| 臺大學術典藏 |
2020-02-06T10:53:30Z |
Structure-based design, synthesis and biological evaluation of novel anthra[1,2-d]imidazole-6,11-dione homologues as potential antitumor agents
|
Chen T.-C.;Yu D.-S.;Huang K.-F.;Fu Y.-C.;Lee C.-C.;Chen C.-L.;Huang F.-C.;Hsieh H.-H.;Jing-Jer Lin;Huang H.-S.; Chen T.-C.; Yu D.-S.; Huang K.-F.; Fu Y.-C.; Lee C.-C.; Chen C.-L.; Huang F.-C.; Hsieh H.-H.; JING-JER LIN; Huang H.-S. |
| 臺大學術典藏 |
2020-02-06T10:53:30Z |
Structure-based design, synthesis and biological evaluation of novel anthra[1,2-d]imidazole-6,11-dione homologues as potential antitumor agents
|
Chen T.-C.;Yu D.-S.;Huang K.-F.;Fu Y.-C.;Lee C.-C.;Chen C.-L.;Huang F.-C.;Hsieh H.-H.;Jing-Jer Lin;Huang H.-S.; Chen T.-C.; Yu D.-S.; Huang K.-F.; Fu Y.-C.; Lee C.-C.; Chen C.-L.; Huang F.-C.; Hsieh H.-H.; JING-JER LIN; Huang H.-S. |
| 臺大學術典藏 |
2020-02-06T10:53:30Z |
Development and evaluation of novel phosphotyrosine mimetic inhibitors targeting the Src homology 2 domain of signaling lymphocytic activation molecule (SLAM) associated protein
|
Chu C.-Y.;Chang C.-P.;Chou Y.-T.;Handoko, Hu Y.-L.;Lo L.-C.;Jing-Jer Lin; Chu C.-Y.; Chang C.-P.; Chou Y.-T.; Handoko, Hu Y.-L.; Lo L.-C.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:30Z |
Development and evaluation of novel phosphotyrosine mimetic inhibitors targeting the Src homology 2 domain of signaling lymphocytic activation molecule (SLAM) associated protein
|
Chu C.-Y.;Chang C.-P.;Chou Y.-T.;Handoko, Hu Y.-L.;Lo L.-C.;Jing-Jer Lin; Chu C.-Y.; Chang C.-P.; Chou Y.-T.; Handoko, Hu Y.-L.; Lo L.-C.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:30Z |
Structure-based design, synthesis and evaluation of novel anthra[1,2-d]imidazole-6,11-dione derivatives as telomerase inhibitors and potential for cancer polypharmacology
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Huang H.-S.; JING-JER LIN; Guh J.-H.; Huang K.-F.; Huang F.-C.; Hsieh H.-H.; Lee C.-C.; Chen T.-C.; Chang D.-M.; Chen C.-L.; Chen C.-L.;Chang D.-M.;Chen T.-C.;Lee C.-C.;Hsieh H.-H.;Huang F.-C.;Huang K.-F.;Guh J.-H.;Jing-Jer Lin;Huang H.-S. |
| 臺大學術典藏 |
2020-02-06T10:53:30Z |
Structure-based design, synthesis and evaluation of novel anthra[1,2-d]imidazole-6,11-dione derivatives as telomerase inhibitors and potential for cancer polypharmacology
|
Huang H.-S.; JING-JER LIN; Guh J.-H.; Huang K.-F.; Huang F.-C.; Hsieh H.-H.; Lee C.-C.; Chen T.-C.; Chang D.-M.; Chen C.-L.; Chen C.-L.;Chang D.-M.;Chen T.-C.;Lee C.-C.;Hsieh H.-H.;Huang F.-C.;Huang K.-F.;Guh J.-H.;Jing-Jer Lin;Huang H.-S. |
| 臺大學術典藏 |
2020-02-06T10:53:29Z |
Conformational transition of a hairpin structure to G-quadruplex within the WNT1 gene promoter
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Chang T.-C.; Kuo M.H.-J.;Wang Z.-F.;Tseng T.-Y.;Li M.-H.;Hsu S.-T.D.;Jing-Jer Lin;Chang T.-C.; Kuo M.H.-J.; Wang Z.-F.; Tseng T.-Y.; Li M.-H.; Hsu S.-T.D.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:29Z |
