Browsing by Author Newbold, RF

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Issue DateTitleAuthor(s)
2013The fetal mouse is a sensitive genotoxicity model that exposes lentiviral-associated mutagenesis resulting in liver oncogenesisNowrouzi, A; Cheung, WT; Li, T; Zhang, X; Arens, A; Paruzynski, A; Waddington, SN; Osejindu, E; Reja, S; von Kalle, C; Wang, Y; Al-Allaf, F; Gregory, L; Themis, M; Holder, M; Dighe, N; Ruthe, A; Buckley, SM; Bigger, B; Montini, E; Thrasher, AJ; Andrews, R; Roberts, TP; Newbold, RF; Coutelle, C; Schmidt, M; Themis, M
9-Nov-2016Functional and prognostic significance of the genomic amplification of frizzled receptor 6 ( FZD6 ) in breast cancerCorda, G; Sala, G; Lattanzio, R; Iezzi, M; Sallese, M; Fragassi, G; Lamolinara, A; Mirza, H; Barcaroli, D; Ermler, S; Silva, E; Yasaei, H; Newbold, RF; Vagnarelli, P; Mottolese, M; Natali, PG; Perracchio, L; Quist, J; Grigoriadis, A; Marra, P; Tutt, AN; Piantelli, M; Iacobelli, S; De Laurenzi, V; Sala, A
2002Functional evidence for a squamous cell carcinoma mortality gene(s) on human chromosome 4Forsyth, NR; Morrison, V; Craig, NJ; Fitzsimmons, SA; Barr, NI; Ireland, H; Gordon, KE; Dowen, S; Cuthbert, AP; Newbold, RF
1999Functional evidence of novel tumor suppressor genes for cutaneous malignant melanomaParris, CN; Harris, JD; Griffin, DK; Cuthbert, AP; Silver, AJ; Newbold, RF
2010Functional identification and mapping of a gene that represses telomerase hTERT transcription in prostate cancer cellsHasan, Rana
2008Genetic polymorphisms in the DNA repair genes XRCC1, XRCC2 and XRCC3 and risk of breast cancer in CyprusNewbold, RF; Loizidou, MA; Neuhausen, SL; Michael, T; Marcou, Y; Kakouri, E; Papadopoulos, M; Kyriacou, K; Hadjisavvas, A
2010Genetic variation in genes interacting with BRCA1/2 and risk of breast cancer in Cypriot population.Newbold, RF; Loizidou, MA; Cariolou, MA; Neuhausen, SL; Bashiardes, E; Marcou, Y; Michael, T; Daniel, M; Kakouri, E; Hadjisavvas, A
2005hTERT protein expression is independent of clinicopathological parameters and c-Myc protein expression in human breast cancerElkak, AE; Meligonis, G; Salhab, M; Mitchell, B; Blake, JRS; Newbold, RF; Mokbel, K
2001Human acrocentric chromosomes with transcriptionally silent nucleolar organizer regions associate with nucleoliSullivan, GJ; Bridger, JM; Cuthbert, AP; Newbold, RF; Bickmore, WA; McStay, B
1998Human chromosome 16 suppresses metastasis but not tumorigenesis in rat prostatic tumor cellsMashimo, T; Watabe, M; Cuthbert, AP; Newbold, RF; Rinker-Schaeffer, CW; Helfer, E; Watabe, K
2003Human squamous cell carcinomas lose a mortality gene from chromosome 6q14.3 to q15Fitzsimmons, SA; Ireland, H; Barr, NI; Cuthbert, AP; Going, JJ; Newbold, RF; Parkinson, EK
2003Is telomerase reactivation associated with the down-regulatoin of TGFβ receptor-II expression in human breast cancer?Elkak, AE; Newbold, RF; Thomas, V; Mokbel, K
2016A mechanistic evaluation of the Syrian hamster embryo cell transformation assay (pH 6.7) and molecular events leading to senescence bypass in SHE cellsNewbold, RF; Pickles, JC
2002A mortality gene(s) for the human adenocarcinoma line HeLa maps to a 130-kb region of human chromosome 4q22-q23Bryce, SD; Morrison, V; Craig, NJ; Forsyth, NR; Fitzsimmons, SA; Ireland, H; Cuthbert, AP; Newbold, RF; Parkinson, EK
2004The mRNA expression of hTERT in human breast carcinomas correlates with VEGF expressionKirkpatrick, KL; Newbold, RF; Mokbel, K
2009The mRNA expression of SETD2 in human breast cancer: Correlation with clinico-athological parametersNewbold, RF; Al Sarakbi, W; Sassi, W; Jiang, WG; Roberts, T; Mokbel, K
2003The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatasesNewbold, RF; Cosma, MP; Pepe, S; Annunziata, I; Grompe, M; Parenti, G; Ballabio, A
2004Mutant mitochondrial elongation factor G1 and combined oxidative phosphorylation deficiencyNewbold, RF; Coenen, MJH; Antonicka, H; Ugalde, C; Sasarman, F; Rossi, R; Heister, A; Trijbels, FJMF; van den Heuvel, LP; Shoubridge, EA; Smeitink, JAM
2008Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial diseaseSugiana, C; Pagliarini, DJ; McKenzie, M; Kirby, DM; Salemi, R; Abu-Amero, KK; Dahl, HH; Hutchison, WM; Vascotto, KA; Newbold, RF
2009A novel splice variant of the DNA-PKcs gene is associated with clinical and cellular radiosensitvity in a xeroderma pigmentosum patientAbbaszadeh, F; Clingen, PH; Arlett, CF; Plowman, PN; Bourton, EC; Themis, M; Makarov, EM; Newbold, RF; Green, MHL; Parris, CN