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Results 1-10 of 38 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2011Molecular mechanisms underlying insulin-like growth factor action: How mutations in the GH: IGF axis lead to short statureForbes, B.
2011Stenotrophomonas maltophilia: emerging disease patterns and challenges for treatmentAbbott, I.; Slavin, M.; Turnidge, J.; Thursky, K.; Worth, L.
2011Late-onset variant fibrodysplasia ossificans progressiva leading to misdiagnosis of ankylosing spondylitisBarnett, C.; Dugar, M.; Haan, E.
2011The antiviral protein viperin inhibits hepatitis C virus replication via interaction with nonstructural protein 5AHelbig, K.; Eyre, N.; Yip, L.; Narayana, S.; Li, K.; Fiches, G.; McCartney, E.; Jangra, R.; Lemon, S.; Beard, M.
2011Clonality and α-a recombination in the Australian Cryptococcus gattii VGII population - an emerging outbreak in AustraliaCarriconde, F.; Gilgado, F.; Arthur, I.; Ellis, D.; Malik, R.; van de Wiele, N.; Robert, V.; Currie, B.; Meyer, W.; Nielsen, K.
2011MLVA and phage typing as complementary tools in the epidemiological investigation of Salmonella enterica serovar typhimurium clustersRoss, I.; Davos, D.; Mwanri, L.; Raupach, J.; Heuzenroeder, M.
2011Actomyosin-mediated cellular tension drives increased tissue stiffness and B-catenin activation to induce interfollicular epidermal hyperplasia and tumor growthSamuel, M.; Lopez, J.; McGhee, E.; Croft, D.; Strachan, D.; Timpson, P.; Munro, J.; Schroder, E.; Zhou, J.; Brunton, V.; Barker, N.; Clevers, H.; Sansom, O.; Anderson, K.; Weaver, V.; Olson, M.
2011A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxiaCorbett, M.; Schwake, M.; Bahlo, M.; Dibbens, L.; Lin, M.; Gandolfo, L.; Vears, D.; O'Sullivan, J.; Robertson, T.; Bayly, M.; Gardner, A.; Vlaar, A.; Korenke, G.; Bloem, B.; de Coo, I.; Verhagen, J.; Lehesjoki, A.; Gecz, J.; Berkovic, S.
2011Sphingosine kinase localization in the control of sphingolipid metabolismSiow, D.; Anderson, C.; Berdyshev, E.; Skobeleva, A.; Natarajan, V.; Pitson, S.; Wattenberg, B.; Cocco, L.; Weber, G.; Weber, C.E.F.
2011Tmprss3, a transmembrane serine protease deficient in human DFNB8/10 deafness, is critical for cochlear hair cell survival at the onset of hearingFasquelle, L.; Scott, H.; Lenoir, M.; Wang, J.; Rebillard, G.; Gaboyard, S.; Venteo, S.; Francois, F.; Masset-Bonnefont, A.; Antonarakis, S.; Neidhart, E.; Chabbert, C.; Puel, J.; Guipponi, M.; Delprat, B.