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miRBase |
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![]() 16 publications mentioning oar-let-7fOpen access articles that are associated with the species Ovis aries and mention the gene name let-7f. Click the [+] symbols to view sentences that include the gene name, or the word cloud on the right for a summary. |
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Other miRNAs from this paper: oar-mir-431, oar-mir-127, oar-mir-432, oar-mir-136, oar-let-7b, oar-let-7c, oar-mir-133, oar-mir-493, oar-mir-379, oar-mir-329b, oar-mir-329a, oar-mir-323b, oar-mir-323c, oar-let-7a, oar-let-7d, oar-let-7g, oar-let-7i
Then Reinhart et al. [2] found another small RNA that possessed a posttranscriptional regulatory function, which was named let-7. In the following years, more and more researchers have successfully discovered this kind of RNAs and named these small RNAs miRNAs, which are noncoding and have specific temporal and spatial expressions.
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Obvious differences were noted in the expression levels of the let-7 family.
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The loss of let-7 gene activity causes reiteration of larval cell fates during the adult stage, whereas increased let-7 gene dosage leads to precocious expression of adult fates during larval stages.
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The let-7 family of miRNAs comprises one of the key regulatory elements in the developmental process.
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Phylogenetic analyses have demonstrated that the let-7 family is highly conserved in both sequence and function among mammals, and it plays a critical role during animal development.
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A comparison of these eight let-7 family types between Ovis aries and 12 other mammals illustrated that the let-7 family sequences had high similarity within Mammalia (see Figure S4).
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B. Alignments of the nine kinds of sequenced let-7-3p miRNAs and the corresponding homologous let-7-3p miRNAs.
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This study also found that the let-7 family of miRNAs possessed the same seed sequence (5′-GAGGTA-3′) reported in previous studies.
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For example, let-7 was identified as a heterochronic switch gene.
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A. Alignments of the seven kinds of sequenced let-7-5p miRNAs and the corresponding homologous let-7-5p miRNAs.
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These let-7-5p miRNAs possessed the same seed sequence (the 2nd to 7th bases at 5′ end, 5′-GAGGTA-3′).
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To date, nine kinds of let-7 family genes have been identified [i. e., let-7a, let-7b, let-7c, let-7d, let-7e, let-7f, let-7g, let-7i, and let-7j (only identified in dogs)] in mammals.
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Eight kinds of Ovis aries let-7 family genes were discovered during this research: oar-let-7a-2 (427,369.75 reads), oar-let-7a-3 (288 reads), oar-let-7b (84,793.63 reads), oar-let-7c-1 (86,997.63 reads), oar-let-7d (28,816 reads), oar-let-7e (18,198.73 reads), oar-let-7f-1 (156,359.98 reads), oar-let-7g (19 reads), and oar-let-7i (148,896.89 reads).
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This study also found that the Ovis aries let-7 family miRNAs possessed the same seed sequence (5′-GAGGTA-3′).
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Figure S4 Alignment of the let-7 family of miRNAs sequenced in this study and the corresponding homologous let-7 family of miRNAs recorded in miRBase v17.0.
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The let-7 family has been studied in many species, including mammals, birds, insects, and plants.
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Other miRNAs from this paper: oar-let-7b, oar-let-7c, oar-mir-29a, oar-mir-133, oar-mir-433, oar-let-7a, oar-let-7d, oar-let-7g, oar-let-7i, oar-mir-143, oar-mir-199a, oar-mir-22, oar-mir-26a, oar-mir-29b-1, oar-mir-99a, oar-mir-29b-2
Five highly expressed miRNAs (miR-1, miR-206, miR-133, miR-29 and let-7) and three lowly expressed miRNAs (miR-155, miR-15 and miR-146) were chosen, and their expression levels in the biceps femoris muscle of adult (12-month-old) Altay sheep were determined using qRT-PCR according to an approach called miR-Q [41].
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To validate the accuracy of the microarray data, five highly expressed miRNAs (miR-1, miR-206, miR-133, miR-29 and let-7) and three lowly expressed miRNAs (miR-155, miR-15 and miR-146) were chosen, and their expression in the biceps femoris muscle of adult (12-month-old) Altay sheep were detected using qRT-PCR.
