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3061por Mäder, Lisa, Blank, Anna E., Capper, David, Jansong, Janina, Baumgarten, Peter, Wirsik, Naita M., Zachskorn, Cornelia, Ehlers, Jakob, Seifert, Michael, Klink, Barbara, Liebner, Stefan, Niclou, Simone, Naumann, Ulrike, Harter, Patrick N., Mittelbronn, Michel“…We investigated 350 glioma patients for the expression of the key EMT factors SLUG and TWIST by immunohistochemistry and immunofluorescence related to morpho-genetic alterations such as EGFR-amplification, IDH-1 (R132H) mutation and 1p/19q LOH. Furthermore, transcriptional cluster and survival analyses were performed. …”
Publicado 2018
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3062por Brogna, Christian, Lavrador, José Pedro, Patel, Sabina, Vergani, Francesco, Bassi, Sanjeev, Grahovac, Gordan, Bhangoo, Ranjeev, Ashkan, Keyoumars“…BACKGROUND: Intradural disc herniations (IDH) are rare, particularly in the cervical spine, where they account for less than 5% of all discs. …”
Publicado 2018
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3063“…Mutations in certain mitochondrial proteins, such as IDH2 have been shown to contribute to leukemogenesis. …”
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3064por Kong, Min Jung, Bak, Sang Hong, Han, Ki-Hwan, Kim, Jee In, Park, Jeen-Woo, Park, Kwon Moo“…In contrast, isocitrate dehydrogenase 2 (Idh2) gene deletion, which results in defect of the NADPH-associated mitochondrial antioxidant system, exacerbated cisplatin-induced changes in mice. …”
Publicado 2018
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3065por Kuthuru, Srikanth, Deaderick, William, Bai, Harrison, Su, Chang, Vu, Tiep, Monga, Vishal, Rao, Arvind“…Using a publicly available data set of magnetic resonance imaging images from patients diagnosed with low-grade gliomas, we demonstrated that the dictionary-based model performs well in predicting 2 biomarkers of interest (1p/19q codeletion and IDH1 mutation). Furthermore, the visual regions (atoms) associated with these dictionaries show association with key molecular pathways implicated in gliomagenesis. …”
Publicado 2018
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3066por Li, Benyi“…So far, multiple efforts have focused on single specific metabolic enzymes responsible for the altered Krebs cycle in human cancers, including metformin for ETC complex I, IDH1/2 inhibitors, PDH inhibitor CPI-613, MPC1/2 inhibitor UK5099, MCT1 inhibitor AZD3965, CPT1 inhibitors etomoxir/perhexiline/ST1326, FASN inhibitor orlistat/TVB-2640, MCD inhibitor CBM-301106, ACAA2 inhibitor trimetazidine. …”
Publicado 2018
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3067“…However, CAP also affected bacterioferritin (Bfr), Isocitrate dehydrogenase (Idh), Trigger factor (Tig) and a chemotaxis protein, which may be involved in P. aeruginosa’s specific response to CAP. …”
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3068por Fei, Dennis Liang, Zhen, Tao, Durham, Benjamin, Ferrarone, John, Zhang, Tuo, Garrett, Lisa, Yoshimi, Akihide, Abdel-Wahab, Omar, Bradley, Robert K., Liu, Paul, Varmus, Harold“…Sequencing DNA from the three AMLs revealed somatic mutations homologous to those considered to be drivers of human AML, including predicted loss- or gain-of-function mutations in Tet2, Gata2, Idh1, and Ikzf1. However, the engineered U2af1(S34F) missense mutation reverted to WT in two of the three AML cases, implying that U2af1(S34F) is dispensable, or even selected against, once leukemia is established.…”
Publicado 2018
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3069por Petzold, Johannes, Severus, Emanuel, Meyer, Shirin, Bauer, Michael, Daubner, Dirk, Krex, Dietmar, Juratli, Tareq A.“…The patient underwent urgent tumor resection, and histologic results revealed an IDH-mutant glioblastoma multiforme. The patient was discharged with a substantially improved psychopathology and without neurological deficits. …”
Publicado 2018
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3070por Zhao, Zheng, Zhang, Ke-Nan, Chai, Rui-Chao, Wang, Kuan-Yu, Huang, Ruo-Yu, Li, Guan-Zhang, Wang, Yong-Zhi, Chen, Jing, Jiang, Tao“…RESULTS: We found that ADAMTSL4 was enriched in GBM (WHO grade IV), especially for those with IDH1/2 wild-type and MGMT unmethylated groups. According to the TCGA classification scheme, ADAMTSL4 can act as a potential marker for subtypes with poorer prognosis. …”
Publicado 2019
