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The growing use of clusters in diverse applications, many of which have real-time constraints, requires quality-of-service (QoS) support from the underlying cluster interconnect.
However, Hox colinearity is not universal [29], and no single mechanism has been identified that can explain Hox colinearity or the persistence of Hox clusters in diverse metazoan lineages [30].
The identification of paralogous genes in the flanking regions of the two globin clusters in diverse teleosts supports the proposed teleost-specific duplication of the vertebrate globin cluster.
These data are consistent with previous results that suggested that the majority of gene clusters in diverse organisms are formed by a string of two to four genes [ 30, 31].
Among them, 10 are particularly biased (δ*-differences ≥90 [ 30]), suggesting an external acquisition from a distantly related organism, notably CF-3 in Synechococcus sp. WH8016, CF-8 in Fischerella sp. PCC 9339, CF-10 in Cylindrospermopsis raciborskii CS-505, CF-20 in WH5701 and 6 orphan clusters in diverse cyanobacterial morphotypes.
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L-Cysteine desulfurase and D-cysteine desulfhydrase likewise cluster in diverse bacteria with RidA, or sometimes Rid1.
p53 negatively regulates the activity of a large number of these genes that are also part of a core proliferation cluster in diverse human cancers.
Expression profiling studies have also revealed widespread overexpression of the miR-17-92 miR-17-92 miR-17-92tumor subtypes, incluster both hematopointic malignancies andiverse tumorsubtypess those derincluding bothst, colon, lung, pancreas, prostate, and stomachematopoietic
We identified five vaginal microbiota clusters in a diverse group of women from four African countries.
Clades A and C are the two clusters in which diverse hemolysin encoding genes have been grouped.
We sought to characterize the genomic regions encompassing Otop1 and the Ush1g-Otop2-Otop3 cluster in a diverse set of vertebrates.
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