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2101por Bąk, Aneta, Skonieczka, Katarzyna, Jaśkowiec, Anna, Junkiert-Czarnecka, Anna, Heise, Marta, Pilarska-Deltow, Maria, Potoczek, Stanisław, Czyżewska, Maria, Haus, Olga“…Eight pathogenic germline mutations were detected in 7 AML patients, in three genes: CEBPA, ETV6, and IDH2. One patient had two pathogenic germinal mutations, one in ETV6 and one in CEBPA gene. …”
Publicado 2021
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2102por Zhou, Weiyan, Huang, Qi, Wen, Jianbo, Li, Ming, Zhu, Yuhua, Liu, Yan, Dai, Yakang, Guan, Yihui, Zhou, Zhirui, Hua, Tao“…Three independent radiomics models (PET-Rad Model, CT-Rad Model and PET/CT-Rad Model) predicting IDH mutation status were generated using the least absolute shrinkage and selection operator (LASSO) regression analysis based on machine learning algorithms. …”
Publicado 2021
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2103por Haubold, Johannes, Hosch, René, Parmar, Vicky, Glas, Martin, Guberina, Nika, Catalano, Onofrio Antonio, Pierscianek, Daniela, Wrede, Karsten, Deuschl, Cornelius, Forsting, Michael, Nensa, Felix, Flaschel, Nils, Umutlu, Lale“…Using an MRI with non-contrast and post-contrast T1-weighted sequences and FLAIR, our workflow automatically predicts the IDH1/2 mutation, the ATRX expression loss, the 1p19q co-deletion and the MGMT methylation status. …”
Publicado 2021
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2104“…T3 of leg/total% was associated with 49% lower, 41% lower, and unchanged relative odds of isolated diastolic hypertension (IDH), systolic-diastolic hypertension (SDH), and isolated systolic hypertension (ISH) compared to T1 (IDH: 0.51, 0.37–0.70; SDH: 0.59, 0.43–0.80; ISH: 1.06, 0.70–1.59). …”
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2105“…There were16 cases of WHO III, 40 cases of WHO IV, 13 cases of IDH mutation (IDHmt), 30 cases of wildtype (wt) and 13 cases of NOS. …”
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2106por Walker, Jamie M., Kazempour Dehkordi, Shiva, Fracassi, Anna, Vanschoiack, Alison, Pavenko, Anna, Taglialatela, Giulio, Woltjer, Randall, Richardson, Timothy E., Zare, Habil, Orr, Miranda E.“…Analyses of 86 proteins associated with CNS cell-typing or known neurodegenerative changes in 168 ROIs from 14 individuals identified 11 proteins displaying differential expression in NFT-bearing neurons of the resilient when compared to the demented (including APP, IDH1, CD68, GFAP, SYP and Histone H3). In addition, IDH1, CD68, and SYP were differentially expressed in the environment of NFT-bearing neurons when comparing resilient to demented. …”
Publicado 2022
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2107por Karajannis, Matthias, Onar-Thomas, Arzu, Baxter, Patricia, Butingan, Nina, Fuller, Christine, Gajjar, Amar, Haque, Sofia, Jabado, Nada, Lin, Tong, Lucas, John, MacDonald, Shannon, Matsushima, Celeste, Patel, Namrata, Pierson, Christopher, Springer, Linda, Stark, Eileen, Souweidane, Mark, Walsh, Michael, Zaky, Wafik, Fouladi, Maryam, Cohen, Kenneth“…Eligible patients without somatic H3 K27M or BRAF mutations were enrolled on Stratum 1 (IDH wild-type) or Stratum 2 (IDH mutant). Protocol radiochemotherapy consisted of involved field radiotherapy with concurrent veliparib at 65 mg/m(2) twice daily. …”
Publicado 2022
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2108por Bennett, Julie, Nobre, Liana, Sheth, Javal, Ryall, Scott, Fang, Karen, Johnson, Monique, Negm, Logine, Chung, Jiil, Komosa, Martin, Nunes, Nuno M, Fat, Mary Jane Lim, Perry, James, Sahgal, Arjun, Detsky, Jay, Bouffet, Eric, Naz-Hazrati, Lili, Dirks, Peter, Ertl-Wagner, Birgit, Kongkham, Paul, Zadeh, Gelareh, Mason, Warren, Climans, Seth, Cusimano, Michael, Das, Sunit, Gao, Andrew, Tsang, Derek, Nguyen, Lananh, Laperriere, Normand, Keith, Julia, Munoz, David, Tabori, Uri, Hawkins, Cynthia“…Ongoing analysis reveals genetic alterations in 95% of available tumours. IDH-mutant tumours account for only 53%, while paediatric-type mutations were found in 35% of AYA tumours with IDH-WT GBM accounting for the remaining 12%. …”
Publicado 2022
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2109“…Moreover, the concentrations of Gln and NE in follicular fluid showed significantly positive correlation with IDH1 expression in GCs (R = 0.3822, R = 0.4009, P < 0.05). …”
