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Results 81-90 of 90 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2018BAK/BAX macropores facilitate mitochondrial herniation and mtDNA efflux during apoptosisMcArthur, K.; Whitehead, L.; Heddleston, J.; Li, L.; Padman, B.; Oorschot, V.; Geoghegan, N.; Chappaz, S.; Davidson, S.; Chin, H.; Lane, R.; Dramicanin, M.; Saunders, T.; Sugiana, C.; Lessene, R.; Osellame, L.; Chew, T.; Dewson, G.; Lazarou, M.; Ramm, G.; et al.
2019Dietary zinc and the control of Streptococcus pneumoniae infectionEijkelkamp, B.A.; Morey, J.R.; Neville, S.L.; Tan, A.; Pederick, V.G.; Cole, N.; Singh, P.P.; Ong, C.-.L.Y.; Gonzalez de Vega, R.; Clases, D.; Cunningham, B.A.; Hughes, C.E.; Comerford, I.; Brazel, E.B.; Whittall, J.J.; Plumptre, C.D.; McColl, S.R.; Paton, J.C.; McEwan, A.G.; Doble, P.A.; et al.
2017Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biasesStessman, H.; Xiong, B.; Coe, B.; Wang, T.; Hoekzema, K.; Fenckova, M.; Kvarnung, M.; Gerdts, J.; Trinh, S.; Cosemans, N.; Vives, L.; Lin, J.; Turner, T.; Santen, G.; Ruivenkamp, C.; Kriek, M.; Van Haeringen, A.; Aten, E.; Friend, K.; Liebelt, J.; et al.
2007Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardationTarpey, P.; Raymond, F.; Nguyen, L.; Rodriguez, J.; Hackett, A.; Vandeleur, L.; Smith, R.; Shoubridge, C.; Edkins, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Hills, K.; Jones, D.; Mironenko, T.; Perry, J.; et al.
2007A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsyCavalleri, G.; Walley, N.; Soranzo, N.; Mulley, J.; Doherty, C.; Kapoor, A.; Depondt, C.; Lynch, J.; Scheffer, I.; Heils, A.; Gehrmann, A.; Kinirons, P.; Gandhi, S.; Satishchandra, P.; Wood, N.; Anand, A.; Sander, T.; Berkovic, S.; Delanty, N.; Goldstein, D.; et al.
2016Clinical and molecular analyses of Beckwith–Wiedemann syndrome: comparison between spontaneous conception and assisted reproduction techniquesTenorio, J.; Romanelli, V.; Martin-Trujillo, A.; Fernández, G.; Segovia, M.; Perandones, C.; Pérez Jurado, L.; Esteller, M.; Fraga, M.; Arias, P.; Gordo, G.; Dapía, I.; Mena, R.; Palomares, M.; Pérez de Nanclares, G.; Nevado, J.; García-Miñaur, S.; Santos-Simarro, F.; Martinez-Glez, V.; Vallespín, E.; et al.
2017Proposed primary endpoints for use in clinical trials that compare treatment options for bloodstream infection in adults: a consensus definitionHarris, P.; McNamara, J.; Paterson, D.; Harris, P.; McNamara, J.; Lye, D.; Davis, J.; Tong, S.; Davis, J.; Bernard, L.; Cheng, A.; Cheng, A.; Doi, Y.; Fowler, V.; Kaye, K.; Leibovici, L.; Leibovici, L.; Lipman, J.; Lipman, J.; Lipman, J.; et al.
2014Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodiesBras, J.; Guerreiro, R.; Darwent, L.; Parkkinen, L.; Ansorge, O.; Escott-Price, V.; Hernandez, D.G.; Nalls, M.A.; Clark, L.N.; Honig, L.S.; Marder, K.; Van Der Flier, W.M.; Lemstra, A.; Scheltens, P.; Rogaeva, E.; St George-Hyslop, P.; Londos, E.; Zetterberg, H.; Ortega-Cubero, S.; Pastor, P.; et al.
2019Quantifying between-cohort and between-sex genetic heterogeneity in major depressive disorderTrzaskowski, M.; Mehta, D.; Peyrot, W.; Hawkes, D.; Davies, D.; Howard, D.; Kemper, K.; Sidorenko, J.; Maier, R.; Ripke, S.; Mattheisen, M.; Baune, B.; Grabe, H.; Heath, A.; Jones, L.; Jones, I.; Madden, P.; McIntosh, A.; Breen, G.; Lewis, C.; et al.
2019Zinc-binding to the cytoplasmic PAS domain regulates the essential WalK histidine kinase of Staphylococcus aureusMonk, I.; Shaikh, N.; Begg, S.; Gajdiss, M.; Sharkey, L.; Lee, J.; Pidot, S.; Seemann, T.; Kuiper, M.; Winnen, B.; Hvorup, R.; Collins, B.; Bierbaum, G.; Udagedara, S.; Morey, J.; Pulyani, N.; Howden, B.; Maher, M.; McDevitt, C.; King, G.; et al.