Adelaide Research & Scholarship: Search

Search

Results 1-10 of 36 (Search time: 0.002 seconds).

previous
1
2
3
4
next

Item hits:

Preview	Issue Date	Title	Author(s)
	2001	Glucose-regulated insulin expression in diabetic rats	Barry, S.; Ramesh, N.; Lejnieks, D.; Simonson, W.; Kemper, L.; Lernmark, A.; Osborne, W.
	2008	The Effect of the JNK Inhibitor, JIP Peptide, on Human T Lymphocyte Proliferation and Cytokine Production	Melino, M.; Hii, C.; McColl, S.; Ferrante, A.
	2001	The CF salt controversy: In vivo observations and therapeutic approaches	Tarran, R.; Grubb, B.; Parsons, D.; Picher, M.; Hirsch, A.; Davis, C.; Boucher, R.
	2010	Genome-wide identification of human FOXP3 target genes in natural regulatory T cells	Sadlon, T.; Wilkinson, B.; Pederson, S.; Brown, C.; Bresatz, S.; Gargett, T.; Melville, E.; Peng, K.; D'Andrea, R.; Glonek, G.; Goodall, G.; Zola, H.; Shannon, F.; Barry, S.
	1997	Expression, Purification and Characterization of Recombinant Caprine N-Acetylglucosamine-6-Sulphatase	Litjens, T.; Bielicki, J.; Anson, D.; Friderici, K.; Jones, M.; Hopwood, J.
	2009	Characterisation and Developmental Potential of Ovine Bone Marrow Derived Mesenchymal Stem Cells	Mc Carty, R.; Gronthos, S.; Zannettino, A.; Foster, B.; Xian, C.
	2004	Mutational analysis of mucopolysaccharidosis type VI patients undergoing a trial of enzyme replacement therapy	Karageorgos, L.; Harmatz, P.; Simon, J.; Pollard, A.; Clements, P.; Brooks, D.; Hopwood, J.
	2004	Mouse orthologue of ARX, a gene mutated in several X-linked forms of mental retardation and epilepsy, is a marker of adult neural stem cells and forebrain GABAergic neurons	Colombo, E.; Galli, R.; Cossu, G.; Gecz, J.; Broccoli, V.
	2016	X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes	Hu, 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.
	2015	HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain.	Jolly, L.; Nguyen, L.; Domingo, D.; Sun, Y.; Barry, S.; Hancarova, M.; Plevova, P.; Vlckova, M.; Havlovicova, M.; Kalscheuer, V.; Graziano, C.; Pippucci, T.; Bonora, E.; Sedlacek, Z.; Gecz, J.