| 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
|
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
|
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
|
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
|
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
|
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. |
| 臺大學術典藏 |
2020-02-06T10:53:32Z |
Development of a plate-based assay platform to monitor cellular SHP2 phosphatase activity during erythroid differentiation
|
Chu C.-Y.; Kuo C.-C.; Chen M.-H.; Chen K.-J.; Lo L.-C.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:32Z |
Synthesis, telomerase evaluation and anti-proliferative studies on various series of diaminoanthraquinone-lkinked aminoacyl residue derivatives
|
Huang F.-C.; Huang K.-F.; Chen R.-H.; Wu J.-E.; Chen T.-C.; Chen C.-L.; Lee C.-C.; Chen J.-Y.; JING-JER LIN; Huang H.-S. |
| 臺大學術典藏 |
2020-02-06T10:53:32Z |
Association of pituitary tumor transforming gene expression with early oral tumorigenesis and malignant progression of precancerous lesions
|
Lou P.-J.; Chang L.-C.; JING-JER LIN; Liao L.-J.;Hsu Y.-H.;Yu C.-H.;Chiang C.-P.;Jhan J.-R.;Chang L.-C.;Jing-Jer Lin;Lou P.-J.; Liao L.-J.; Hsu Y.-H.; Yu C.-H.; Chiang C.-P.; Jhan J.-R. |
| 臺大學術典藏 |
2020-02-06T10:53:32Z |
Association of pituitary tumor transforming gene expression with early oral tumorigenesis and malignant progression of precancerous lesions
|
Lou P.-J.; Chang L.-C.; JING-JER LIN; Liao L.-J.;Hsu Y.-H.;Yu C.-H.;Chiang C.-P.;Jhan J.-R.;Chang L.-C.;Jing-Jer Lin;Lou P.-J.; Liao L.-J.; Hsu Y.-H.; Yu C.-H.; Chiang C.-P.; Jhan J.-R. |
| 臺大學術典藏 |
2020-02-06T10:53:31Z |
Induction of senescence in cancer cells by the G-quadruplex stabilizer, BMVC4, is independent of its telomerase inhibitory activity
|
JING-JER LIN; Chang T.-C.; Wang J.-M.; Chang C.-C.; Huang F.-C. |
| 臺大學術典藏 |
2020-02-06T10:53:31Z |
Design, synthesis and evaluation of telomerase inhibitory, hTERT repressing, and anti-proliferation activities of symmetrical 1,8-disubstituted amidoanthraquinones
|
Lee C.-C.; Huang K.-F.; Chang D.-M.; Hsu J.-J.; Huang F.-C.; Shih K.-N.; Chen C.-L.; Chen T.-C.; Chen R.-H.; JING-JER LIN; Huang H.-S. |
| 臺大學術典藏 |
2020-02-06T10:53:31Z |
Depleting components of the THO complex causes increased telomere length by reducing the expression of the telomere-associated protein Rif1p
|
Yu T.-Y.; Wang C.-Y.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:30Z |
Yin Yang 1 is a target of microRNA-34 family and contributes to gastric carcinogenesis
|
Wang A.-M.; Huang T.-T.; Hsu K.-W.; Huang K.-H.; Fang W.-L.; Yang M.-H.; Lo S.-S.; Chi C.-W.; JING-JER LIN; Yeh T.-S. |
| 臺大學術典藏 |
2020-02-06T10:53:30Z |
Synthesis and evaluation of activity-based probes carrying a 5′-fluorosulfonylbenzoyl adenosine moiety for protein kinases
|
Hsu Y.-L.;Yang C.-C.;Lan C.-Y.;Jing-Jer Lin;Lo L.-C.; Hsu Y.-L.; Yang C.-C.; Lan C.-Y.; JING-JER LIN; Lo L.-C. |
| 臺大學術典藏 |
2020-02-06T10:53:30Z |
Synthesis and evaluation of activity-based probes carrying a 5′-fluorosulfonylbenzoyl adenosine moiety for protein kinases
|
Hsu Y.-L.;Yang C.-C.;Lan C.-Y.;Jing-Jer Lin;Lo L.-C.; Hsu Y.-L.; Yang C.-C.; Lan C.-Y.; JING-JER LIN; Lo L.-C. |
| 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
|
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
|
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
|
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
|
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
|
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
|
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. |
