Collection's Items (Sorted by Submit Date in Descending order): 351 to 400 of 457
| Issue Date | Title | Author(s) |
| 2010 | Genetic 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 |
| 2010 | Congenital imperforate hymen with hydrocolpos and hydronephrosis associated with severe hydramnios and increase of maternal ovarian steroidogenic enzymes | Karteris, E; Foster, H; Karamouti, M; Goumenou, A |
| 2009 | Analysis of telomere maintenance in artemis defective human cell lines | Yasaei, Hemad |
| 1974 | Studies on the changes in protein fluorescence and enzymic activity of aspartate aminotransferase on binding of pyridoxal 5'-Phosphate | Evans, RW; Holbrook, J |
| 1980 | The electrophoresis of transferrins in urea/polyacrylamide gels | Evans, RW; Williams, J |
| 1978 | Studies of the binding of different iron donors to human serum transferrin and isolation of iron-binding fragments from the N- and C-Terminal regions of the protein | Evans, RW; Williams, J |
| 1978 | Iron-binding fragments from the N-Terminal and C-Terminal regions of human lactoferrin | Bluard-Deconinck, JM; Williams, J; Evans, RW; Snick, JV; Osinski, PA; Massont, PL |
| 1975 | Differences in the protein fluorescence of the two iron(lI1)-binding sites of ovotransferrin | Evans, RW |
| 1995 | Identification and characterisation of an extrachromosomal element from a multidrug-resistant isolate of Trypanosoma brucei brucei | Jamnadass, Harmanjeet Ramni |
| 1972 | Protein fluorescence of nicotinamide nucleotide-dependent dehydrogenases | Holbrook, BJJ; Yates, DW; Reynolds, SJ; Evans, RW; Greenwood, C; Gore, MG |
| 2009 | Examining the suitability of molecular and metabolomic-based techniques as tools for assessing the effects of pharmaceuticals in the aquatic environment | Eccles, Paul David |
| 2005 | Homology modelling of transferrin-binding protein A from Neisseria meningitidis | Oakhill, JS; Gorringe, AR; Sutton, BJ; Evans, RW |
| 2008 | Identification of an iron–hepcidin complex | Farnaud, SJ; Rapisarda, C; Bui, TT; Drake, AF; Cammack, R; Evans, RW |
| 2008 | Chelator-facilitated removal of iron from transferrin: Relevance to combined chelation therapy | Devanur, LD; Evans, RW; Evans, PJ; Hider, RC |
| 2009 | Chromosome territory position and active relocation in normal and hutchinson-gilford progeria fibroblasts | Mehta, Ishita Shailesh |
| 2009 | Quantitative investigations of FXN transcription and epigenetic modifications, including histone acetylation and methylation, in FRDA human and mouse tissues | Trabzuni, Daniah M |
| 2009 | The mRNA expression of SETD2 in human breast cancer: Correlation with clinico-athological parameters | Newbold, RF; Al Sarakbi, W; Sassi, W; Jiang, WG; Roberts, T; Mokbel, K |
| 2010 | Rapid chromosome territory relocation by nuclear motor activity in response to serum removal in primary human fibroblasts | Mehta, IS; Amira, M; Harvey, AJ; Bridger, JM |
| 2009 | Determination of wave speed and distensibility of flexible tubes using diameter and velocity | Li, Y; Khir, AW |
| 2005 | A new approach to investigate wave dissipation in viscoelastic tubes: Application of wave intensity analysis | Feng, J; Khir, AW |
| 2009 | A novel splice variant of the DNA-PKcs gene is associated with clinical and cellular radiosensitvity in a xeroderma pigmentosum patient | Abbaszadeh, F; Clingen, PH; Arlett, CF; Plowman, PN; Bourton, EC; Themis, M; Makarov, EM; Newbold, RF; Green, MHL; Parris, CN |
| 2010 | Internalisation of membrane progesterone receptor-α after treatment with progesterone: Potential involvement of a clathrin-dependent pathway | Foster, H; Reynolds, A; Stenbeck, G; Dong, J; Thomas, P; Karteris, E |
| 2010 | Expression of mTOR and downstream signalling components in the JEG-3 and BeWo human placental choriocarcinoma cell lines | Mparmpakas, D; Zachariades, E; Foster, H; Kara, A; Harvey, AJ; Goumenou, A; Karteris, E |
| 2009 | Brk protects breast cancer cells from autophagic cell death induced by loss of anchorage | Harvey, AJ; Pennington, C; Porter, S; Burmi, RS; Edwards, DE; Eccles, SA; Crompton, MR |
| 1996 | Role of cytokines in the pathogenesis of type 1 diabetes | Hussain, Munther Jaffar |
| 2005 | Role of Ca2+ in the electrostatic stability and functional activity of the globular domain of human C1q | Roumenina, LT; Kantardjiev, AA; Atanasov, BP; Waters, P; Gadjeva, M; Reid, KBM; Mantovani, A; Kishore, U; Kojouharova, MS |
| 2008 | Interaction of the globular domain of human C1q with Salmonella typhimurium lipopolysaccharide | Roumenina, LT; Popov, KT; Bureeva, SV; Kojouharova, MS; Gadjeva, M; Rabheru, S; Thakrar, R; Kaplun, A; Kishore, U |
