Zobrazeno 1 - 10
of 206
pro vyhledávání: '"Aitman TJ"'
Autor:
Wei, W, Tuna, S, Keogh, MJ, Smith, KR, Aitman, TJ, Beales, PL, Bennett, DL, Gale, DP, Bitner-Glindzicz, MAK, Black, GC, Brennan, P, Elliott, P, Flinter, FA, Floto, RA, Houlden, H, Irving, M, Koziell, A, Maher, ER, Markus, HS, Morrell, NW, Newman, WG, Roberts, I, Sayer, JA, Smith, KGC, Taylor, JC, Watkins, H, Webster, AR, Wilkie, AOM, Williamson, C, Attwood, A, Brown, M, Brod, NC, Crisp-Hihn, A, Davis, J, Deevi, SVV, Dewhurst, EF, Edwards, K, Erwood, M, Fox, J, Frary, AJ, Hu, F, Jolley, J, Kingston, N, Linger, R, Mapeta, R, Martin, J, Meacham, S, Papadia, S, Rayner-Matthews, PJ, Samarghitean, C, Shamardina, O, Simeoni, I, Staines, S, Staples, E, Stark, H, Stephens, J, Titterton, C, Von Ziegenweidt, J, Watt, C, Whitehorn, D, Wood, Y, Yates, K, Yu, P, James, R, Ashford, S, Penkett, CJ, Stirrups, KE, Bariana, T, Lentaigne, C, Sivapalaratnam, S, Westbury, SK, Allsup, DJ, Bakchoul, T, Biss, T, Boyce, S, Collins, J, Collins, PW, Curry, NS, Downes, K, Dutt, T, Erber, WN, Evans, G, Everington, T, Favier, R, Gomez, K, Greene, D, Gresele, P, Hart, D, Kazmi, R, Kelly, AM, Lambert, M, Madan, B, Mangles, S, Mathias, M, Millar, C, Obaji, S, Peerlinck, K, Roughley, C, Schulman, S, Scully, M, Shapiro, SE, Sibson, K, Sims, MC, Tait, RC, Talks, K, Thys, C, Toh, C-H, Van Geet, C, Westwood, J-P, Mumford, AD, Ouwehand, WH, Freson, K, Laffan, MA, Tan, RYY, Harkness, K, Mehta, S, Muir, KW, Hassan, A, Traylor, M, Drazyk, AM, Parry, D, Ahmed, M, Kazkaz, H, Vandersteen, AM, Ormondroyd, E, Thomson, K, Dent, T, Buchan, RJ, Bueser, T, Carr-White, G, Cook, S, Daniels, MJ, Harper, AR, Ware, JS, Dixon, PH, Chambers, J, Cheng, F, Estiu, MC, Hague, WM, Marschall, H-U, Vazquez-Lopez, M, Arno, G, French, CE, Michaelides, M, Moore, AT, Sanchis-Juan, A, Carss, K, Raymond, FL, Chinnery, PF, Griffiths, P, Horvath, R, Hudson, G, Jurkute, N, Pyle, A, Yu-Wai-Man, P, Whitworth, J, Adlard, J, Armstrong, R, Brewer, C, Casey, R, Cole, TRP, Evans, DG, Greenhalgh, L, Hanson, HL, Hoffman, J, Izatt, L, Kumar, A, Lalloo, F, Ong, KR, Park, S-M, Searle, C, Side, L, Snape, K, Woodward, E, Tischkowitz, M, Grozeva, D, Kurian, MA, Themistocleous, AC, Gosal, D, Marshall, A, Matthews, E, McCarthy, MI, Renton, T, Rice, ASC, Vale, T, Walker, SM, Woods, CG, Thaventhiran, JE, Allen, HL, Savic, S, Alachkar, H, Antrobus, R, Baxendale, HE, Browning, MJ, Buckland, MS, Cooper, N, Edgar, JDM, Egner, W, Gilmour, KC, Goddard, S, Gordins, P, Grigoriadou, S, Hackett, S, Hague, R, Hayman, G, Herwadkar, A, Huissoon, AP, Jolles, S, Kelleher, P, Kumararatne, D, Longhurst, H, Lorenzo, LE, Lyons, PA, Maimaris, J, Noorani, S, Richter, A, Sargur, RB, Sewell, WAC, Thomas, D, Thomas, MJ, Worth, A, Yong, PFK, Kuijpers, TW, Thrasher, AJ, Levine, AP, Sadeghi-Alavijeh, O, Wong, EKS, Cook, HT, Chan, MMY, Hall, M, Harris, C, McAlinden, P, Marchbank, KJ, Marks, S, Maxwell, H, Mozere, M, Wessels, J, Johnson, SA, Bleda, M, Hadinnapola, C, Haimel, M, Swietlik, E, Bogaard, H, Church, C, Coghlan, G, Condliffe, R, Corris, P, Danesino, C, Eyries, M, Gall, H, Ghofrani, H-A, Gibbs, JSR, Girerd, B, Holden, S, Houweling, A, Howard, LS, Humbert, M, Kiely, DG, Kovacs, G, Lawrie, A, Ross, RVM, Moledina, S, Montani, D, Newnham, M, Olschewski, A, Olschewski, H, Peacock, A, Pepke-Zaba, J, Scelsi, L, Seeger, W, Soubrier, F, Suntharalingam, J, Toshner, M, Treacy, C, Trembath, R, Noordegraaf, AV, Waisfisz, Q, Wharton, J, Wilkins, MR, Wort, SJ, Graf, S, Louka, E, Roy, NB, Rao, A, Ancliff, P, Babbs, C, Layton, DM, Mead, AJ, O'Sullivan, J, Okoli, S, Saleem, M, Bierzynska, A, Diz, CB, Colby, E, Ekani, MN, Satchell, S, Fowler, T, Rendon, A, Scott, R, Smedley, D, Thomas, E, Caulfield, M, Abbs, S, Burrows, N, Chitre, M, Gattens, M, Gurnell, M, Kelsall, W, Poole, KES, Ross-Russell, R, Spasic-Boskovic, O, Twiss, P, Wagner, A, Banka, S, Clayton-Smith, J, Douzgou, S, Abulhoul, L, Aurora, P, Bockenhauer, D, Cleary, M, Dattani, M, Ganesan, V, Pilkington, C, Rahman, S, Shah, N, Wedderburn, L, Compton, CJ, Deshpande, C, Fassihi, H, Haque, E, Josifova, D, Mohammed, SN, Robert, L, Rose, SJ, Ruddy, DM, Sarkany, RN, Sayer, G, Shaw, AC, Campbell, C, Gibson, K, Koelling, N, Lester, T, Nemeth, AH, Palles, C, Patel, S, Sen, A, Taylor, J, Tomlinson, IP, Malka, S, Browning, AC, Burn, J, De Soyza, A, Graham, J, Pearce, S, Quinton, R, Schaefer, AM, Wilson, BT, Wright, M, Simpson, M, Syrris, P, Bradley, JR, Turro, E
Publikováno v:
NIHR BioResource–Rare Diseases, 100,000 Genomes Project–Rare Diseases Pilot & Daniels, M J 2019, ' Germline selection shapes human mitochondrial DNA diversity ', Science (New York, N.Y.), vol. 364, no. 6442 . https://doi.org/10.1126/science.aau6520
Science, 364(6442). American Association for the Advancement of Science
Science
Tomlinson, I 2019, ' Germline selection shapes human mitochondrial DNA diversity ', Science, vol. 364, no. 6442, pp. 749-+ . https://doi.org/10.1126/science.aau6520
Science, 364(6442). American Association for the Advancement of Science
Science
Tomlinson, I 2019, ' Germline selection shapes human mitochondrial DNA diversity ', Science, vol. 364, no. 6442, pp. 749-+ . https://doi.org/10.1126/science.aau6520
INTRODUCTION Only 2.4% of the 16.5-kb mitochondrial DNA (mtDNA) genome shows homoplasmic variation at >1% frequency in humans. Migration patterns have contributed to geographic differences in the frequency of common genetic variants, but population g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd0acfee6b4573c8d6320d0057b56790
Autor:
