pre-miRNA Information | |
---|---|
pre-miRNA | mmu-mir-125a |
Genomic Coordinates | chr17: 17830812 - 17830879 |
Description | Mus musculus miR-125a stem-loop |
Comment | The mature sequence shown here represents the most commonly cloned form from large-scale cloning studies . |
RNA Secondary Structure |
Mature miRNA Information | |
---|---|
Mature miRNA | mmu-miR-125a-5p |
Sequence | 6| UCCCUGAGACCCUUUAACCUGUGA |29 |
Evidence | Experimental |
Experiments | Cloned |
Putative Targets |
Gene Information | |||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Gene Symbol | Hif1an | ||||||||||||||||||||
Synonyms | 2310046M24Rik, A830014H24Rik, FIH, FIH1 | ||||||||||||||||||||
Description | hypoxia-inducible factor 1, alpha subunit inhibitor | ||||||||||||||||||||
Transcript | NM_176958 | ||||||||||||||||||||
Expression | |||||||||||||||||||||
Putative miRNA Targets on Hif1an | |||||||||||||||||||||
3'UTR of Hif1an (miRNA target sites are highlighted) |
>Hif1an|NM_176958|3'UTR 1 CCTGCCAGAGGTCAAGGCCTCCTGTCAGGTGACTGCTATCCTGTCCACATGCTTCGTTGATGAGGACAGGACACTCCAAG 81 CACTAGTATTGCACGCTGCACTTAATGGACTGGACTCTTGCCATGGCCCTGGAGGCAGGTGTCTGAGGCAAGGCAGGGTA 161 GTTGACTCCACTCCCATTTGGAAAGGTTTCTCACCCTTGCCTCTTGAGCCCCAGAACCTTCCCTCTGCCCCCCTGAAGTC 241 CTGCATTTAGTGTGTGGAGTCCCAGCTTCTGGTTGTAATCATGTCTGTGTTAGTCTGTTAACCTCAGGGTGTGTGTGTGT 321 GTGTACATGTGTGCATATGCATGTGTGTATACACACACATGCATGTATCTGTTCCTTGTTCCCTCTTCCTGGGTCAGGAT 401 GTCACTTCTGGCTCTCAGCTCCTGTCTCCTGAAGCCTCAGTGCCTCAGCCTGGGAGGAGAGATGCTCCTGTGTCCCTACA 481 ACATCTGGGCTGTGGTGCCAGAATGACTCTGCACATGAGTCTGCCTTCTGCCAGTTTTTGCAGCATAGTCAGGCTACAAA 561 CCAGGTGGCAATAACTGCTGGGGCCCTAATGGGGACATTGAGAAGGAGGCTTATCTTTGGGAGGTAGCCTTCTAGTGGAA 641 GAGGATTAGATAAGATTCCAGTTGAGAACTACATGCTTAAGCCATACATAGAAGGAAAACTTGGGGACCTGAAACCAGGA 721 TTGTGCATATGTCCAAATACAGGCATTTGCAGCCGTTCTCTTCAGTACCAGCTCCTGTCCCTGTGCTGCAATGAGGGATT 801 CTAGCTCTGACTTTTTTGGGCTCGAGGGGTATGAACCTCTGCATGTGTGTGTACACATCTGCACACTTGTATGCATGTGT 881 GATCACACTTGCCATCCTTCTTGCTTACTAAGGTTCTCAACTGCTAACATTGTCCAGTGTGGCAGTACAGCGTGAACCCC 961 AGATACTGCCTGACTCAGCCTAGAGCTTTTACACTCGGATTTTAGCCATCCCGTCTTGGTCAGATCTTACTGCAGCCTAC 1041 CTAAAGCTGACTGGCTCAAGCCTCCCAGTCCTGTGTCTTTCCCTGTCTGAACCACATCCCTGCTCCTGCTGAGCTTCCTG 