| 臺大學術典藏 |
2020-02-06T10:53:37Z |
The telomerase-recruitment domain of the telomere binding protein Cdc13 is regulated by Mec1p/Tel1p-dependent phosphorylation
|
Tseng S.-F.;Jing-Jer Lin;Teng S.-C.; Tseng S.-F.; JING-JER LIN; Teng S.-C. |
| 臺大學術典藏 |
2020-02-06T10:53:37Z |
The telomerase-recruitment domain of the telomere binding protein Cdc13 is regulated by Mec1p/Tel1p-dependent phosphorylation
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Tseng S.-F.;Jing-Jer Lin;Teng S.-C.; Tseng S.-F.; JING-JER LIN; Teng S.-C. |
| 臺大學術典藏 |
2020-02-06T10:53:37Z |
The tea polyphenols EGCG and EGC repress mRNA expression of human telomerase reverse transcriptase (hTERT) in carcinoma cells
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Lin S.-C.;Li W.-C.;Shih J.-W.;Hong K.-F.;Pan Y.-R.;Jing-Jer Lin; Lin S.-C.; Li W.-C.; Shih J.-W.; Hong K.-F.; Pan Y.-R.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:37Z |
The tea polyphenols EGCG and EGC repress mRNA expression of human telomerase reverse transcriptase (hTERT) in carcinoma cells
|
Lin S.-C.;Li W.-C.;Shih J.-W.;Hong K.-F.;Pan Y.-R.;Jing-Jer Lin; Lin S.-C.; Li W.-C.; Shih J.-W.; Hong K.-F.; Pan Y.-R.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:37Z |
Facile synthesis toward the construction of an activity probe library for glycosidases
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Chiang Y.-L.; JING-JER LIN; Li Y.-K.; Lo L.-C.; Shie T.-H.;Chiang Y.-L.;Jing-Jer Lin;Li Y.-K.;Lo L.-C.; Shie T.-H. |
| 臺大學術典藏 |
2020-02-06T10:53:37Z |
Facile synthesis toward the construction of an activity probe library for glycosidases
|
Chiang Y.-L.; JING-JER LIN; Li Y.-K.; Lo L.-C.; Shie T.-H.;Chiang Y.-L.;Jing-Jer Lin;Li Y.-K.;Lo L.-C.; Shie T.-H. |
| 臺大學術典藏 |
2020-02-06T10:53:37Z |
Rapid and selective isolation of β-xylosidase through an activitybased chemical approach
|
Lo L.-C.;Chu C.-Y.;Pan Y.-R.;Wan C.-F.;Li Y.-K.;Jing-Jer Lin; Lo L.-C.; Chu C.-Y.; Pan Y.-R.; Wan C.-F.; Li Y.-K.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:37Z |
Rapid and selective isolation of β-xylosidase through an activitybased chemical approach
|
Lo L.-C.;Chu C.-Y.;Pan Y.-R.;Wan C.-F.;Li Y.-K.;Jing-Jer Lin; Lo L.-C.; Chu C.-Y.; Pan Y.-R.; Wan C.-F.; Li Y.-K.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:37Z |
Synthesis of activity probes for β-xylosidase
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Lo L.-C.;Chu C.-Y.;Lin F.-A.;Pan Y.-R.;Li Y.-K.;Jing-Jer Lin; Lo L.-C.; Chu C.-Y.; Lin F.-A.; Pan Y.-R.; Li Y.-K.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:37Z |
Synthesis of activity probes for β-xylosidase
|
Lo L.-C.;Chu C.-Y.;Lin F.-A.;Pan Y.-R.;Li Y.-K.;Jing-Jer Lin; Lo L.-C.; Chu C.-Y.; Lin F.-A.; Pan Y.-R.; Li Y.-K.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:37Z |
Telomere and telomerase as targets for anti-cancer and regeneration therapies
|
Hsu Y.-H.;Jing-Jer Lin; Hsu Y.-H.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:37Z |
Telomere and telomerase as targets for anti-cancer and regeneration therapies
|
Hsu Y.-H.;Jing-Jer Lin; Hsu Y.-H.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:36Z |
The U3 small nucleolar ribonucleoprotein component Imp4p is a telomeric DNA-binding protein
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Kuo C.-C.; Lin Y.-C.; Wu C.-F.; JING-JER LIN; Hsieh Y.-C.; Tu P.-J.; Lee Y.-Y. |
| 臺大學術典藏 |
2020-02-06T10:53:36Z |
A concise paradigm for the construction of amide linker of 2,7-diamidoanthraquinone derivatives as potential telomerase inhibitors