| 2003 | A chromosome 3-encoded repressor of the human telomerase reverse transcriptase (hTERT) gene controls the state of hTERT chromatin | Szutorisz, H; Lingner, J; Cuthbert, AP; Trott, DA; Newbold, RF; Nabholz, M |
| 2001 | Human acrocentric chromosomes with transcriptionally silent nucleolar organizer regions associate with nucleoli | Sullivan, GJ; Bridger, JM; Cuthbert, AP; Newbold, RF; Bickmore, WA; McStay, B |
| 2008 | Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease | Sugiana, C; Pagliarini, DJ; McKenzie, M; Kirby, DM; Salemi, R; Abu-Amero, KK; Dahl, HH; Hutchison, WM; Vascotto, KA; Newbold, RF |
| 1998 | SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome | Zhu, Z; Yao, J; Johns, T; Fu, K; De Brie, I; MacMillan, C; Cuthbert, AP; Newbold, RF; Wang, J; Cheverette, M |
| 1998 | A telomere-independent senescence mechanism is the sole barrier to Syrian hamster cell immortalization | Russo, I; Silver, AR; Cuthbert, AP; Griffin, DK; Trott, DA; Newbold, RF |
| 2001 | A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13 | Seyda, A; Newbold, RF; Hudson, TJ; Verner, A; MacKay, N; Winter, S; Feigenbaum, A; Malaney, S; Gonzalez-Halphen, D; Cuthbert, AP |
| 1999 | Functional evidence of novel tumor suppressor genes for cutaneous malignant melanoma | Parris, CN; Harris, JD; Griffin, DK; Cuthbert, AP; Silver, AJ; Newbold, RF |
| 2001 | Telomere length abnormalities in mammalian radiosensitive cells | McIllrath, J; Bouffler, SD; Samper, E; Cuthbert, AP; Wojcik, A; Szumiel, I; Bryant, PE; Riches, AC; Slijepcevic, P; Newbold, RF |
| 1998 | Human chromosome 16 suppresses metastasis but not tumorigenesis in rat prostatic tumor cells | Mashimo, T; Watabe, M; Cuthbert, AP; Newbold, RF; Rinker-Schaeffer, CW; Helfer, E; Watabe, K |
| 2002 | Functional evidence for a squamous cell carcinoma mortality gene(s) on human chromosome 4 | Forsyth, NR; Morrison, V; Craig, NJ; Fitzsimmons, SA; Barr, NI; Ireland, H; Gordon, KE; Dowen, S; Cuthbert, AP; Newbold, RF |
| 2003 | Human squamous cell carcinomas lose a mortality gene from chromosome 6q14.3 to q15 | Fitzsimmons, SA; Ireland, H; Barr, NI; Cuthbert, AP; Going, JJ; Newbold, RF; Parkinson, EK |
| 2002 | A mortality gene(s) for the human adenocarcinoma line HeLa maps to a 130-kb region of human chromosome 4q22-q23 | Bryce, SD; Morrison, V; Craig, NJ; Forsyth, NR; Fitzsimmons, SA; Ireland, H; Cuthbert, AP; Newbold, RF; Parkinson, EK |
| 2001 | Regulation of human telomerase activity: Repression by normal chromosome 3 abolishes nuclear telomerase reverse transcriptase transcripts but does not affect c-Myc activity | Ducrest, AL; Amacker, M; Mathieu, YD; Cuthbert, AP; Trott, DA; Newbold, RF; Nabholz, M; Lingner, J |
| 1999 | Telomerase repressor sequences on chromosome 3 and induction of permanent growth arrest in human breast cancer cells | Cuthbert, AP; Bond, J; Trott, DA; Gill, S; Broni, J; Marriott, A; Khoudoli, G; Parkinson, EK; Cooper, CS; Newbold, RF |
| 2006 | The journals of importance to UK clinicians: A questionnaire survey of surgeons | Jones, TH; Hanney, S; Buxton, MJ |
| 1977 | Analysis of candicidin and related polyene antibiotics by means of the coil planet centrifuge | Lightbown, JW; Newland, P; Sutherland, IA; Dymond, JWA |
| 1993 | The gene responsible for Werner syndrome may be a cell division "counting" gene | Faragher, RG; Kill, IR; Hunter, JA; Pope, FM; Tannock, C; Shall, S |
| 2005 | Chromosome positioning is largely unaffected in lymphoblastoid cell lines containing emerin or A-type lamin mutations | Meaburn, KJ; Levy, N; Toniolo, D; Bridger, JM |
| 2001 | The spatial relationship of human chromosomes within the nuclei of normal and emerin-mutant cells | Boyle, S; Gilchrist, S; Bridger, JM; Mahy, N; Ellis, J; Bickmore, WA |
| 2007 | Endogenous retrotransposon sequences of the schistosoma mansoni intermediate snail host | Knight, M; Bridger, JM; Ittiprasert, W; Odoemelam, E; Masabanda, J; Miller, A; Raghavan, N |
| 1998 | Putting the genome on the map | Bridger, JM; Bickmore, WA |
| 1997 | Nuclear RNA accumulations represent released transcripts and exhibit specific distributions with respect to Sm antigens domains | Lampel, S; Bridger, JM; Zirbel, R; Mathieu, U; Lichter, P |
| 2005 | Non-random chromosome positioning in mammalian sperm nuclei, with migration of the sex chromosomes during late spermatogenesis | Foster, H; Abeydeera, L; Griffin, DK; Bridger, JM |
Collection's Items (Sorted by Submit Date in Descending order): 351 to 400 of 457