1121 GCTGAGTAGATGAAATGGGGTCAGACTTAGGCAGCTAACTCAATACCTTTCATCCACCTCAGGGCAAGGGGAAAAAAAAT 1201 GTCCTCTTGCCTCTTAGAGCCAGCGCCTCTGCCAGACCCAACAAAGCGTCGCATGTGAGCTGGAGTAGAGCTGGGAGAGC 1281 TTGGAGATAGAATTTACTTTTCTGTTGGTAGCTGTTTATGGGAGCCCTCCTCGGGGCTGCAGCTTATAGCTCTGTGTTAC 1361 ACAACACAGAGCGCAATCATTTGTATCTGTTAAGAGGGAATGGGGCCCCAGCAGCTTGGCAGAGTGGTGGCCCCGTGTCC 1441 ACTTACCTCAAGTCCCTTCCTTCTCTGTCAACCTTTTTTCTCTAAAATTGGAGTTGGAAGTCTGATTTTATTCTTTTCTT 1521 TGCCACCTTTTAGTCCCCTTCCCTGTAGATTTGACCTCCCGTGTTCAAGCTGTGGGTCTTAGCCCTGAAGCTCAGCTTAC 1601 AGCGCCCCATGGACTGAACAGATGCAGGCGAATGCTTGTGCACCCGTGTGCGTTTAGGGGCGGGAGCTCTAGCCCCCACT 1681 CTGGGCTCTGCAGTGTGGTTGCGCAGACTTGGTACCTTCTTGAGTATGGCTCTTTAAATACAGCCCGTGCTGGGCAGTGT 1761 GATCGCGGCAAACGCATGCCTCCATCTCTTTTGGGAACGAGGGATGCAGCAGAAGAGGGAGGCAGAGTGGTATTAGTTTG 1841 GCCACCGTGGCGGATTTTCATTCTCCGCAGATCTATGGTCCTGGCTCTGCCCTCAAAGGTGTCTGGGATGTGTGGCAGGG 1921 AGTCTGGATCTGCTCGGTTGACCCTTCAGTATAACTCTGCTCTCACAGGTCTGACCTAGGGTGGCTGAGGGCAGCGAGAG 2001 AGAAGGTGAGCTTAGGCACCATCACAGGATTGGCCCTGATGCTGGGATGATGTCATGGCTGTTCCTGGTCTTAGACACCT 2081 GATGTGTACCTGTTGTTTCTAGCTCTGTCCCTCACAGTGCTGCGTGGTAGTCAAGAGCAAACCTAATGCCATTTAGCTAT 2161 AAACCCACTACTCCCTGCTCCTCCATTTCTTCCAAATGCTGTTGGTTCTCTACCTCACCTCAAGCCTTGTTCCCTAGAGA 2241 GTGTGCAGGTAGACTCAGGCAAGAGGGTGTGGAAGGGTGAAAGGCTTTGGGGGTTCAGCTAGAGACATGGAAAAGCTGCC 2321 TAGAAAGCCATCTTAACAAGCTAAGGGTTCTGGGAAGAAGCAGAAGAGTGAGCTTCGGCCCTGCGGGGGAAAGGGGTGCT 2401 GTAGGTCCTGTAGCTCCTCTCACCACACCTCTGCATGCTGAGAGGAAGCTCTGGTAACCCGATTCATATTCTGCTGGGCC 2481 ACTTCCTCCTGGGGATGGCAAGCAGGGACTCACCTAGGCTAGGGTCTCAACCCTAGGGCTGTTGAGGCTCCAGTTGTACT 2561 TGCAGCAGAGCAGGCATCACTATTGTGTACCCATTCTAGCCAACAGCCTGGGAGTCAGACGTGCCAAGGAAGGTGGAGAC 2641 CTGGGCTTGTCCAGGGGTCAGCCATCTTGCAGGCTCTCGTGTTTATACCAGCAGTACAGTGAAAACTACTGTTTTGTGAA 2721 GTCAAATATTTGCTGGGGGGTTAGAGTTATGGGGTGGAGGAGGGGCTGTTCTGGGCATCAGTTGAGCAGATGCCCAGGAT 2801 GCCTGGGGGAGACCAGCTTCCCCTACAAATCAGAGCTCTAAATTACAAGGTTTTTACCAACGCGAACAGTTGGGGGAAGT 2881 CGTCTGCTCTCATTTGCGTAATGGTTTCTGTCACTGGTGATTAGACACAGGATGAAGGAAAAGAAATTTGACAATTAGGA 2961 ATGAGCCATCATTAATCTGAATCTGTTAGGAGACAGAGAGGGGAAGGCTCCTTACTATTGGGCCAACCTAGTATGGGGAG 3041 ACACTCCCTATTTCTGACCCCAGAATCTTGTGGGCCAGGTACCCTTTTGGAGTTCCCACAAGTGTGGGTGGAGTTTGTAT 