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Results 11-20 of 82 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2015Mutational analysis of the Shigella flexneri O-antigen polymerase Wzy: Identification of Wzz-dependent Wzy mutantsNath, P.; Tran, E.; Morona, R.; Parkinson, J.S.
1995Lipopolysaccharide with an altered O-antigen produced in Escherichia coli K-12 harbouring mutated, cloned Shigella flexneri rfb genesMorona, R.; Macpherson, D.; Van Den Bosch, L.; Carlin, N.; Manning, P.
2005NmlR of Neisseria gonorrhoeae : a novel redox responsive transcription factor from the MerR familyKidd, S.; Potter, A.; Apicella, M.; Jennings, M.; McEwan, A.
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.
2005Twenty-six novel EFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS)Wieland, I.; Reardon, W.; Jakubiczka, S.; Franco, B.; Kress, W.; Vincent-Delorme, C.; Theirry, P.; Edwards, M.; Konig, R.; Rusu, C.; Schweiger, S.; Thompson, E.; Tinschert, S.; Stewart, F.; Wieacker, P.
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.

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