Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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A randomised, phase II study of nintedanib or sunitinib in previously untreated patients with advanced renal cell cancer: 3-year resultsEisen, T ; Loembé, A-B ; Shparyk, Y ; MacLeod, N ; Jones, R J ; Mazurkiewicz, M ; Temple, G ; Dressler, H ; Bondarenko, IBritish journal of cancer, 2015-10, Vol.113 (8), p.1140-1147 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
2 |
Material Type: Artigo
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Broader incorporation of bioinformatics in education: opportunities and challengesCummings, Michael P ; Temple, Glena GBriefings in bioinformatics, 2010-11, Vol.11 (6), p.537-543 [Periódico revisado por pares]England: Oxford Publishing Limited (England)Texto completo disponível |
3 |
Material Type: Artigo
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Use of phage antibodies to distinguish closely related species of protozoan parasitesPaget, T ; Khan, N ; Temple, G ; Hough, V ; Greenman, JDisease markers, 2000, Vol.16 (1-2), p.83-90 [Periódico revisado por pares]United States: IOS PressTexto completo disponível |
4 |
Material Type: Artigo
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Organ Preservation in Rectal Adenocarcinoma: a phase II randomized controlled trial evaluating 3-year disease-free survival in patients with locally advanced rectal cancer treated with chemoradiation plus induction or consolidation chemotherapy, and total mesorectal excision or nonoperative managementSmith, J Joshua ; Chow, Oliver S ; Gollub, Marc J ; Nash, Garrett M ; Temple, Larissa K ; Weiser, Martin R ; Guillem, José G ; Paty, Philip B ; Avila, Karin ; Garcia-Aguilar, JulioBMC cancer, 2015-10, Vol.15 (1), p.767-767, Article 767 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
5 |
Material Type: Artigo
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Genetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie SyndromeAnsari, Morad ; Rainger, Jacqueline ; Hanson, Isabel M ; Williamson, Kathleen A ; Sharkey, Freddie ; Harewood, Louise ; Sandilands, Angela ; Clayton-Smith, Jill ; Dollfus, Helene ; Bitoun, Pierre ; Meire, Francoise ; Fantes, Judy ; Franco, Brunella ; Lorenz, Birgit ; Taylor, David S ; Stewart, Fiona ; Willoughby, Colin E ; McEntagart, Meriel ; Khaw, Peng Tee ; Clericuzio, Carol ; Van Maldergem, Lionel ; Williams, Denise ; Newbury-Ecob, Ruth ; Traboulsi, Elias I ; Silva, Eduardo D ; Madlom, Mukhlis M ; Goudie, David R ; Fleck, Brian W ; Wieczorek, Dagmar ; Kohlhase, Juergen ; McTrusty, Alice D ; Gardiner, Carol ; Yale, Christopher ; Moore, Anthony T ; Russell-Eggitt, Isabelle ; Islam, Lily ; Lees, Melissa ; Beales, Philip L ; Tuft, Stephen J ; Solano, Juan B ; Splitt, Miranda ; Hertz, Jens Michael ; Prescott, Trine E ; Shears, Deborah J ; Nischal, Ken K ; Doco-Fenzy, Martine ; Prieur, Fabienne ; Temple, I Karen ; Lachlan, Katherine L ; Damante, Giuseppe ; Morrison, Danny A ; van Heyningen, Veronica ; FitzPatrick, David R Anderson, Michael GPloS one, 2016-04, Vol.11 (4), p.e0153757-e0153757 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |
6 |
Material Type: Artigo
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Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2 H19-imprinting control region, ICR1POOLE, Rebecca L ; LEITH, Donald J ; DOCHERTY, Louise E ; SHMELA, Mansur E ; GICQUEL, Christine ; SPLITT, Miranda ; KAREN TEMPLE, I ; MACKAY, Deborah JgEuropean journal of human genetics : EJHG, 2012-02, Vol.20 (2), p.240-243 [Periódico revisado por pares]Basingstoke: Nature Publishing GroupTexto completo disponível |
7 |
Material Type: Artigo
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Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndromeBLIEK, Jet ; VERDE, Gaetano ; FISCHETTO, Rita ; LALATTA, Faustina ; GIORDANO, Lucio ; FERRARI, Paola ; CUBELLIS, Maria Vittoria ; LARIZZA, Lidia ; TEMPLE, I. Karen ; MANNENS, Marcel M. A. M ; MACKAY, Deborah J. G ; RICCIO, Andrea ; CALLAWAY, Jonathan ; MAAS, Saskia M ; DE CRESCENZO, Agostina ; SPARAGO, Angela ; CERRATO, Flavia ; RUSSO, Silvia ; FERRAIUOLO, Serena ; MICHELA RINALDI, MariaEuropean journal of human genetics : EJHG, 2009-05, Vol.17 (5), p.611-619 [Periódico revisado por pares]Basingstoke: Nature Publishing GroupTexto completo disponível |
8 |
Material Type: Artigo
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Very small deletions within the NESP55 gene in pseudohypoparathyroidism type 1bRezwan, Faisal I ; Poole, Rebecca L ; Prescott, Trine ; Walker, Joanna M ; Karen Temple, I ; Mackay, Deborah J GEuropean journal of human genetics : EJHG, 2015-04, Vol.23 (4), p.494-499 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
9 |
Material Type: Artigo
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Evidence for anticipation in Beckwith-Wiedemann syndromeBerland, Siren ; Appelbäck, Mia ; Bruland, Ove ; Beygo, Jasmin ; Buiting, Karin ; Mackay, Deborah J G ; Karen Temple, I ; Houge, GunnarEuropean journal of human genetics : EJHG, 2013-12, Vol.21 (12), p.1344-1348 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
10 |
Material Type: Artigo
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Active nuclear receptors exhibit highly correlated AF-2 domain motionsTeotico, Denise G ; Frazier, Monica L ; Ding, Feng ; Dokholyan, Nikolay V ; Temple, Brenda R S ; Redinbo, Matthew R Fetrow, Jacquelyn S.PLoS computational biology, 2008-07, Vol.4 (7), p.e1000111-e1000111 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |