep78/68 proteins of adeno-associated virus type 2 (AAV-2) are involved in many aspects of t...
AbstractResolution of the covalently closed terminus of adeno-associated Virus (AAV) DNA is mediated...
AbstractAdeno-associated virus (AAV) replication proteins Rep78 and Rep68 play major roles in the li...
AbstractAdeno-associated virus (AAV) replication (Rep) proteins are pleiotropic effectors of viral D...
The adeno-associated virus type 2 (AAV) replication (Rep) proteins Rep78 and 68 (Rep78/68) exhibit a...
AbstractThe Rep68 and Rep78 proteins of adeno-associated virus type-2 (AAV) are multifunctional DNA ...
The life cycle of the human parvovirus adeno-associated virus (AAV) is orchestrated by four Rep prot...
Die molekularen Mechanismen der vielfältigen Effekte der Rep Proteine des Adeno-assoziierten Virus (...
The adeno-associated virus (AAV) Rep protein is required for both viral DNA replication and transact...
We previously reported the development of an in vitro adeno-associated virus (AAV) DNA replication s...
AbstractInteraction between the adenoassociated virus (AAV) replication proteins, Rep68 and 78, and ...
AbstractThe adeno-associated virus (AAV) terminal repeats (TR) are cis required, and the AAV encoded...
Adeno-associated virus (AAV) uses three promoters, p5, p19, and p40, to regulate viral gene expressi...
Recent success achieving long-term in vivo gene transfer without a significant immune response by us...
AbstractThe adeno-associated virus (AAV) replication proteins Rep78 and Rep68 regulate viral gene ex...
AbstractRep78/68 proteins of adeno-associated virus type 2 (AAV-2) are involved in many aspects of t...
AbstractResolution of the covalently closed terminus of adeno-associated Virus (AAV) DNA is mediated...
AbstractAdeno-associated virus (AAV) replication proteins Rep78 and Rep68 play major roles in the li...
AbstractAdeno-associated virus (AAV) replication (Rep) proteins are pleiotropic effectors of viral D...
The adeno-associated virus type 2 (AAV) replication (Rep) proteins Rep78 and 68 (Rep78/68) exhibit a...
AbstractThe Rep68 and Rep78 proteins of adeno-associated virus type-2 (AAV) are multifunctional DNA ...
The life cycle of the human parvovirus adeno-associated virus (AAV) is orchestrated by four Rep prot...
Die molekularen Mechanismen der vielfältigen Effekte der Rep Proteine des Adeno-assoziierten Virus (...
The adeno-associated virus (AAV) Rep protein is required for both viral DNA replication and transact...
We previously reported the development of an in vitro adeno-associated virus (AAV) DNA replication s...
AbstractInteraction between the adenoassociated virus (AAV) replication proteins, Rep68 and 78, and ...
AbstractThe adeno-associated virus (AAV) terminal repeats (TR) are cis required, and the AAV encoded...
Adeno-associated virus (AAV) uses three promoters, p5, p19, and p40, to regulate viral gene expressi...
Recent success achieving long-term in vivo gene transfer without a significant immune response by us...