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2901“…RESULTS: Body and relative wing size and IDH1 allozyme data show that the intraspecific variation in P. chalceus is high and in the same range as the interspecific variation (P. chalceus versus P. littoralis). …”
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2902por Feingold, Kenneth R., Wang, Yuwei, Moser, Arthur, Shigenaga, Judy K., Grunfeld, Carl“…Expression of PGC1 α and β, coactivators required for PPARs and TR, was also decreased in kidneys of LPS-treated mice, as were mitochondrial genes regulated by PGC1 (Atp5g1, COX5a, Idh3a, and Ndufs8). Decreased renal FA oxidation could be a by-product of the systemic coordinated host response to increase FAs and TGs available for host defense and/or tissue repair. …”
Publicado 2008
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2903por O'Keefe, Louise V., Colella, Alex, Dayan, Sonia, Chen, Qingwen, Choo, Amanda, Jacob, Reuben, Price, Gareth, Venter, Deon, Richards, Robert I.“…Functional relationships between Wwox and either CG6439/isocitrate dehydrogenase (Idh) or Cu–Zn superoxide dismutase (Sod) were confirmed by genetic interactions. …”
Publicado 2011
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2904por Tefferi, A, Abdel-Wahab, O, Cervantes, F, Crispino, J D, Finazzi, G, Girodon, F, Gisslinger, H, Gotlib, J, Kiladjian, J-J, Levine, R L, Licht, J D, Mullally, A, Odenike, O, Pardanani, A, Silver, R T, Solary, E, Mughal, T“…We provide a detailed overview of new mutations with putative epigenetic effects (TET oncogene family member 2 (TET2), additional sex comb-like 1 (ASXL1), isocitrate dehydrogenase (IDH) and enhancer of zeste homolog 2 (EZH2)) and an update on treatment with Janus kinase (JAK) inhibitors, pomalidomide, everolimus, interferon-α, midostaurin and cladribine. …”
Publicado 2011
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2905por Bittencourt, Rosane Isabel, Vassallo, Jose, Chauffaille, Maria de Lourdes Lopes Ferrari, Xavier, Sandra Guerra, Pagnano, Katia Borgia, Nascimento, Ana Clara Kneese, De Souza, Carmino Antonio, Chiattone, Carlos Sergio“…In addition to the JAK2 mutation, other mutations involving TET2 (ten-eleven translocation), LNK (a membrane-bound adaptor protein); IDH1/2 (isocitrate dehydrogenase 1/2 enzyme); ASXL1 (additional sex combs-like 1) genes were found in myeloproliferative neoplasms thus showing the importance of identifying molecular genetic alterations to confirm diagnosis, guide treatment and improve our understanding of the biology of these diseases. …”
Publicado 2012
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2906por Fasan, Annette, Alpermann, Tamara, Haferlach, Claudia, Grossmann, Vera, Roller, Andreas, Kohlmann, Alexander, Eder, Christiane, Kern, Wolfgang, Haferlach, Torsten, Schnittger, Susanne“…CEBPA distal PM was less frequent in patients with mutations in FLT3, NPM1 and TET2 and more frequent in cases with RUNX1 and IDH2R140 mutations. Overall, no association of methylation to prognosis was seen. …”
Publicado 2013
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2907por Gonçalves, Daniela Dib, Benitez, Aline, Lopes-Mori, Fabiana Maria Ruiz, Alves, Lucimara Aparecida, Freire, Roberta Lemos, Navarro, Italmar Teodorico, Santana, Maria Aparecida Zanella, dos Santos, Luís Roberto Alves, Carreira, Teresa, Vieira, Maria Luísa, de Freitas, Julio Cesar“…Although the town of Jataizinho has a human development index (IDH) that was considered to be average (0.733) in the state of Parana, the low social, economic and cultural conditions of the population from small rural properties have resulted in lack of basic information on animal health and direct or indirect contact with the various species of domestic animals, wildlife and ticks have probably contributed to the prevalence levels found. …”
Publicado 2013
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2908por Mao, Pingping, Hever-Jardine, Mary P., Rahme, Gilbert J., Yang, Eric, Tam, Janice, Kodali, Anita, Biswal, Bijesh, Fadul, Camilo E., Gaur, Arti, Israel, Mark A., Spinella, Michael J.“…STK17A overexpression is associated with a significant survival disadvantage among patients with glioma which is independent of age, molecular phenotype, IDH1 mutation, PTEN loss, and alterations in the p53 pathway and partially independent of grade. …”
Publicado 2013
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2909“…There is evidence that genetic mutations in epigenetic regulators (such as DNMT3, IDH1/2 or H3.3) mediate or contribute to these patterns, although a unifying molecular mechanism underlying the global alterations of DNA methylation has largely been elusive. …”