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Other miRNAs from this paper: oar-let-7b, oar-let-7c, oar-mir-21, oar-mir-125b, oar-mir-154a, oar-mir-154b, oar-let-7a, oar-let-7d, oar-let-7g, oar-let-7i, oar-mir-10a, oar-mir-10b, oar-mir-143, oar-mir-200a, oar-mir-26a, oar-mir-26b, oar-mir-374b
In addition, the apoptosis, Wnt signaling, and C21-Steroid hormone metabolism pathways, which contain target genes of the let-7 family, are important for granulosa cell proliferation, follicular growth and development, and luteinic formation and regression.
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The mir-10 (MIPF0000033), mir-143 (MIPF0000094), let-7 (MIPF0000002) and mir-26 (MIPF0000043) families were found to be preferentially expressed in ovine ovary.
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For example, the expression abundance of let-7 family members varied from 0 to 344,318 reads.
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Some of the abundant miRNAs in the anestrous ovary of Tan sheep, including miR-143, miR-26a, let-7 and miR-21, were also reported to be highly abundant in ovaries of human, cow [23– 25], pig [26], adult and neonatal mouse [27, 28] and sheep [2, 3].
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Other miRNAs from this paper: oar-let-7b, oar-let-7c, hco-mir-5885a, hco-mir-40b, hco-mir-50, hco-mir-61, hco-mir-43, hco-mir-5895, hco-mir-45, hco-mir-5899, hco-lin-4, hco-mir-87a, hco-mir-87b, hco-mir-83, hco-mir-71, hco-mir-5908, hco-mir-84a, hco-mir-5352, hco-mir-228, hco-mir-5885b, hco-mir-5960, hco-mir-60, hco-mir-5885c, oar-let-7a, oar-let-7d, oar-let-7g, oar-let-7i, oar-mir-103, oar-mir-26a
In the L4 libraries, hco-miR-5885a-3p, hco-miR-5885b-3p, hco-miR-5885c-3p, hco-miR-5908-3p, hco-lin-4-5p, hco-miR-83-3p and sequences homologous to cel-let-7-5p and asu-miR-100a-5p, not previously identified from H. contortus, are all highly expressed in the L4 EV-enriched and have lower read counts in the L4 EV -depleted libraries.
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Interestingly, some of these (let-7, miR-100) have identity within the seed region to mammalian miRNAs, implying that they could potentially regulate host genes [21], or alternatively compete in host miRNA -mediated regulation.
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Interestingly a number of these (asu- miR-100a-5p, miR-60-3p, miR-71-5p, let-7-5p, lin-4-5p and miR-5885a, b, c-3p) were also present in EV libraries prepared from H. polygyrus adult stage [9], while miR-100a-5p and let-7-5p were recently identified in adult EV of the clade I nematode Trichuris muris [21].
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This is consistent with data on secreted miRNAs of H. polygyrus that showed enrichment of let-7, mir-100 and mir-60 in the vesicle rather than supernatant fraction [9].
