This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .
This human miRNA was predicted by computational methods using conservationwith mouse and Fugu rubripes sequences . Expression of the excised miRwas validated in zebrafish, and the ends mapped by cloning. Subsequentcloning studies have also verified the expression of miR-222 in human EScells. The mature sequence shown here represents the most commonly clonedform from large-scale cloning studies .