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In our previous study, we investigated gene expression changes in the BLA underlying the acquisition of learned safety and reported a specific "fingerprint" of mRNA expression in the BLA2.
Several other studies investigated gene expression changes in postmortem tissue of patients with MD, with or without suicide (Table 1).
Many of these studies investigated gene expression changes in PC12 but few have evaluated the suitability of HKGs as normalizers in this model.
To address this point, we investigated gene expression changes of the 53 qPCR-validated Klf5 targets, following KD of each single Klf.
Two groups have investigated gene expression changes during differentiation of long slender trypomastigotes to stumpy forms, then procyclic forms using microarrays [ 6, 7]; Capewell et al. [ 13] extended the analysis of stumpy differentiation to polysomal RNA.
We have recently investigated gene expression changes at several time-points after chronic administration of heroin or methamphetamine to associate drug-induced molecular changes with long-term behavioral adaptations e [ 32].
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Thereafter, transcriptional study including cDNA microarray in combination with suppression subtraction hybridization (SSH) was used to investigate gene expression changes in the mutant, and a total of 267 differentially expressed genes were detected [ 12].
Therefore, a transcriptional study including a cDNA macroarray in combination with suppression subtraction hybridization (SSH) was used to investigate gene expression changes in the MT, and a total of 368 differentially expressed genes were detected [ 22- 25].
Therefore, we referred the expression data from mature gland to investigate gene expression changes in epithelium.
Investigating gene expression changes underlying these phenotypes, we establish compelling correlations with widespread shifts in chromatin accessibility and H3.3 composition, whose positioning strikingly corresponds to the normal distribution pattern of Atrx binding.
To investigate gene expression changes possibly related to the growth rate recovery, quantitative reverse transcriptase PCR and 2DE proteomic studies were performed.
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