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Other miRNAs from this paper: hsa-let-7a-1, hsa-let-7a-2, hsa-let-7a-3, hsa-let-7f-1, hsa-let-7f-2, hsa-mir-15a, hsa-mir-16-1, hsa-mir-21, hsa-mir-23a, hsa-mir-24-1, hsa-mir-24-2, hsa-mir-26a-1, hsa-mir-29a, hsa-mir-30a, hsa-mir-31, hsa-mir-99a, hsa-mir-29b-1, hsa-mir-29b-2, hsa-mir-103a-2, hsa-mir-103a-1, hsa-mir-16-2, hsa-mir-192, hsa-mir-148a, hsa-mir-10b, hsa-mir-181a-2, hsa-mir-181a-1, hsa-mir-215, hsa-mir-223, hsa-mir-224, hsa-mir-200b, hsa-mir-15b, hsa-mir-27b, hsa-mir-125b-1, hsa-mir-141, hsa-mir-143, hsa-mir-152, hsa-mir-125b-2, hsa-mir-126, hsa-mir-146a, hsa-mir-184, hsa-mir-200c, hsa-mir-155, hsa-mir-29c, hsa-mir-200a, hsa-mir-99b, hsa-mir-296, hsa-mir-30e, hsa-mir-26a-2, hsa-mir-378a, hsa-mir-342, hsa-mir-148b, hsa-mir-451a, ssc-mir-125b-2, ssc-mir-148a, ssc-mir-15b, ssc-mir-184, ssc-mir-224, ssc-mir-23a, ssc-mir-24-1, ssc-mir-26a, ssc-mir-29b-1, ssc-let-7f-1, ssc-mir-103-1, ssc-mir-21, ssc-mir-29c, hsa-mir-486-1, hsa-mir-499a, hsa-mir-671, hsa-mir-378d-2, bta-mir-26a-2, bta-mir-29a, bta-let-7f-2, bta-mir-103-1, bta-mir-148a, bta-mir-16b, bta-mir-21, bta-mir-499, bta-mir-99a, bta-mir-125b-1, bta-mir-126, bta-mir-181a-2, bta-mir-27b, bta-mir-31, bta-mir-15b, bta-mir-215, bta-mir-30e, bta-mir-148b, bta-mir-192, bta-mir-200a, bta-mir-200c, bta-mir-23a, bta-mir-29b-2, bta-mir-29c, bta-mir-10b, bta-mir-24-2, bta-mir-30a, bta-mir-200b, bta-let-7a-1, bta-mir-342, bta-let-7f-1, bta-let-7a-2, bta-let-7a-3, bta-mir-103-2, bta-mir-125b-2, bta-mir-15a, bta-mir-99b, hsa-mir-664a, ssc-mir-99b, hsa-mir-103b-1, hsa-mir-103b-2, ssc-mir-15a, ssc-mir-16-2, ssc-mir-16-1, bta-mir-141, bta-mir-143, bta-mir-146a, bta-mir-152, bta-mir-155, bta-mir-16a, bta-mir-184, bta-mir-24-1, bta-mir-223, bta-mir-224, bta-mir-26a-1, bta-mir-296, bta-mir-29d, bta-mir-378-1, bta-mir-451, bta-mir-486, bta-mir-671, bta-mir-29e, bta-mir-29b-1, bta-mir-181a-1, ssc-mir-181a-1, ssc-mir-215, ssc-mir-30a, bta-mir-2318, bta-mir-2339, bta-mir-2430, bta-mir-664a, bta-mir-378-2, ssc-let-7a-1, ssc-mir-378-1, ssc-mir-29a, ssc-mir-30e, ssc-mir-499, ssc-mir-143, ssc-mir-10b, ssc-mir-486-1, ssc-mir-152, ssc-mir-103-2, ssc-mir-181a-2, ssc-mir-27b, ssc-mir-24-2, ssc-mir-99a, ssc-mir-148b, ssc-mir-664, ssc-mir-192, ssc-mir-342, ssc-mir-125b-1, oar-mir-21, oar-mir-29a, oar-mir-125b, oar-mir-181a-1, hsa-mir-378b, hsa-mir-378c, ssc-mir-296, ssc-mir-155, ssc-mir-146a, bta-mir-148c, ssc-mir-126, ssc-mir-378-2, ssc-mir-451, hsa-mir-378d-1, hsa-mir-378e, hsa-mir-378f, hsa-mir-378g, hsa-mir-378h, hsa-mir-378i, hsa-mir-451b, hsa-mir-499b, ssc-let-7a-2, ssc-mir-486-2, hsa-mir-664b, hsa-mir-378j, ssc-let-7f-2, ssc-mir-29b-2, ssc-mir-31, ssc-mir-671, bta-mir-378b, bta-mir-378c, hsa-mir-486-2, oar-let-7a, oar-mir-103, oar-mir-10b, oar-mir-143, oar-mir-148a, oar-mir-152, oar-mir-16b, oar-mir-181a-2, oar-mir-200a, oar-mir-200b, oar-mir-200c, oar-mir-23a, oar-mir-26a, oar-mir-29b-1, oar-mir-30a, oar-mir