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PreviewIssue DateTitleAuthor(s)
2017Getting it right when budgets are tight: Using optimal expansion pathways to prioritize responses to concentrated and mixed HIV epidemicsStuart, R.; Kerr, C.; Haghparast-Bidgoli, H.; Estill, J.; Grobicki, L.; Baranczuk, Z.; Prieto, L.; Montañez, V.; Reporter, I.; Gray, R.; Skordis-Worrall, J.; Keiser, O.; Cheikh, N.; Boonto, K.; Osornprasop, S.; Lavadenz, F.; Benedikt, C.; Martin-Hughes, R.; Hussain, S.; Kelly, S.; et al.
2017YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunctionGabriele, M.; Vulto-van Silfhout, A.; Germain, P.; Vitriolo, A.; Kumar, R.; Douglas, E.; Haan, E.; Kosaki, K.; Takenouchi, T.; Rauch, A.; Steindl, K.; Frengen, E.; Misceo, D.; Pedurupillay, C.; Stromme, P.; Rosenfeld, J.; Shao, Y.; Craigen, W.; Schaaf, C.; Rodriguez-Buritica, D.; et al.
2017Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domainsGeisheker, M.; Heymann, G.; Wang, T.; Coe, B.; Turner, T.; Stessman, H.; Hoekzema, K.; Kvarnung, M.; Shaw, M.; Friend, K.; Liebelt, J.; Barnett, C.; Thompson, E.; Haan, E.; Guo, H.; Anderlid, B.; Nordgren, A.; Lindstrand, A.; Vandeweyer, G.; Alberti, A.; et al.
2015Tc17 cells are a proinflammatory, plastic lineage of pathogenic CD8⁺ T cells that induce GVHD without antileukemic effectsGartlan, K.; Markey, K.; Varelias, A.; Bunting, M.; Koyama, M.; Kuns, R.; Raffelt, N.; Olver, S.; Lineburg, K.; Cheong, M.; Teal, B.; Lor, M.; Comerford, I.; Teng, M.; Smyth, M.; McCluskey, J.; Rossjohn, J.; Stockinger, B.; Boyle, G.; Lane, S.; et al.
2012Prognostically significant fusion oncogenes in Pakistani patients with adult acute lymphoblastic leukemia and their association with disease biology and outcomeSabir, N.; Iqbal, Z.; Aleem, A.; Awan, T.; Naeem, T.; Asad, S.; Tahir, A.; Absar, M.; Hasanato, R.; Basit, S.; Chishti, M.; Ul-Haque, M.; Khalid, A.; Sabar, M.; Rasool, M.; Karim, S.; Khan, M.; Samreen, B.; Akram, A.; Siddiqi, M.; et al.
1997Ancient missense mutations in a new member of the RoRet gene family are likely to cause Familial Mediterranean FeverAksentijevich, I.; Centola, M.; Deng, Z.; Sood, R.; Balow, J.; Wood, G.; Zaks, N.; Mansfield, E.; Chen, X.; Eisenberg, S.; Vedula, A.; Shafran, N.; Raben, N.; Pras, E.; Pras, M.; Kastner, D.; Blake, T.; Baxevanis, A.; Robbins, C.; Krizman, D.; et al.
2014The founding charter of the Genomic Observatories NetworkDavies, N.; Field, D.; Amaral-Zettler, L.; Clark, M.; Deck, J.; Drummond, A.; Faith, D.; Geller, J.; Gilbert, J.; Glöckner, F.; Hirsch, P.; Leong, J.; Meyer, C.; Obst, M.; Planes, S.; Scholin, C.; Vogler, A.; Gates, R.; Toonen, R.; Berteaux-Lecellier, V.; et al.
1997A high-resolution genetic map of the familial Mediterranean fever candidate region allows identification of haplotype-sharing among ethnic groupsBalow Jnr., J.; Shelton, D.; Orsborn, A.; Mangelsdorf, M.; Aksentijevich, I.; Blake, T.; Sood, R.; Gardner, D.; Liu, R.; Pras, E.; Levy, E.; Centola, M.; Deng, Z.; Zaks, N.; Wood, G.; Chen, X.; Richards, N.; Shohat, M.; Livneh, A.; Pras, M.; et al.
1999Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromesMcDermott, M.; Aksentijevich, I.; Galon, J.; McDermott, E.; Ogunkolade, B.; Centola, M.; Mansfield, E.; Gadina, M.; Karenko, L.; Petterson, T.; McCarthy, J.; Frucht, D.; Aringer, M.; Torosyan, Y.; Teppo, A.; Wilson, M.; Karaarslan, H.; Wan, Y.; Todd, I.; Wood, G.; et al.
1997Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the Familial Mediterranean Fever Locus (MEFV) on chromosome 16p13.3Sood, R.; Blake, T.; Aksentijevich, I.; Wood, G.; Chen, X.; Gardner, D.; Shelton, D.; Mangelsdorf, M.; Orsborn, A.; Pras, E.; Balow, J.; Centola, M.; Deng, Z.; Zaks, N.; Chen, X.; Richards, N.; Fischel-Ghodsian, N.; Rotter, J.; Pras, M.; Shohat, M.; et al.