Search


Current filters:


Start a new search
Add filters:

Use filters to refine the search results.


Results 1-10 of 60 (Search time: 0.002 seconds).
Item hits:
PreviewIssue DateTitleAuthor(s)
2002Using genomic resources to guide research directions. The arabinogalactan protein gene family as a test caseSchultz, C.; Rumsewicz, M.; Johnson, K.; Jones, B.; Gaspar, Y.; Bacic, A.
2003Molecular characterization and analysis of the acrB gene of Aspergillus nidulans: A gene identified by genetic interaction as a component of the regulatory network that includes the CreB deubiquitination enzymeBoase, N.; Lockington, R.; Adams, J.; Rodbourn, L.; Kelly, J.
2000FMR3 is a novel gene associated with FRAXE CpG island and transcriptionally silent in FRAXE full mutationsGecz, J.
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.
2004Inhibition of generation of cytotoxic T lymphocyte activity by a CCL19/macrophage inflammatory protein (MIP)-3beta antagonistPilkington, K.; Clark-Lewis, I.; McColl, S.
2002Asparagine hydroxylation of the HIF transactivation domain: A hypoxic switchLando, D.; Peet, D.; Whelan, D.; Gorman, J.; Whitelaw, M.
2005Cytoplasmic ATP-sensing domains regulate gating of skeletal muscle ClC-1 chloride channelsBennetts, B.; Rychkov, G.; Ng, H.; Morton, C.; Stapleton, D.; Parker, M.; Cromer, B.
2007Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a marfanoid habitusRaymond, F.; Tarpey, P.; Edkins, S.; Tofts, C.; O'Meara, S.; Teague, J.; Butler, A.; Stevens, C.; Barthorpe, S.; Buck, G.; Cole, J.; Dicks, E.; Gray, K.; Harrison, R.; Hills, K.; Hinton, J.; Jones, D.; Menzies, A.; Perry, J.; Raine, K.; et al.
2005Drosophila starvin encodes a tissue-specific BAG-domain protein required for larval food uptakeCoulson, M.; Robert, S.; Saint, R.
2007Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardationTarpey, 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.