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Alternative splicing, which produces multiple mRNAs from a single gene, occurs in most human genes and contributes to protein diversity.
We have demonstrated that in self-reactive human anti-CXCR4 antibodies, tyrosine sulfation occurs in novel areas of the V-region genes and contributes bidirectionally to antibody binding activity [17].
MIZ1 globally accumulates on MYC target genes and contributes to repression of MYC-activated target genes upon HUWE1 inhibition.
In the present study, we provide evidence that NRF2 regulates many ARE-dependent genes and contributes to resistance to iAs3+-induced cytotoxicity and apoptosis in human keratinocytes.
These findings support the notion that IRF1 selectively regulates a distinct set of BV6-induced NF- κB target genes and contributes to NF- κB activation.
It seems likely that some functional specificity has evolved between the different RR genes and contributes to their retention in plant genomes.
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QTLs serve as placeholders for genes and contribute to the functional characterization of the genome.
The human indigenous microbiota could thereby potentially serve as a reservoir of resistance genes and contribute towards antibiotic resistance development [12], [13].
Single Hex-positive ESCs coexpressed epiblast and extraembryonic genes and contributed to all lineages in chimeras.
XY performed searches for additional GH genes and contributed to the writing of the manuscript.
JDS conceived the study, performed sequence analysis of var genes, and contributed to the projects design and coordination.
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