Search


Current filters:

Start a new search
Add filters:

Use filters to refine the search results.


Results 1-10 of 55 (Search time: 0.003 seconds).
Item hits:
PreviewIssue DateTitleAuthor(s)
2017NAD deficiency, congenital malformations, and niacin supplementationShi, H.; Enriquez, A.; Rapadas, M.; Martin, E.; Wang, R.; Moreau, J.; Lim, C.; Szot, J.; Ip, E.; Hughes, J.; Sugimoto, K.; Humphreys, D.; McInerney-Leo, A.; Leo, P.; Maghzal, G.; Halliday, J.; Smith, J.; Colley, A.; Mark, P.; Collins, F.; et al.
2017Two SUMO proteases SUMO PROTEASE RELATED TO FERTILITY1 and 2 are required for fertility in arabidopsisLiu, L.; Jiang, Y.; Zhang, X.; Wang, X.; Wang, Y.; Han, Y.; Coupland, G.; Jin, J.; Searle, I.; Fu, Y.; Chen, F.
2014Understanding the undelaying mechanism of HASubtyping in the level of physic-chemal characteristics of proteinEbrahimi, M.; Aghagolzadeh, P.; Shamabadi, N.; Tahmasebi, A.; Alsharifi, M.; Adelson, D.; Hemmatzadeh, F.; Ebrahimie, E.; Tompkins, S.
2017Structure aided design of a Neu5Gc specific lectinDay, C.; Paton, A.; Higgins, M.; Shewell, L.; Jen, F.; Schulz, B.; Herdman, B.; Paton, J.; Jennings, M.
2015Detection of Wzy/Wzz interaction in Shigella flexneriNath, P.; Morona, R.
2015Structural and biochemical analysis of a single amino-acid mutant of WzzBSF that alters lipopolysaccharide O-antigen chain length in shigella flexneriChang, C.; Tran, E.; Ericsson, D.; Casey, L.; Lonhienne, T.; Benning, F.; Morona, R.; Kobe, B.; Dobson, R.
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.
2016The First Histidine Triad Motif of PhtD Is Critical for Zinc Homeostasis in Streptococcus pneumoniaeEijkelkamp, B.; Pederick, V.; Plumptre, C.; Harvey, R.; Hughes, C.; Paton, J.; McDevitt, C.; Camilli, A.
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.
2015Biochemical effects of mutations in the gene encoding the alpha subunit of eukaryotic initiation factor (eIF) 2B associated with Vanishing White Matter diseaseWortham, N.; Proud, C.