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> > We have further generated extensive bioinformatics annotation data for the plant CAZyme sequences by running various bioinformatics tools against different databases.
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More recently, time-resolved techniques from pulse-labeling based quantitative mass-spectrometry (QMS) (Mulder et al., 2010; Talkington et al., 2005) and synchrotron X-ray footprinting (Adilakshmi et al., 2008) have further generated a large amount of real-time data for various protein binding and rRNA folding events in the process of the in vitro 30S subunit assembly.
Continuing refinements in radiotherapy treatment planning techniques as well as technical advances in ultrasound have further generated the resurgence of enthusiasm for using prostate brachytherapy to treat clinically localised prostate cancer.
In order to understand and interpret these data and to test our hypothesis on the systemic response of the proteomes we have generated, we have further classified and filtered the list of identified proteins for pathway abundances.
We will have further reports.
It is possible that the pathogen-inducible later increase in LYS1 activity could have further roles for generating diffusible signals that might serve innate immune activation, not only in cells that are directly in contact with invading microbes but also in cell layers adjacent to infection sites.
Applying analogous genetic crossing schemes, we have generated three further deletions: An ∼44-kb deletion between two FRT sites located in ap f08090 and ap e01573.
To investigate this further we have generated over a dozen mutations in the poliovirus Sabin 2 strain polymerase and carried out in vitro biochemical assays to show that these can either increase or decrease polymerase fidelity while having minor effects on elongation rates and processivity.
To address this further, we have generated mice that are double-deficient in Mmp13 and Plau, the plasminogen activator most important for Plg activation in tissues.
To test the GeminiDistances program further, we have generated the GeminiDistances output for the β-spiral trimeric interfaces of the shaft domain of the adenovirus type 2 (PDB code: 1QIU), for which the key amino acids involved in the interfaces have been well described [25].
Further, we have generated a Cre-reporter mouse in which SYNbglA is expressed following recombination to demonstrate the general utility of SYNbglA for in vivo analyses.
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