Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Frank J. O'Neill"'
Autor:
John E. Greenlee, Frank J. O'Neill
Publikováno v:
Clinical Virology. :581-601
Publikováno v:
Virology. 245:289-302
Using a series of modified wtSV40 and early region SV40 DNAs, we assayed the effect of viral late region sequences on T-antigen production by the SV40 early region. We found that SV40 late region (L-SV40) DNA sequences reduced T-antigen (T-Ag) produc
Publikováno v:
Oncogene. 14:955-965
In several clones of SV40-transformed human cells, we investigated the relative amounts of large T-Antigen (T-Ag) and p53 proteins, both unbound and associated within complexes, with the goal of identifying changes associated with transformation and
Publikováno v:
Virus Research. 34:237-263
SV40 containing recombinant vectors were introduced into permissive simian, non-permissive rodent and semi-permissive human cell lines, and assayed for transformation. All mouse and human cell clones expressed T-antigen (T-Ag) and were morphologicall
Publikováno v:
Virus Research. 25:169-187
Simian virus 40 (SV40) propagates poorly in cells from human embryonic kidney (HEK) and human fetal fibroblasts (HFF) while BK virus grows well in many human cell types. It has been suggested that sequences within the SV40 late region but not within
Publikováno v:
Intervirology. 31:175-187
WtSV40 and its variant EL-SV40 (contains two complementing defective genomes) fail to productively infect human embryonic kidney cells or human fibroblasts. However, early SV40 (E-SV40) genomes can propagate in human cells when complemented by a part
Publikováno v:
Journal of neurovirology. 9(5)
In immunologically normal individuals, the polyomavirus, JC virus (JCV), produces an asymptomatic primary infection followed by lifelong persistence of the virus in renal tubular epithelial cells. In some immunocompromised patients, however, in parti
Autor:
Helen Carney, Frank J. O'Neill
Publikováno v:
Journal of Neurovirology. 5:324-324
Autor:
S.A. Nachtigal, T. Brennan, J. Camilleri, John R. Martin, Michael D. Dority, Ronald Glaser, D.R. Mayo, M. Fons, Joseph F. Metcalf, Karen D. Cockley, William C. Wallen, Frank J. Jenkins, Savio L.C. Woo, XiaoLing Xu, John E. Oakes, C.Z. Deng, K.J. Johnson, John J. Docherty, Herman F. Staats, A. Legrand, P.R. Knight, S. AbuBakar, Laura A. Burdett, Antonia R. Sepulveda, Brian Wigdahl, Milton J. Finegold, M. Nachtigal, Anamaris M. Colberg-Poley, MaryAnn Jerkofsky, Marshall V. Williams, Linda E. Fisher, I. Boldogh, Scott L. Barmat, Daniel J. Tenney, Ching-Hwa Ann Tsai, Navin M. Patel, Thomas Albrecht, A.M. Penna, Peter L. Abt, Satvir S. Tevethia, Joan M. Cory, Jeffrey P. Iltis, Robert N. Lausch, Janet S. Butel, T. Albrecht, Betsy M. Ohlsson-Wilhelm, Frank J. O'Neill, Thomas H. Miller, I.H. Gomolin, Fred Rapp, Yuetsu Tanaka, Helena Wrzos, Stephen R. Lee, S.P. Sirpenski, Mary K. Howett, P. Greenspan, John W. Kreider, Charles Kunsch, M.L. Nagpal, L.A. Weymouth
Publikováno v:
Intervirology. 31:65-65
Autor:
Thomas H. Miller, Frank J. O'Neill
Publikováno v:
Virology. 143:75-87
Wild-type (wt) BK virus was introduced into permissive BSC-1 cells along with either early or late defective SV40 genomes. The defectives contained all of the late (L-SV40) or all of the early (E-SV40) coding sequences. Persistently infected (PI) BSC