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PreviewIssue DateTitleAuthor(s)
2012Nonredundant regulation of rice arbuscular mycorrhizal symbiosis by two members of the PHOSPHATE TRANSPORTER1 gene familyYang, S.; Gronlund, M.; Jakobsen, I.; Grotemeye, M.; Rentsch, D.; Miyao, A.; Hirochika, H.; Kumar, C.; Sundaresan, V.; Salamin, N.; Catausan, S.; Mattes, N.; Heuer, S.; Paszkowski, U.
2015Mutational analysis of the Shigella flexneri O-antigen polymerase Wzy: Identification of Wzz-dependent Wzy mutantsNath, P.; Tran, E.; Morona, R.; Parkinson, J.S.
2010The structure of the talin/integrin complex at a lipid bilayer: an NMR and MD simulation studyKalli, A.; Wegener, K.; Goult, B.; Anthis, N.; Campbell, I.; Sansom, 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.
2013H-NS plays a role in expression of Acinetobacter baumannii virulence featuresEijkelkamp, B.; Stroeher, U.; Hassan, K.; Elbourne, L.; Paulsen, I.; Brown, M.; Payne, S.M.
2012A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disabilityHuang, L.; Jolly, L.; Willis-Owen, S.; Gardner, A.; Sharma, R.; Douglas, E.; Shoubridge, C.; Wieczorek, D.; Tzschach, A.; Cohen, M.; Hackett, A.; Field, M.; Froyen, G.; Hu, H.; Haas, S.; Ropers, H.; Kalscheuer, V.; Corbett, M.; Gecz, J.
2015HCFC1 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.
2014Differential, dominant activation and inhibition of Notch signalling and APP cleavage by truncations of PSEN1 in human diseaseNewman, M.; Wilson, L.; Verdile, G.; Lim, A.; Khan, I.; Nik, S.; Pursglove, S.; Chapman, G.; Martins, R.; Lardelli, 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.
2011A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxiaCorbett, M.; Schwake, M.; Bahlo, M.; Dibbens, L.; Lin, M.; Gandolfo, L.; Vears, D.; O'Sullivan, J.; Robertson, T.; Bayly, M.; Gardner, A.; Vlaar, A.; Korenke, G.; Bloem, B.; de Coo, I.; Verhagen, J.; Lehesjoki, A.; Gecz, J.; Berkovic, S.