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1801por Draaisma, Kaspar, Wijnenga, Maarten M. J., Weenink, Bas, Gao, Ya, Smid, Marcel, Robe, P., van den Bent, Martin J., French, Pim J.“…RESULTS: Of the molecular markers investigated (all genes mutated at a population frequency >1.7 % and frequent chromosomal imbalances) in the entire glioma dataset, 57 were significantly associated with overall survival. Of these, IDH1 or IDH2 mutations are associated with lowest hazard ratio, which confirms IDH as the most important prognostic marker in diffuse gliomas. …”
Publicado 2015
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1802por Reinhardt, Annekathrin, Stichel, Damian, Schrimpf, Daniel, Koelsche, Christian, Wefers, Annika K., Ebrahimi, Azadeh, Sievers, Philipp, Huang, Kristin, Casalini, M. Belén, Fernández-Klett, Francisco, Suwala, Abigail, Weller, Michael, Gramatzki, Dorothee, Felsberg, Joerg, Reifenberger, Guido, Becker, Albert, Hans, Volkmar H., Prinz, Marco, Staszewski, Ori, Acker, Till, Dohmen, Hildegard, Hartmann, Christian, Paulus, Werner, Heß, Katharina, Brokinkel, Benjamin, Schittenhelm, Jens, Buslei, Rolf, Deckert, Martina, Mawrin, Christian, Hewer, Ekkehard, Pohl, Ute, Jaunmuktane, Zane, Brandner, Sebastian, Unterberg, Andreas, Hänggi, Daniel, Platten, Michael, Pfister, Stefan M., Wick, Wolfgang, Herold-Mende, Christel, Korshunov, Andrey, Reuss, David E., Sahm, Felix, Jones, David T. W., Capper, David, von Deimling, Andreas“…In comparison to supratentorial localization, the MC GBM IDH wildtype subclass midline was overrepresented, whereas the MCs GBM IDH wildtype subclass mesenchymal and subclass RTK II were underrepresented in the cerebellum. …”
Publicado 2019
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1803“…It can occur due to sporadic, de novo, mosaic pathogenic variants in the gene encoding isocitrate dehydrogenase 1 (IDH1) or isocitrate dehydrogenase 2 (IDH2). IDH1 variants are associated with endocrine manifestations, such as pituitary adenomas. …”
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1804por Clavreul, Anne, Lemée, Jean-Michel, Soulard, Gwénaëlle, Rousseau, Audrey, Menei, Philippe“…Methods: Eighty-five patients with primary IDH-wildtype GB treated with the standard therapy between 2012 and 2019 were analyzed retrospectively. …”
Publicado 2021
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1805“…High 5MC and DNMT1, and low IDH1 levels were associated with poorer outcome when looking at all canine MCT cases. …”
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1806por Allwohn, Luisa, Wolfgang, Josy, Onken, Julia, Wasilewski, David, Roohani, Siyer, Zips, Daniel, Ehret, Felix, Kaul, David“…MATERIAL AND METHODS: Patients treated for a 1p/19q-codeleted and IDH-mutant ODG were evaluated. The patient and tumor characteristics were analyzed for their influence on PFS and OS. …”
Publicado 2023
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1807“…BACKGROUND: Intradural disc herniations (IDH) are uncommon and can be found in the cervical spine. …”
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1808por Hua, Rongxuan, Li, Qiuxuan, Gao, Han, Wang, Boya, He, Chengwei, Wang, Ying, Zhang, Sitian, Gao, Lei, Shang, Hongwei, Wang, Wen, Xu, Jingdong“…For subgroup analysis, we analyzed multiple factors including iso-citrate dehydrogenase (IDH) genotype, age, diagnosis, pTERT region, so as to locate the sources of heterogeneity. …”
Publicado 2023
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1809por Valery, Marine, Vasseur, Damien, Fachinetti, Francesco, Boilève, Alice, Smolenschi, Cristina, Tarabay, Anthony, Antoun, Leony, Perret, Audrey, Fuerea, Alina, Pudlarz, Thomas, Boige, Valérie, Hollebecque, Antoine, Ducreux, Michel“…About 40% of BTC bear a targetable molecular alteration, the most frequent being FGFR2 fusions and IDH1 mutations in about 15% of intrahepatic cholangiocarcinomas. …”
Publicado 2023
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1810por Ottoman, Oscar, Chalamila, Athuman, Mgaya, Evarista, Kanji, Raheel, Magambo, Magreth, Rambau, Peter“…Molecular genetics study of IDH-mutant is used for WHO grading and management of the oligodendrogliomas lesions. …”
