Contributions de l’utilisateur
- 1 mars 2018 à 07:10 (diff | hist) . . (-99) . . m Otherwise wild-type background treated with BM(PEG2) (X), but not with
- 27 février 2018 à 14:07 (diff | hist) . . (+4 042) . . N D-type IpaB is expected for secretion regulation, inducibility and host cell (Page créée avec « Cheung et al.et al., 2010), the 4 IpaD:1 IpaB TC subpopulation have to represent the functionally relevant a single. Organisation of TCs within needle [http://armor-team.c... ») (actuel)
- 26 février 2018 à 06:42 (diff | hist) . . (+3 865) . . N Otherwise wild-type background treated with BM(PEG2) (X), but not with (Page créée avec « Again, [https://dx.doi.org/10.3332/ecancer.2016.651 title= ecancer.2016.651] the size of those bands didn't precisely correspond to these anticipated for multimers of IpaD... »)
- 26 février 2018 à 06:27 (diff | hist) . . (+3 752) . . N S, their location colour coded as in Fig. 1A (right), i. (Page créée avec « the lightest [http://eaamongolia.org/vanilla/discussion/747588/oposed-order-of-insertion-with-getting-the-lowest-and-hence-almost-certainly Oposed order of insertion (with... ») (actuel)
- 26 février 2018 à 05:25 (diff | hist) . . (-195) . . m A 1:5 to 1:ten molar ratio in isolated needles and antibodies to IpaB (actuel)
- 24 février 2018 à 07:19 (diff | hist) . . (+3 761) . . N A 1:five to 1:ten molar ratio in isolated needles and antibodies to IpaB (Page créée avec « S2A and B), maybe on account of partial disruption of their secretion signals/chaperone binding regions (Lokareddy et al., 2010). Also, avidin-binding may well destabilise... ») (actuel)
- 8 février 2018 à 06:28 (diff | hist) . . (+119) . . m Ogen genotype combinations pooled, but we also located that sign and (actuel)
- 6 février 2018 à 18:10 (diff | hist) . . (+3 928) . . N Ogen genotype combinations pooled, but we also found that sign and (Page créée avec « We believe that taking into account this complexity might help much better have an understanding of the variables [http://besocietal.com/members/coppershrimp7/activity/463... ») (actuel)
- 6 février 2018 à 17:22 (diff | hist) . . (-121) . . m Allel coiled coil (Barta et al., 2012) fits neatly into the bigger (actuel)
- 5 février 2018 à 05:55 (diff | hist) . . (+3 605) . . N R domains of IpaD, though white arrows indicate reduced bulges assumed (Page créée avec « Furthermore, cross-sections via the map showed comparable capabilities to corresponding sections in the ipaB map (Fig. 4A, ideal).?2014 The Authors. Molecular Microbiology... ») (actuel)
- 5 février 2018 à 05:21 (diff | hist) . . (+67) . . m Allel coiled coil (Barta et al., 2012) fits neatly into the bigger
- 3 février 2018 à 14:42 (diff | hist) . . (+333) . . m Authors. Molecular Microbiology published by John Wiley Sons Ltd., Molecular Microbiology (actuel)
- 3 février 2018 à 14:12 (diff | hist) . . (+3 715) . . N S with needles of wild-type length, to make sure they also carried (Page créée avec « In addition, when it's lost, it could be stochastically additional [https://dx.doi.org/10.1002/cam4.798 title= cam4.798] likely to be replaced by an IpaD than by a brand n... ») (actuel)