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Results 241-250 of 267 (Search time: 0.002 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.
2016Association between transcatheter aortic valve replacement and subsequent infective endocarditis and in-hospital deathRegueiro, A.; Linke, A.; Latib, A.; Ihlemann, N.; Urena, M.; Walther, T.; Husser, O.; Herrmann, H.; Nombela-Franco, L.; Cheema, A.; Le Breton, H.; Stortecky, S.; Kapadia, S.; Bartorelli, A.; Sinning, J.; Amat-Santos, I.; Munoz-Garcia, A.; Lerakis, S.; Gutiérrez-Ibanes, E.; Abdel-Wahab, M.; 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.
2017Parallel palaeogenomic transects reveal complex genetic history of early European farmersLipson, M.; Szécsényi-Nagy, A.; Mallick, S.; Pósa, A.; Stégmár, B.; Keerl, V.; Rohland, N.; Stewardson, K.; Ferry, M.; Michel, M.; Oppenheimer, J.; Broomandkhoshbacht, N.; Harney, E.; Nordenfelt, S.; Llamas, B.; Gusztáv, B.; Köhler, K.; Oross, K.; Bondár, M.; Marton, T.; et al.
2018Congenital Titinopathy: Comprehensive characterization and pathogenic insightsOates, E.C.; Jones, K.J.; Donkervoort, S.; Charlton, A.; Brammah, S.; Smith, J.E.; Ware, J.S.; Yau, K.S.; Swanson, L.C.; Whiffin, N.; Peduto, A.J.; Bournazos, A.; Waddell, L.B.; Farrar, M.A.; Sampaio, H.A.; Teoh, H.L.; Lamont, P.J.; Mowat, D.; Fitzsimons, R.B.; Corbett, A.J.; et al.
2007Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: A population-based studyJenkins, M.; Hayashi, S.; O'Shea, A.; Burgart, L.; Smyrk, T.; Shimizu, D.; Waring, P.; Ruszkiewicz, A.; Pollett, A.; Redston, M.; Barker, M.; Baron, J.; Casey, G.; Dowty, J.; Giles, G.; Limburg, P.; Newcomb, P.; Young, J.; Walsh, M.; Thibodeau, S.; et al.
2022Probiotic peanut oral immunotherapy versus oral immunotherapy and placebo in children with peanut allergy in Australia (PPOIT-003): a multicentre, randomised, phase 2b trialLoke, P.; Orsini, F.; Lozinsky, A.C.; Gold, M.; O'Sullivan, M.D.; Quinn, P.; Lloyd, M.; Ashley, S.E.; Pitkin, S.; Axelrad, C.; Metcalfe, J.R.; Su, E.L.; Tey, D.; Robinson, M.N.; Allen, K.J.; Prescott, S.L.; Galvin, A.D.; Tang, M.L.K.; O'Sullivan, M.; Fahy-Scheer, S.; 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.

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