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Huang H.-S.; JING-JER LIN; Huang K.-F.; Li C.-L. |
| 臺大學術典藏 |
2020-02-06T10:53:36Z |
Synthesis and human telomerase inhibition of a series of regioisomeric disubstituted amidoanthraquinones
|
Huang H.-S.; Chen I.-B.; Huang K.-F.; Lu W.-C.; Shieh F.-Y.; Huang Y.-Y.; Huang F.-C.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:35Z |
Synthesis, cytotoxicity and human telomerase inhibition activities of a series of 1,2-heteroannelated anthraquinones and anthra[ 1,2-d]imidazole-6,11 -dione homologues
|
Huang H.-S.; Chen T.-C.; Chen R.-H.; Huang K.-F.; Huang F.-C.; Jhan J.-R.; Chen C.-L.; Lee C.-C.; Lo Y.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:35Z |
Ten1p promotes the telomeric DNA-binding activity of Cdc13p: Implication for its function in telomere length regulation
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Qian W.; Wang J.; Jin N.-N.; Fu X.-H.; Lin Y.-C.; JING-JER LIN; Zhou J.-Q. |
| 臺大學術典藏 |
2020-02-06T10:53:35Z |
Synthesis and cytotoxic properties of 4,11-bis[(aminoethyl)amino]anthra[2,3-b]thiophene-5,10-diones, novel analogues of antitumor anthracene-9,10-diones
|
JING-JER LIN; Huang H.-S.; Shtil A.A.; Preobrazhenskaya M.N.; Balzarini J.; Huang F.-C.; Buyanov V.N.; Kovalenko L.V.; Sinkevich Y.B.; Luzikov Y.N.; Glazunova V.A.; Dezhenkova L.G.; Shchekotikhin A.E. |
| 臺大學術典藏 |
2020-02-06T10:53:35Z |
Synthesis, human telomerase inhibition and anti-proliferative studies of a series of 2,7-bis-substituted amido-anthraquinone derivatives
|
Huang F.-C.; Chiang Y.-H.; Huang Y.-Y.; Li C.-L.; Huang H.-S.; Huang K.-F.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:34Z |
Overexpression of the pituitary tumor transforming gene induces p53-dependent senescence through activating DNA damage response pathway in normal human fibroblasts
|
Hsu Y.-H.;Liao L.-J.;Yu C.-H.;Chiang C.-P.;Jhan J.-R.;Chang L.-C.;Chen Y.-J.;Lou P.-J.;Jing-Jer Lin; Hsu Y.-H.; Liao L.-J.; Yu C.-H.; Chiang C.-P.; Jhan J.-R.; Chang L.-C.; Chen Y.-J.; Lou P.-J.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:34Z |
Overexpression of the pituitary tumor transforming gene induces p53-dependent senescence through activating DNA damage response pathway in normal human fibroblasts
|
Hsu Y.-H.;Liao L.-J.;Yu C.-H.;Chiang C.-P.;Jhan J.-R.;Chang L.-C.;Chen Y.-J.;Lou P.-J.;Jing-Jer Lin; Hsu Y.-H.; Liao L.-J.; Yu C.-H.; Chiang C.-P.; Jhan J.-R.; Chang L.-C.; Chen Y.-J.; Lou P.-J.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:34Z |
NSC746364, NSC746365, and NSC746366: The spectra of cytotoxicity and molecular correlates of response to telomerase activity
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JING-JER LIN; Li C.-L.; Chen C.-L.; Lee C.-C.; Huang K.-F.; Huang H.-S.; Huang H.-S.;Huang K.-F.;Lee C.-C.;Chen C.-L.;Li C.-L.;Jing-Jer Lin |
| 臺大學術典藏 |
2020-02-06T10:53:34Z |
NSC746364, NSC746365, and NSC746366: The spectra of cytotoxicity and molecular correlates of response to telomerase activity
|
JING-JER LIN; Li C.-L.; Chen C.-L.; Lee C.-C.; Huang K.-F.; Huang H.-S.; Huang H.-S.;Huang K.-F.;Lee C.-C.;Chen C.-L.;Li C.-L.;Jing-Jer Lin |
| 臺大學術典藏 |
2020-02-06T10:53:34Z |
Selective activation of SHP2 activity by cisplatin revealed by a novel chemical probe-based assay
|
Kuo C.-C.;Chu C.-Y.;Jing-Jer Lin;Lo L.-C.; Kuo C.-C.; Chu C.-Y.; JING-JER LIN; Lo L.-C. |
| 臺大學術典藏 |
2020-02-06T10:53:34Z |
Selective activation of SHP2 activity by cisplatin revealed by a novel chemical probe-based assay
|
Kuo C.-C.;Chu C.-Y.;Jing-Jer Lin;Lo L.-C.; Kuo C.-C.; Chu C.-Y.; JING-JER LIN; Lo L.-C. |
