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The expression of basal markers identifies a distinct subgroup of triple-negative breast cancer (TNBC), representing almost 75% of cases [ 23].
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The present study using the Dongnong422/Kongyu131 RIL population and a genetic linkage map containing 158 SSR markers identified a novel major QTL qPSST6 for cold tolerance at the booting stage of rice in the 28.4 cM region on chromosome 6.
First, multiple housekeeping genetic markers identify a large clonal group of identical genotypes coexisting with a diverse set of rare genotypes.
These markers identify a population of "stem cells" with different kinetics, suggesting a more complex regulation of the intestinal stem cell hierarchy[ 48].
The combined use of APC and E-cadherin methylation markers identified a subgroup of cancer patients with worse prognosis (median survival 3.3 vs 16.1 months, P=0.006).
The coexpression of Isl-1 and SM-MHC in the early EGF-induced ATMCs is very interesting because these markers identify a population of VSMCs progenitors in the developing human heart and in differentiating ESCs cultures.
These individuals with morphotype R exhibit the mitochondrial haplotype of form S (for both cyt b and COI) but all polymorphic microsatellite markers identified a form R nuclear DNA origin (genotype 1) for both specimens.
Marker-trait association analysis of RphC in the CI 9214/Stirling DH population using 4,500 DArT-seq markers identified a highly significant (−log10Pvalue > 17) single peak on the long arm of chromosome 5H (5HL).
Each marker identifies a unique rather than common population of cancer cells.
Thus, each marker identifies a unique sub-population of cancer cells, rather than identifying the same population of cells.
These data indicate that each marker identifies a different cell sub-population, making the precise biology of each population uncertain.
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