Showing results 431 to 446 of 446
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Preview | Issue Date | Title | Author(s) |
| 2017 | Unique presentation of cutis laxa with Leigh-like syndrome due to ECHS1 deficiency | Balasubramaniam, S.; Riley, L.; Bratkovic, D.; Ketteridge, D.; Manton, N.; Cowley, M.; Gayevskiy, V.; Roscioli, T.; Mohamed, M.; Gardeitchik, T.; Morava, E.; Christodoulou, J. |
| 2015 | Unravelling complexity in seagrass systems for management: Australia as a microcosm | Kilminster, K.; McMahon, K.; Waycott, M.; Kendrick, G.; Scanes, P.; McKenzie, L.; O'Brien, K.; Lyons, M.; Ferguson, A.; Maxwell, P.; Glasby, T.; Udy, J. |
| 2017 | Unravelling mummies: cryptic diversity, host specificity, trophic and coevolutionary interactions in psyllid-parasitoid food webs | Hall, A.; Steinbauer, M.; Taylor, G.; Johnson, S.; Cook, J.; Riegler, M. |
| 2014 | Using the zebrafish model for Alzheimer's disease research | Newman, M.; Ebrahimie, E.; Lardelli, M. |
| 2009 | Variation in Giardia: towards a taxonomic revision of the genus | Monis, P.; Caccio, S.; Thompson, R. |
| 1998 | A very high density microsatellite map (1 STR/41kb) of 1.7 Mb on Xp22 spanning the microphthalmia with linear skin defects (MLS) syndrome critical region | Cox, Timothy C.; Cox, Liza L.; Ballabio, Andrea |
| 2015 | Vulnerability to climate change adaptation in rural Bangladesh | Shaw, Jennie,; Grubb, Michael, |
| 2014 | Whole exome sequencing of extreme morbid obesity patients: translational implications for obesity and related disorders | Paz-Filho, G.; Boguszewski, M.; Mastronardi, C.; Patel, H.; Johar, A.; Chuah, A.; Huttley, G.; Boguszewski, C.; Wong, M.; Arcos-Burgos, M.; Licinio, J. |
| 2016 | Whole genome comparison reveals high levels of inbreeding and strain redundancy across the spectrum of commercial wine strains of Saccharomyces cerevisiae | Borneman, A.; Forgan, A.; Kolouchova, R.; Fraser, J.; Schmidt, S. |
| 2015 | Whole genome sequences are required to fully resolve the linkage disequilibrium structure of human populations | Pengelly, R.; Tapper, W.; Gibson, J.; Knut, M.; Tearle, R.; Collins, A.; Ennis, S. |
| 2015 | WWOX, the chromosomal fragile site FRA16D spanning gene: its role in metabolism and contribution to cancer | Richards, R.I.; Choo, A.; Lee, C.S.; Dayan, S.; O Keefe, L. |
| 1995 | X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome | Gedeon, A.; Wilson, M.; Colley, A.; Sillence, D.; Mulley, J. |
| 1995 | X-Y chromosome dissociation in mice and rats exposed to increased testicular or environmental temperatures | Van Zelst, S.; Zupp, J.; Hayman, D.; Setchell, B. |
| 2013 | Y-Chromosome and mtDNA genetics reveal significant contrasts in affinities of modern Middle Eastern populations with European and African populations | Badro, D.; Douaihy, B.; Haber, M.; Youhanna, S.; Salloum, A.; Ghassibe-Sabbagh, M.; Johnsrud, B.; Khazen, G.; Matisoo-Smith, E.; Soria-Hernanz, D.; Wells, R.; Tyler-Smith, C.; Platt, D.; Zalloua, P.; Caramelli, D. |
| 2017 | YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction | Gabriele, M.; Vulto-van Silfhout, A.; Germain, P.; Vitriolo, A.; Kumar, R.; Douglas, E.; Haan, E.; Kosaki, K.; Takenouchi, T.; Rauch, A.; Steindl, K.; Frengen, E.; Misceo, D.; Pedurupillay, C.; Stromme, P.; Rosenfeld, J.; Shao, Y.; Craigen, W.; Schaaf, C.; Rodriguez-Buritica, D.; et al. |
| 2009 | Zebrafish aplnra functions in epiboly | Nornes, S.; Tucker, B.; Lardelli, M. |