French, CE, Delon, I, Dolling, H, Sanchis-Juan, A, Shamardina, O, Mégy, K, Abbs, S, Austin, T, Bowdin, S, Branco, RG, Firth, H, Tuna, S, Aitman, TJ, Ashford, S, Astle, WJ, Bennet, DL, Bleda, M, Carss, KJ, Chinnery, PF, Deevi, SVV, Fletcher, D, Gale, DP, Gräf, SF, Hu, F, James, R, Kasanicki, MA, Kingston, N, Koziell, AB, Allen, HL, Maher, ER, Markus, HS, Meacham, S, Morrell, NW, Penkett, CJ, Roberts, I, Smith, KGC, Stark, H, Stirrups, KE, Turro, E, Watkins, H, Williamson, C, Young, T, Bradley, JR, Ouwehand, WH, Raymond, FL, Agrawal, S, Armstrong, R, Beardsall, K, Belteki, G, Bohatschek, M, Broster, S, Campbell, R, Chaudhary, R, Costa, C, D’Amore, A, Fitzsimmons, A, Hague, J, Harley, J, Hoodbhoy, S, Kayani, R, Kelsall, W, Mehta, SG, O’Donnell, R, O’Hare, S, Ogilvy-Stuart, A, Papakostas, S, Park, SM, Parker, A, Pathan, N, Prapa, M, Sammut, A, Sandford, R, Schon, K, Singh, Y, Spike, K, Tavares, ALT, Wari-Pepple, D, Wong, HS, Woods, CG, Rowitch, DH
Publikováno v:
2019, ' Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children ', Intensive Care Medicine, vol. 45, no. 5, pp. 627-636 . https://doi.org/10.1007/s00134-019-05552-x
Intensive Care Medicine
French, C E, Delon, I, Dolling, H, Sanchis-Juan, A, Shamardina, O, Mégy, K, Abbs, S, Austin, T, Bowdin, S, Branco, R G, Firth, H, Williamson, C & Rowitch, D H & Raymond, F L & Dixon, P 2019, ' Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children ', Intensive Care Medicine, vol. 45, no. 5, pp. 627-636 . https://doi.org/10.1007/s00134-019-05552-x
Intensive Care Medicine
French, C E, Delon, I, Dolling, H, Sanchis-Juan, A, Shamardina, O, Mégy, K, Abbs, S, Austin, T, Bowdin, S, Branco, R G, Firth, H, Williamson, C & Rowitch, D H & Raymond, F L & Dixon, P 2019, ' Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children ', Intensive Care Medicine, vol. 45, no. 5, pp. 627-636 . https://doi.org/10.1007/s00134-019-05552-x
Purpose With growing evidence that rare single gene disorders present in the neonatal period, there is a need for rapid, systematic, and comprehensive genomic diagnoses in ICUs to assist acute and long-term clinical decisions. This study aimed to ide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fea855d42d553df60c3de14262258d3
https://doi.org/10.1007/s00134-019-05552-x
https://doi.org/10.1007/s00134-019-05552-x
Autor:
Chen, T, Rotival, M, Behmoaras, JV, Chiu, LY, Bagnati, M, Jo, JH, Srivastava, PK, Petretto, E, Pusey, CD, Lai, PC, Aitman, TJ, Cook, HT, Behmoaras, J
Crescentic glomerulonephritis (Crgn) is a complex disorder where macrophage activity and infiltration are significant effector causes. In previous linkage studies using the uniquely susceptible Wistar Kyoto (WKY) rat strain, we have identified multip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1032::8897683b7c27cfe5785c879b5cb9a05b
