Browsing by Author Newbold, RF

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Issue DateTitleAuthor(s)
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
2001A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13Seyda, A; Newbold, RF; Hudson, TJ; Verner, A; MacKay, N; Winter, S; Feigenbaum, A; Malaney, S; Gonzalez-Halphen, D; Cuthbert, AP
2008Positioning of human chromosomes in murine cell hybrids according to syntenyNewbold, RF; Meaburn, KJ; Bridger, JM
2001Regulation of human telomerase activity: Repression by normal chromosome 3 abolishes nuclear telomerase reverse transcriptase transcripts but does not affect c-Myc activityDucrest, AL; Amacker, M; Mathieu, YD; Cuthbert, AP; Trott, DA; Newbold, RF; Nabholz, M; Lingner, J
1998SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndromeZhu, Z; Yao, J; Johns, T; Fu, K; De Brie, I; MacMillan, C; Cuthbert, AP; Newbold, RF; Wang, J; Cheverette, M
1998Telomerase activity in melanoma and non-melanoma skin cancerNewbold, RF; Parris, CN; Jezzard, S; Silver, A; Mackie, R; MacGregor, J