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2910por Liu, Yanwei, Hu, Huimin, Wang, Kuanyu, Zhang, Chuanbao, Wang, Yinyan, Yao, Kun, Yang, Pei, Han, Lei, Kang, Chunsheng, Zhang, Wei, Jiang, Tao“…Established biomarkers of astrocytomas, like IDH1 and TP53 mutation, were not associated with malignant progression. …”
Publicado 2014
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2911por Engle, Elizabeth K., Fisher, Daniel A.C., Miller, Christopher A., McLellan, Michael D., Fulton, Robert S., Moore, Deborah M., Wilson, Richard K., Ley, Timothy J., Oh, Stephen T.“…The fourth clonal group (including IDH1 and RUNX1) was acquired at sAML transformation and was predominantly absent at sAML remission/relapsed PMF. …”
Publicado 2014
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2912por Wan, Shaogui, Wu, Yousheng, Zhou, Xingchun, Chen, Yibing, An, Jiaze, Yu, Xiaohe, Zhang, Huiqing, Yang, Hushan, Xing, Jinliang“…We identified 7 SNPs in SDHC, SDHD, FH, and IDH2 genes to be significantly associated with the RFS of HCC patients. …”
Publicado 2015
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2913“…The TCR subtype was characterized by no IDH1 mutation, and EGFR and Ki-67 overexpression. …”
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2914por Wu, Yi-Hsuan, Chiu, Daniel Tsun-Yee, Lin, Hsin-Ru, Tang, Hsiang-Yu, Cheng, Mei-Ling, Ho, Hung-Yao“…Treatment of G6PD-knockdown cells with siRNA against HSCARG enhanced the DNA binding activity of NF-κB and the expression of TNF-α and MX1, but suppressed the expression of viral genes; however, the overexpression of HSCARG inhibited the antiviral response. Exogenous G6PD or IDH1 expression inhibited the expression of HSCARG, resulting in increased expression of TNF-α and MX1 and reduced viral gene expression upon virus infection. …”
Publicado 2015
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2915por Zhang, Feng, Liu, Yifan, Zhang, Zhiwen, Li, Jie, Wan, Yi, Zhang, Liying, Wang, Yangmei, Li, Xia, Xu, Yuqiao, Fu, Xin, Zhang, Xiumin, Zhang, Ming, Zhang, Zhekai, Zhang, Jing, Yan, Qingguo, Ye, Jing, Wang, Zhe, Chen, Charlie Degui, Lin, Wei, Li, Qing“…In addition, we detected that IDH1 mutation by DNA sequencing was associated with favorable survival within DA. …”
Publicado 2016
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2916por Cao, Chan, Shuai, Ling-Ying, Xin, Xiao-Ping, Liu, Zhi-Tao, Song, Yan-Ling, Zeng, Zhi-Gao“…We did not detect a humped relationship between small mammal diversity and disturbance levels predicted by the intermediate disturbance hypothesis (IDH). Our study highlighted the necessity of conducting manipulated experiments under multiple grazing intensities.…”
Publicado 2016
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2917por Naseri, Nima N., Bonica, Joseph, Xu, Hui, Park, Larry C., Arjomand, Jamshid, Chen, Zhengming, Gibson, Gary E.“…Furthermore, message levels for isocitrate dehydrogenase 1 (IDH1) were markedly increased in in HD lymphoblasts and were responsive to treatments. …”
Publicado 2016
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2918por Nguyen, Quoc-Bao D., Perry, Avital, Graffeo, Christopher S., Nesvick, Cody L., Raghunathan, Aditya, Jentoft, Mark E., O'Neill, Brian P., Morris, Padraig P., Morris, Jonathan M., Van Gompel, Jamie J.“…Pathology confirmed the diagnosis of gliosarcoma, IDH-wildtype (WHO grade IV). Her postoperative course was uneventful and she was discharged at preoperative neurologic baseline. …”
Publicado 2016
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2919por Shahid, Muhammad, Cho, Kyoung Min, Nguyen, Minh Nam, Choi, Tae Gyu, Jo, Yong Hwa, Aryal, Saurav Nath, Yoo, Ji Youn, Yun, Hyeong Rok, Lee, Jae Woong, Eun, Young Gyu, Lee, Ju-Seog, Kang, Insug, Ha, Joohun, Yoon, Hwi-Joong, Kim, Si-Young, Kim, Sung Soo“…By incorporating into histological classification and molecular marker, the 89-gene signature could further stratify patients with 1p/19q co-deletion and IDH1 mutation. Additionally, subset analyses suggested that the 89-gene signature could predict patients who would benefit from adjuvant chemotherapy. …”
Publicado 2016
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2920por Wang, Ming, Zhang, Shaowei, Chuang, Shih-Sung, Ashton-Key, Margaret, Ochoa, Eguzkine, Bolli, Niccolo, Vassiliou, George, Gao, Zifen, Du, Ming-Qing“…We confirmed frequent mutations in TET2 (9/9), DNMT3A (3/9), IDH2 (3/9), RHOA (3/9) and PLCG1 (2/9) as recently reported by others. …”
Publicado 2017
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