Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Joseph S. Orlando"'
Publikováno v:
Journal of Virology. 83:8733-8743
Of the five herpes simplex virus type 1 immediate early (IE) proteins, the least is known about the function of ICP22 during productive infection and latency. Research characterizing the physical and functional properties of the protein has been limi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b96247e4947f0e45190bde6f8d6cb795
https://doi.org/10.1128/jvi.00810-09
https://doi.org/10.1128/jvi.00810-09
Autor:
Joseph S. Orlando, David A. Ornelles
Publikováno v:
Journal of Virology. 76:1475-1487
The E4orf6 protein of group C adenovirus is an oncoprotein that, in association with the E1B 55-kDa protein and by E1B-independent means, promotes virus replication. An arginine-faced amphipathic α-helix in the E4orf6 protein is required for the E4o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3390588c72611d5ded089c10eab3ed6
https://doi.org/10.1128/jvi.76.3.1475-1487.2002
https://doi.org/10.1128/jvi.76.3.1475-1487.2002
Autor:
Janice M. Zabolotny, Dimcho Bachvarov, Sang Wook Yoo, Martin Lange, Makoto Hiromura, Anna S. Kushnir, Vladimir Gelev, Anny Usheva, Eric Paquet, Priscilla A. Schaffer, Nobuo Horikoshi, Joseph S. Orlando
Publikováno v:
Scientific Reports
Experimental and bioinformatic studies of transcription initiation by RNA polymerase II (RNAP2) have revealed a mechanism of RNAP2 transcription initiation less uniform across gene promoters than initially thought. However, the general transcription
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d01fb5750269821617a3998bf7b98728
http://europepmc.org/articles/PMC3895905
http://europepmc.org/articles/PMC3895905
Autor:
Magdalena Kosz-Vnenchak, David M. Knipe, Todd L. Astor, Joseph S. Orlando, Anna S. Kushnir, Stephen A. Rice, Priscilla A. Schaffer, John W. Balliet
Publikováno v:
Journal of virology. 80(19)
The immediate-early regulatory protein ICP22 is required for efficient replication of herpes simplex virus type 1 in some cell types (permissive) but not in others (restrictive). In mice infected via the ocular route, the pathogenesis of an ICP22 −
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80fa12f2b1f58dd610411080384849a4
https://pubmed.ncbi.nlm.nih.gov/16973544
https://pubmed.ncbi.nlm.nih.gov/16973544
Publikováno v:
Journal of virology. 80(8)
Herpes simplex virus type 1 ICP22 − /U S 1.5 − mutants initiate viral gene expression in all cells; however, in most cell types, the replication process stalls due to an inability to express γ 2 late proteins. Although the function of ICP22/U S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d164380bc0f36e897eab523d4dc42d5c
https://pubmed.ncbi.nlm.nih.gov/16571817
https://pubmed.ncbi.nlm.nih.gov/16571817
Autor:
David A. Ornelles, Steven M. Yannone, Stephen B. Waters, Joseph S. Orlando, Steven A. Akman, Constantinos Koumenis, David J. Chen, Lori S. Hart, Christine Naczki
Publikováno v:
The Journal of biological chemistry. 280(2)
The adenoviral protein E4orf6 has been shown to inhibit both in vitro V(D)J recombination and adenoviral DNA concatenation, two processes that rely on cellular DNA double strand break repair (DSBR) proteins. Most of the known activities of E4orf6 dur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bbaa4edbb80d9af37868e301e24891c
https://pubmed.ncbi.nlm.nih.gov/15507430
https://pubmed.ncbi.nlm.nih.gov/15507430
Autor:
David A. Ornelles, Joseph S. Orlando
Publikováno v:
Journal of virology. 73(6)
A region in the carboxy terminus of the protein encoded by open reading frame 6 in early region 4 (E4orf6) of adenovirus type 5 was determined to be required for directing nuclear localization of the E1B 55-kDa protein and for efficient virus replica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a18e987e8e584d04cc409df911c54c89
https://pubmed.ncbi.nlm.nih.gov/10233919
https://pubmed.ncbi.nlm.nih.gov/10233919
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