3121 GCCTTCATAGACTGGAGTCCAGGCCCAGCTTGAGGTGGGTTTGCAAACAGACATCTTTCTGCCTGAGCCCTCGCAGTTGA 3201 AGGTAGGTAGGCTGGTTACTGCGTGTGCTCAGTTACAGGAAGGATCTCTGTAGTAGTCAGCACTGTTGCGCCCCACCTGT 3281 GACAGGGATCTGTCACTTCGAAGCACTTGAGCTTGTGTGGGAAGCCTGAGCTTCATCAAACCCCAGACACTGGTGGAAGT 3361 TGGAAAGGAAACCGTATGAAGAGTAGCAGAGCCTAGGTATGTGCAAGGAGGGGTGTGAGGAAGAGCTGGTCCAGCACAGG 3441 CTGTCTGGGAGGAGACTCGGCCTCTCAGCAGCGTTGTCTTACTCTGGATCAGCGAGCCATTGCTGTGGGGAACACTGAGG 3521 TTCCTGGCTCAGTGACCCAGTGATGTGGCTATTGAAAAATGGAGAGTCCAGCGTAGATCTTCCAGTGTTTGCAAGTTACC 3601 TCACCACTCACCCCCATCCCTTCAAACGCCTAAGAATATTAGTCTGTACCAAGTAGTGGTCCTCACCATTAGTGTGTTCC 3681 TTAGACCCCAGCCCCCCCAAGGTTTGGAGGGGGCTCCTCTGTCTCCTTTCATAATGTGAACTTCTCAAGGATGGTGCTAT 3761 CTCAGTCCTTGGTAAGTTCCCTACCTCTGTTGTCTTTCATCCTTCAAAACTTGGTGCAGAATTTAGCAAGGGCTACCAGC 3841 AGTGACCCTCTGACCAGTTTTTCCTACATGGCCAGGGGTGGGGATGGGGATAGCTCAGGGTTGTAGAGGCCAGGCCTTTC 3921 CAGTTCCTGTTTCTCTTGGTGTCCTCTTGACCCATCTTTAAGAGGATCCTTGAGCTTTCTCCTAACTAGGCTCTCAGTGG 4001 CCTCTTTACCAAGGCTCTTTTCCTCAAAGACGCTCTCTGGCTCCAAGTGCTGGGCAGCCTGGCTGGAGGATCCCTCTCCA 4081 CAGGGTCTGTCCCTGCCCCTGCTTCACTTCTGACCTCAGGTAGCTCTGTTGCTGTGTCCCTGCTGAGTTGCTATGTCCGT 4161 CTGCTCTGTCCACTTACCATTCCTCAGTCTTTCCATGCTGGGCCGTTGTCTTACCATGGCCATCCTTCCTACCTTTTCTT 4241 CAGCCAGCTCTGTTTAATTATAGACCCATAGGGTCCTGACTGGAGCCCCATTGAGCACTTTGGGGACGTTTCTGGAGGAA 4321 CAGAGGCTCAGAAACTGGTGTCCTCAAGGCCCATGGGCCTGTGGTTAGCGAAGCCTCGGAGACAACTGGGGAGGAACTTG 4401 GAGAGGTGAAGGACTTGGTGAGAGACTTGGAGAAAGAGGCCAGGCTTGGGAAAGCAGGGTGGCAGGAGCGAGCTCTGTTT 4481 TCCATGAGTGTGTCCTTGTGCCTTAGGGTCCAGCAGTTCAGGTATGAGGGGCATTTTCTGAATGCCTCCTAATTTCTCTC 4561 AGGTCTTTGGCTCAGTGTCACCAAGTTTGACAGACCCCTTCGTTCCTGAGCTTGCTAGAAGGGAAGCAGCACGTTGAGTG 4641 GTGTGGTGTGGTGCGAGAGCGGAGGCCTCCCATGCAGAAGGCTGGGGTGGTGGACAAGAGAAAGGGCCCGGTGGTCAGCT 4721 TCTCACCGATGACTCTCCATGCCTCAAGAGACTGAGTATAGTAGTTGGTTCAAGAAGTTACTCTAAAACTGCCTGCCCTC 4801 TTCACCTAAAGTCTGTTCTCATTTCGGGGAGGAATGCAAGTCCTTAATTTTCAAGGGAAGACAGTCTAGTGTTTAAAAGC 4881 ATGTGTCTGGGGTCTGGTCCCTTTGGTACATTTCTAGCTTGCTACTTACCAGCTGGGTTTGACCTTGGTTGATTGATTGA 4961 ACCCGAGTCTCGGTTTCCTTTCCTATAATGACTTGTGGGGGTGGGGGTTTGAAAATATCTACCTCAGGGTTGCTGGATGA 5041 ACTGAAATAATGTCTGTAAAGCTTTAGCACAGTGCCTGGCAAGCACTTAATAAACGGCTGTGGTGGTGGTGGTTTA Target sites
