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Results 101-109 of 109 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2016Distinct evolution and dynamics of epigenetic and genetic heterogeneity in acute myeloid leukemiaLi, S.; Garrett-Bakelman, F.E.; Chung, S.S.; Sanders, M.A.; Hricik, T.; Rapaport, F.; Patel, J.; Dillon, R.; Vijay, P.; Brown, A.L.; Perl, A.E.; Cannon, J.; Bullinger, L.; Luger, S.; Becker, M.; Lewis, I.D.; To, L.B.; Delwel, R.; Löwenberg, B.; Döhner, H.; et al.
2018Augmented capacity for peripheral serotonin release in human obesityYoung, R.; Lumsden, A.; Martin, A.; Schober, G.; Pezos, N.; Thazhath, S.; Isaacs, N.; Cvijanovic, N.; Sun, E.; Wu, T.; Rayner, C.; Nguyen, Q.N.; Fontgalland, D.; Rabbitt, P.; Hollington, P.; Sposato, L.; Due, S.; Wattchow, D.; Liou, A.; Jackson, V.; et al.
2017Adults with Philadelphia chromosome-like acute lymphoblastic leukemia frequently have IGH-CRLF2 and JAK2 mutations, persistence of minimal residual disease and poor prognosisHerold, T.; Schneider, S.; Metzeler, K.; Neumann, M.; Hartmann, L.; Roberts, K.; Konstandin, N.; Greif, P.; Braeundl, K.; Ksienzyk, B.; Huk, N.; Schneider, I.; Zellmeier, E.; Jurinovic, V.; Mansmann, U.; Hiddemann, W.; Mullighan, C.; Bohlander, S.; Spiekermann, K.; Hoelzer, D.; et al.
2013SMAD2, SMAD3 and SMAD4 mutations in colorectal cancerFleming, N.; Jorissen, R.; Mouradov, D.; Christie, M.; Sakthianandeswaren, A.; Palmieri, M.; Day, F.; Li, S.; Tsui, C.; Lipton, L.; Desai, J.; Jones, I.; McLaughlin, S.; Ward, R.; Hawkins, N.; Ruszkiewicz, A.; Moore, J.; Zhu, H.; Mariadason, J.; Burgess, A.; et al.
2015Effects of diabetes definition on global surveillance of diabetes prevalence and diagnosis: a pooled analysis of 96 population-based studies with 331 288 participantsNCD Risk Factor Collaboration (NCD-RisC),; Danaei, G.; Fahimi, S.; Lu, Y.; Zhou, B.; Hajifathalian, K.; Cesare, M.; Lo, W.; Reis-Santos, B.; Cowan, M.; Shaw, J.; Bentham, J.; Lin, J.; Bixby, H.; Magliano, D.; Bovet, P.; Miranda, J.; Khang, Y.; Stevens, G.; Riley, L.; et al.
2015Global, regional, and national incidence, prevalence, and years lived with disability for 301 acute and chronic diseases and injuries in 188 countries, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013Global Burden of Disease Study 2013 Collaborators,; Vos, T.; Barber, R.; Bell, B.; Bertozzi-Villa, A.; Biryukov, S.; Bolliger, I.; Charlson, F.; Davis, A.; Degenhardt, L.; Dicker, D.; Duan, L.; Erskine, H.; Feigin, V.; Ferrari, A.; Fitzmaurice, C.; Fleming, T.; Graetz, N.; Guinovart, C.; Haagsma, J.; et al.
2015Antiplatelet treatment compared with anticoagulation treatment for cervical artery dissection (CADISS): a randomised trialCADISS trial investigators,; Markus, H.; Hayter, E.; Levi, C.; Feldman, A.; Venables, G.; Norris, J.; Peycke, J.; Willson, M.; Hicks, C.; Hayter, E.; Madigan, J.; Clifton, A.; Menon, R.; Kennedy, F.; Khan, U.; Feldman, A.; Hollocks, M.; Markus, H.; King, A.; et al.
2019A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delayMucha, B.E.; Banka, S.; Ajeawung, N.F.; Molidperee, S.; Chen, G.G.; Koenig, M.K.; Adejumo, R.B.; Till, M.; Harbord, M.; Perrier, R.; Lemyre, E.; Boucher, R.M.; Skotko, B.G.; Waxler, J.L.; Thomas, M.A.; Hodge, J.C.; Gecz, J.; Nicholl, J.; McGregor, L.; Linden, T.; et al.
2008Interferon autoantibodies associated with AIRE deficiency decrease the expression of IFN-stimulated genesKisand, K.; Link, M.; Wolff, A.; Meager, A.; Tserel, L.; Org, T.; Murumagi, A.; Uibo, R.; Willcox, N.; Podkrajek, K.; Battelino, T.; Lobell, A.; Kampe, O.; Lima, K.; Meloni, A.; Ergun-Longmire, B.; Maclaren, N.; Perheentupa, J.; Krohn, K.; Scott, H.; et al.

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