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Examination of the read mappings revealed that the mapped reads were not evenly distributed along the viral genome for any of the three sequencing platforms.
Flexible alignment; electrostatic and hydrophobic mappings revealed that the obtained model could be useful for the development of new DHFR inhibitors.
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RNase A/T1 mappings revealed a weak accumulation for each mutant U1 RNA.
Mapping studies revealed that the N-terminus of L-terminase ATPase domain (residues 1 58) contains a minimal S-terminase binding domain sufficient for stoichiometric association with residues 140 162 of S-terminase, the L-terminase binding domain.
Mapping studies revealed that the peptide invariably induces strong proliferation of NZB CD4 T cells in vitro, and is the only sequence to stimulate responses by T cells from NZB mice prior to the onset of disease [8].
Mapping experiments revealed that the same determinants in Nef govern its ability to prevent TCR induced actin remodeling, IS recruitment of Lck and reduction of TCR signal transmission.
Mapping studies revealed that all three mAbs bind discontinuous epitopes within the highly conserved fusion-loop region of DII (contacting residues W101, L107, and/or G109) [ 37].
Mapping studies revealed that a unique extreme N-terminal portion of ELMO is involved in the nucleotide-state specific interaction with RhoG.
Mapping experiments revealed that only those regions of Atg13 coprecipitate with Atg101 that contain amino acids 1 230, whereas the unstructured middle and C-terminal regions do not show binding and 7(b)).
Furthermore, genome-wide nucleosome-mapping analysis revealed that nucleosome occupancy for Htz1p-bound genes decreases upon deleting htz1 or chz1, suggesting that Htz1 is required for nucleosome structure at the specific genome loci.
Mapping analysis revealed that rhizobial fhbs and thbs are flanked by a variety of genes whereas several rhizobial sdgbs and gcss are flanked by genes coding for proteins involved in the metabolism of nitrates and nitrites and chemotaxis, respectively.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com