-99a, bta-mir-664b, chi-let-7a, chi-let-7f, chi-mir-103, chi-mir-10b, chi-mir-125b, chi-mir-126, chi-mir-141, chi-mir-143, chi-mir-146a, chi-mir-148a, chi-mir-148b, chi-mir-155, chi-mir-15a, chi-mir-15b, chi-mir-16a, chi-mir-16b, chi-mir-184, chi-mir-192, chi-mir-200a, chi-mir-200b, chi-mir-200c, chi-mir-215, chi-mir-21, chi-mir-223, chi-mir-224, chi-mir-2318, chi-mir-23a, chi-mir-24, chi-mir-26a, chi-mir-27b, chi-mir-296, chi-mir-29a, chi-mir-29b, chi-mir-29c, chi-mir-30a, chi-mir-30e, chi-mir-342, chi-mir-378, chi-mir-451, chi-mir-499, chi-mir-671, chi-mir-99a, chi-mir-99b, bta-mir-378d, ssc-mir-378b, oar-mir-29b-2, ssc-mir-141, ssc-mir-200b, ssc-mir-223, bta-mir-148d
Ye et al. (2012) examined miRNA expression in the duodenum of E. coli F18-sensitive and -resistant weaned piglets and identified 12 candidate miRNA (ssc-miR-143, ssc-let-7f, ssc-miR-30e, ssc-miR-148a, ssc-miR-148b, ssc-miR-181a, ssc-miR-192, ssc-miR-27b, ssc-miR-15b, ssc-miR-21, ssc-miR-215, and ssc-miR-152) disease markers.
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Additionally, a number of miRNAs including miR-148a, miR-26a, miR-21-5p, miR-27b, miR-143, bta-miR-30a-5p, let-7a-5p, let-7f, miR-10b, and miR-99a-5p are highly expressed in bovine mammary gland/mammary epithelial cells (Li et al., 2012a, 2014a; Jin et al., 2014a; Le Guillou et al., 2014) suggesting roles in the lactation process and mammary gland functions.
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Other miRNAs from this paper: hsa-let-7a-1, hsa-let-7a-2, hsa-let-7a-3, hsa-let-7b, hsa-let-7c, hsa-let-7d, hsa-let-7e, hsa-let-7f-1, hsa-let-7f-2, hsa-mir-22, hsa-mir-23a, hsa-mir-29a, hsa-mir-30a, hsa-mir-29b-1, hsa-mir-29b-2, hsa-mir-200b, hsa-let-7g, hsa-let-7i, hsa-mir-125b-1, hsa-mir-125a, hsa-mir-125b-2, hsa-mir-127, hsa-mir-150, hsa-mir-200c, hsa-mir-29c, hsa-mir-200a, oar-mir-127, oar-mir-432, hsa-mir-432, hsa-mir-1185-2, hsa-mir-1185-1, oar-let-7b, oar-let-7c, oar-mir-29a, oar-mir-125b, oar-mir-1185, oar-mir-323c, oar-let-7a, oar-let-7d, oar-let-7g, oar-let-7i, oar-mir-150, oar-mir-200a, oar-mir-200b, oar-mir-200c, oar-mir-22, oar-mir-23a, oar-mir-29b-1, oar-mir-30a, oar-mir-29b-2
For example, members of the let-7 family (let-7a, let-7b and let-7c) were detected to be less abundant in lambs with curly fleece than in adults with non-curling fleece, consistent with previous observation that let-7 miRNAs showed decreased expression from small waves to medium waves and medium waves to large wave in Hu sheep [32].
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Therefore, we speculate that let-7 miRNAs may function by altering the expression profiles in hair cells, thereby changing hair cell differentiation and function and facilitating the hair curvature.
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Other studies also showed that let-7 genes are related to the growth of hair follicles and hair quality in skin tissue [33, 34].
