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Results 1-10 of 15 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2010Increased IL-17 A secretion in response to candida albicans in APS1 and its animal modelAhlgren, K.; Moretti, S.; Lundgren, B.; Karlsson, I.; Ahlin, E.; Norling, A.; Hallgren, A.; Perheentupa, J.; Gustafsson, J.; Rorsman, F.; Crewther, P.; Ronnelid, J.; Bensing, S.; Scott, H.; Kampe, O.; Romani, L.; Lobell, A.; Scientific meeting of the Australasian Society for Immunology (40th : 2010 : Perth W.A.) )
2010Detection of low level nilotinib or dasatinib resistant BCR-ABL mutations by mass spectrometry in CML patients who fail Imatinib is highly predivtive of their subsequent clonal expansion when treated with the drug for which their mutation confers resistanceParker, W.; Ho, M.; Lawrence, R.; Irwin, D.; Scott, H.; Hughes, T.; Branford, S.; American Society of Hematology Meeting (52nd : 2010 : Florida, CA.)
2010One of the reasons why humans, and not sponges or worms, get psychiatric disorders?Scott, H.
2010Transplantation of autoimmune regulator-encoding bone marrow cells delays the onset of experimental autoimmune encephalomyelitisKo, H.; Kinkel, S.; Hubert, F.; Nasa, Z.; Chan, J.; Siatskas, C.; Hirubalan, P.; Toh, B.; Scott, H.; Alderuccio, F.
2010Diversity and clonotypic composition of influenza-specific CD8⁺ TCR repertoires remain unaltered in the absence of AireKedzierska, K.; Valkenburg, S.; Guillonneau, C.; Hubert, F.; Cukalac, T.; Curtis, J.; Stambas, J.; Scott, H.; Kedzierski, L.; Venturi, V.; Davenport, M.
2010SAGE analysis of genes differentially expressed in presymptomatic TgSOD1(G93A) transgenic mice identified cellular processes involved in early stage of ALS pathologyGuipponi, M.; Li, Q.; Hyde, L.; Beissbarth, T.; Smyth, G.; Masters, C.; Scott, H.
2010A serial analysis of gene expression profile of the Alzheimer's disease Tg2576 mouse modelGeorge, A.; Gordon, L.; Beissbarth, T.; Koukoulas, I.; Holsinger, R.; Perreau, V.; Cappai, R.; Tan, S.; Masters, C.; Scott, H.; Li, Q.
2010Poor prognosis in familial acute myeloid leukaemia with combined biallelic CEBPA mutations and downstream events affecting the ATM, FLT3 and CDX2 genesCarmichael, C.; Wilkins, E.; Bengtsson, H.; Horwitz, M.; Speed, T.; Vincent, P.; Young, G.; Hahn, C.; Escher, J.; Scott, H.
2010Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndromeJongmans, M.; Kuiper, R.; Carmichael, C.; Wilkins, E.; Dors, N.; Carmagnac, A.; Schouten-van Meeteren, N.; Li, X.; Stankovic, M.; Kamping, E.; Bengtsson, H.; Schoenmakers, M.; Geurts van Kessel, A.; Hoogerbrugge, P.; Hahn, C.; Brons, P.; Scott, H.; Hoogerbrugge, N.
2010Ultrastructure of medullary thymic epithelial cells of autoimmune regulator (Aire)-deficient miceMilicevic, Z.; Milicevic, N.; Laan, M.; Peterson, P.; Kisand, K.; Scott, H.; Westermann, J.