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PreviewIssue DateTitleAuthor(s)
2013A novel prion disease associated with diarrhea and autonomic neuropathyMead, S.; Gandhi, S.; Beck, J.; Caine, D.; Gallujipali, D.; Carswell, C.; Hyare, H.; Joiner, S.; Ayling, H.; Lashley, T.; Linehan, J.M.; Al-Doujaily, H.; Sharps, B.; Revesz, T.; Sandberg, M.K.; Reilly, M.M.; Koltzenburg, M.; Forbes, A.; Rudge, P.; Brandner, S.; et al.
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.
2013A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndromeBuchovecky, C.; Turley, S.; Brown, H.; Kyle, S.; McDonald, J.; Liu, B.; Pieper, A.; Huang, W.; Katz, D.; Russell, D.; Shendure, J.; Justice, M.
2013A tudor domain protein SPINDLIN1 interacts with the mRNA-binding protein SERBP1 and is involved in mouse oocyte meiotic resumptionChew, T.; Peaston, A.; Lim, A.; Lorthongpanich, C.; Knowles, B.; Solter, D.; Sun, Q.-Y.
2013ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticityHirata, H.; McMichael, G.; Haan, E.; MacLennan, A.; Yap, T.; Nguyen, L.; Shaw, M.; Gecz, J.
2013A transcription factor contributes to pathogenesis and virulence in streptococcus pneumoniaeMahdi, L.; Ebrahimie, E.; Adelson, D.; Paton, J.; Ogunniyi, A.; Skurnik, M.
2013Characterization of mutants of a highly cross-reactive calcium-binding protein from Brassica pollen for allergen-specific immunotherapyGarmatiuk, T.; Swoboda, I.; Twardosz-Kropfmüller, A.; Dall’Antonia, F.; Keller, W.; Singh, M.B.; Bhalla, P.L.; Okada, T.; Toriyama, K.; Weber, M.; Ghannadan, M.; Sperr, W.R.; Blatt, K.; Valent, P.; Klein, B.; Niederberger, V.; Curin, M.; Balic, N.; Spitzauer, S.; Valenta, R.
2013A heterozygous moth genome provides insights into herbivory and detoxificationYou, M.; Baxter, S.
2013Mutations in DEPDC5 cause familial focal epilepsy with variable fociDibbens, L.; de Vries, B.; Donatello, S.; Heron, S.; Hodgson, B.; Chintawar, S.; Crompton, D.; Hughes, J.; Bellows, S.; Klein, K.; Callenbach, P.; Corbett, M.; Gardner, A.; Kivity, S.; Iona, X.; Regan, B.; Weller, C.; Crimmins, D.; O'Brien, T.; Guerrero-Lopez, R.; et al.
2013Interplay between manganese and iron in pneumococcal pathogenesis: Role of the orphan response regulator ritROng, C.; Potter, A.; Trappetti, C.; Walker, M.; Jennings, M.; Paton, J.; McEwan, A.; Payne, S.M.

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