The fasting-refeeding regimen increased Akt phosphorylation. by Tucker Hopkins (20790529)

RT-qPCR Primer. by Dequan Wang (6007007)

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CCND1 is a target gene of miR-1247-3p. by Dequan Wang (6007007)

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miR-1247-3p was downregulated in CRC resistant cells. by Dequan Wang (6007007)

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miR-1247-3p plasmid. by Dequan Wang (6007007)

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RNA-sequencing data screening for miR-1247-3p target genes. by Dequan Wang (6007007)

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Dual luciferase primer. by Dequan Wang (6007007)

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shCCND1 plasmid. by Dequan Wang (6007007)

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CCND1 promoted chemoresistance in CRC. by Dequan Wang (6007007)

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Overexpression of miR-1247-3p promoted apoptosis and inhibited resistance in drug-resistant cells. by Dequan Wang (6007007)

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Effect of miR-1247-3p on survival in colorectal cancer patients. by Dequan Wang (6007007)

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S1 Raw images - by Dequan Wang (6007007)

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Introduction to the dataset. by Dequan Wang (6007007)

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Downregulation of miR-1247-3p inhibited apoptosis and reduced chemosensitivity in cells. by Dequan Wang (6007007)

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miR-1247-3p was downregulated in tissues of patients with CRC and was associated with prognosis and drug resistance. by Dequan Wang (6007007)

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<b>The loss of insulin-positive cell clusters precedes the decrease of islet frequency and beta cell area in type 1 diabetes</b> by Denise M. Drotar (21679539)

Group-level narrow- and broad-band spectral changes after hemispherotomy reveal a marked EEG slowing of the isolated cortex, robust across patients. by Michele Angelo Colombo (22446342)

Discovery of Novel [1,2,4]Triazolo[1,5‑<i>a</i>]pyrimidine Derivatives as Novel Potent S‑Phase Kinase-Associated Protein 2 (SKP2) Inhibitors for the Treatment of Cancer by Kaizhao Hu (15670612)

“…Mechanistically, compound <b>E35</b> markedly decreased the expression of Skp2, as well as increased the expression of its substrates p21 and p27. …”

Discovery of Novel [1,2,4]Triazolo[1,5‑<i>a</i>]pyrimidine Derivatives as Novel Potent S‑Phase Kinase-Associated Protein 2 (SKP2) Inhibitors for the Treatment of Cancer by Kaizhao Hu (15670612)

“…Mechanistically, compound <b>E35</b> markedly decreased the expression of Skp2, as well as increased the expression of its substrates p21 and p27. …”

Discovery of Novel [1,2,4]Triazolo[1,5‑<i>a</i>]pyrimidine Derivatives as Novel Potent S‑Phase Kinase-Associated Protein 2 (SKP2) Inhibitors for the Treatment of Cancer by Kaizhao Hu (15670612)

“…Mechanistically, compound <b>E35</b> markedly decreased the expression of Skp2, as well as increased the expression of its substrates p21 and p27. …”