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Recent studies in multiple species have unveiled diverse roles of the FT/TFL1 gene family in developmental processes other than flowering regulation.
Pre-clinical studies in multiple species have confirmed the safety of H2S-releasing NSAIDs, supporting the initiation of human clinical trials.
Several studies, that have combined data from multiple species, have found that the first intron is,on average, longer that other introns [20].
The few studies that have combined intron data from multiple species have found that the first intron is - on average - longer than later introns [8], [9], and that introns from the 5' UTR region of a gene tend to be longer than introns from within the CDS or 3' UTR [10], [11].
Studies comparing the transcriptomes of multiple species have provided insights on phenotypic variation and accompanying expression variation.
Fortunately, new alignment methods that compare sequences from multiple species have been developed to minimize these drawbacks.
Similar(41)
Sequence conservation among multiple species has been proven to constrain functional TFBS [16], [17], [40].
This lack of phenotype across multiple species has led to the hypothesis that the three mammalian Anp32 orthologues are functionally redundant such that no one factor is essential for development.
The potent developmental toxicity of dioxin in multiple species has been known for a number of years.
Having a complete set of orthologous tRNAs across multiple species has enabled the detection of several functional changes in nuclear tRNA genes.
Supporting this notion, our analysis of DBC1 and CCAR1 from multiple species has established evidence that both proteins have evolved from one common nematode ancestor, LST-3.
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