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2921por Sinha, Subarna, Thomas, Daniel, Chan, Steven, Gao, Yang, Brunen, Diede, Torabi, Damoun, Reinisch, Andreas, Hernandez, David, Chan, Andy, Rankin, Erinn B., Bernards, Rene, Majeti, Ravindra, Dill, David L.“…We extensively validate a SL interaction identified by MiSL between the IDH1 mutation and ACACA in leukaemia using gene targeting and patient-derived xenografts. …”
Publicado 2017
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2922por Murnyák, Balázs, Kouhsari, Mahan C., Hershkovitch, Rotem, Kálmán, Bernadette, Marko-Varga, György, Klekner, Álmos, Hortobágyi, Tibor“…We collected genomic and clinical data from the latest glioma datasets of The Cancer Genome Atlas and performed PARP1, ATRX, IDH1, and p53 immunohistochemistry on GBM tissue samples. …”
Publicado 2017
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2923“…In an analysis further stratified by clinical characteristics at baseline, the association between lower levels of 5-mC% and glioma risk was evident only among younger participants (age <52 years), women, and those with aggressive tumor characteristics, such as glioblastoma subtype, high tumor grade (grade III or IV), and absence of IDH1 mutation. Our findings indicate that global DNA hypomethylation in leukocytes may contribute to the development of glioma and that the association is affected by age, sex, and tumor aggressiveness.…”
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2924por Helbig, Doris, Quaas, Alexander, Mauch, Cornelia, Merkelbach-Bruse, Sabine, Büttner, Reinhard, Emberger, Michael, Wobser, Marion, Rüsseler, Vanessa, Pütz, Katharina, Binot, Elke, Rehker, Jan, Budczies, Jan, Ihle, Michaela Angelika“…In addition to BRAF, KNSTRN, IDH1 and PDGFRA amplification, CNV analyses revealed deletions in the CDKN2A, KIT and PDGFRA genes. …”
Publicado 2017
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2925por Stasik, S., Schuster, C., Ortlepp, C., Platzbecker, U., Bornhäuser, M., Schetelig, J., Ehninger, G., Folprecht, G., Thiede, C.“…The integration of NGS results for several common point mutations in various oncogenes (i.e. IDH1 and 2, c-KIT, DNMT3A, NRAS, KRAS, BRAF) revealed that the prevalent transition vs. transversion bias (3.57:1) has an impact on site-specific detection limits of low-level mutations. …”
Publicado 2018
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2926“…These include fibroblast growth factor receptor (FGFR), isocitrate dehyrogenase 1 (IDH1), epidermal growth factor receptor (EGFR), and BRAF genetic aberrations. …”
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2927por Ceccon, Garry, Werner, Jan-Michael, Dunkl, Veronika, Tscherpel, Caroline, Stoffels, Gabriele, Brunn, Anna, Deckert, Martina, Fink, Gereon R., Galldiks, Norbert“…At this time point, recurrent tumor histology revealed an epithelioid glioblastoma, without a mutation in the isocitrate dehydrogenase gene (IDH wild-type). In order to identify a potential target for an experimental salvage therapy, mutational tumor analysis showed a BRAF V600E mutation. …”
Publicado 2018
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2928por Han, Mingzhi, Xu, Ran, Wang, Shuai, Yang, Ning, Ni, Shilei, Zhang, Qing, Xu, Yangyang, Zhang, Xin, Zhang, Chao, Wei, Yuzhen, Ji, Jianxiong, Huang, Bin, Zhang, Di, Chen, Anjing, Li, Wenjie, Bjerkvig, Rolf, Li, Xingang, Wang, Jian“…Through analysis of publicly available databases, we found that STEAP3 was highly expressed in malignant gliomas, especially in the mesenchymal glioma molecular subtype and isocitrate dehydrogenase 1/2 (IDH1/2) wild-type gliomas. Expression levels of STEAP3 in gliomas correlated inversely with patient overall survival (OS) and served as an independent prognostic marker by multivariate Cox regression analysis. …”
Publicado 2018
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2929por Saif, Aneeqa, Kazmi, Syed Faheem Ali, Naseem, Rabia, Shah, Haider, Butt, Mohammad Omar“…Moreover, mutations affecting cellular metabolism like isocitrate dehydrogenase (IDH1), lysine-specific demethylase 1 (LSD 1), and nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) have become a huge success by providing targets for novel therapeutic drugs. …”
Publicado 2018
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2930“…Third, by identifying the biologically consistent phenotype among the WGS-profiled tumors, the GBM pattern proves to be a technology-independent predictor of survival and response to chemotherapy and radiation, statistically better than the patient's age and tumor's grade, the best other indicators, and MGMT promoter methylation and IDH1 mutation. We conclude that by using the complex structure of the data, comparative spectral decompositions underlie a mathematically universal description of the genotype-phenotype relations in cancer that other methods miss.…”
