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1801por Lee, Zheng Wei, Zhou, Jianbiao, Chen, Chien-Shing, Zhao, Yujun, Tan, Choon-Hong, Li, Ling, Moore, Philip Keith, Deng, Lih-Wen“…The slow-releasing hydrogen sulfide (H(2)S) donor, GYY4137, caused concentration-dependent killing of seven different human cancer cell lines (HeLa, HCT-116, Hep G2, HL-60, MCF-7, MV4-11 and U2OS) but did not affect survival of normal human lung fibroblasts (IMR90, WI-38) as determined by trypan blue exclusion. …”
Publicado 2011
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1802“…CBP was not comparably enriched in Lea1-containing U2 snRNPs from tgs1Δ cells. Moreover, CBP was not associated with mature Nop58-containing C/D snoRNPs or mature Cbf5- and Gar1-containing H/ACA snoRNPs from tgs1Δ cells. …”
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1803por Chen, Feng, Zhang, Xinli, Sun, Shan, Zara, Janette N., Zou, Xuan, Chiu, Robert, Culiat, Cymbelin T., Ting, Kang, Soo, Chia“…Moreover, NELL-1 mRNA levels were significantly decreased when Osterix was overexpressed in Saos-2, U2OS, Hela and Glioma cells. Correspondingly, knockdown of Osterix increased NELL-1 transcription and osteoblastic differentiation in both Saos-2 cells and primary human osteoblasts. …”
Publicado 2011
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1804por Shieh, Grace S, Pan, Chin-Hua, Wu, Jia-Hong, Sun, Yun-Ju, Wang, Chia-Chang, Hsiao, Wei-Chun, Lin, Chia-Yeh, Tung, Luh, Chang, Tien-Hsien, Fleming, Alastair B, Hillyer, Cory, Lo, Yi-Chen, Berger, Shelley L, Osley, Mary Ann, Kao, Cheng-Fu“…In addition, the deletion of genes encoding the U2 snRNP subunits, Lea1 or Msl1, in combination with an htb-K123R mutation, leads to synthetic lethality. …”
Publicado 2011
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1805por Lee, Hyun Ju, Rho, Jasung, Gui, Shao Ran, Kim, Mi Kyung, Lee, Yu Kyoung, Lee, Yeon Sook, Kim, Jeong Eun, Cho, Euna, Cho, Mong, Hwang, Tae-Ho“…RESULTS: Simultaneous treatment with JX-594 and aldosterone significantly increased viral replication in A2780, PC-3, and HepG2 cell lines, but not in U2OS cell lines. Furthermore, the aldosterone treatment time altered the JX-594 replication according to the cell line. …”
Publicado 2011
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1806“…Inos affected anticipatory activity preceding lights-off, suggesting a possible clock-dependent function. BM-40-SPARC, U2af50 and fax affected peak activity at dawn without affecting anticipation or overall inactivity (proportion of 15-min intervals without activity), suggesting that these effects may depend on the day-night light cycle. …”
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1807por Indig, Fred E., Rybanska, Ivana, Karmakar, Parimal, Devulapalli, Chakravarty, Fu, Haiqing, Carrier, France, Bohr, Vilhelm A.“…Furthermore, treatment of U2OS cells with 15 µM of the Topoisomerase I inhibitor, camptothecin, causes the dissociation of the nucleolin-Werner complex in the nucleolus, followed by partial re-association in the nucleoplasm. …”
Publicado 2012
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1808por Kumar, Priyadarsina, Lindberg, Louise, Thirkill, Twanda L., Ji, Jennifer W., Martsching, Lindsay, Douglas, Gordon C.“…More detailed examination of its intranuclear distribution using a proximity ligation assay, subcellular fractionation, and immunoprecipitation suggests that MUC1-N is located in nuclear speckles (interchromatin granule clusters) and closely associates with the spliceosome protein U2AF65. Nuclear localization of MUC1-N was abolished when cells were treated with RNase A and nuclear localization was altered when cells were incubated with the transcription inhibitor 5,6-dichloro-1-b-d-ribofuranosylbenzimidazole (DRB). …”
Publicado 2012
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1809“…Introduction of point mutations into the mapped BPS led to reduced U2 binding to the BPS and thereby inhibition of the second step of E6E7 splicing at the nt 409 3′ ss. …”
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1810por Groth-Pedersen, Line, Aits, Sonja, Corcelle-Termeau, Elisabeth, Petersen, Nikolaj H. T., Nylandsted, Jesper, Jäättelä, Marja“…Importantly, all seven siRNAs also killed human cervix cancer (HeLa) and osteosarcoma (U-2-OS) cells and sensitized cancer cells to other lysosome-destabilizing treatments, i.e. photo-oxidation, siramesine, etoposide or cisplatin. …”
Publicado 2012
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1811“…The cellular intrinsic DNA/protein complex (as detected for U2 DNA) showed no association with ND10. Furthermore, our examination of PML−/−, Daxx−/−, and Sp100-negative cells led to our discovering that DNA/protein complexes recruit ND10 protein independently. …”
