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PreviewIssue DateTitleAuthor(s)
1988Mitogenic effects of growth hormone in cultured human fibroblasts: evidence for action via local insulin-like growth factor 1 productionCouper, J.; Haynes, K.; Werther, G.
2020HOPX regulates bone marrow-derived mesenchymal stromal cell fate determination via suppression of adipogenic gene pathwaysHng, C.H.; Camp, E.; Anderson, P.; Breen, J.; Zannettino, A.; Gronthos, S.
2008Multipotential human adipose-derived stromal stem cells exhibit a perivascular phenotype in vitro and in vivoZannettino, A.; Paton, S.; Arthur, A.; Khor, F.; Itescu, S.; Gimble, J.; Gronthos, S.
2016X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesHu, H.; Haas, S.; Chelly, J.; Van Esch, H.; Raynaud, M.; De Brouwer, A.; Weinert, S.; Froyen, G.; Frints, S.; Laumonnier, F.; Zemojtel, T.; Love, M.; Richard, H.; Emde, A.; Bienek, M.; Jensen, C.; Hambrock, M.; Fischer, U.; Langnick, C.; Feldkamp, M.; et al.
2013Sensory neuro-immune interactions differ between Irritable Bowel Syndrome subtypesHughes, P.; Harrington, A.; Castro Kraftchenko, J.; Liebregts, T.; Adam, B.; Grasby, D.; Isaacs, N.; Maldeniya, M.; Martin, C.; Persson, J.; Andrews, J.; Holtmann, G.; Blackshaw, L.; Brierley, S.
2013Characterization of mutants of a highly cross-reactive calcium-binding protein from Brassica pollen for allergen-specific immunotherapyGarmatiuk, T.; Swoboda, I.; Twardosz-Kropfmüller, A.; Dall’Antonia, F.; Keller, W.; Singh, M.B.; Bhalla, P.L.; Okada, T.; Toriyama, K.; Weber, M.; Ghannadan, M.; Sperr, W.R.; Blatt, K.; Valent, P.; Klein, B.; Niederberger, V.; Curin, M.; Balic, N.; Spitzauer, S.; Valenta, R.
2010Serum testosterone bioassay evaluation in a large male cohortNeed, E.; O'Loughlin, P.; Armstrong, D.; Haren, M.; Martin, S.; Tilley, W.; Wittert, G.; Buchanan, G.
2011Small bowel homing T cells are associated with symptoms and delayed gastric emptying in functional dyspepsiaLiebregts, T.; Adam, B.; Bredack, C.; Gururatsakul, M.; Pilkington, K.; Brierley, S.; Blackshaw, L.; Gerken, G.; Talley, N.; Holtmann, G.
2013Mutations in DEPDC5 cause familial focal epilepsy with variable fociDibbens, L.; de Vries, B.; Donatello, S.; Heron, S.; Hodgson, B.; Chintawar, S.; Crompton, D.; Hughes, J.; Bellows, S.; Klein, K.; Callenbach, P.; Corbett, M.; Gardner, A.; Kivity, S.; Iona, X.; Regan, B.; Weller, C.; Crimmins, D.; O'Brien, T.; Guerrero-Lopez, R.; et al.
2004CYP3A4 mediates dextropropoxyphene N-demethylation to nordextropropoxyphene: human in vitro and in vivo studies and lack of CYP2D6 involvementSomogyi, A.; Menelaou, A.; Fullston, S.