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PreviewIssue DateTitleAuthor(s)
2019A comprehensive screening of copy number variability in dementia with Lewy bodiesKun-Rodrigues, C.; Orme, T.; Carmona, S.; Hernandez, D.G.; Ross, O.A.; Eicher, J.D.; Shepherd, C.; Parkkinen, L.; Darwent, L.; Heckman, M.G.; Scholz, S.W.; Troncoso, J.C.; Pletnikova, O.; Dawson, T.; Rosenthal, L.; Ansorge, O.; Clarimonm, J.; Lleo, A.; Morenas-Rodriguez, E.; Clark, L.; et al.
2017High prevalence of relapse in children with Philadelphia-like acute lymphoblastic leukemia despite risk-adapted treatmentHeatley, S.; Sadras, T.; Kok, C.; Nievergall, E.; Quek, K.; Dang, P.; McClure, B.; Venn, N.; Moore, S.; Suttle, J.; Law, T.; Ng, A.; Muskovic, W.; Norris, M.; Revesz, T.; Osborn, M.; Moore, A.; Suppiah, R.; Fraser, C.; Alvaro, F.; et al.
2019PHF6 regulates hematopoietic stem and progenitor cells and its loss synergizes with expression of TLX3 to cause leukemiaMcRae, H.; Garnham, A.; Hu, Y.; Witkowski, M.; Corbett, M.; Dixon, M.; May, R.; Sheikh, B.; Chiang, W.; Kueh, A.; Nguyen, T.; Man, K.; Gloury, R.; Aubrey, B.; Policheni, A.; Di Rago, L.; Alexander, W.; Gray, D.; Strasser, A.; Hawkins, E.; et al.
2018Antenatal IL-1-dependent inflammation persists postnatally and causes retinal and sub-retinal vasculopathy in progenyBeaudry-Richard, A.; Nadeau-Vallée, M.; Prairie, É.; Maurice, N.; Heckel, É.; Nezhady, M.; Pundir, S.; Madaan, A.; Boudreault, A.; Hou, X.; Quiniou, C.; Sierra, E.; Beaulac, A.; Lodygensky, G.; Robertson, S.; Keelan, J.; Adams-Waldorf, K.; Olson, D.; Rivera, J.; Lubell, W.; et al.
2011SHP-1 expression accounts for resistance to imatinib treatment in Philadelphia chromosome-positive cells derived from patients with chronic myeloid leukemiaEsposito, N.; Colavita, I.; Quintarelli, C.; Sica, A.; Peluso, A.; Luciano, L.; Picardi, M.; Vecchio, L.; Buonomo, T.; Hughes, T.; White, D.; Radich, J.; Russo, D.; Branford, S.; Saglio, G.; Vaz de Melo, J.; Martinelli, R.; Ruoppolo, M.; Kalebic, T.; Martinelli, G.; et al.
2015Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiencyTan, C.; Shard, C.; Ranieri, E.; Hynes, K.; Pham, D.; Leach, D.; Buchanan, G.; Corbett, M.; Shoubridge, C.; Kumar, R.; Douglas, E.; Nguyen, L.; Mcmahon, J.; Sadleir, L.; Specchio, N.; Marini, C.; Guerrini, R.; Moller, R.; Depienne, C.; Haan, E.; et al.
2017MicroRNA-194 promotes prostate cancer metastasis by inhibiting SOCS2Das, R.; Gregory, P.; Fernandes, R.; Denis, I.; Wang, Q.; Townley, S.; Zhao, S.; Hanson, A.; Pickering, M.; Armstrong, H.; Lokman, N.; Ebrahimie, E.; Davicioni, E.; Jenkins, R.; Karnes, R.; Ross, A.; Den, R.; Klein, E.; Chi, K.; Ramshaw, H.; et al.
2019Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2Corbett, M.A.; Kroes, T.; Veneziano, L.; Bennett, M.F.; Florian, R.; Schneider, A.L.; Coppola, A.; Licchetta, L.; Franceschetti, S.; Suppa, A.; Wenger, A.; Mei, D.; Pendziwiat, M.; Kaya, S.; Delledonne, M.; Straussberg, R.; Xumerle, L.; Regan, B.; Crompton, D.; van Rootselaar, A.-.F.; et al.
2019Recurrent TTN metatranscript-only c.39974-11T>G splice variant associated with autosomal recessive arthrogryposis multiplex congenita and myopathyBryen, S.J.; Ewans, L.; Pinner, J.; MacLennan, S.C.; Donkervoort, S.; Castro, D.; Töpf, A.; O'Grady, G.; Cummings, B.; Chao, K.R.; Weisburd, B.; Francioli, L.; Faiz, F.; Bournazos, A.M.; Hu, Y.; Malicki, D.M.; Doyle, H.; Witting, N.; Vissing, J.; Claeys, K.G.; et al.
2019Autoimmune psychosis: an international consensus on an approach to the diagnosis and management of psychosis of suspected autoimmune originPollak, T.A.; Lennox, B.R.; Müller, S.; Benros, M.E.; Prüss, H.; Tebartz van Elst, L.; Klein, H.; Steiner, J.; Frodl, T.; Bogerts, B.; Tian, L.; Groc, L.; Hasan, A.; Baune, B.T.; Endres, D.; Haroon, E.; Yolken, R.; Benedetti, F.; Halaris, A.; Meyer, J.H.; et al.