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It is noteworthy that bulk soil and endosphere host similar bacterial communities, in terms of size, suggesting that the ability to thrive in plant tissues requires specific genetic requirements [ 39].
Over the last decade, genetically engineered mouse models have been extensively used to dissect the genetic requirements for neoplastic initiation and progression of diffuse gliomas.
We show that the genetic requirements for MG and glyoxal resistance are distinct and that different carbonyl stresses require distinct genetic cohorts for cell survival.
The SCF (Skp1 Cullin F-box) E3 ubiquitin ligaSkp1 Cullin F-boxcovE3ed throubiquitinic requirements for celigasele progression in budding yeast.
However, in case of Mycobacterium tuberculosis (Mtb) infection the role of biofilms and the genetic requirements for biofilm formation remains largely unknown.
It has been shown that these two regions have different genetic requirements [10], [11].
Here, we compared genetic requirements for germ cell development in vitro and in vivo.
We next tested the genetic requirements for LST-4 localization during phagosome maturation (Figure 2P).
To test this hypothesis, we used RNA blot hybridization to analyze genetic requirements for IGS siRNA biogenesis (Figure 1D).
Although there has been extensive analysis of the genetic requirements for these cellular processes, biochemical characterization of the proteins involved in these processes has lagged behind.
Yet a major limitation remains with the lack of evidence to correlate differentiation in vitro with landmark events and genetic requirements in vivo.
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