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2110Publicado 2019Tabla de Contenidos: “…/ Marina Montoto Ugarte -- La antropología forense ante la Corte IDH / Ana Buriano Castro.…”
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2111por Grogan, Patrick T., Helgager, Jeffrey J., Deming, Dustin A., Howard, Steven P., Jenkins, Robert B., Robins, H. Ian“…Here, we describe two cases of RIG diagnosed as glioblastoma (GB), IDH-wildtype, in adults who had previously received central nervous system radiation for childhood cancers. …”
Publicado 2023
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2112por Madaci, Lamia, Gard, Charlyne, Nin, Sébastien, Venton, Geoffroy, Rihet, Pascal, Puthier, Denis, Loriod, Béatrice, Costello, Régis“…However, advancements in medical research have introduced targeted therapies, initially employing monoclonal antibodies such as ant-CD52 and anti-CD123, and subsequently utilizing specific inhibitors that target molecular mutations like anti-IDH1, IDH2, or FLT3. The challenge lies in determining the role of these therapeutic options, considering the inherent tumor heterogeneity associated with leukemia diagnosis and the clonal drift that this type of tumor can undergo. …”
Publicado 2023
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2113“…In particular, S100A6 upregulation in glioma tissues exhibited a significant and positive correlation with the World Health Organization (WHO) grade, histological type, age, sex, primary treatment outcomes, 1p/19q codeletion, isocitrate dehydrogenase (IDH) status, overall survival (OS), progression-free interval and disease-specific survival. …”
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2114“…CONCLUSION: PRAME expression statuses may dictate different biological and clinicopathological profiles in IDH-wildtype glioblastoma.…”
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2115por Fala, Maria, Ros, Susana, Sawle, Ashley, Rao, Jyotsna U, Tsyben, Anastasia, Tronci, Laura, Frezza, Christian, Mair, Richard, Brindle, Kevin M“…BACKGROUND: Branched-chain aminotransferase 1 (BCAT1) has been proposed to drive proliferation and invasion of isocitrate dehydrogenase (IDH) wild-type glioblastoma cells. However, the Cancer Genome Atlas (TCGA) dataset shows considerable variation in the expression of this enzyme in glioblastoma. …”
Publicado 2023
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2116“…The risk score was stratified by age, gender, WHO grade, IDH1 mutation, MGMT promoter methylation, and 1p/19q codeletion status, and a nomogram was constructed and validated. …”
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2117por Batchu, Sai, Hanafy, Khalid A., Redjal, Navid, Godil, Saniya S., Thomas, Ajith J.“…Furthermore, the interactions discovered herein are compared to IDH-mutant astrocytoma, allowing for focus on the cellular ecosystem unique to GBM. …”
Publicado 2023
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2118“…Interestingly, these rare intravascular cells showing EGFR amplification by CISH or mutant IDH1 protein by immunohistochemistry were located in the middle or outer portions of vessel walls, but not amongst the morphologic boundaries of the endothelial lining. …”
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2119por Castells, X, Acebes, J J, Majós, C, Boluda, S, Julià-Sapé, M, Candiota, A P, Ariño, J, Barceló, A, Arús, C“…This was repeated for two other published signatures and the performance of LDA equations was evaluated on an independent test set, which contained status of IDH1 mutation, EGFR amplification, MGMT methylation and gene VEGF expression, among other clinical and molecular information. …”
Publicado 2012
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2120por Berghoff, Anna S., Stefanits, Harald, Woehrer, Adelheid, Heinzl, Harald, Preusser, Matthias, Hainfellner, Johannes A.“…Applying this levels-of-evidence system to MGMT, IDH1, 1p19q, Ki67, MYCC, MYCN and β-catenin, only immunohistochemical IDH1 mutation testing in patients with diffuse gliomas is supported by sufficient evidence in order to be unequivocally qualified for clinical use. …”
Publicado 2013
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