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3281por Chakravarty, Sumana, Reddy, Bommana R., Sudhakar, Sreesha R., Saxena, Sandeep, Das, Tapatee, Meghah, Vuppalapaty, Brahmendra Swamy, Cherukuvada V., Kumar, Arvind, Idris, Mohammed M.“…The most affected process was mitochondrial function, 4 of the 18 differentially regulated proteins were mitochondrial proteins: PHB2, SLC25A5, VDAC3 and IDH2, as reported in rodent and clinical samples. …”
Publicado 2013
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3282por Bieńkowski, Michał, Piaskowski, Sylwester, Stoczyńska-Fidelus, Ewelina, Szybka, Małgorzata, Banaszczyk, Mateusz, Witusik-Perkowska, Monika, Jesień-Lewandowicz, Emilia, Jaskólski, Dariusz J., Radomiak-Załuska, Anna, Jesionek-Kupnicka, Dorota, Sikorska, Beata, Papierz, Wielisław, Rieske, Piotr, Liberski, Paweł P.“…The aim of our study was to analyse whether the molecular markers of glioblastoma (i.e. TP53 and IDH1 mutations, CDKN2A deletion, EGFR amplification, chromosome 7 polysomy and EGFRvIII expression) could be associated with distinct prognosis and/or response to the therapy. …”
Publicado 2013
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3283por Torres-Martín, Miguel, Peña-Granero, Carolina, Carceller, Fernando, Gutiérrez, Manuel, Burbano, Rommel R, Pinto, Giovanny R, Castresana, Javier S, Melendez, Bárbara, Rey, Juan A“…No sequence changes for R132 and R172 of the IDH1/2 genes were identified. CONCLUSIONS: The molecular findings in this pediatric anaplastic glioma do not allow for a clearly definitive pathological diagnosis. …”
Publicado 2014
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3284por Chen, T-C, Hou, H-A, Chou, W-C, Tang, J-L, Kuo, Y-Y, Chen, C-Y, Tseng, M-H, Huang, C-F, Lai, Y-J, Chiang, Y-C, Lee, F-Y, Liu, M-C, Liu, C-W, Liu, C-Y, Yao, M, Huang, S-Y, Ko, B-S, Hsu, S-C, Wu, S-J, Tsay, W, Chen, Y-C, Tien, H-F“…ASXL1 mutation was closely associated with trisomy 8 and mutations of RUNX1, EZH2, IDH, NRAS, JAK2, SETBP1 and SRSF2, but was negatively associated with SF3B1 mutation. …”
Publicado 2014
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3285por Wang, Hongjun, Zhao, Yan, Zhang, Chuanbao, Li, Mingyang, Jiang, Chuanlu, Li, Yongli“…Rab27a also showed a mesenchymal subtype, G3 subtype and isocitrate dehydrogenase 1 (IDH1) wild-type preference and association with migration. …”
Publicado 2014
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3286por Renneville, Aline, Abdelali, Raouf Ben, Chevret, Sylvie, Nibourel, Olivier, Cheok, Meyling, Pautas, Cécile, Duléry, Rémy, Boyer, Thomas, Cayuela, Jean-Michel, Hayette, Sandrine, Raffoux, Emmanuel, Farhat, Hassan, Boissel, Nicolas, Terre, Christine, Dombret, Hervé, Castaigne, Sylvie, Preudhomme, Claude“…In the present study, we performed mutational analysis of 11 genes (FLT3, NPM1, CEBPA, MLL, WT1, IDH1/2, RUNX1, ASXL1, TET2, DNMT3A), EVI1 overexpression screening, and 6.0 single-nucleotide polymorphism array (SNP-A) analysis in diagnostic samples of the 278 AML patients enrolled in the ALFA-0701 trial. …”
Publicado 2014
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3287por Holmberg Olausson, Karl, Maire, Cecile L., Haidar, Sam, Ling, Jason, Learner, Emily, Nistér, Monica, Ligon, Keith L.“…Within proneural subclass tumors, high PROM1 expression correlates inversely with IDH1 (R132H) mutation. These findings support PROM1 as a tumor cell-intrinsic marker related to GBM survival, independent of its stem cell properties, and highlight potentially divergent roles for this protein in normal mouse and human glia.…”
Publicado 2014
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3290por Rodón, Jordi, Carducci, Michael, Sepulveda-Sánchez, Juan M., Azaro, Analía, Calvo, Emiliano, Seoane, Joan, Braña, Irene, Sicart, Elisabet, Gueorguieva, Ivelina, Cleverly, Ann, Pillay, N. Sokalingum, Desaiah, Durisala, Estrem, Shawn T., Paz-Ares, Luis, Holdhoff, Matthias, Blakeley, Jaishri, Lahn, Michael M., Baselga, Jose“…Of the 5 patients with IDH1/2 mutation, 4 patients had a clinical benefit as defined by CR/PR and SD ≥6 cycles. …”
Publicado 2014