Conformational transition of a hairpin structure to G-quadruplex within the WNT1 gene promoter
|
Chang T.-C.; Kuo M.H.-J.;Wang Z.-F.;Tseng T.-Y.;Li M.-H.;Hsu S.-T.D.;Jing-Jer Lin;Chang T.-C.; Kuo M.H.-J.; Wang Z.-F.; Tseng T.-Y.; Li M.-H.; Hsu S.-T.D.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:29Z |
Direct evidence of mitochondrial G-quadruplex DNA by using fluorescent anti-cancer agents
|
Chang T.-C.; Lou P.-J.; Huang W.-C.;Tseng T.-Y.;Chen Y.-T.;Chang C.-C.;Wang Z.-F.;Wang C.-L.;Hsu T.-N.;Li P.-T.;Chen C.-T.;Jing-Jer Lin;Lou P.-J.;Chang T.-C.; Huang W.-C.; Tseng T.-Y.; Chen Y.-T.; Chang C.-C.; Wang Z.-F.; Wang C.-L.; Hsu T.-N.; Li P.-T.; Chen C.-T.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:29Z |
Direct evidence of mitochondrial G-quadruplex DNA by using fluorescent anti-cancer agents
|
Chang T.-C.; Lou P.-J.; Huang W.-C.;Tseng T.-Y.;Chen Y.-T.;Chang C.-C.;Wang Z.-F.;Wang C.-L.;Hsu T.-N.;Li P.-T.;Chen C.-T.;Jing-Jer Lin;Lou P.-J.;Chang T.-C.; Huang W.-C.; Tseng T.-Y.; Chen Y.-T.; Chang C.-C.; Wang Z.-F.; Wang C.-L.; Hsu T.-N.; Li P.-T.; Chen C.-T.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:29Z |
Pif1 regulates telomere length by preferentially removing telomerase from long telomere ends
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JING-JER LIN; Li H.-W.; Lu C.-Y.; Chien I.-C.; Yu T.-Y.; Li J.-R.; Li J.-R.;Yu T.-Y.;Chien I.-C.;Lu C.-Y.;Jing-Jer Lin;Li H.-W. |
| 臺大學術典藏 |
2020-02-06T10:53:29Z |
Pif1 regulates telomere length by preferentially removing telomerase from long telomere ends
|
JING-JER LIN; Li H.-W.; Lu C.-Y.; Chien I.-C.; Yu T.-Y.; Li J.-R.; Li J.-R.;Yu T.-Y.;Chien I.-C.;Lu C.-Y.;Jing-Jer Lin;Li H.-W. |
| 臺大學術典藏 |
2020-02-06T10:53:29Z |
Inhibition of cancer cell migration and invasion through suppressing the wnt1-mediating signal pathway by G-quadruplex structure stabilizers
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Wang J.M.;Huang F.C.;Kuo M.H.-J.;Wang Z.-F.;Tseng T.-Y.;Chang L.-C.;Yen S.-J.;Chang T.-C.;Jing-Jer Lin; Wang J.M.; Huang F.C.; Kuo M.H.-J.; Wang Z.-F.; Tseng T.-Y.; Chang L.-C.; Yen S.-J.; Chang T.-C.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:29Z |
Inhibition of cancer cell migration and invasion through suppressing the wnt1-mediating signal pathway by G-quadruplex structure stabilizers
|
Wang J.M.;Huang F.C.;Kuo M.H.-J.;Wang Z.-F.;Tseng T.-Y.;Chang L.-C.;Yen S.-J.;Chang T.-C.;Jing-Jer Lin; Wang J.M.; Huang F.C.; Kuo M.H.-J.; Wang Z.-F.; Tseng T.-Y.; Chang L.-C.; Yen S.-J.; Chang T.-C.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:28Z |
Identification of a new class of WNT1 inhibitor: Cancer cells migration, G-quadruplex stabilization and target validation
