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3921por Jurmeister, Philipp, Glöß, Stefanie, Roller, Renée, Leitheiser, Maximilian, Schmid, Simone, Mochmann, Liliana H., Payá Capilla, Emma, Fritz, Rebecca, Dittmayer, Carsten, Friedrich, Corinna, Thieme, Anne, Keyl, Philipp, Jarosch, Armin, Schallenberg, Simon, Bläker, Hendrik, Hoffmann, Inga, Vollbrecht, Claudia, Lehmann, Annika, Hummel, Michael, Heim, Daniel, Haji, Mohamed, Harter, Patrick, Englert, Benjamin, Frank, Stephan, Hench, Jürgen, Paulus, Werner, Hasselblatt, Martin, Hartmann, Wolfgang, Dohmen, Hildegard, Keber, Ursula, Jank, Paul, Denkert, Carsten, Stadelmann, Christine, Bremmer, Felix, Richter, Annika, Wefers, Annika, Ribbat-Idel, Julika, Perner, Sven, Idel, Christian, Chiariotti, Lorenzo, Della Monica, Rosa, Marinelli, Alfredo, Schüller, Ulrich, Bockmayr, Michael, Liu, Jacklyn, Lund, Valerie J., Forster, Martin, Lechner, Matt, Lorenzo-Guerra, Sara L., Hermsen, Mario, Johann, Pascal D., Agaimy, Abbas, Seegerer, Philipp, Koch, Arend, Heppner, Frank, Pfister, Stefan M., Jones, David T. W., Sill, Martin, von Deimling, Andreas, Snuderl, Matija, Müller, Klaus-Robert, Forgó, Erna, Howitt, Brooke E., Mertins, Philipp, Klauschen, Frederick, Capper, David“…This includes two classes with neuroendocrine differentiation, characterized by IDH2 or SMARCA4/ARID1A mutations with an overall favorable clinical course, one class composed of highly aggressive SMARCB1-deficient carcinomas and another class with tumors that represent potentially previously misclassified adenoid cystic carcinomas. …”
Publicado 2022
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3922por Zhu, Qinghui, Shen, Shaoping, Yang, Chuanwei, Li, Mingxiao, Zhang, Xiaokang, Li, Haoyi, Zhao, Xuzhe, Li, Ming, Cui, Yong, Ren, Xiaohui, Lin, Song“…BACKGROUND: The diagnosis of oligodendroglioma based on the latest World Health Organization Classification of Tumors of the Central Nervous System (WHO CNS 5) criteria requires the codeletion of chromosome arms 1p and 19q and isocitrate dehydrogenase gene (IDH) mutation (mut). Previously identified prognostic indicators may not be completely suitable for patients with oligodendroglioma based on the new diagnostic criteria. …”
Publicado 2022
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3923por Murugesan, K., Necchi, A., Burn, T.C., Gjoerup, O., Greenstein, R., Krook, M., López, J.A., Montesion, M., Nimeiri, H., Parikh, A.R., Roychowdhury, S., Schwemmers, S., Silverman, I.M., Vogel, A.“…In intrahepatic cholangiocarcinoma, FGFR2 REs significantly co-occurred with BAP1 alterations, whereas KRAS, TP53, IDH1, and ARID1A alterations were mutually exclusive. …”
Publicado 2022
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3924por Krigers, Aleksandrs, Demetz, Matthias, Moser, Patrizia, Kerschbaumer, Johannes, Brawanski, Konstantin R., Fritsch, Helga, Thomé, Claudius, Freyschlag, Christian F.“…Tumors with higher expression of GAP-43 (p = 0.024, HR = 1.71/rank) and actin (p < 0.001, HR = 2.28/rank) showed significantly reduced OS. IDH1 wildtype glioma demonstrated significantly more expression of all proteins: GAP-43 (p = 0.009), Cx43 (p = 0.003) and actin (p < 0.001). …”
Publicado 2023
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3925por Boele, Florien W, den Otter, Patricia W M, Reijneveld, Jaap C, de Witt Hamer, Philip C, van Thuijl, Hinke F, Lorenz, Linda M C, Wesseling, Pieter, Lagerwaard, Frank J, Taphoorn, Martin J B, Kouwenhoven, Mathilde C M, Snijders, Tom J, Douw, Linda, Klein, Martin“…Where available, histology of the initial tumor was revised and immunohistochemical staining for IDH1 R132H mutant protein was performed. RESULTS: Thirty patients and nineteen caregivers participated. …”
Publicado 2022
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3926por Li, Junhong, Zhang, Shuxin, Chen, Siliang, Yuan, Yunbo, Zuo, Mingrong, Li, Tengfei, Wang, Zhihao, Liu, Yanhui“…The LRS was demonstrated to be an independent prognostic predictor for glioma patients, and a nomogram consisting of the LRS, IDH mutational status, WHO grade, and radiotherapy showed a C-index of 0.852. …”
Publicado 2023
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3927por Yang, Long, Dong, Xia, Abuduaini, Baiheremujiang, Jiamali, Nueraihemaiti, Seyiti, Zulihuma, Shan, Xue-Feng, Gao, Xiao-Ming“…Currently, most studies have focused on factors influencing IDH or mortality risk, while few predictive models have been used for mortality risk in IHD patients. …”
Publicado 2023
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3928por Park, Jihye, An, Hongyul, Lim, Jiwoo, Park, I Seul, Kim, Mi Hyun, Kim, Ji Hyung, Kim, Seung Won, Koh, Young Il, Lee, Eun Young, Cheon, Jae Hee“…Among the BD patients of our cohort, five variants (DNMT3A, TET2, ASXL1, STAG2, and IDH2) were detected. DNMT3A mutations were the most common, followed by TET2 mutations. …”
