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3761por Alcaniz, Joshua, Winkler, Lars, Dahlmann, Mathias, Becker, Michael, Orthmann, Andrea, Haybaeck, Johannes, Krassnig, Stefanie, Skofler, Christina, Kratzsch, Tobias, Kuhn, Susanne A., Jödicke, Andreas, Linnebacher, Michael, Fichtner, Iduna, Walther, Wolfgang, Hoffmann, Jens“…Molecular characterization of 23 PDX identified all of them as IDH-wt (R132) with frequent mutations in EGFR, TP53, FAT1, and within the PI3K/Akt/mTOR pathway. …”
Publicado 2023
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3762por Hosono, Naoko, Chi, SungGi, Yamauchi, Takahiro, Fukushima, Kentaro, Shibayama, Hirohiko, Katagiri, Seiichiro, Gotoh, Akihiko, Eguchi, Motoki, Morishita, Takanobu, Ogasawara, Reiki, Kondo, Takeshi, Yanada, Masamitsu, Yamamoto, Kazuhito, Kobayashi, Tsutomu, Kuroda, Junya, Usuki, Kensuke, Utsu, Yoshikazu, Yoshimitsu, Makoto, Ishitsuka, Kenji, Ono, Takaaki, Takahashi, Naoto, Iyama, Satoshi, Kojima, Kensuke, Nakamura, Yukinori, Fukuhara, Suguru, Izutsu, Koji, Abutani, Hikaru, Yamauchi, Nobuhiko, Yuda, Junichiro, Minami, Yosuke“…As for the detection of actionable mutations, 38% (n = 69) of patients had useful genetic mutation (FLT3‐ITD/TKD, IDH1/2, and DNMT3A (R822)) for treatment selection. …”
Publicado 2023
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3763por Gerritsen, Jasper K W, Zwarthoed, Rosa H, Kilgallon, John L, Nawabi, Noah Lee, Versyck, Georges, Jessurun, Charissa A C, Pruijn, Koen P, Fisher, Fleur L, Larivière, Emma, Solie, Lien, Mekary, Rania A, Satoer, Djaina D, Schouten, Joost W, Bos, Eelke M, Kloet, Alfred, Tewarie, Rishi Nandoe, Smith, Timothy R, Dirven, Clemens M F, De Vleeschouwer, Steven, Vincent, Arnaud J P E, Broekman, Marike L D“…GTR based on RTV improved median OS in the overall cohort (19.0 months, P < .0001), and in the subgroups with IDH wildtype tumors (18.5 months, P = .00055), MGMT methylated tumors (35.0 months, P < .0001), aged <70 (20.0 months, P < .0001), NIHSS 0–1 (19.0 months, P = .0038), KPS 90–100 (19.5 months, P = .0012), and KPS ≤80 (17.0 months, P = .036). …”
Publicado 2022
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3764por Li, Junnan, Pei, Li, Liang, Simin, Xu, Shuangnian, Wang, Yi, Wang, Xiao, Liao, Yi, Zhan, Qian, Cheng, Wei, Yang, Zesong, Tang, Xiaoqiong, Zhang, Hongbin, Xiao, Qing, Chen, Jianbin, Liu, Lin, Wang, Li“…Further analysis showed TET2, NPM1, SRSF2, and IDH1 gene mutations, and epigenetic genes (p < 0.050) presented significantly higher frequency in older patients. …”
Publicado 2023
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3765por Phon, Brandon Wee Siang, Bhuvanendran, Saatheeyavaane, Ayub, Qasim, Radhakrishnan, Ammu Kutty, Kamarudin, Muhamad Noor Alfarizal“…Additionally, EMT-related genes were upregulated in GBM archetypes (wild-type IDH1(R132) ) that historically have poorer treatment responses, with said genes being significant predictors of poorer survival in the TCGA cohort. …”
Publicado 2023
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3766por Nobre, Liana, Sait, Sameer Farouk, Bennet, Julie, Larsen, Alexandra Gianyini, Ho, I-Chen, Gianno, Francesca, Lin, Andrew, Mellinghoff, Ingo, Miller, Alexandra, Siddaway, Robert, Karijannis, Matthias, Tabori, Uri, Bale, Tejus, Hawkins, Cynthia“…From a population-based cohort of over 1800 pediatric and AYA (adolescent and young adult) gliomas, FGFR mutations were found in 6% of pediatric low-grade gliomas (LGG) and 16 % of IDH-WT AYA gliomas. Given the frequency of FGFR driver alterations, we assembled a large cohort of 370 FGFR mutated glioma across all ages (6 months to 87 years) 53% of which were LGG. …”
