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Results 1-10 of 64 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2004Interleukin 18 receptorSergi, B.; Penttila, I.
2004A2 milk is allergenicSmith, W.; Thompson, D.; Kummerow, M.; Quinn, P.; Gold, M.
2004TM4SF10 gene sequencing in XLMR patients identifies common polymorphisms but no disease-associated mutationChristophe-Hobertus, C.; Kooy, F.; Gecz, J.; Abramowicz, M.; Holinski-Feder, E.; Schwartz, C.; Christophe, D.
2004De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiencyMcFarland, R.; Kirby, D.; Fowler, K.; Ohtake, A.; Ryan, M.; Amor, D.; Fletcher, J.; Dixon, J.; Collins, F.; Turnbull, D.; Taylor, R.; Thorburn, A.
2004Characterization of the MEK5-ERK5 module in human neutrophils and its relationship to ERK1/ERK2 in the chemotactic responseHii, C.; Anson, D.; Costabile, M.; Mukaro, V.; Dunning, K.; Ferrante, A.
2004Insuflon versus subcutaneous injection for cytokine administration in children and adolescents: a randomised crossover studyDyer, S.; Collins, C.; Baghurst, P.; Saxon, B.; Meachan, B.
2004Aberrant CBFA2T3B gene promoter methylation in breast tumorsBais, A.; Gardner, A.; McKenzie, O.; Callen, D.; Sutherland, G.; Kremmidiotis, G.
2004The molecular basis of intellectual disability: novel genes with naturally occurring mutations causing altered gene expression in the brainGecz, J.
2004A combined 13CO2/H2 breath test can be used to assess starch digestion and fermentation in humansSymonds, E.; Kritas, S.; Omari, T.; Butler, R.
2004Enzyme replacement therapy in mucopolysaccharidosis VI (Maroteaux-Lamy Syndrome)Harmatz, P.; Whitley, C.; Waber, L.; Pais, R.; Steiner, R.; Plecko, B.; Kaplan, P.; Simon, J.; Butensky, E.; Hopwood, J.