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Other miRNAs from this paper: oar-let-7b, oar-let-7c, oar-mir-181a-1, oar-let-7a, oar-let-7d, oar-let-7g, oar-let-7i, oar-mir-10a, oar-mir-143, oar-mir-181a-2, oar-mir-199a, oar-mir-25
let-7c and let-7i belong to the let-7 family, which is an important tumor-suppressor miRNA, and both are downregulated.
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Other miRNAs from this paper: oar-let-7b, oar-let-7c, oar-let-7a, oar-let-7d, oar-let-7g, oar-let-7i, oar-mir-10a, oar-mir-10b, oar-mir-143, oar-mir-199a, oar-mir-200a, oar-mir-200b, oar-mir-200c
MiR-let-7, which includes miR-let-7i, miR-let-7c, and miR-let-7b, is expressed in the skin of goats, sheep, and mice, and its target genes were related to the growth of hair follicles and hair quality.
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Other miRNAs from this paper: hsa-let-7a-1, hsa-let-7a-2, hsa-let-7a-3, hsa-let-7b, hsa-let-7c, hsa-let-7d, hsa-let-7e, hsa-let-7f-1, hsa-let-7f-2, hsa-mir-20a, hsa-mir-96, hsa-let-7g, hsa-let-7i, hsa-mir-1-2, hsa-mir-133a-1, hsa-mir-133a-2, hsa-mir-1-1, hsa-mir-216b, oar-let-7b, oar-let-7c, oar-let-7a, oar-let-7d, oar-let-7g, oar-let-7i
However, low expression of 12 members of another common miRNA family, let-7 (not found in T. saginata[51]), was shared among T. multiceps (17,125 counts), E. granulosus and E. multilocularis.
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Considering that T. saginata and T. multiceps belong to the same genus, Taenia, the absence of let-7 miRNAs in T. saginata, their presence in T. multiceps and their universal existence in some other species suggest that non-recovery of let-7 in T. saginata may be attributed to the specific stage of the parasite examined or experimental methods.
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Other miRNAs from this paper: hsa-let-7a-1, hsa-let-7a-2, hsa-let-7a-3, hsa-let-7b, hsa-let-7c, hsa-let-7f-1, hsa-let-7f-2, hsa-mir-31, mmu-let-7g, mmu-mir-1a-1, mmu-mir-133a-1, mmu-mir-144, hsa-mir-196a-1, mmu-mir-199a-1, hsa-mir-199a-1, mmu-mir-200b, mmu-mir-203, mmu-mir-206, mmu-mir-122, mmu-mir-143, hsa-mir-196a-2, hsa-mir-199a-2, hsa-mir-203a, hsa-mir-222, hsa-mir-200b, mmu-mir-299a, hsa-let-7g, hsa-mir-1-2, hsa-mir-122, hsa-mir-133a-1, hsa-mir-133a-2, hsa-mir-143, hsa-mir-144, hsa-mir-206, hsa-mir-320a, mmu-mir-196a-1, mmu-mir-196a-2, mmu-let-7a-1, mmu-let-7a-2, mmu-let-7b, mmu-let-7c-1, mmu-let-7c-2, mmu-let-7f-1, mmu-let-7f-2, mmu-mir-31, mmu-mir-331, hsa-mir-1-1, mmu-mir-1a-2, mmu-mir-222, mmu-mir-199a-2, hsa-mir-299, hsa-mir-374a, hsa-mir-331, mmu-mir-133a-2, mmu-mir-133b, hsa-mir-133b, hsa-mir-455, hsa-mir-92b, mmu-mir-374b, mmu-mir-455, mmu-mir-92b, hsa-mir-374b, mmu-mir-1b, mmu-mir-374c, oar-let-7b, oar-let-7c, oar-mir-133, hsa-mir-4286, hsa-mir-374c, oar-mir-299, hsa-mir-203b, mmu-mir-299b, mmu-mir-133c, oar-let-7a, oar-let-7g, oar-mir-143, oar-mir-199a, oar-mir-200b, oar-mir-374a, oar-mir-374b, chi-let-7a, chi-let-7b, chi-let-7c, chi-let-7f, chi-let-7g, chi-mir-1, chi-mir-122, chi-mir-133a, chi-mir-133b, chi-mir-143, chi-mir-144, chi-mir-196a, chi-mir-199a, chi-mir-200b, chi-mir-206, chi-mir-222, chi-mir-331, chi-mir-374a, chi-mir-374b, chi-mir-455, chi-mir-502a, chi-mir-92b
In the whole hair cycle, the abundance of expression of let-7a-5p, let-7f, let-7b, let-7c, let-7g, miR-199a-3p, miR-143, miR-1, and miR-320a reached their highest levels in the present study (Table 2).
