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| Preview | Issue Date | Title | Author(s) |
| 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. |
| 2002 | Nonspecific, nested suppression PCR method for isolation of unknown flanking DNA ("Cold-start method") | Lardelli, M. |
| 2006 | Novel DNA binding by a basic helix-loop-helix protein - The role of the dioxin receptor PAS domain | Chapman-Smith, A.; Whitelaw, M. |
| 2002 | Nutrition as therapy: let's look at the evidence | Moran, J.; Peter, J.; Solomon, P. |
| 2000 | On the conservation of function of the Drosophila Fat facets deubiquitinating enzyme and Fam, its mouse homolog | Chen, Xiaoguang; Overstreet, Erin; Wood, Stephen Andrew; Fischer, J. A. |
| 2004 | Oxygen-dependent asparagine hydroxylation | Peet, D.; Lando, D.; Whelan, D.; Whitelaw, M.; Gorman, J. |
| 2003 | Oxygen-dependent regulation of hypoxia-inducible factors by prolyl and asparaginyl hydroxylation | Lando, D.; Gorman, J.; Whitelaw, M.; Peet, D. |
