Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Matthew Wigan"'
Autor:
Kee Ming Chia, Brian Gabrielli, Sandra Pavey, Mitchell S. Stark, Kelly Brooks, Loredana Spoerri, Matthew Wigan, Pamela Mukhopadhyay
Publikováno v:
Journal of Investigative Dermatology. 134(1):150-158
A hallmark of cancer is genomic instability that is considered to provide the adaptive capacity of cancers to thrive under conditions in which the normal precursors would not survive. Recent genomic analysis has revealed a very high degree of genomic
Autor:
Andrew Burgess, ShuShyan Wong, Brian Gabrielli, Sandra Pavey, Nichole Giles, Alex Pinder, Matthew Wigan, Richard A. Sturm
Publikováno v:
Journal of Investigative Dermatology. 132:1681-1688
UVR is a major environmental risk factor for the development of melanoma. Here we describe a coupled DNA-damage tolerance (DDT) mechanism and G2-phase cell cycle checkpoint induced in response to suberythemal doses of UVR that is commonly defective i
Autor:
Nicole Giles, Brian Gabrielli, Pamela Mukhopadhyay, Matthew Wigan, Max V. Ranall, Kelly Brooks, Sandra Pavey
Publikováno v:
Molecular Cancer Therapeutics. 10:A65-A65
In Australia melanomas account for 10% of all reported cancers and 3% of cancer mortalities. Current treatments offer Using ICRF-193, an inhibitor of Topoisomerase II, a panel of melanoma cell lines were investigated for decatenation checkpoint funct
Autor:
Brian Gabrielli, Kelly Brooks, Matthew Wigan, Richard A. Sturm, Andrew Burgess, Nichole Giles, Sandra Pavey
Publikováno v:
Cancer Research. 71:4197-4197
Ultraviolet radiation (UVR) is a major environmental risk factor in the development of skin cancer. Here we describe a G2 phase cell cycle checkpoint response to suberythemal doses of UVR that is defective in a majority of melanoma cell lines tested.
Autor:
Nichole Giles, Brian Gabrielli, Wanda DePinto, Andrew Burgess, Matthew Wigan, Paul Gillespie, Frankie Stevens
Publikováno v:
Melanoma Research. 16:S5
Cyclin-dependent kinase 4 (CDK4)/cyclin D has a key role in regulating progression through late G(1) into S phase of the cell cycle. CDK4-cyclin D complexes then persist through the latter phases of the cell cycle, although little is known about thei