Showing results 102 to 121 of 189
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| Preview | Issue Date | Title | Author(s) |
| 2007 | Know thy fly | O'Keefe, L.; Smibert, P.; Colella, A.; Chataway, T.; Saint, R.; Richards, R. |
| 2007 | Light-responsive cryptochromes from a simple multicellular animal, the coral Acropora millepora | Levy, O.; Appelbaum, L.; Leggat, W.; Gothilf, Y.; Hayward, David C.; Miller, David James; Hoegh-Guldberg, O |
| 2003 | Lineage specific differentiation of mouse ES cells: formation and differentiation of early primitive ectoderm-like (epl) cells | Rathjen, Joy R.; Rathjen, Peter David |
| 2001 | Lineage specific differentiation of pluripotent cells in vitro: a role for extraembryonic cell types | Rathjen, Joy R.; Dunn, S. M.; Bettess, Michael David; Rathjen, Peter David |
| 2002 | Localized expression of a dpp/BMP2/4 ortholog in a coral embryo | Hayward, D.; Samuel, G.; Pontynen, P.; Catmull, J.; Saint, R.; Miller, D.; Ball, E. |
| 2006 | Loss of Atrx affects trophoblast development and the pattern of x-inactivation in extraembryonic tissues | Garrick, David; Sharpe, Jackie A.; Arkell, Ruth; Dobbie, Lorraine; Smith, Andrew J. H.; Wood, William G.; Higgs, Douglas R.; Gibbons, Richard J. |
| 2005 | Maintenance of ancestral complexity and non-metazoan genes in two basal cnidarians | Technau, U.; Rudd, S.; Maxwell, P.; Gordon, P.; Saina, M.; Grasso, L.; Hayward, D.; Sensen, C.; Saint, R.; Holstein, T.; Ball, E.; Miller, D. |
| 2002 | Mammalian two-hybrid assay showing redox control of HIF-like factor | Lando, D.; Peet, D.; Pongratz, I.; Whitelaw, M. |
| 2001 | Meta-analysis, overviews and publication bias | Solomon, P.; Hutton, J. |
| 2002 | MID1 and MID2 homo- and heterodimerise to tether the rapamycin-sensitive PP2A regulatory subunit, Alpha 4, to microtubules: implications for the clinical variability of X-linked Opitz GBBB syndrome and other developmental disorders | Short, Kieran Matthew; Hopwood, Blair; Yi, Zou; Cox, Timothy Chilton |
| 2005 | Mild phenotypes in a series of patients with opitz GBBB syndrome with MID1 mutations | So, Joyce; Suckow, Vanessa; Kijas, Zofia; Kalscheuer, Vera M.; Moser, Bettina; Winter, Jennifer; Baars, Marieke; Firth, Helen; Lunt, Peter; Hamel, Ben C. J.; Meinecke, Peter; Moraine, Claude; Odent, Sylvie; Schinzel, Albert; van der Smagt, J. J.; Devriendt, Koen; Albrecht, Beate; Gillessen-Kaesbach, Gabriele; van der Burgt, Ineke; Petrij, Fred; Faivre, Laurence; McGaughran, Julie; McKenzie, Fiona; Opitz, John M.; Cox, Timothy Chilton; Schweiger, Susann |
| 2001 | Molecular characterisation of a new case of microphthalmia with linear skin defects (MLS) | Kayserili, Hulya; Cox, Timothy Chilton; Cox, Liza L.; Basaran, Seher; Kilic, Gulleyla; Ballabio, Andrea; Yuksel-Apak, Memnune |
| 2005 | Molecular genetics of pseudoxanthoma elasticum: Type and frequency of mutations in ABCC6 | Miksch, S.; Lumsden, A.; Guenther, U.; Foernzler, D.; Christen-Zach, S.; Daugherty, C.; Ramesar, R.; Lebwohl, M.; Hohl, D.; Neldner, K.; Lindpaintner, K.; Richards, R.; Struk, B. |
| 2000 | Motor axon pathfinding in the peripheral nervous system | Krull, C.; Koblar, S. |
| 2001 | Mouse ES cells: experimental exploitation of pluripotent differentiation potential | Rathjen, Joy R.; Rathjen, Peter David |
| 2007 | Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation | Tarpey, 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. |
| 2007 | Neural plate morphogenesis during mouse neurulation is regulated by antagonism of Bmp signalling | Ybot-Gonzalez, Patricia; Gaston-Massuet, Carles; Girdler, Gemma; Klingensmith, John; Arkell, Ruth; Greene, Nicholas D. E.; Copp, Andrew J. |
| 2000 | New mutations in MID1 provide support for loss of function as the cause of X-linked Optiz syndrome | Cox, T.; Allen, L.; Cox, L.; Hopwood, B.; Goodwin, B.; Haan, E.; Suthers, G. |
| 2003 | A new X-linked syndrome with agenesis of the corpus callosum, mental retardation, coloboma, micrognathia, and a mutation in the Alpha 4 gene at Xq13 | Graham, J. M.; Wheeler, P.; Tackels-Horne, Darci; Lin, Angela E.; Hall, Bryan D.; May, Melanie; Short, K. M.; Schwartz, Charles E.; Cox, T. C. |
| 2000 | Non-specific, nested suppression PCR method for isolation of unknown flanking DNA | Tamme, R.; Camp-Dotlic, E.; Kortschak, R.; Lardelli, M. |