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1812por Janssen, Ole, Schaumann, Frank, Holz, Olaf, Lavae-Mokhtari, Bianca, Welker, Lutz, Winkler, Carla, Biller, Heike, Krug, Norbert, Hohlfeld, Jens M“…It was therefore the aim of this study to test the effect and reproducibility of a low-dose LPS challenge (20,000 E.U.; 2 μg) using a flow- and volume-controlled inhalation technique to increase LPS deposition. …”
Publicado 2013
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1813“…In the canonical assembly model, the U4/U6.U5 triple snRNP binds only after joining of the U1 and, subsequently, U2 snRNPs to the intron-containing pre-mRNA. Catalytic activation requires the exchange of U6 for U1 snRNA at the 5′ splice site, which is promoted by the DEAD-box protein Prp28. …”
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1814por Kuijjer, Marieke L, van den Akker, Brendy EWM, Hilhorst, Riet, Mommersteeg, Monique, Buddingh, Emilie P, Serra, Massimo, Bürger, Horst, Hogendoorn, Pancras CW, Cleton-Jansen, Anne-Marie“…This resulted in inhibition of proliferation of osteosarcoma cell lines U-2 OS and HOS, but not of 143B, which harbors a KRAS oncogenic transformation. …”
Publicado 2014
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1815por Aesoy, Reidun, Gradin, Katarina, Aasrud, Kathrine S, Hoivik, Erling A, Ruas, Jorge L, Poellinger, Lorenz, Bakke, Marit“…Our results also establish CDKN2B as a hypoxia regulated gene, as endogenous CDKN2B mRNA and protein levels were reduced by hypoxic treatment of U2OS cells. CONCLUSIONS: Our data reveal a novel mode of regulation by protein-protein interaction that directly ties together, at the transcriptional level, the Myc- and hypoxia-dependent signaling pathways and expands our understanding of the roles of hypoxia and cell cycle alterations during tumorigenesis.…”
Publicado 2014
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1816por Arrey Tarkang, Protus, Franzoi, Kathrin Diehl, Lee, Sukjun, Lee, Eunyoung, Vivarelli, Diego, Freitas-Junior, Lucio, Liuzzi, Michel, Nolé, Tsabang, Ayong, Lawrence S., Agbor, Gabriel A., Okalebo, Faith A., Guantai, Anastasia N.“…Cytotoxicity testing of Nefang and the solvent extracts on two human cell lines (Hep G2 and U2OS) revealed no significant toxicity relative to their antiplasmodial activities (SI > 20). …”
Publicado 2014
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1817por Fu, Zeze, Deng, Biyong, Liao, Yuxin, Shan, Liancheng, Yin, Fei, Wang, Zhuoying, Zeng, Hui, Zuo, Dongqing, Hua, Yingqi, Cai, Zhengdong“…After 8-hour treatment of shikonin, the expression levels of RIP1 and RIP3 were increased while caspase-3, caspase-6 and PARP were not activated in K7 and U2OS cells determined by Western blot. Size of primary tumor and lung metastasis in shikonin treated group were significantly reduced. …”
Publicado 2013
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1818por Bumke-Vogt, Christiane, Osterhoff, Martin A., Borchert, Andrea, Guzman-Perez, Valentina, Sarem, Zeinab, Birkenfeld, Andreas L., Bähr, Volker, Pfeiffer, Andreas F. H.“…Apigenin and luteolin were identified in our U-2 OS (human osteosarcoma) cell screening assay for micronutrients triggering rapid intracellular translocation of the forkhead box transcription factor O1 (FOXO1), an important mediator of insulin signal transduction. …”
Publicado 2014
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1819Vertebrate Ssu72 Regulates and Coordinates 3′-End Formation of RNAs Transcribed by RNA Polymerase IIpor Wani, Shotaro, Yuda, Masamichi, Fujiwara, Yosuke, Yamamoto, Masaya, Harada, Fumio, Ohkuma, Yoshiaki, Hirose, Yutaka“…Ssu72 depletion in DT40 cells caused defects in 3′-end formation of U2 and U4 snRNAs and GAPDH mRNA. Surprisingly, however, Ssu72 inactivation increased the efficiency of 3′-end formation of non-polyadenylated replication-dependent histone mRNA. …”
Publicado 2014
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1820Clusterin inhibition using OGX-011 synergistically enhances zoledronic acid activity in osteosarcomapor Lamoureux, Francois, Baud'huin, Marc, Ory, Benjamin, Guiho, Romain, Zoubeidi, Amina, Gleave, Martin, Heymann, Dominique, Rédini, Françoise“…METHODS: The combined effects of OGX-011 and ZOL were investigated in vitro on cell growth, viability, apoptosis and cell cycle repartition of ZOL-sensitive or -resistant human OS cell lines (SaOS2, U2OS, MG63 and MNNG/HOS). RESULTS: In OS cell lines, ZOL increased levels of HSPs, especially CLU, in a dose- and time-dependent manner by mechanism including increased HSF1 transcription activity. …”
Publicado 2014
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