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By pushing polymerising actin filaments into the vesicle neck in conjunction with accessory proteins like dynamin, myosin VI could lead to vesicle scission and could subsequently transport the clathrin-coated vesicle into the actin rich terminal web region where it is uncoated.
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In this work, arb-PIB with short isoprene-rich terminal sequences (arb-PIB-co-IP) was functionalized to provide arborescent epoxide, allylic alcohol, and carboxylic acid derivatives of PIB.
In the highly conserved and purine-rich terminal SRL loop, multiple stop sites arise in RNA isolated from cells treated with increasing cisplatin concentrations.
21 Accordingly, we observed a trend that let-7 members with long uridine-rich terminal loops (let-7b, let-7d, let-7f, let-7g, let-7i and miR-98) decreased more remarkably in Lin28-positive cases, than let-7 members with short terminal loops (let-7a, let-7c and let-7e) (Suppl. Fig. S3).
Chromosome 4B is polymorphic for a pericentric inversion in T. aestivum [ 65], and homoeologous group 4 has a lower number of genes than the remaining six Triticeae homoeologous groups [ 29], presumably due to the translocation of the gene-rich terminal region of the short arm of chromosome 4 to the long arm of chromosome 5 [ 30].
The presence of AU-rich 5' terminal region of the antisense strand was proposed to be one of the criteria for designing potent siRNAs [ 3].
For example, Ui-Tei et al. [ 3] proposed several criteria for potent siRNAs, including the presence of AU-rich 5' terminal region and G/C at the 3' end of the antisense strand, and the absence of long GC stretches (>9 base pairs).
Individual MITEs are usually less than 600 bp and A/T rich, with terminal inverted repeats (TIRs) and 2 11 bp target site duplication (TSD) sequences [ 1, 10].
This binding occurs between the 3rd SH3 domain of vinexin and the proline rich C-terminal region of β-dystroglycan, specifically the most C-terminal SH3 binding domain [ 48].
Structurally, metazoan H1s are divided into three domains: a short, flexible N-terminal, a globular domain containing a winged-helix fold and a long, lysine rich C-terminal tail.
The ETK-CD had the auto-phosphorylation site Tyr574 and a tyrosine rich C-terminal tail (Lee et al., 2008) (Fig. 1A).
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