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Chang L.-C.; Chen T.-C.; Chen S.-J.; Chen C.-L.; Lee C.-C.; Wu S.-H.; Yen Y.; Huang H.-S.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:28Z |
A fluorescent anti-cancer agent, 3,6-bis(1-methyl-4-vinylpyridinium) carbazole diiodide, stains g-quadruplexes in cells and inhibits tumor growth
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Tseng T.-Y.;Chang C.-C.;Jing-Jer Lin;Chang T.-C.; Tseng T.-Y.; Chang C.-C.; JING-JER LIN; Chang T.-C. |
| 臺大學術典藏 |
2020-02-06T10:53:28Z |
A fluorescent anti-cancer agent, 3,6-bis(1-methyl-4-vinylpyridinium) carbazole diiodide, stains g-quadruplexes in cells and inhibits tumor growth
|
Tseng T.-Y.;Chang C.-C.;Jing-Jer Lin;Chang T.-C.; Tseng T.-Y.; Chang C.-C.; JING-JER LIN; Chang T.-C. |
| 臺大學術典藏 |
2020-02-06T10:53:28Z |
The addition of a spin column step in the telomeric repeat application protocol removes telomerase inhibitors
|
Chen Y.-C.; Huang F.-C.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:28Z |
Design, synthesis, and evaluation of cell permeable probes for protein kinases
|
Hsu Y.-L.; Yang C.-C.; Chou T.-C.; Tai C.-H.; Chen L.-Y.; Fu S.-L.; JING-JER LIN; Lo L.-C. |
| 臺大學術典藏 |
2020-02-06T10:53:27Z |
A Low-Toxicity DNA-Alkylating N-Mustard-Quinoline Conjugate with Preferential Sequence Specificity Exerts Potent Antitumor Activity Against Colorectal Cancer
|
Chen T.-L.;Lin Y.-W.;Chen Y.-B.;Jing-Jer Lin;Su T.-L.;Shen C.-N.;Lee T.-C.; Chen T.-L.; Lin Y.-W.; Chen Y.-B.; JING-JER LIN; Su T.-L.; Shen C.-N.; Lee T.-C. |
| 臺大學術典藏 |
2020-02-06T10:53:27Z |
A Low-Toxicity DNA-Alkylating N-Mustard-Quinoline Conjugate with Preferential Sequence Specificity Exerts Potent Antitumor Activity Against Colorectal Cancer
|
Chen T.-L.;Lin Y.-W.;Chen Y.-B.;Jing-Jer Lin;Su T.-L.;Shen C.-N.;Lee T.-C.; Chen T.-L.; Lin Y.-W.; Chen Y.-B.; JING-JER LIN; Su T.-L.; Shen C.-N.; Lee T.-C. |
| 臺大學術典藏 |
2020-02-06T10:53:27Z |
GATA3 interacts with and stabilizes HIF-1α to enhance cancer cell invasiveness
|
Lin M.-C.;Jing-Jer Lin;Hsu C.-L.;Juan H.-F.;Lou P.-J.;Huang M.-C.; Lin M.-C.; JING-JER LIN; Hsu C.-L.; Juan H.-F.; Lou P.-J.; Huang M.-C. |
| 臺大學術典藏 |
2020-02-06T10:53:27Z |
GATA3 interacts with and stabilizes HIF-1α to enhance cancer cell invasiveness
|
Lin M.-C.;Jing-Jer Lin;Hsu C.-L.;Juan H.-F.;Lou P.-J.;Huang M.-C.; Lin M.-C.; JING-JER LIN; Hsu C.-L.; Juan H.-F.; Lou P.-J.; Huang M.-C. |
| 臺大學術典藏 |
2020-02-06T10:53:27Z |
The serine protease inhibitor serpinB2 binds and stabilizes p21 in senescent cells
|
Hsieh H.-H.;Chen Y.-C.;Jhan J.-R.;Jing-Jer Lin; Hsieh H.-H.; Chen Y.-C.; Jhan J.-R.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:27Z |
The serine protease inhibitor serpinB2 binds and stabilizes p21 in senescent cells
|
Hsieh H.-H.;Chen Y.-C.;Jhan J.-R.;Jing-Jer Lin; Hsieh H.-H.; Chen Y.-C.; Jhan J.-R.; JING-JER LIN |
