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Preview	Issue Date	Title	Author(s)
	2016	Quantification of heterogeneity in lung disease with image-based pulmonary function testing	Stahr, C.; Samarage, C.; Donnelley, M.; Farrow, N.; Morgan, K.; Zosky, G.; Boucher, R.; Siu, K.; Mall, M.; Parsons, D.; Dubsky, S.; Fouras, A.
	2014	A single whole-body low dose X-irradiation does not affect L1, B1 and IAP repeat element DNA methylation longitudinally	Newman, M.; Sykes, P.; Blyth, B.; Bezak, E.; Lawrence, M.; Morel, K.; Ormsby, R.; Suter, C.
	2014	Comparative analyses of lung transcriptomes in patients with alveolar capillary dysplasia with misalignment of pulmonary veins and in foxf1 heterozygous knockout mice	Sen, P.; Dharmadhikari, A.; Majewski, T.; Mohammad, M.; Kalin, T.; Zabielska, J.; Ren, X.; Bray, M.; Brown, H.; Welty, S.; Thevananther, S.; Langston, C.; Szafranski, P.; Justice, M.; Kalinichenko, V.; Gambin, A.; Belmont, J.; Stankiewicz, P.; Koval, M.
	2018	Differential effects on gene transcription and hematopoietic differentiation correlate with GATA2 mutant disease phenotypes	Chong, C.-E.; Venugopal, P.; Stokes, P.; Lee, Y.; Brautigan, P.; Yeung, D.; Babic, M.; Engler, G.; Lane, S.; Klingler-Hoffmann, M.; Matthews, J.; D'Andrea, R.; Brown, A.; Hahn, C.; Scott, H.
	2015	Seminal plasma promotes lesion development in a xenograft model of endometriosis	McGuane, J.T.; Watson, K.M.; Zhang, J.; Johan, M.Z.; Wang, Z.; Kuo, G.; Sharkey, D.J.; Robertson, S.A.; Hull, M.L.
	2018	Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder	Frints, S.G.M.; Ozanturk, A.; Rodríguez Criado, G.; Grasshoff, U.; de Hoon, B.; Field, M.; Manouvrier-Hanu, S.; E Hickey, S.; Kammoun, M.; Gripp, K.W.; Bauer, C.; Schroeder, C.; Toutain, A.; Mihalic Mosher, T.; Kelly, B.J.; White, P.; Dufke, A.; Rentmeester, E.; Moon, S.; Koboldt, D.C.; et al.
	2013	Mammalian sex determination and gonad development	Wilhelm, D.; Yang, J.; Thomas, P.
	2015	Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome	Walz, K.; Cohen, D.; Neilsen, P.; Foster, J.; Brancati, F.; Demir, K.; Fisher, R.; Moffat, M.; Verbeek, N.; Bjørgo, K.; Lo Castro, A.; Curatolo, P.; Novelli, G.; Abad, C.; Lei, C.; Zhang, L.; Diaz-Horta, O.; Young, J.; Callen, D.; Tekin, M.
	2017	Incorrect dosage of IQSEC2, a known intellectual disability and epilepsy gene, disrupts dendritic spine morphogenesis	Hinze, S.; Jackson, M.; Lie, S.; Jolly, L.; Field, M.; Barry, S.; Harvey, R.; Shoubridge, C.
	2017	A frailty index based on deficit accumulation quantifies mortality risk in humans and in mice	Rockwood, K.; Blodgett, J.M.; Theou, O.; Sun, M.H.; Feridooni, H.A.; Mitnitski, A.; Rose, R.A.; Godin, J.; Gregson, E.; Howlett, S.E.