Publicado 2023
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3767por Geyer, Lucas, Wolf, Thibaut, Chenard, Marie Pierre, Cebula, Helene, Schott, Roland, Noel, Georges, Guerin, Eric, Pencreach, Erwan, Reita, Damien, ENTZ-WERLE, Natacha, Lhermitte, Benoit“…Indeed, it was associated to a better prognosis in MAPK-induced tumors, but to a worse survival in IDH-wild-type glioblastomas. CDKN2A homozygous deletion present in all type of high grade pediatric or adult gliomas was significantly linked to a worse outcome in the entire population. …”
Publicado 2023
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3768por Haldar, Debanjan, Kazerooni, Anahita Fathi, Mahtabfar, Aria, Khalili, Nastaran, Familiar, Ariana, Kraya, Adam, Kim, Meen Chul, Tu, Wenxin, Haldar, Shuvanjan, Bagheri, Sina, Anderson, Hannah, Viswanathan, Karthik, Shaikh, Ibraheem, Ware, Jeffrey, Storm, Phillip, Vossough, Arastoo, Resnick, Adam, Nabavizadeh, Ali“…Categorical variables included sex (male vs female), genetic mutation status for 10 selected genes (BRAF, FGFR1, TSC1, TSC2, NF1, MYB, EGFR, ALK, IDH1, and RB1) that are known to play a role in the pathogenesis of pLGG (mutated vs non-mutated), and tumor location (9 categories). …”
Publicado 2023
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3769“…Specific HOXAs could distinguish IDH mutation (HOXA1-7, HOXA9, HOXA13) and molecular GBM subtypes (HOXA1-2, HOXA9-11, HOXA13). …”
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3770por Ong, W L, Stewart, J, Sahgal, A, Soliman, H, Tseng, C L, Detsky, J, Ho, L, Das, S, Maralani, P, Lipsman, N, Stanisz, G, Perry, J, Chen, H, Atenafu, E, Lau, A, Ruschin, M, Myrehaug, S“…Age, sex, MGMT methylation and IDH-mutation status were not associated with tumor dynamics during treatment. …”
Publicado 2023
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3771por Bennett, J, Nobre, L, Sheth, J, Ryall, S, Fang, K, Johnson, M, Negm, L, Chung, J, Komosa, M, Nunes, N, Lim Fat, M J, Perry, J, Sahgal, A, Detsky, J, Bouffet, E, Naz-Hazrati, L, Dirks, P, Ertl-Wagner, B, Kongkham, P, Zadeh, G, Mason, W, Cusimano, M, Das, S, Gao, A, Tsang, D, Nguyen, L, Laperriere, N, Keith, J, Munoz, D, Tabori, U, Hawkins, C“…The most common paediatric alterations included BRAF p.V600E (11%) and FGFR alterations (7%) while BRAF fusions (4%), H3 p.K27M (4%) and H3.3 p.G34R (1%) were rare. IDH mutation was found in 57% of tumours. Molecular GBM accounted for 7%. …”
Publicado 2023
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3772“…Final pathological diagnosis including molecular diagnostics was consistent with WHO grade 4 IDH-wildtype H3G34 mutant diffuse hemispheric glioma with osseous metastases. …”
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3773por Lee, Hye In, Kim, Jina, Kim, In Ah, Lee, Joo Ho, Cho, Jaeho, Yoon, Hong In, Wee, Chan Woo“…Patients aged ≥65 years who underwent radiotherapy for IDH-wildtype eGBM between 2006 and 2021 were included. …”
Publicado 2023
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3774por Zhang, Chun, Xiao, Jing, Fa, Luzhong, Jiang, Fanwen, Jiang, Hui, Zhou, Lin, Xu, Zhuping“…In conclusion, the proposed four-gene (PTPN12, IDH2, P2RX4, and KDELR2) prognostic hazard model had satisfactory prognostic ability. …”
Publicado 2023
