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Results 1-10 of 48 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2017Dominant protection from HLA-linked autoimmunity by antigen-specific regulatory T cellsOoi, J.; Petersen, J.; Tan, Y.; Huynh, M.; Willett, Z.; Ramarathinam, S.; Eggenhuizen, P.; Loh, K.; Watson, K.; Gan, P.; Alikhan, M.; Dudek, N.; Handel, A.; Hudson, B.; Fugger, L.; Power, D.; Holt, S.; Coates, P.; Gregersen, J.; Purcell, A.; et al.
2018Characterization of the Mel1c melatoninergic receptor in platypus (Ornithorhynchus anatinus)Gautier, C.; Guenin, S.; Riest-Fery, I.; Perry, T.; Legros, C.; Nosjean, O.; Simonneaux, V.; Grützner, F.; Boutin, J.; Janke, A.
2010Genome-wide identification of human FOXP3 target genes in natural regulatory T cellsSadlon, T.; Wilkinson, B.; Pederson, S.; Brown, C.; Bresatz, S.; Gargett, T.; Melville, E.; Peng, K.; D'Andrea, R.; Glonek, G.; Goodall, G.; Zola, H.; Shannon, F.; Barry, S.
2012CDP-diacylglycerol synthetase-controlled phosphoinositide availability limits VEGFA signaling and vascular morphogenesisPan, W.; Pham, V.; Stratman, A.; Castranova, D.; Kamei, M.; Kidd, K.; Lo, B.; Shaw, K.; Torres-Vazquez, J.; Mikelis, C.; Gutkind, J.; Davis, G.; Weinstein, B.
2014Identification of highly conserved putative developmental enhancers bound by SOX3 in neural progenitors using ChIP-SeqMcAninch, D.; Thomas, P.; Zheng, D.
2014Copy number variation in the horse genomeGhosh, S.; Qu, Z.; Das, P.; Fang, E.; Juras, R.; Cothran, E.; McDonell, S.; Kenney, D.; Lear, T.; Adelson, D.; Chowdhary, B.; Raudsepp, T.; Barsh, G.
2015Diversity of aquatic pseudomonas species and their activity against the fish pathogenic oomycete saprolegniaLiu, Y.; Rzeszutek, E.; van der Voort, M.; Wu, C.; Thoen, E.; Skaar, I.; Bulone, V.; Dorrestein, P.; Raaijmakers, J.; de Bruijn, I.; Almeida, A.
2018Eimeria taggarti n. sp., a novel coccidian (Apicomplexa: Eimeriorina) in the prostate of an Antechinus flavipesAmery-Gale, J.; Devlin, J.; Tatarczuch, L.; Taggart, D.; Schultz, D.; Charles, J.; Beveridge, I.
2013The genomic landscape of hypodiploid acute lymphoblastic leukemiaTo, L.
2013Yunis-Varón Syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphataseCampeau, P.; Lenk, G.; Lu, J.; Bae, Y.; Burrage, L.; Turnpenny, P.; Corona-Rivera, J.; Morandi, L.; Mora, M.; Reutter, H.; Vulto-van Silfhout, A.; Faivre, L.; Haan, E.; Gibbs, R.; Meisler, M.; Lee, B.

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