公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
2013 | 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 | Chen C.-L.; Chang D.-M.; Chen T.-C.; Lee C.-C.; Hsieh H.-H.; Huang F.-C.; Huang K.-F.; JIH-HWA GUH ; JING-JER LIN ; Huang H.-S. | European Journal of Medicinal Chemistry | 35 | 34 | |
2001 | Studies on anthracenes. 1. Human telomerase inhibition and lipid peroxidation of 9-acyloxy 1,5-dichloroanthracene derivatives | Huang H.-S.; Hwang J.-M.; Jen Y.-M.; JING-JER LIN ; Lee K.-Y.; Shi C.-H.; Hsu H.-C. | Chemical and Pharmaceutical Bulletin | 26 | 22 | |
2005 | Study of the preferred modification sites of the quinone methide intermediate resulting from the latent trapping device of the activity probes for hydrolases | Lo, Lee-Chiang; Chiang, Ying-Ling; Kuo, Chi-Hsien; Liao, Hsin-Kai; Chen, Yu-Ju; Lin, Jing-Jer; JING-JER LIN ; LEE-CHIANG LO | Biochemical & Biophysical Research Communications | 30 | 28 | |
2023 | Suppressing c-FOS expression by G-quadruplex ligands inhibits osimertinib-resistant non-small cell lung cancer | Lu, Kai; Wang, Hsin-Chiao; Tu, Yi-Chen; Chang, Cheng-Chung; PEI-JEN LOU ; Chang, Ta-Chau; JING-JER LIN | Journal of the National Cancer Institute | 2 | | |
2019 | Synthesis and biological evaluation of anthra[1,9-cd]pyrazol-6(2H)-one scaffold derivatives as potential anticancer agents | Chen T.-C.; JIH-HWA GUH ; Hsu H.-W.; Chen C.-L.; Lee C.-C.; Wu C.-L.; Lee Y.-R.; JING-JER LIN ; Yu D.-S.; Huang H.-S. | Arabian Journal of Chemistry | 8 | 7 | |
2009 | 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 | Shchekotikhin A.E.; Glazunova V.A.; Dezhenkova L.G.; Luzikov Y.N.; Sinkevich Y.B.; Kovalenko L.V.; Buyanov V.N.; Balzarini J.; Huang F.-C.; JING-JER LIN ; Huang H.-S.; Shtil A.A.; Preobrazhenskaya M.N. | Bioorganic and Medicinal Chemistry | 42 | 37 | |
2013 | 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. | Journal of the Chinese Chemical Society | 6 | 6 | |
2007 | 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 | Chemical and Pharmaceutical Bulletin | 48 | 44 | |
2006 | 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 | Journal of the Chinese Chemical Society | 3 | 2 | |
2012 | Synthesis, antiproliferative activities and telomerase inhibition evaluation of novel asymmetrical 1,2-disubstituted amidoanthraquinone derivatives | Lee C.-C.; Huang K.-F.; Lin P.-Y.; Huang F.-C.; Chen C.-L.; Chen T.-C.; JIH-HWA GUH ; JING-JER LIN ; Huang H.-S. | European Journal of Medicinal Chemistry | 27 | 23 | |
2009 | 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 | Bioorganic and Medicinal Chemistry | 56 | 51 | |
2008 | Synthesis, human telomerase inhibition and anti-proliferative studies of a series of 2,7-bis-substituted amido-anthraquinone derivatives | Huang H.-S.; Huang K.-F.; Li C.-L.; Huang Y.-Y.; Chiang Y.-H.; Huang F.-C.; JING-JER LIN | Bioorganic and Medicinal Chemistry | 48 | 41 | |
2012 | 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. | Archiv der Pharmazie | 8 | 8 | |
2006 | 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 | Cancer Letters | 42 | 38 | |
2006 | The telomerase-recruitment domain of the telomere binding protein Cdc13 is regulated by Mec1p/Tel1p-dependent phosphorylation | Tseng S.-F.; JING-JER LIN ; Chiou S.-H.; Liu C.-J.; Chi C.-W.; Chen P.-M.; SHU-CHUN TENG ; Wu K.-J. | Nucleic Acids Research | 97 | 96 | |
2005 | Telomere and telomerase as targets for anti-cancer and regeneration therapies | Hsu Y.-H.; JING-JER LIN | Acta Pharmacologica Sinica | 20 | 17 | |
2000 | Telomere-binding and Stn1p-interacting activities are required for the essential function of Saccharomyces cerevisiae Cdc13p | Wang M.-J.; Lin Y.-C.; Pang T.-L.; Lee J.-M.; Chou C.-C.; JING-JER LIN | Nucleic Acids Research | 29 | | |
2014 | Telomeric transcripts stimulate telomere recombination to suppress senescence in cells lacking telomerase | Yu T.-Y.; Kao Y.-W.; JING-JER LIN | Proceedings of the National Academy of Sciences of the United States of America | 98 | 92 | |
2009 | 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. | Cell Research | 17 | 17 | |
1988 | A trans-acting gene is required for the phenotypic expression of a tyrosinase gene in Streptomyces | Lee Y.-H.W.; Chen B.-F.; Wu S.-Y.; Leu W.-M.; JING-JER LIN ; Chen C.W.; Lo S.J. | Gene | 41 | 49 | |