Publicado 2023
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1811“…Almost 70% of the cases were both IDH-1 and p53 wild-type, and we observed the presence of both mutations in only 3.7% of the cases. …”
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1812por Zhang, Nengyi, Gur, Amit, Gibon, Yves, Sulpice, Ronan, Flint-Garcia, Sherry, McMullen, Michael D., Stitt, Mark, Buckler, Edward S.“…Using candidate gene association mapping, we identified that this non-synonymous polymorphism was associated with IDH activity variation. The proposed mechanism for the IDH activity variation includes additional components regulating protein level. …”
Publicado 2010
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1813por Munthe, Sune, Petterson, Stine Asferg, Dahlrot, Rikke Hedegaard, Poulsen, Frantz Rom, Hansen, Steinbjørn, Kristensen, Bjarne Winther“…We identified 26 gliomas having the R132 mutation in Isocitrate DeHydrogenase 1 (mIDH1). A double immunofluorescence approach identifying mIDH1 positive tumor cells and a panel of markers was used. …”
Publicado 2016
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1814por Lohkamp, Laura-Nanna, Schinz, Maren, Gehlhaar, Claire, Guse, Katrin, Thomale, Ulrich-Wilhelm, Vajkoczy, Peter, Heppner, Frank L., Koch, Arend“…BRAF V600E mutations were detected in 50% of the PXA but not in any of the gcGBM (50% vs. 0%, p-value < 0.001). IDH1 R132 and IDH R172 mutations were not present in any of the PXA and gcGBM cases. …”
Publicado 2016
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1815por Nguyen, T B, Sakata-Yanagimoto, M, Asabe, Y, Matsubara, D, Kano, J, Yoshida, K, Shiraishi, Y, Chiba, K, Tanaka, H, Miyano, S, Izutsu, K, Nakamura, N, Takeuchi, K, Miyoshi, H, Ohshima, K, Minowa, T, Ogawa, S, Noguchi, M, Chiba, S“…TET2 and DNMT3A mutations were identified in both the PD1+ cells and the CD20+ cells in 15/16 and 4/7 cases, respectively. All the RHOA and IDH2 mutations were confined to the PD1+ cells, indicating that some, including RHOA and IDH2 mutations, being specific events in tumor cells. …”
Publicado 2017
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1816“…METHODS: We retrospectively reviewed 143 cases with both molecular information (IDH1/TERT/1p19q) and MRI images diagnosed as cerebral diffuse gliomas. …”
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1817por Cedena, M. Teresa, Rapado, Inmaculada, Santos-Lozano, Alejandro, Ayala, Rosa, Onecha, Esther, Abaigar, María, Such, Esperanza, Ramos, Fernando, Cervera, José, Díez-Campelo, María, Sanz, Guillermo, Rivas, Jesús Hernández, Lucía, Alejandro, Martínez-López, Joaquin“…However, total number of mutations/patient was negatively associated with overall drug response (odds ratio [OR]: 0.56, 95% confidence interval [CI]: 0.33–0.94; p=0.028), and a positive association was found for having ≥1 mutation in a DNA methylation-related gene: TET2, DNMT3A, IDH1 and/or IDH2 (OR: 4.76, 95%CI: 1.31–17.27; p=0.017). …”
Publicado 2017
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1818por Bronk, Julianna K., Guha-Thakurta, Nandita, Allen, Pamela K., Mahajan, Anita, Grosshans, David R., McGovern, Susan L.“…There was no difference in PsP rate based on radiation type, radiation dose, tumor grade, 1p19q codeletion, or IDH status. PsP occurred earlier in oligodendroglioma patients treated with protons compared to photons, 48 days vs. 131 days, p < .01. …”
Publicado 2018
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1819por Manso, Rebeca, González-Rincón, Julia, Rodríguez-Justo, Manuel, Roncador, Giovanna, Gómez, Sagrario, Sánchez-Beato, Margarita, Piris, Miguel A., Rodríguez-Pinilla, Socorro M.“…PLCG1 was mutated in 14.3%, IDH2 in 11.2% and DNMT3A in 7.1% of cases, respectively. …”
Publicado 2018
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1820“…In 36 patients with isocitrate dehydrogenases 1 and 2 (IDH1/2) data, only one had IDH1 mutation and no patient had IDH2 mutation. …”
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