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Results 1-10 of 13 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2004Rise and fall of the Beringian steppe bisonShapiro, B.; Drummond, A.; Rambaut, A.; Wilson, M.; Matheus, P.; Sher, A.; Pybus, O.; Gilbert, M.; Barnes, I.; Binladen, J.; Willerslev, E.; Hansen, A.; Baryshnikov, G.; Burns, J.; Davydov, S.; Driver, J.; Froese, D.; Harington, C.; Keddie, G.; Kosintsev, P.; et al.
2008X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentDibbens, L.; Tarpey, P.; Hynes, K.; Bayly, M.; Scheffer, I.; Smith, R.; Bomar, J.; Sutton, E.; Vandeleur, L.; Shoubridge, C.; Edkins, S.; Turner, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Jones, D.; et al.
2004Proceedings of the Oxygen Homeostasis/Hypoxia MeetingKaufman, B.; Scharf, O.; Arbeit, J.; Ashcroft, M.; Brown, J.; Bruick, R.; Chapman, J.; Evans, S.; Giaccia, A.; Harris, A.; Huang, E.; Johnson, R.; Kaelin Jr., W.; Koch, C.; Maxwell, P.; Mitchell, J.; Neckers, L.; Powis, G.; Rajendran, J.; Semenza, G.; et al.
2008Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosisBerkovic, S.; Dibbens, L.; Oshlack, A.; Silver, J.; Katerelos, M.; Vears, D.; Lullmann-Rauch, R.; Blanz, J.; Zhang, K.; Stankovich, J.; Kalnins, R.; Dowling, J.; Andermann, E.; Andermann, F.; Faldini, E.; D'Hooge, R.; Vadlamudi, L.; Macdonnell, R.; Hodgson, B.; Bayly, M.; et al.
2008Genome analysis of the platypus reveals unique signatures of evolutionWarren, W.; Hillier, L.; Graves, J.; Birney, E.; Ponting, C.; Grutzner, F.; Belov, K.; Miller, W.; Clarke, L.; Chinwall, A.; Yang, S.; Heger, A.; Locke, D.; Miethke, P.; Waters, P.; Veyrunes, F.; Fulton, L.; Fulton, B.; Graves, T.; Wallis, J.; et al.
2009Lin28 promotes transformation and is associated with advanced human malignanciesViswanathan, S.; Powers, J.; Einhorn, W.; Hoshida, Y.; Ng, T.; Toffanin, S.; O'Sullivan, M.; Lu, J.; Philips, L.; Lockhart, V.; Sha, S.; Tanwar, P.; Mermel, C.; Beroukhim, R.; Azam, M.; Teixeira, J.; Meyerson, M.; Hughes, T.; Llovet, J.; Mullighan, C.; et al.
2008Progress and prospects in rat genetics: a community viewAitman, T.; Critser, J.; Cuppen, E.; Dominiczak, A.; Fernandez-Suarez, X.; Flint, J.; Gauguier, D.; Geurts, A.; Gould, M.; Harris, P.; Holmdahl, R.; Hubner, N.; Izsvák, Z.; Jacob, H.; Kuramoto, T.; Kwitek, A.; Marrone, A.; Mashimo, T.; Moreno, C.; Mullins, J.; et al.
2003Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardationBurdon, K.; McKay, J.; Sale, M.; Russell-Eggitt, I.; Mackey, D.; Wirth, G.; Elder, J.; Nicoll, A.; Clarke, M.; FitzGerald, L.; Stankovich, J.; Shaw, M.; Sharma, S.; Gajovic, S.; Gruss, P.; Ross, S.; Thomas, P.; Voss, A.; Thomas, T.; Gecz, J.; et al.
2002Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndromeLower, K.; Turner, G.; Kerr, B.; Mathews, K.; Shaw, M.; Gedeon, A.; Schelley, S.; Hoyme, H.; White, S.; Delatycki, M.; Lampe, A.; Clayton-Smith, J.; Stewart, H.; van Ravenswaay, C.; de Vries, B.; Cox, B.; Grompe, M.; Ross, S.; Thomas, P.; Mulley, J.; et al.
2004The sequence and analysis of duplication-rich human chromosome 16Martin, J.; Han, C.; Gordon, L.; Terry, A.; Prabhakar, S.; She, X.; Xie, G.; Hellsten, U.; Man, Y.; Altherr, M.; Couronne, O.; Aerts, A.; Bajorek, E.; Black, S.; Blumer, H.; Branscomb, E.; Brown, N.; Bruno, W.; Buckingham, J.; Callen, D.; et al.

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