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	1.	IL-2/CD40-activated macrophages rescue age and tumor-induced T cell dysfunction in elderly mice. [electronic resource] by Jackaman, C Dye, D E Nelson, D J Producer: 20150715 In: Age (Dordrecht, Netherlands) vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The triple challenges associated with age-related comorbidities in Down syndrome. [electronic resource] by Glasson, E J Dye, D E Bittles, A H Producer: 20141027 In: Journal of intellectual disability research : JIDR vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Dystrophin gene transcripts skipping the mdx mutation. [electronic resource] by Wilton, S D Dye, D E Laing, N G Producer: 19970605 In: Muscle & nerve vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Revertant fibres: a possible genetic therapy for Duchenne muscular dystrophy? [electronic resource] by Wilton, S D Dye, D E Blechynden, L M Laing, N G Producer: 19971009 In: Neuromuscular disorders : NMD vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	hShroom1 links a membrane bound protein to the actin cytoskeleton. [electronic resource] by Dye, D E Karlen, S Rohrbach, B Staub, O Braathen, L R Eidne, K A Coombe, D R Producer: 20090323 In: Cellular and molecular life sciences : CMLS vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	The impact of single gene and chromosomal disorders on hospital admissions of children and adolescents: a population-based study. [electronic resource] by Dye, D E Brameld, K J Maxwell, S Goldblatt, J Bower, C Leonard, H Bourke, J Glasson, E J O'Leary, P Producer: 20110901 In: Public health genomics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Myosin storage myopathy: slow skeletal myosin (MYH7) mutation in two isolated cases. [electronic resource] by Laing, N G Ceuterick-de Groote, C Dye, D E Liyanage, K Duff, R M Dubois, B Robberecht, W Sciot, R Martin, J-J Goebel, H H Producer: 20050919 In: Neurology vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)