1. Adelaide Research & Scholarship

Search


Current filters:




Start a new search
Add filters:

Use filters to refine the search results.

 | 
Results 1-10 of 36 (Search time: 0.006 seconds).
Item hits:
PreviewIssue DateTitleAuthor(s)
2006Novel DNA binding by a basic helix-loop-helix protein - The role of the dioxin receptor PAS domainChapman-Smith, A.; Whitelaw, M.
2008Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoformSharma, S.; Burdon, K.; Dave, A.; Jamieson, R.; Yaron, Y.; Billson, F.; van Maldergem, L.; Lorenz, B.; Gecz, J.; Craig, J.
2001An orphaned mammalian b-globin gene of ancient evolutionary originWheeler, D.; Hope, R.; Cooper, S.; Dolman, G.; Webb, G.; Bottema, C.; Gooley, A.; Goodman, M.; Holland, R.
2002Characterization of a novel type IV pilus locus encoded on the large plasmid of locus of enterocyte effacement-negative shiga-toxigenic Escherichia coli strains that are virulent for humansSrimanote, P.; Paton, A.; Paton, J.
2000Ovine interleukin 12 has biological activity on ovine and human activated peripheral blood mononuclear cellsSwinburne, S.; Russ, G.; Krishnan, R.
2008PU.1 and NFATc1 mediate osteoclastic induction of the mouse β₃ integrin promoterCrotti, T.; Sharma, S.; Fleming, J.; Flannery, M.; Ostrowski, M.; Goldring, S.; McHugh, K.
2003Nova regulates GABA(A) receptor gamma 2 alternative splicing via a distal downstream UCAU-rich intronic splicing enhancerDredge, B.; Darnell, R.
2006Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardationHagens, O.; Dubos, A.; Abidi, F.; Barbi, G.; Van Zutven, L.; Hoeltzenbein, M.; Tommerup, N.; Moraine, C.; Fryns, J.; Chelly, J.; van Bokhoven, H.; Gecz, J.; Dollfus, H.; Ropers, H.; Schwartz, C.; de Cassia Stocco dos Santos, R.; Kalscheuer, V.; Hanauer, A.
2000Gene encoding the mouse sulphamidase: cDNA cloning, structure, and chromosomal mappingCostanzi, E.; Beccari, T.; Stinchi, S.; Bibi, L.; Hopwood, J.; Orlacchio, A.
2004Glycogen branching enzyme (GBE1) mutation causing equine glycogen storage disease IVWard, T.; Valberg, S.; Adelson, D.; Abbey, C.; Binns, M.; Mickelson, J.

Discover