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Other miRNAs from this paper: oar-mir-411b, oar-let-7a, oar-mir-10b, oar-mir-143, oar-mir-148a, oar-mir-26a, oar-mir-26b, oar-mir-99a
The ten most highly ranked miRNAs are relatively well conserved across species – for example, four miRNAs (miR-143, let-7a, let-7f, miR-148a) in pig testis 47 and two miRNAs (let-7a, let-7f) in human testis 48 ranked within the ten most highly expressed miRNAs found in this study.
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Other miRNAs from this paper: oar-let-7b, oar-let-7c, oar-mir-21, oar-mir-370, oar-let-7a, oar-let-7d, oar-let-7g, oar-let-7i, oar-mir-150, oar-mir-221, oar-mir-27a, chi-let-7a, chi-let-7b, chi-let-7c, chi-let-7d, chi-let-7e, chi-let-7f, chi-let-7g, chi-let-7i, chi-mir-122, chi-mir-130a, chi-mir-140, chi-mir-144, chi-mir-146b, chi-mir-150, chi-mir-155, chi-mir-196b, chi-mir-199b, chi-mir-21, chi-mir-217, chi-mir-221, chi-mir-223, chi-mir-27a, chi-mir-27b, chi-mir-320, chi-mir-328, chi-mir-34b, chi-mir-363, chi-mir-451
PPRV infection in spleen and lung triggered the expression of many immune-related miRNAs, including, miR-21, miR-150, miR-146b, and let-7 family as reported in Japanese encephalitis virus infection (Cai et al., 2015).
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Other miRNAs from this paper: oar-let-7b, oar-let-7c, oar-mir-21, oar-mir-376b, oar-mir-369, oar-let-7a, oar-let-7d, oar-let-7g, oar-let-7i, oar-mir-106b, oar-mir-30a, oar-mir-30d
These include miR-126-5p, miR-30a-5p, and miR-30d (Guay et al. 2011), as well as miR-27b, miR-21, miR-206 (Herrera et al. 2010), and let-7 family (Frost and Olson 2011), each of which is altered in the states of insulin resistance, glucose intolerance, and/or type-2 diabetes in adult life.
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We selected the following nine miRNAs including miR-1, miR-206, miR-378, miR-486-5p, miR-140, miR-191, miR-16, let-7b, and let-7f.
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Other miRNAs from this paper: hsa-let-7a-1, hsa-let-7a-2, hsa-let-7a-3, hsa-let-7b, hsa-let-7c, hsa-let-7d, hsa-let-7e, hsa-let-7f-1, hsa-let-7f-2, hsa-let-7g, hsa-let-7i, hsa-mir-146a, hsa-mir-155, hsa-mir-146b, oar-let-7b, oar-let-7c, oar-let-7a, oar-let-7d, oar-let-7g, oar-let-7i
In later years, another short RNA let-7 was identified [98], with a large number of small RNAs being revealed in 2001 [92], which subsequently opened the lid to the world of the microRNA biotechnology [93, 99- 102].
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Other miRNAs from this paper: oar-let-7b, oar-let-7c, oar-mir-21, oar-mir-133, oar-let-7a, oar-let-7d, oar-let-7g, oar-let-7i, oar-mir-10a, oar-mir-10b, oar-mir-143, oar-mir-148a, oar-mir-194, oar-mir-200b, oar-mir-26a, oar-mir-26b
In the DU, CE, and CO libraries, miR-143 had the largest number of reads, while the miR-21, miR-148a, miR-26, and let-7 families were the next most abundant.
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