Publicado 2023
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3930por Wang, Xinzhuang, Zhang, Hong, Zhang, Mingchu, Zhang, Xuezhi, Mao, Wenbin, Gao, Ming“…We observed that some mutation-specific ferroptosis regulators, such as down-regulated ACSL4 in EGFR-mutated patients and up-regulated FADS2 in IDH1-mutated patients, were linked to the inhibited ferroptosis activity in GBM. …”
Publicado 2023
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3931por Li, J., Mi, L., Ran, B., Sui, C., Zhou, L., Li, F., Dionigi, G., Sun, H., Liang, N.“…Finally, five validated DEPs showed a potential prognostic role after examining The Cancer Genome Atlas database: FN1, IDH2, VDAC1, FABP4, and TG. Accordingly, a nomogram was constructed whose concordance index was 0.685 (confidence interval: 0.645–0.726). …”
Publicado 2022
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3932por Sampson, John H, Singh Achrol, Achal, Aghi, Manish K, Bankiewicz, Krystof, Bexon, Martin, Brem, Steven, Brenner, Andrew, Chandhasin, Chandtip, Chowdhary, Sajeel, Coello, Melissa, Ellingson, Benjamin M, Floyd, John R, Han, Seunggu, Kesari, Santosh, Mardor, Yael, Merchant, Fahar, Merchant, Nina, Randazzo, Dina, Vogelbaum, Michael, Vrionis, Frank, Wembacher-Schroeder, Eva, Zabek, Miroslaw, Butowski, Nicholas“…METHODS: MDNA55-05 is an open-label, single-arm phase IIb study of MDNA55 in recurrent GBM (rGBM) patients with an aggressive form of GBM (de novo GBM, IDH wild-type, and nonresectable at recurrence) on their 1st or 2nd recurrence. …”
Publicado 2023
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3933por Li, Junsheng, Wang, Siyu, Chi, Xiaojing, He, Qiheng, Tao, Chuming, Ding, Yaowei, Wang, Jia, Zhao, Jizong, Wang, Wen“…The mutant frequencies of IDH were significantly lower in cluster 1 (P<0.05). …”
Publicado 2023
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3934“…RESULTS: A total of 24 AML patients were involved in the study, of whom 13 (54.2%) were in the unfit group, and 11 (45.8%) were in the R/R group. FLT3 and IDH (8/24, 33.3%) were the most common gene aberrations. …”
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3935por Wong, Eric T., Rosenberg, Harry, Dawood, Olivia, Hertan, Lauren, Vega, Rafael A., Anderson, Matthew, Uhlmann, Erik J.“…Gross total resection of the tumor revealed IDH-1 wild-type glioblastoma. After treatment with radiation and temozolomide chemotherapy, his cognitive status deteriorated rapidly, and he died from unexpected sudden death 2 months after radiation. …”
Publicado 2023
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3936“…Meanwhile, advances in the molecular profiling of BTCs has contributed to the recent proliferation of molecularly targeted therapeutics for the subset of BTCs harboring alterations in IDH1, FGFR2, MAP kinase signaling, HER2, and beyond, and there has been great interest in investigating combinations of these agents with immunotherapy. …”
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3937por Choi, Haeyoun, Baek, In-Cheol, Park, Soon A, Park, Jae-Sung, Jeun, Sin-Soo, Kim, Tai-Gyu, Ahn, Stephen“…The GB group was comprised of 77 patients with newly diagnosed IDH-wildtype GB at our institution, and the control group consisted of 200 healthy Korean volunteers. …”
Publicado 2023
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3938por Carstam, Louise, Latini, Francesco, Solheim, Ole, Bartek, Jiri, Pedersen, Lars K., Zetterling, Maria, Beniaminov, Stanislav, Sjåvik, Kristin, Ryttlefors, Mats, Jensdottir, Margret, Rydenhag, Bertil, Smits, Anja, Jakola, Asgeir S.“…PURPOSE: Since the introduction of the molecular definition of oligodendrogliomas based on isocitrate dehydrogenase (IDH)-status and the 1p19q-codeletion, it has become increasingly evident how this glioma entity differs much from other diffuse lower grade gliomas and stands out with longer survival and often better responsiveness to adjuvant therapy. …”
Publicado 2023
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3939por Shan, Enfang, Cao, Yi-nan, Zhang, Yang, Chen, Wen, Ren, Xurui, Zhu, Shanjie, Xi, Xueru, Mu, Shuai, Ma, Mian, Zhi, Tongle, Li, Xianwen“…The expression level of CACNG3 in the IDH1 wide-type group, 1p/19q non-codel group, and mesenchymal subtype group was significantly reduced, and the results showed that CACNG3 could serve as a biomarker for the mesenchymal molecular subtype. …”
Publicado 2023
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3940por Zou, Yining, Zhu, Kun, Pang, Yanrui, Han, Jing, Zhang, Xin, Jiang, Zhengzeng, Huang, Yufeng, Gu, Wenyi, Ji, Yuan“…BAP1, CDKN2A, and CDKN2B were the most common concomitant genetic alterations of FGFR2, whereas KRAS and IDH1 mutations were mutually exclusive to FGFR2 rearrangements. …”
Publicado 2023
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