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3291por Mock, Andreas, Warta, Rolf, Geisenberger, Christoph, Bischoff, Ralf, Schulte, Alexander, Lamszus, Katrin, Stadler, Volker, Felgenhauer, Thomas, Schichor, Christian, Schwartz, Christoph, Matschke, Jakob, Jungk, Christine, Ahmadi, Rezvan, Sahm, Felix, Capper, David, Glass, Rainer, Tonn, Jörg-Christian, Westphal, Manfred, von Deimling, Andreas, Unterberg, Andreas, Bermejo, Justo Lorenzo, Herold-Mende, Christel“…Next, survival associations were investigated in two retrospective independent multicenter validation sets (n=61, n=129, all IDH1-wildtype). Reliability of measurements was tested using a second array technology (spotted arrays). …”
Publicado 2015
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3292“…Based on transcriptomic sequencing data from O. fragrans buds at four developmental stages, six reference genes (OfACT, OfEF1α, OfIDH, OfRAN1, OfTUB, and OfUBC2) with stable expression (0.5 to 2 fold change in expression levels between any two developmental stages), as well as the commonly used reference gene Of18S, were selected as candidates for gene expression normalization in the RT-qPCR analysis of O. fragrans. …”
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3293por Ayenew, Biruk, Degu, Asfaw, Manela, Neta, Perl, Avichai, Shamir, Michal O., Fait, Aaron“…The trend of increment in TCA cycle genes like ATCs, ACo1, and IDH in the combined treatment might support the observed increment in organic acids, GABA shunt, and their derivatives. …”
Publicado 2015
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3294“…Following the Intermediate Disturbance Hypothesis (IDH), moderate levels of disturbance (either frequency or intensity) are expected to enhance species richness. …”
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3295por Pan, Qiong, Hu, Hao, Han, Liangrong, Jing, Xin, Liu, Hailiang, Yang, Chuanchun, Zhang, Fengting, Hu, Yue, Yue, Hongni, Ning, Ying“…In particular, TPM1, SMAD6, SMAD3, and HCN4 may be associated with her heart defects, and HEXA, KIF7, and IDH2 are responsible for her developmental and mental retardation. …”
Publicado 2016
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3296por Inoue, Akihiro, Ohnishi, Takanori, Kohno, Shohei, Mizuno, Yosuke, Kitazawa, Riko, Nakamura, Yawara, Ohue, Shiro“…Immunohistochemistry revealed that most tumor cells were positively stained for both p53 and EGFR but negatively stained for isocitrate dehydrogenase 1 (IDH1). CONCLUSIONS: We reported a case of multicentric gliomas occurring in both supra- and infratentorial regions with different histopathology. …”
Publicado 2016
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3297por Iqbal, Zeeshan Muhammad, Akbar, Haji, Hosseini, Afshin, Bichi Ruspoli Forteguerri, Elena, Osorio, Johan S., Loor, Juan J.“…Along with the upregulation of G6PD and IDH1, important for NADPH synthesis during lipogenesis, and the basal glucose transporter SLC2A1, these data indicated a pro-lipogenic response in the digital cushion with OVE. …”
Publicado 2016
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3298por Martínez‐Sáez, Elena, Peg, Vicente, Ortega‐Aznar, Arantxa, Martínez‐Ricarte, Francisco, Camacho, Jessica, Hernández‐Losa, Javier, Ferreres Piñas, Joan Carles, Ramón y Cajal, Santiago“…Immunohistochemistry and PCR were used for IDH1 mutations. Statistical analysis was based on the following tests: chi‐square, Student's t, Pearson correlation, Spearman's rho, and Mann–Whitney; ROC and Kaplan–Meier curves were constructed. …”
Publicado 2016
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3299por Sun, Q-Y, Ding, L-W, Tan, K-T, Chien, W, Mayakonda, A, Lin, D-C, Loh, X-Y, Xiao, J-F, Meggendorfer, M, Alpermann, T, Garg, M, Lim, S-L, Madan, V, Hattori, N, Nagata, Y, Miyano, S, Yeoh, A E J, Hou, H-A, Jiang, Y-Y, Takao, S, Liu, L-Z, Tan, S-Z, Lill, M, Hayashi, M, Kinoshita, A, Kantarjian, H M, Kornblau, S M, Ogawa, S, Haferlach, T, Yang, H, Koeffler, H P“…Interestingly, clonality analysis suggests that IDH2/1, DNMT3A, U2AF1 and TET2 mutations are clonal and occur early, and MLL-PTD likely arises after these initial mutations. …”
Publicado 2017
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3300por Nazha, A, Zarzour, A, Al-Issa, K, Radivoyevitch, T, Carraway, H E, Hirsch, C M, Przychodzen, B, Patel, B J, Clemente, M, Sanikommu, S R, Kalaycio, M, Maciejewski, J P, Sekeres, M A“…Overall, mutations in FLT3, DNMT3A, NPM1 and IDH2 were more specific for pAML whereas UTAF1, STAG2, BCORL1, BCOR, EZH2, JAK2, CBL, PRPF8, SF3B1, ASXL1 and DHX29 were more specific for sAML. …”
Publicado 2016
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