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Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by distinctive tissue pathology.
No macroscopically identifiable masses were generated in the remaining 22 mice transplanted with ESP cells; however, histological and microscopic analyses of the transplantation sites revealed the existence of three distinctive tissue subtypes within this area.
Furthermore, each gene has distinctive tissue distribution patterns.
It will be interesting to extend detailed tissue specific comparisons to mouse/human embryonic stages to find out if distinctive tissue specific patterning is observed during prenatal development.
These three ER subtypes have been shown in many cases to have distinctive tissue distribution patterns, dissimilar ligand affinities, and different patterns of gene regulation following ligand exposure.
The human CD36 gene exhibits six alternative promoters yielding transcripts 1A 1F, with distinctive tissue distribution as shown in Fig. 1 A and B. The most ubiquitous transcript is 1B, which is nearly exclusive in liver, monocytes, and macrophages.
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Furthermore, most plastid genes expressed in higher level in leaf than that in flower, but it might not reflect to the protein level in the plastids of distinctive tissues in moth orchid.
Therefore, the variation of gene copy number and steady state transcript level probably did not reflect to the protein level in the plastids of distinctive tissues in moth orchid.
Rather than acting as housekeeping genes with uniform and ubiquitous expression, ncRNAs have distinctive, tissue-specific, expression patterns.
The majority of identified ETS represents unknown noncoding sequences in intergenic regions on BTA6 displaying a distinctive tissue-specific expression profile.
In accordance with expression patterns mentioned previously, grna only acquires distinctive tissue-specificity at 24 hpf, as is the case for its prevalence within the caudal ICM, restricting its involvement to definitive hematopoietic waves.
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