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PreviewIssue DateTitleAuthor(s)
2013Identification Of KLHL41 mutations implicates BTB-Kelch-Mediated Ubiquitination as an alternate pathway to myofibrillar disruption in nemaline myopathyGupta, V.; Ravenscroft, G.; Shaheen, R.; Todd, E.; Swanson, L.; Shiina, M.; Ogata, K.; Hsu, C.; Clarke, N.; Darras, B.; Farrar, M.; Hashem, A.; Manton, N.; Muntoni, F.; North, K.; Sandaradura, S.; Nishino, I.; Hayashi, Y.; Sewry, C.; Thompson, E.; et al.
2013Differential effects of exposure to maternal obesity or maternal weight loss during the periconceptional period in the sheep on insulin signalling molecules in skeletal muscle of the offspring at 4 months of ageNicholas, L.; Morrison, J.; Rattanatray, L.; Ozanne, S.; Kleemann, D.; Walker, S.; MacLaughlin, S.; Zhang, S.; Martin-Gronert, M.; McMillen, I.; Torrens, C.
2013Distinct roles for Toll and autophagy pathways in double-stranded RNA toxicity in a Drosophila model of expanded repeat neurodegenerative diseasesSamaraweera, S.; O'Keefe, L.; Price, G.; Venter, D.; Richards, R.
2013The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowthJolly, L.; Homan, C.; Jacob, R.; Barry, S.; Gecz, J.
2013Tropomyosin regulates cell migration during skin wound healingLees, J.; Ching, Y.; Adams, D.; Bach, C.; Samuel, M.; Kee, A.; Hardeman, E.; Gunning, P.; Cowin, A.; O'Neill, G.
2013Loss of Usp9x disrupts cortical architecture, hippocampal development and TGFβ-mediated axonogenesisStegeman, S.; Jolly, L.; Premarathne, S.; Gecz, J.; Richards, L.; Mackay-Sim, A.; Wood, S.; Alsina, B.

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