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Loss of programmed death ligand-1 expression on donor T cells lessens acute graft-versus-host disease lethality by Saha, A, O'Connor, R, Thangavelu, G, Lovitch, S, Dandamudi, D, Wilson, C, Vincent, B, Aoyama, K, Taylor, P, Panoskaltsis-Mortari, A, Foncea, R, Burrill, J, Guo, L, Sacristan, C, Furlan, S, Snyder, N, Blair, I, Milone, M, Dustin, M, Riley, J, Bernlohr, D, Turka, L, Murphy, W, Fife, B, Munn, D, Miller, J, Serody, J, Kean, L, Freeman, G, Sharpe, A, Blazar, B
Published 2015Conference item -
2
Programmed death ligand-1 expression on donor T cells drives graft-versus-host disease lethality. by Saha, A, O'Connor, R, Thangavelu, G, Lovitch, S, Dandamudi, D, Wilson, C, Vincent, B, Tkachev, V, Pawlicki, J, Furlan, S, Kean, L, Aoyama, K, Taylor, P, Panoskaltsis-Mortari, A, Foncea, R, Ranganathan, P, Devine, S, Burrill, J, Guo, L, Sacristan, C, Snyder, N, Blair, I, Milone, M, Dustin, M, Riley, J, Bernlohr, D, Murphy, W, Fife, B, Munn, D, Miller, J, Serody, J, Freeman, G, Sharpe, A, Turka, L, Blazar, B
Published 2016Journal article -
3
Programmed death ligand-1 expression on donor T cells drives graft-versus-host disease lethality. by Saha, A, O'Connor, R, Thangavelu, G, Lovitch, S, Dandamudi, D, Wilson, C, Vincent, B, Tkachev, V, Pawlicki, J, Furlan, S, Kean, L, Aoyama, K, Taylor, P, Panoskaltsis-Mortari, A, Foncea, R, Ranganathan, P, Devine, S, Burrill, J, Guo, L, Sacristan, C, Snyder, N, Blair, I, Milone, M, Dustin, M, Riley, J, Bernlohr, D, Murphy, W, Fife, B, Munn, D, Miller, J, Serody, J, Freeman, G, Sharpe, A, Turka, L, Blazar, B
Published 2016Journal article -
4
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis by Kenna, P, van Doormaal PTC, P, Dekker, A, Ticozzi, N, Kenna, B, Diekstra, F, van Rheenen, W, van Eijk, K, Jones, A, Keagle, P, Shatunov, A, Sproviero, W, Smith, B, van Es, M, Topp, S, Kenna, A, Miller, J, Fallini, C, Tiloca, C, McLaughlin, R, Vance, C, Troakes, C, Colombrita, C, Mora, G, Calvo, A, Verde, F, Al-Sarraj, S, King, A, Calini, D, de Belleroche, J, Baas, F, van der Kooi, A, de Visser, M, ten Asbroek, A, Sapp, P, McKenna-Yasek, D, Polak, M, Asress, S, Munoz-Blanco, J, SLAGEN Consortium, Lauria, G, Williams, K, Leigh, P, Nicholson, G, Blair, I, Leblond, C, Dion, P, Rouleau, G, Pall, H, Shaw, P, Turner, M, Talbot, K, Taroni, F, Boylan, K, Van Blitterswijk, M, Rademakers, R, Esteban-Perez, J, Garcia-Redondo, A, Van Damme, P, Robberecht, W, Chio, A, Gellera, C, Drepper, C, Sendtner, M, Ratti, A, Glass, J, Mora, J, Basak, A, Hardiman, O, Ludolph, A, Andersen, P, Wesihaupt, J, Brown, R, Al-Chalabi, A, Silani, V, Shaw, C, van den Berg, L, Veldink, J, Landers, J
Published 2016Journal article -
5
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis by Lin, K, Pulit, SL, Van Rheenen, W, Shatunov, A, Dekker, AM, McLaughlin, RL, Diekstra, FP, Van Der Spek, RAA, Võsa, U, De Jong, S, Robinson, MR, Yang, J, Fogh, I, Van Doormaal, PT, Tazelaar, GHP, Koppers, M, Blokhuis, AM, Sproviero, W, Jones, AR, Kenna, KP, Van Eijk, KR, Harschnitz, O, Schellevis, RD, Brands, WJ, Medic, J, Menelaou, A, Vajda, A, Ticozzi, N, Rogelj, B, Vrabec, K, Ravnik-Glavač, M, Koritnik, B, Zidar, J, Leonardis, L, Grošelj, LD, Millecamps, S, Salachas, F, Meininger, V, De Carvalho, M, Pinto, S, Mora, JS, Rojas-García, R, Polak, M, Chandran, S, Colville, S, Swingler, R, Morrison, KE, Shaw, PJ, Hardy, J, Orrell, RW, Pittman, A, Sidle, K, Fratta, P, Malaspina, A, Topp, S, Petri, S, Abdulla, S, Drepper, C, Sendtner, M, Meyer, T, Ophoff, RA, Staats, KA, Wiedau-Pazos, M, Lomen-Hoerth, C, Van Deerlin, VM, Trojanowski, JQ, Elman, L, McCluskey, L, Basak, AN, Tunca, C, Hamzeiy, H, Parman, Y, Meitinger, T, Lichtner, P, Radivojkov-Blagojevic, M, Andres, CR, Maurel, C, Bensimon, G, Landwehrmeyer, B, Brice, A, Payan, CAM, Saker-Delye, S, Dürr, A, Wood, NW, Tittmann, L, Lieb, W, Franke, A, Rietschel, M, Cichon, S, Nöthen, MM, Amouyel, P, Tzourio, C, Dartigues, J-F, Uitterlinden, AG, Rivadeneira, F, Estrada, K, Hofman, A, Curtis, C, Blauw, HM, Van Der Kooi, AJ, De Visser, M, Goris, A, Weber, M, Shaw, CE, Smith, BN, Pansarasa, O, Cereda, C, Del Bo, R, Comi, GP, D'Alfonso, S, Bertolin, C, Sorarù, G, Mazzini, L, Pensato, V, Gellera, C, Tiloca, C, Ratti, A, Calvo, A, Moglia, C, Brunetti, M, Arcuti, S, Capozzo, R, Zecca, C, Lunetta, C, Penco, S, Riva, N, Padovani, A, Filosto, M, Muller, B, Stuit, RJ, Registry, P, Slalom Group, Registry, S, Fals Sequencing Consortium, Slagen Consortium, Nnipps Study Group, Blair, I, Zhang, K, McCann, EP, Fifita, JA, Nicholson, GA, Rowe, DB, Pamphlett, R, Kiernan, MC, Grosskreutz, J, Witte, OW, Ringer, T, Prell, T, Stubendorff, B, Kurth, I, Hübner, CA, Leigh, PN, Casale, F, Chio, A, Beghi, E, Pupillo, E, Tortelli, R, Logroscino, G, Powell, J, Ludolph, AC, Weishaupt, JH, Robberecht, W, Van Damme, P, Franke, L, Pers, TH, Brown, RH, Glass, JD, Landers, JE, Hardiman, O, Andersen, PM, Corcia, P, Vourc'H, P, Silani, V, Wray, NR, Visscher, PM, De Bakker, PIW, Van Es, MA, Pasterkamp, RJ, Lewis, CM, Breen, G, Al-Chalabi, A, Van Den Berg, LH, Veldink, JH
Published 2016Journal article