Provided by authors
Predicted by miRanda
DRVs
SNPs
DRVs & SNPs
|
||||||||||||||||||||
miRNA-target interactions (Predicted by miRanda) |
|
Experimental Support 1 for Functional miRNA-Target Interaction | |||||||
---|---|---|---|---|---|---|---|
miRNA:Target | ---- | ||||||
Validation Method |
|
||||||
Conditions | CD4+ T cells (C57BL/6) | ||||||
Disease | MIMAT0000135 | ||||||
Location of target site | 3'UTR | ||||||
Tools used in this research | TargetScan , miRTarCLIP , Piranha | ||||||
Original Description (Extracted from the article) |
...
"HITS-CLIP data was present in GSM1013576. RNA binding protein: AGO2. Condition:CD4+ T cells
... - Loeb GB; Khan AA; Canner D; Hiatt JB; et al., 2012, Molecular cell. |
||||||
miRNA-target interactions (Provided by authors) |
|
||||||
Article |
- Loeb GB; Khan AA; Canner D; Hiatt JB; et al. - Molecular cell, 2012
MicroRNAs (miRNAs) are essential components of gene regulation, but identification of miRNA targets remains a major challenge. Most target prediction and discovery relies on perfect complementarity of the miRNA seed to the 3' untranslated region (UTR). However, it is unclear to what extent miRNAs target sites without seed matches. Here, we performed a transcriptome-wide identification of the endogenous targets of a single miRNA-miR-155-in a genetically controlled manner. We found that approximately 40% of miR-155-dependent Argonaute binding occurs at sites without perfect seed matches. The majority of these noncanonical sites feature extensive complementarity to the miRNA seed with one mismatch. These noncanonical sites confer regulation of gene expression, albeit less potently than canonical sites. Thus, noncanonical miRNA binding sites are widespread, often contain seed-like motifs, and can regulate gene expression, generating a continuum of targeting and regulation.
LinkOut: [PMID: 23142080]
|
Experimental Support 2 for Functional miRNA-Target Interaction | |
---|---|
miRNA:Target | ---- |
Validation Method |
|
Conditions | liver tissue of C57BL/6 |
Disease | MIMAT0000135 |
Tools used in this research | TargetScan |
Original Description (Extracted from the article) |
...