http://hdl.handle.net/10044/1/47836
http://hdl.handle.net/10044/1/47836
Autor:
Todd, JA, Aitman, TJ, Cornall, RJ, Ghosh, S, Hall, JR, Hearne, CM, Knight, AM, Love, JM, McAleer, MA, Prins, JB, Rodrigues, N, Lathrop, M, Pressey, A, DeLarato, NH, Peterson, LB, Wicker, LS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::f87e06d2890dbe26ca4259fc98f41011
https://ora.ox.ac.uk/objects/uuid:743d7f7a-fa55-4bfd-923d-812ab1b8adbe
https://ora.ox.ac.uk/objects/uuid:743d7f7a-fa55-4bfd-923d-812ab1b8adbe
Autor:
Todd, JA, Aitman, TJ, Cornall, RJ, Ghosh, S, Hall, JRS, Hearne, CM, Knight, AM, Love, JM, McAleer, MA, Prins, J-B, Rodrigues, N, Lathrop, M, Pressey, A, DeLarato, NH, Peterson, LB, Wicker, LS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4b0a0cae86ae2c9422e6ed797de83ad0
https://ora.ox.ac.uk/objects/uuid:4839a6e1-28f7-4353-91a9-dee22ab52d00
https://ora.ox.ac.uk/objects/uuid:4839a6e1-28f7-4353-91a9-dee22ab52d00
Autor:
Chambers, JC, Abbott, J, Zhang, W, Turro, E, Scott, WR, Tan, ST, Afzal, U, Afaq, S, Loh, M, Lehne, B, O'Reilly, P, Gaulton, KJ, Pearson, RD, Li, X, Lavery, A, Vandrovcova, J, Wass, MN, Miller, K, Sehmi, J, Oozageer, L, Kooner, IK, Al-Hussaini, A, Mills, R, Grewal, J, Panoulas, V, Lewin, AM, Northwood, K, Wander, GS, Geoghegan, F, Li, Y, Wang, J, Aitman, TJ, McCarthy, MI, Scott, J, Butcher, S, Elliott, P, Kooner, JS
Publikováno v:
Chambers, J C, Abbott, J, Zhang, W, Turro, E, Scott, W R, Tan, S, Afzal, U, Afaq, S, Loh, M, Lehne, B, O'reilly, P, Gaulton, K J, Pearson, R D, Li, X, Lavery, A, Vandrovcova, J, Wass, M N, Miller, K, Sehmi, J, Oozageer, L, Kooner, I K, Al-hussaini, A, Mills, R, Grewal, J, Panoulas, V, Lewin, A M, Northwood, K, Wander, G S, Geoghegan, F, Li, Y, Wang, J, Aitman, T J, Mccarthy, M I, Scott, J, Butcher, S, Elliott, P & Kooner, J S 2014, ' The South Asian Genome ', PLoS ONE, vol. 9, no. 8, pp. e102645 . https://doi.org/10.1371/journal.pone.0102645
PloS one, vol 9, iss 8
PLoS ONE
PLoS ONE, Vol 9, Iss 8, p e102645 (2014)
PloS one, vol 9, iss 8
PLoS ONE
PLoS ONE, Vol 9, Iss 8, p e102645 (2014)
Genetics of disease Microarrays Variant genotypes Population genetics Sequence alignment Alleles The genetic sequence variation of people from the Indian subcontinent who comprise one-quarter of the world's population, is not well described. We carri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca8425144e34e61c1566ee94ff45b7cb
http://bura.brunel.ac.uk/handle/2438/11182
http://bura.brunel.ac.uk/handle/2438/11182
Autor:
Reynolds J, Cook PR, Behmoaras J, Smith J, Bhangal G, Tadros S, Tee J, Salama AD, Evans DJ, Aitman TJ, Cook TH, Pusey CD.
Publikováno v:
American Journal of Pathology.
Akademický článek
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Akademický článek
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