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3071por Alieva, Maria, Leidgens, Verena, Riemenschneider, Markus J., Klein, Christoph A., Hau, Peter, van Rheenen, Jacco“…Primary brain tumor initiating cell lines from IDH-wild type GBM stably expressing H2B-Dendra2 were implanted orthotopically in the brains of SCID mice. …”
Publicado 2019
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3072por Ugele, Ines, Cárdenas-Conejo, Zugey Elizabeth, Hammon, Kathrin, Wehrstein, Monika, Bruss, Christina, Peter, Katrin, Singer, Katrin, Gottfried, Eva, Boesch, Jakob, Oefner, Peter, Dettmer, Katja, Renner, Kathrin, Kreutz, Marina“…Mutations in isocitrate dehydrogenase (IDH) or a reduced expression of L-2-hydroxyglutarate (HG)-dehydrogenase result in accumulation of D-2-HG or L-2-HG, respectively, in tumor tissues. …”
Publicado 2019
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3073por Montano, Nicola, D’Alessandris, Quintino Giorgio, Izzo, Alessandro, Fernandez, Eduardo, Pallini, Roberto“…Isocitrate dehydrogenase (IDH) mutation is the most recently introduced molecular marker and is important for the GBM classification because distinguishes primary (de novo) from secondary GBM. …”
Publicado 2016
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3074por Cardoso, Adauto Lima, Fantinatti, Bruno Evaristo de Almeida, Venturelli, Natália Bortholazzi, Carmello, Bianca de Oliveira, de Oliveira, Rogério Antonio, Martins, Cesar“…Based on the transcriptional quantification of DNA modification genes (dnmt, tet, and tdg) and their candidate regulators (idh genes, microRNAs, and long non-coding RNAs) and on RNA-protein interaction prediction, we suggest the occurrence of passive demethylation in gonads of FB+ and 5hmC loss by Tet inhibition or by 5hmC oxidation in MB+ muscle. …”
Publicado 2019
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3075por Gallego Hernanz, Maria Pilar, Torregrosa Diaz, José Miguel, Sorel, Nathalie, Bobin, Arthur, Dindinaud, Elodie, Bouyer, Sabrina, Desmier, Deborah, Brizard, Françoise, Leleu, Xavier, Maillard, Natacha, Chomel, Jean‐Claude“…Targeted high‐throughput sequencing revealed the presence of IDH1, SRSF2, and WT1 additional pathogenic mutations. …”
Publicado 2019
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3076por Zhang, Gaoqi, Zhang, Jilei, Yang, Xinrui, Zhang, Xinpei, Yang, Siyuan, Wang, Jing, Hu, Kai, Shi, Jinlong, Ke, Xiaoyan, Fu, Lin“…Results: High DOCK1 expression was associated with older age (P=0.019), wild-type CEBPA (P=0.002), IDH1/2 mutations (P=0.010) and RUNX1 mutation (P=0.005). …”
Publicado 2019
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3077“…In addition, multiple targeted agents are opening opportunities to treat subgroups of patients whose disease harbors mutations in TP53, IDH, FLT3, and genes involved in splicing machinery. …”
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3078por Yuan, Qing, Cai, Hong-Qing, Zhong, Yi, Zhang, Min-Jie, Cheng, Zhi-Jian, Hao, Jia-Jie, Wang, Ming-Rong, Wan, Jing-Hai“…Furthermore, expression of IGFBP2 mRNA was related to the occurrence of isocitrate dehydrogenase 1 (IDH1) mutation, high heat shock protein 27 (Hsp27) expression and telomerase reverse transcriptase (TERT) promoter mutation (TERTp(+)) (P=0.013, 0.015 and 0.016, respectively), and patients with TERTp(+)/IGFBP2(high) showed the shortest survival. …”
Publicado 2019
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3079“…This risk signature was identified to independently predict the outcome of GBM patients, as well as stratified by IDH1 status, MGMT promoter status, and radio-chemotherapy. …”
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3080por Kim, Hyung‐Jin, Cao, Wa, Oh, Gi‐Su, Lee, SeungHoon, Shen, AiHua, Khadka, Dipendra, Lee, Su‐Bin, Sharma, Subham, Kim, Seon Young, Choe, Seong‐Kyu, Kwak, Tae Hwan, Kim, Jin‐Man, Park, Raekil, So, Hong‐Seob“…We elucidated that the reduction of cellular NAD(+) during the aging process was an important contributor for ARHL; it facilitated oxidative stress and pro‐inflammatory responses in the cochlear tissue through regulating sirtuins that alter various signaling pathways, such as NF‐κB, p53, and IDH2. However, augmentation of NAD(+) by β‐lap effectively prevented ARHL and accompanying deleterious effects through reducing inflammation and oxidative stress, sustaining mitochondrial function, and promoting mitochondrial biogenesis in rodents. …”
Publicado 2019
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