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Local asymmetries in tyrosine kinase receptor activity in axonal branch, driven by differential distribution of active receptor molecules in filopodia, generate dynamical behavior and drive branch pruning.
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The regulatory networks that drive branching morphogenesis employ cell-generated and passive mechanical forces, which integrate extracellular signals from the microenvironment into morphogenetic movements.
Using synthetic materials to model physicochemical and spatiotemporal features of buckling and clefting morphogenesis might facilitate our understanding of the physical mechanisms that drive branching morphogenesis across different organs and species.
Lineage-tracing experiments have shown that Sox9-positive or Id2-positive progenitor cells present at the tip of the epithelial tree before E15 behave as multipotent progenitor cells and drive branching morphogenesis (Alanis et al., 2014; Rawlins et al., 2009a).
Studies to identify transcription factors and signaling pathways that drive branching morphogenesis and lineage specification have shown that lung morphogenesis is orchestrated by intrinsic epithelial signaling pathways as well as crosstalk between the epithelium and the mesenchyme (Hogan et al., 2014; Rock and Hogan, 2011).
Beyond PR 3A, several drives branch off as loops accessing campsites, staff residences, and other park facilities.
Thus, we propose a bidirectional model for WRN helicase driven branch migration of mobile D-loops (Fig. 9).
In this study we identified mobile plasmid-based D-loops as novel substrates for both WRN helicase driven branch migration and exonuclease activities, and found that telomeric D-loops were disrupted less efficiently than non-telomeric D-loops.
The hexameric form of RuvB acts as motor protein that drives branch migration by utilizing the energy of ATP hydrolysis., Helicases are ubiquitous enzymes present in prokaryotes, eukaryotes and viruses and are involved in nucleic acid metabolic pathways including DNA replication, repair, recombination and transcription.
These findings suggest that LOXL2 expression drives branching of MCF10A cells on Matrigel, and inhibition of ErbB2 abrogates this LOXL2-mediated effect.
Yet Drummonds wasn't the first bank to launch a drive-through branch.
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