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PreviewIssue DateTitleAuthor(s)
2008X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentDibbens, L.; Tarpey, P.; Hynes, K.; Bayly, M.; Scheffer, I.; Smith, R.; Bomar, J.; Sutton, E.; Vandeleur, L.; Shoubridge, C.; Edkins, S.; Turner, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Jones, D.; et al.
2008Behavioural characterisation of the alpha-mannosidosis guinea pigRobinson, A.; Crawley, A.; Auclair, D.; Weston, P.; Hirte, C.; Hemsley, K.; Hopwood, J.
2008The mir-200 family and mir-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1Gregory, P.; Bert, A.; Paterson, E.; Barry, S.; Tsykin, A.; Farshid, G.; Vadas, M.; Khew-Goodall, Y.; Goodall, G.
2008A mouse model of human mucopolysaccharidosis IX exhibits osteoarthritisMartin, D.; Atmuri, V.; Hemming, R.; Farley, J.; Mort, J.; Byers, S.; Hombach-Klonisch, S.; Stern, R.; Triggs-Raine, B.
2008Gender specific effects on the actin-remodelling protein Flightless I and TGF-beta 1 contribute to impaired wound healing in aged skinAdams, D.; Studwick, X.; Kopeki, Z.; Hooper-Jones, J.; Matthaei, K.; Campbell, H.; Powell, B.; Cowin, A.
2008Human nocturnal frontal lobe epilepsy: Pharmocogenomic profiles of pathogenic nicotinic acetylcholine receptor β-subunit mutations outside the ion channel poreHoda, J.; Gu, W.; Friedli, M.; Phillips, H.; Bertrand, S.; Antonarakis, S.; Goudie, D.; Roberts, R.; Scheffer, I.; Marini, C.; Patel, J.; Berkovic, S.; Mulley, J.; Steinlein, O.; Bertrand, D.
2008Improved lactational nutrition and postnatal growth ameliorates impairment of glucose tolerance by uteroplacental insufficiency in male rat offspringSiebel, A.; Mibus, A.; De Blasio, M.; Westcott, K.; Morris, M.; Prior, L.; Owens, J.; Wlodek, M.

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