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To identify transactivating regions within ApiAP2 proteins, we used the genetically tractable models yeast and T. gondii to more rapidly screen for active protein sequences.
We have captured information from the basic scientists in Canada that work with five animal models – yeast, fly, worm, zebrafish and mouse.
This family also includes the cytokinin receptors AHK2, AHK3, AHK4 [ 8- 11] and AHK1 which is the first partner of the osmosensing pathway displaying an osmosensor function in both models, yeast and Arabidopsis[ 12, 13].
To facilitate comparison between reconstructions and models, Yeast 6 metabolite and reaction identifiers are consistent with Yeast 5 identifiers (e.g. reaction 'r_0123' in Yeast 5 is the same reaction as 'r_0123' in Yeast 6, and metabolite 's_0042' in Yeast 5 is the same metabolite as 's_0042' in Yeast 6).
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Yarrowia lipolytica is widely studied as a non-conventional model yeast owing to the high level of lipid accumulation.
The validation and refinement of GEMs for a model yeast Scheffersomyces stipitis is used as the case study to demonstrate the effectiveness of the SID framework.
Thereafter, yeasts were inoculated in a lab medium, containing a commercial citrus extract and/or sodium benzoate, and US-treated; finally, a challenge test in pineapple juice was performed, using W. anomalus as a model yeast.
Our past efforts modeling yeast cell polarization [19] were hampered by the complexity of the model.
In this study, we characterized extracellular vesicles produced by the model yeast S. cerevisiae.
The importance of Hsp60 as a chaperone in fungi has been extensively studied in the model yeast Sacharomyces cereviseae [18], [19], [20], [21].
Our results share similarities with the findings of studies investigating interactions among chaperones and other proteins in the model yeast S. cereviseae [62], [63], [64].
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