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2141por Sumitomo, Yasuhiko, Higashitsuji, Hiroaki, Higashitsuji, Hisako, Liu, Yu, Fujita, Takanori, Sakurai, Toshiharu, Candeias, Marco M, Itoh, Katsuhiko, Chiba, Tsutomu, Fujita, Jun“…When 3 copies of MCRE were placed upstream of the CMV promoter and used in transient transfection, reporter gene expression was increased 3- to 7-fold at 32°C relative to 37°C in various cell lines including HEK293, U-2 OS, NIH/3T3, BALB/3T3 and CHO-K1 cells. In stable transfectants, MCRE also enhanced the reporter gene expression at 32°C, although more copy numbers of MCRE were necessary. …”
Publicado 2012
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2142por Zaw, Myo Thura, Yamasaki, Eiki, Yamamoto, Shingo, Nair, G Balakrish, Kawamoto, Keiko, Kurazono, Hisao“…BACKGROUND: The uropathogenic specific protein (Usp) and three OrfU proteins (OrfU1, OrfU2 and OrfU3) are encoded in the putative small pathogenicity island which is closely associated with Uropathogenic Escherichia coli. …”
Publicado 2013
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2143por Grimbizis, Grigoris F., Gordts, Stephan, Di Spiezio Sardo, Attilio, Brucker, Sara, De Angelis, Carlo, Gergolet, Marco, Li, Tin-Chiu, Tanos, Vasilios, Brölmann, Hans, Gianaroli, Luca, Campo, Rudi“…Anomalies are classified into the following main classes, expressing uterine anatomical deviations deriving from the same embryological origin: U0, normal uterus; U1, dysmorphic uterus; U2, septate uterus; U3, bicorporeal uterus; U4, hemi-uterus; U5, aplastic uterus; U6, for still unclassified cases. …”
Publicado 2013
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2144por Rehman, Sadia, Ikram, Muhammad, Khan, Ajmal, Min, Soyoung, Azad, Effat, Hofer, Thomas S, Mok, KH, Baker, Robert J, Blake, Alexander J, Rehman, Saeed Ur“…Both the compounds were studied subsequently for the U2OS tumoricidal activity and it was found that L has LD(50) value of 200 μM whereas the sodium analog cytotoxicity did not drop down below 60%. …”
Publicado 2013
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2145por Dong, Yuan, Cui, Cheng-Bin, Li, Chang-Wei, Hua, Wei, Wu, Chang-Jing, Zhu, Tian-Jiao, Gu, Qian-Qun“…The followed isolation and characterization demonstrated that six metabolites, cyclo(d-Pro-d-Phe) (1), cyclo(d-Tyr-d-Pro) (2), phenethyl 5-oxo-l-prolinate (3), cyclo(l-Ile-l-Pro) (4), cyclo(l-Leu-l-Pro) (5) and 3β,5α,9α-trihydroxy-(22E,24R)-ergosta-7,22-dien-6-one (6), were newly produced by the mutant u2n2h3-3 compared to the parent ZBY-3 strain. Compound 3 was a new compound; 2 was isolated from a natural source for the first time, and all of these compounds were also not yet found in the metabolites of other A. versicolor strains. …”
Publicado 2014
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2146“…The knockdown of S100A9 induced by RNA interference (RNAi) method in three osteosarcoma cell lines (U2OS, 143B, MG63) was applied to analyze the effects of S100A9 on cell proliferation, cell cycle distribution, migration, invasion and xenotransplanted tumors. …”
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2147por Hwang, Sang Mee, Kim, Seon Young, Kim, Jung Ah, Park, Hee-Sue, Park, Si Nae, Im, Kyongok, Kim, Kwantae, Kim, Sung-Min, Lee, Dong Soon“…However, those patients with a high percentage (≥80 %) of cells with short TL showed poorer overall survival (P = 0.021), and this was an independent prognostic factor, along with TP53, U2AF1 mutation, and high BM blast count (P = 0.044, 0.001, 0.004, 0.012, respectively). …”
Publicado 2016
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2148por Celeghin, Andrea, Giunco, Silvia, Freguja, Riccardo, Zangrossi, Manuela, Nalio, Silvia, Dolcetti, Riccardo, De Rossi, Anita“…All these effects occurred within 72 h and were not observed in BIBR-treated TERT-negative 4134/TERT- and U2OS cells. The cell cycle arrest and apoptosis, consequent upon short-term TERT inhibition, were associated with and likely dependent on the activation of the DNA damage response (DDR), highlighted by the increased levels of γH2AX and activation of ATM and ATR pathways. …”
Publicado 2016
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2149por Belayachi, Lamiae, Aceves-Luquero, Clara, Merghoub, Nawel, de Mattos, Silvia Fernández, Amzazi, Saaîd, Villalonga, Priam, Bakri, Youssef“…The plant was extracted using organic solvents, and four different extracts were screened on Jurkat, Jeko-1, TK-6, LN229, SW620, U2OS, PC-3 and NIH3T3 cells. RESULTS: Cell viability assays revealed that, the IC50 values were (11,63±5,37μg/ml) for Jurkat, (13,33±1,67μg/ml) for Jeko-1, (41,67±1,98μg/ml) for LN229 and (19,31±4,88μg/ml) for PC-3 cells upon treatment with Oe-DF and Oe-HE respectively. …”