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2931“…Hot air treatment could induced CitAco2/3, CitIDH2/3, CitGAD4, CitACLs, CitPEPCKs and CitFBPases expression during fruit storage period, but had no significant effect on CitGSs expression, The enhanced expression of degradation-related genes was closely related to the degradation of citric acid. …”
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2932por Breckwoldt, Michael O., Bode, Julia, Sahm, Felix, Krüwel, Thomas, Solecki, Gergely, Hahn, Artur, Wirthschaft, Peter, Berghoff, Anna S., Haas, Maximilian, Venkataramani, Varun, von Deimling, Andreas, Wick, Wolfgang, Herold-Mende, Christel, Heiland, Sabine, Platten, Michael, Bendszus, Martin, Kurz, Felix T., Winkler, Frank, Tews, Björn“…We compare infiltration and neoangiogenesis patterns in four brain tumor models and the human disease: whereas the U87MG glioma model resembles brain metastases with an encapsulated growth and extensive neoangiogenesis, S24 experimental gliomas mimic IDH1 wildtype glioblastomas, exhibiting infiltration into the adjacent parenchyma and along white matter tracts to the contralateral hemisphere. …”
Publicado 2019
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2933por Chai, Rui-Chao, Wu, Fan, Wang, Qi-Xue, Zhang, Shu, Zhang, Ke-Nan, Liu, Yu-Qing, Zhao, Zheng, Jiang, Tao, Wang, Yong-Zhi, Kang, Chun-Sheng“…Compared with the RM1 subgroup, the RM2 subgroup correlates with a poorer prognosis, higher WHO grade, and lower frequency of IDH mutation. Moreover, the hallmarks of epithelial-mesenchymal transition and TNFα signaling via NF-κB are also significantly enriched in the RM2 subgroup. …”
Publicado 2019
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2934por Ainelo, Andres, Porosk, Rando, Kilk, Kalle, Rosendahl, Sirli, Remme, Jaanus, Hõrak, Rita“…Secondly, proteome data indicated that GraT induces downregulation of central carbon metabolism, as suggested by the decreased levels of TCA cycle enzymes isocitrate dehydrogenase Idh, α-ketoglutarate dehydrogenase subunit SucA, and succinate-CoA ligase subunit SucD. …”
Publicado 2019
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2935“…Applied to study reductive glutamine metabolism in cancer cells, shown to mediate fatty acid biosynthesis under hypoxia and defective mitochondria, we find a previously unappreciated role of reductive IDH1 as the sole net contributor of carbons to fatty acid biosynthesis under standard normoxic conditions in HeLa cells. …”
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2936por Wojtas, Bartosz, Gielniewski, Bartlomiej, Wojnicki, Kamil, Maleszewska, Marta, Mondal, Shamba S., Nauman, Pawel, Grajkowska, Wieslawa, Glass, Rainer, Schüller, Ulrich, Herold-Mende, Christel, Kaminska, Bozena“…Gliosarcoma is a very rare brain tumor reported to be a variant of glioblastoma (GBM), IDH-wildtype. While differences in molecular and histological features between gliosarcoma and GBM were reported, detailed information on the genetic background of this tumor is lacking. …”
Publicado 2019
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2937“…RESULTS: Venetoclax has demonstrated promising results in preclinical and clinical trials, especially in patients with poor prognosis and the IDH mutation, with an excellent side-effect profile. …”
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2938“…Comparative analysis showed that the genome of strain DM2 encodes some strain-specific proteins in comparison with B. subtilis subsp. subtilis str. 168, such as carboxymuconolactone decarboxylase family protein, gfo/Idh/MocA family oxidoreductases, GlsB/YeaQ/YmgE family stress response membrane protein, HlyC/CorC family transporters, LLM class flavin-dependent oxidoreductase, and LPXTG cell wall anchor domain-containing protein. …”
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2939por Potharaju, Mahadev, Mathavan, Anugraha, Mangaleswaran, Balamurugan, Patil, Sushama, John, Reginald, Ghosh, Siddhartha, Kalavakonda, Chandrasekhar, Ghosh, Mitra, Verma, Rama Shanker“…We studied the association of immunohistochemical expression of hypoxia inducible factor-1 alpha (HIF-1α), telomerase reverse transcriptase (TERT), isocitrate dehydrogenase 1 (IDH1) and tumor protein p53 with overall survival (OS) in glioblastoma patients uniformly treated by standard of care, with adequate follow-up. …”
Publicado 2019
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2940“…Recurrent genetic mutations found in AML have been intensely studied from a cell intrinsic perspective leading to the genesis of multiple, recently approved targeted therapies including IDH1/2-mutant inhibitors and FLT3-ITD/-TKD inhibitors. …”
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