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3775por Su, Minqiang, Lin, Xiaojue, Xiao, Zupeng, She, Yuanhang, Deng, Ming, Liu, Guangbin, Sun, Baoli, Guo, Yongqing, Liu, Dewu, Li, Yaokun“…According to Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analyses, ten genes (DGAT1, IDH2, CYP11B1, GFUS, CYC1, GPT, PYCR3, OPLAH, ALDH1A3, and NAPRT) associated with lactation fat percentage, milk yield, antioxidant activity, stress resistance, and inflammation and immune response were identified as key candidates for lactation traits. …”
Publicado 2023
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3776por Karschnia, Philipp, Dono, Antonio, Young, Jacob S, Juenger, Stephanie T, Teske, Nico, Häni, Levin, Sciortino, Tommaso, Mau, Christine Y, Bruno, Francesco, Nunez, Luis, Morshed, Ramin A, Haddad, Alexander F, Weller, Michael, van den Bent, Martin, Beck, Juergen, Hervey-Jumper, Shawn, Molinaro, Annette M, Tandon, Nitin, Rudà, Roberta, Vogelbaum, Michael A, Bello, Lorenzo, Schnell, Oliver, Grau, Stefan J, Chang, Susan M, Berger, Mitchel S, Esquenazi, Yoshua, Tonn, Joerg-Christian“…RESULTS: We studied 681 patients with first recurrence of Isocitrate Dehydrogenase (IDH) wild-type glioblastomas, including 310 patients who underwent re-resection. …”
Publicado 2023
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3777por Dimov, Diyan, Brainman, Daniel, Berger, Björn, Coras, Roland, Grote, Alexander, Simon, Matthias“…METHODS: We retrospectively reviewed clinical and imaging data of 71 patients with newly diagnosed primary (IDH1 wildtype) mGBM who underwent operative treatment in 2015–2020 at the authors’ institution. …”
Publicado 2023
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3778por Farzana, Walia, Basree, Mustafa M., Diawara, Norou, Shboul, Zeina A., Dubey, Sagel, Lockhart, Marie M., Hamza, Mohamed, Palmer, Joshua D., Iftekharuddin, Khan M.“…To our knowledge, this study is the first to investigate the potential of conventional radiomics, sophisticated multi-resolution fractal texture features, and different molecular features (MGMT, IDH mutations) as a diagnostic and prognostic tool for prediction of REP from non-REP cases using computational and statistical modeling methods. …”
Publicado 2023
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3779Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With Cancerpor Wadensten, Elisabeth, Wessman, Sandra, Abel, Frida, Diaz De Ståhl, Teresita, Tesi, Bianca, Orsmark Pietras, Christina, Arvidsson, Linda, Taylan, Fulya, Fransson, Susanne, Vogt, Hartmut, Poluha, Anna, Pradhananga, Sailendra, Hellberg, Maria, Lagerstedt-Robinson, Kristina, Raj Somarajan, Praveen, Samuelsson, Sofie, Orrsjö, Sara, Maqbool, Khurram, Henning, Karin, Strid, Tobias, Ek, Torben, Fagman, Henrik, Olsson Bontell, Thomas, Martinsson, Tommy, Puls, Florian, Kogner, Per, Wirta, Valtteri, Pronk, Cornelis Jan, Wille, Joakim, Rosenquist, Richard, Nistér, Monica, Mertens, Fredrik, Sabel, Magnus, Norén-Nyström, Ulrika, Grillner, Pernilla, Nordgren, Ann, Ljungman, Gustaf, Sandgren, Johanna, Gisselsson, David“…Potential treatment targets were found in 31 patients (26%), most commonly ALK mutations/fusions (n = 4), RAS/RAF/MEK/ERK pathway mutations (n = 14), FGFR1 mutations/fusions (n = 5), IDH1 mutations (n = 2), and NTRK2 gene fusions (n = 2). …”
Publicado 2023
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3780por Sheng, Ziyue, Lou, Shang, Cao, Jin, Sun, Weidi, Shen, Yaojia, Xu, Yunhan, Ren, Ziyang, Liu, Wen, Yi, Qian, Song, Peige“…Hypertension phenotypes were categorized as normotension, pre-hypertension, isolated systolic hypertension (ISH), isolated diastolic hypertension (IDH), and systolic-diastolic hypertension (SDH). …”
Publicado 2023
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