Publicado 2017
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2150“…TUG1 knockdown induced miR-144-3p expression in MG63 and U2OS cell lines. Results from dual luciferase reporter assay, RNA-binding protein immuno precipitation (RIP) and applied biotin-avidin pull-down system confirmed TUG1 regulated miR-144-3p expression through direct binding. …”
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2151por Donkers, Joanne M., Zehnder, Benno, van Westen, Gerard J. P., Kwakkenbos, Mark J., IJzerman, Adriaan P., Oude Elferink, Ronald P. J., Beuers, Ulrich, Urban, Stephan, van de Graaf, Stan F. J.“…This study aims to identify clinically-applied compounds intervening with NTCP-mediated bile acid transport and HBV/HDV infection. 1280 FDA/EMA-approved drugs were screened to identify compounds that reduce uptake of taurocholic acid and lower Myrcludex B-binding in U2OS cells stably expressing human NTCP. HBV/HDV viral entry inhibition was studied in HepaRG cells. …”
Publicado 2017
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2152“…We evaluated the RhoA activation in osteosarcoma MG-63 and U2OS cells with RhoA activation assay. A panel of inhibitors of PI3K and Akt treated osteosarcoma cells and blocked kinase activity. …”
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2153“…Six LacI-family transcriptional factors (named AbfR, AauR, AauU1, AauU2, BauR1 and BauR2) and a TetR-family regulator (XsaR) presumably act as local repressors for AOS utilization genes encoding various α- or β-L-arabinofuranosidases and predicted AOS transporters. …”
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2154Disturbed alternative splicing of FIR (PUF60) directed cyclin E overexpression in esophageal cancerspor Ogura, Yukiko, Hoshino, Tyuji, Tanaka, Nobuko, Ailiken, Guzhanuer, Kobayashi, Sohei, Kitamura, Kouichi, Rahmutulla, Bahityar, Kano, Masayuki, Murakami, Kentarou, Akutsu, Yasunori, Nomura, Fumio, Itoga, Sakae, Matsubara, Hisahiro, Matsushita, Kazuyuki“…Conversely, c-myc gene transcriptional repressor FIR (alias PUF60; U2AF-related protein) and its alternative splicing variant form (FIRΔexon2) were overexpressed in ESCC. …”
Publicado 2018
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2155por Maitre, Elsa, Bertrand, Philippe, Maingonnat, Catherine, Viailly, Pierre-Julien, Wiber, Margaux, Naguib, Dina, Salaün, Véronique, Cornet, Edouard, Damaj, Gandhi, Sola, Brigitte, Jardin, Fabrice, Troussard, Xavier“…We selected a panel of 21 relevant genes based on a literature review of whole exome sequencing studies (BRAF, MAP2K1, DUSP2, MAPK15, ARID1A, ARID1B, EZH2, KDM6A, CREBBP, TP53, CDKN1B, XPO1, KLF2, CXCR4, NOTH1, NOTCH2, MYD88, ANXA1, U2AF1, BCOR, and ABCA8). We analyzed 20 HCL-c and 4 HCL-v patients. …”
Publicado 2018
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2156por Tefferi, Ayalew, Guglielmelli, Paola, Nicolosi, Maura, Mannelli, Francesco, Mudireddy, Mythri, Bartalucci, Niccolo, Finke, Christy M., Lasho, Terra L., Hanson, Curtis A., Ketterling, Rhett P., Begna, Kebede H., Naseema Gangat, Pardanani, Animesh, Vannucchi, Alessandro M.“…Among 641 cytogenetically annotated patients with PMF and informative for previously recognized adverse mutations, multivariable analysis identified “VHR” karyotype, “unfavorable” karyotype, absence of type 1/like CALR mutation and presence of ASXL1, SRSF2, or U2AF1Q157 mutation, as inter-independent predictors of inferior survival; the respective HRs (95% CI) were 3.1 (2.1–4.3), 2.1 (1.6–2.7), 2.1 (1.6–2.9), 1.8 (1.5–2.3), 2.4 (1.9–3.2), and 2.4 (1.7–3.3). …”
Publicado 2018
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2157“…Inhibition of CDR1as in OS cell lines U2OS and MG63 with high CDR1as levels, leading to de-repressed miR-7 levels, impaired cell vitality and increased apoptosis and G1/S arrest in parallel with reduced ability of cell migration, which, however, could be restored by miR-7 inhibitor. …”
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2158“…The random variable u ∼ N (0, σ(u)(2)) indicated a pen level HP standard deviation σ(u) = 12.1 kcal/kg(0.68). …”
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2159“…METHODS: A total of 18 fixed-bearing U2 total knee arthroplasty system implants (United Orthopedic Corp., Hsinchu, Taiwan) were used. …”
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2160“…Cubic spline dose-response meta-analysis yielded RRs as follows: across the global range for GL (55-290 g/d), 5.5 (95% CI, 3.1-9.8) (I(2)=0); for GI (47-82 U), 2.71 (95% CI, 1.47-4.40) (I(2)=0); and for the CHD-carbohydrate dependence on GI (50-80 U), 4.57 (95% CI, 1.86-11.4) (I(2)=16%). …”
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