"FIH1 is a target of miR-125a-5p We then determined whether miR- 125a-5p influenced the expression of FIH1. Similar to the miR-NC
... - Li G; Li J; Li C; Qi H; Dong P; Zheng J; Yu F, 2016, Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology. |
Article |
- Li G; Li J; Li C; Qi H; Dong P; Zheng J; Yu F - Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, 2016
BACKGROUND/AIMS: Emerging evidence shows that microRNAs (miRNAs) play a crucial role in the regulation of activation, proliferation and apoptosis of hepatic stellate cells (HSCs). Previous studies have indicated that miR-125a-5p is correlated with hepatitis B virus replication and disease progression. However, little is known about the biological role and underlying mechanism of miR-125a-5p in liver fibrosis. METHODS: We analyzed the level of miR-125a-5p in carbon tetrachloride-induced liver fibrosis and activated HSCs. We analyzed the effects of miR-125a-5p down-regulation on HSC activation and proliferation. We also analyzed the binding of miR-125a-5p to the 3'-untranslated region of factor inhibiting hypoxia-inducible factor 1 (FIH1) mRNA. RESULTS: Up-regulation of miR-125a-5p was observed in the liver tissues of fibrotic mice and activated HSCs. Down-regulation of miR-125a-5p prevented the activation and proliferation of HSCs. FIH1, a negative modulator of hypoxia inducible factor 1, was confirmed to be a target of miR-125a-5p using the luciferase reporter assay. Further studies demonstrated that miR-125a-5p prompted the activation and proliferation of HSCs, at least in part, by down-regulating FIH1. CONCLUSION: Our findings shed new light on miRNAs as a promising therapeutic target in liver fibrosis.
LinkOut: [PMID: 27074047]
|
CLIP-seq Support 1 for dataset GSM4656409 | |
---|---|
Method / RBP | HITS-CLIP / AGO |
Cell line / Condition | mouse liver / Adult |
Location of target site | NM_176958 | 3UTR | AAUGACUUGUGGGGGUGGGGGUUUGAAAAUAUCUACCUCA |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Accession Series | GSE153876 |
CLIP-seq Viewer | Link |
CLIP-seq Support 2 for dataset GSM4656410 | |
---|---|
Method / RBP | HITS-CLIP / AGO |
Cell line / Condition | mouse liver / e185 rep2 |
Location of target site | NM_176958 | 3UTR | GUGGGGGUGGGGGUUUGAAAAUAUCUACCUCA |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Accession Series | GSE153876 |
CLIP-seq Viewer | Link |
CLIP-seq Support 3 for dataset GSM4751757 | |
---|---|
Method / RBP | HITS-CLIP / AGO |
Cell line / Condition | adipose tissue / RNA sequencing of iBAT 2 |
Location of target site | NM_176958 | 3UTR | CUCAGGGUUGUAGAG |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Accession Series | GSE142677 |
CLIP-seq Viewer | Link |
CLIP-seq Support 4 for dataset GSM4751757 | |
---|---|
Method / RBP | HITS-CLIP / AGO |
Cell line / Condition | adipose tissue / RNA sequencing of iBAT 2 |
Location of target site | NM_176958 | 3UTR | GUUGCUGGAUGAACUGAAA |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Accession Series | GSE142677 |
CLIP-seq Viewer | Link |
CLIP-seq Support 5 for dataset GSM4751759 | |
---|---|
Method / RBP | HITS-CLIP / AGO |
Cell line / Condition | adipose tissue / RNA sequencing of iBAT 4 |
Location of target site | NM_176958 | 3UTR | GUGUGUGUGUGUGUGUACAUGU |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Accession Series | GSE142677 |
CLIP-seq Viewer | Link |
CLIP-seq Support 6 for dataset GSM4751760 | |
---|---|
Method / RBP | HITS-CLIP / AGO |
Cell line / Condition | adipose tissue / RNA sequencing of eWAT 1 |
Location of target site | NM_176958 | 3UTR | GUUGCUGGAUGAACUGAAA |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Accession Series | GSE142677 |
