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As a gene monitoring approach, three-base periodicity can be used to predict protein coding sequences [ 15].
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The significant upregulation of p21/CDKN1A CDKs inhibitor gene, monitored by microarray studies, was further investigated at the protein level by immunoblot analysis.
Two types of eQTLs are expected: cis-eQTLs that are located at the same locus that the gene monitored for expression (structural gene) and trans-eQTLs that are located at another locus.
One of the best and most accurate methods for identifying disease-causing genes is monitoring gene expression values in different samples using microarray technology.
Genes monitored were smad2, smad3, TGF-β1, TGF-β3 and glyceraldehyde phosphate dehydrogenase (GAPDH).
More than 60% of the genes monitored in the shoots of all six species responded to NaCl with significant changes in transcript level in at least one genotype.
Full-length antisense genes of gyrA and gyrB were cloned into pAZI9018b and transformed into M. smegmatis and the survival kinetics following the antisense induction of the individual genes monitored.
The genes monitored were: OR 3267, OR 6425, TAAR 3721, V1R 18775, CASR and adenylate cyclase.
Each dataset is characterized by N = 10000 genes monitored over M = 13 time samples.
The levels of Mcl-1 or A1 mRNA (Fig 1A) as well as of all remaining genes monitored were found to be largely unchanged (Supporting Information Table II).
During infection of the plant Arabidopsis by the bacterial pathogen Pseudomonas syringae, approximately 2,000 of the approximately 8,000 genes monitored showed significant expression level changes [ 10].
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