Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Julian V. Melton"'
Autor:
Brett A. Lidbury, Gerald M. McInerney, Andres Merits, Suresh Mahalingam, Liis Karo-Astover, Kuo-Ching Sheng, Julian V. Melton, Bastian Thaa, Michelle Nelson, Lara J. Herrero, Peter W. Gage, Adam Taylor, Gary Ewart
Publikováno v:
Journal of Virology. 90:4150-4159
The alphaviral 6k gene region encodes the two structural proteins 6K protein and, due to a ribosomal frameshift event, the transframe protein (TF). Here, we characterized the role of the 6k proteins in the arthritogenic alphavirus Ross River virus (R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::465b1e3368a2f40502855d8d0b9818b7
https://doi.org/10.1128/jvi.03192-15
https://doi.org/10.1128/jvi.03192-15
Publikováno v:
Annals of the New York Academy of Sciences. 1102:96-108
Alphaviruses such as the Sindbis-group viruses, Scandinavian Ockelbo virus, the African Asian chikungunya virus, the African O'nyong-nyong virus, the South American Mayaro virus, and the Australasian Barmah Forest and Ross River viruses, are commonly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::192d425f2a13b45ba38c17639bfc50d9
https://doi.org/10.1196/annals.1408.007
https://doi.org/10.1196/annals.1408.007
Publikováno v:
Journal of Biological Chemistry. 277:46923-46931
Ross River virus and Barmah Forest virus are Australian arboviruses of the Alphavirus genus. Features of alphavirus infection include an increased permeability of cells to monovalent cations followed by virion budding. Virally encoded ion channels ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d53975aa43041038095c324842d0f647
https://doi.org/10.1074/jbc.m207847200
https://doi.org/10.1074/jbc.m207847200
Autor:
Philip W. Sheard, Michael P. Murphy, Andrew M. James, Serena J. Hyslop, Michael A. Packer, Cheng-Yoong Pang, Julian V. Melton, Carolyn M. Porteous, Yau-Huei Wei, William K. Porteous
Publikováno v:
European Journal of Biochemistry. 257:192-201
Mutations and deletions in mitochondrial DNA (mtDNA) lead to a number of human diseases characterized by neuromuscular degeneration. Accumulation of truncated mtDNA molecules (delta-mtDNA) lacking a specific 4977-bp fragment, the common deletion, lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcc2ff4e1b8e2ba2beba2bb9c49412bb
https://doi.org/10.1046/j.1432-1327.1998.2570192.x
https://doi.org/10.1046/j.1432-1327.1998.2570192.x
Publikováno v:
Protein Reviews ISBN: 9780306484957
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b928d7b985a34e6d6624da2bcfc61c72
https://doi.org/10.1007/0-387-28146-0_15
https://doi.org/10.1007/0-387-28146-0_15