CLIP-seq Viewer | Link |
CLIP-seq Support 7 for dataset GSM4751761 | |
---|---|
Method / RBP | HITS-CLIP / AGO |
Cell line / Condition | adipose tissue / RNA sequencing of eWAT 2 |
Location of target site | NM_176958 | 3UTR | GUUGCUGGAUGAACUGAAA |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Accession Series | GSE142677 |
CLIP-seq Viewer | Link |
CLIP-seq Support 8 for dataset GSM4751763 | |
---|---|
Method / RBP | HITS-CLIP / AGO |
Cell line / Condition | adipose tissue / RNA sequencing of eWAT 4 |
Location of target site | NM_176958 | 3UTR | GUUGCUGGAUGAACUGAAA |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Accession Series | GSE142677 |
CLIP-seq Viewer | Link |
CLIP-seq Support 9 for dataset GSM1013576 | |
---|---|
Method / RBP | HITS-CLIP / AGO2 |
Cell line / Condition | CD4+ T cells (C57BL/6) / CD4+ T cells, 155KO, biological rep2 |
Location of target site | NM_176958 | 3UTR | UCAGGGUGUGUGUGUGUGUGU |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 23142080 / GSE41285 |
CLIP-seq Viewer | Link |
28 mmu-miR-125a-5p Target Genes:
Functional analysis:
ID | Target | Description | Validation methods | |||||||||
Strong evidence | Less strong evidence | |||||||||||
MIRT001716 | Lin28a | lin-28 homolog A (C. elegans) | 1 | 1 | ||||||||
MIRT005597 | Trim71 | tripartite motif-containing 71 | 4 | 3 | ||||||||
MIRT006310 | Cbx7 | chromobox 7 | 2 | 1 | ||||||||
MIRT006967 | 4632428N05Rik | V-set immunoregulatory receptor | 2 | 1 | ||||||||
MIRT054177 | Ptpn18 | protein tyrosine phosphatase, non-receptor type 18 | 2 | 1 | ||||||||
MIRT054178 | Ptpn7 | protein tyrosine phosphatase, non-receptor type 7 | 2 | 1 | ||||||||
MIRT054179 | Ppp1ca | protein phosphatase 1, catalytic subunit, alpha isoform | 2 | 1 | ||||||||
MIRT054180 | Ppp2ca | protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform | 2 | 1 | ||||||||
MIRT054570 | Traf6 | TNF receptor-associated factor 6 | 3 | 1 | ||||||||
MIRT580227 | Tspan12 | tetraspanin 12 | 2 | 2 | ||||||||
MIRT582368 | Mtf1 | metal response element binding transcription factor 1 | 2 | 2 | ||||||||
MIRT582450 | Mgat4a | mannoside acetylglucosaminyltransferase 4, isoenzyme A | 2 | 2 | ||||||||
MIRT584884 | Antxr2 | anthrax toxin receptor 2 | 2 | 2 | ||||||||
MIRT587193 | Foxk1 | forkhead box K1 | 2 | 2 | ||||||||
MIRT588848 | Snrnp40 | small nuclear ribonucleoprotein 40 (U5) | 2 | 2 | ||||||||
MIRT591275 | Lars2 | leucyl-tRNA synthetase, mitochondrial | 2 | 4 | ||||||||
MIRT592914 | Madd | MAP-kinase activating death domain | 2 | 2 | ||||||||
MIRT594893 | Il1rn | interleukin 1 receptor antagonist | 2 | 4 | ||||||||
MIRT596427 | Hif1an | hypoxia-inducible factor 1, alpha subunit inhibitor | 3 | 3 | ||||||||
MIRT599142 | Dqx1 | DEAQ RNA-dependent ATPase | 2 | 2 | ||||||||
MIRT599717 | Aph1c | aph1 homolog C, gamma secretase subunit | 2 | 2 | ||||||||
MIRT600832 | Gm14137 | predicted gene 14137 | 2 | 2 | ||||||||
MIRT604902 | Jmy | junction-mediating and regulatory protein | 2 | 2 | ||||||||
MIRT605441 | Stat1 | signal transducer and activator of transcription 1 | 2 | 2 | ||||||||
MIRT606092 | Wdr25 | WD repeat domain 25 | 2 | 2 | ||||||||
MIRT732537 | Tnfrsf1b | tumor necrosis factor receptor superfamily, member 1b | 4 | 0 | ||||||||
MIRT734700 | VDR | vitamin D receptor | 2 | 0 | ||||||||
MIRT734824 | Sox11 | SRY (sex determining region Y)-box 11 | 2 | 0 |
miRNA-Drug Associations | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
miRNA-Drug Resistance Associations | ||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|