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2141por Nordfors, Kristiina, Haapasalo, Joonas, Afyounian, Ebrahim, Tuominen, Joonas, Annala, Matti, Häyrynen, Sergei, Karhu, Ritva, Helén, Pauli, Lohi, Olli, Nykter, Matti, Haapasalo, Hannu, Granberg, Kirsi J.“…In the astrocytoma case, R132C missense mutation was found in the known hotspot site in isocitrate dehydrogenase 1 (IDH1) and LOH was detected in TP53. The mother carried few other somatic alterations, suggesting that the IDH1 mutation and LOH in TP53 were sufficient to drive tumor development. …”
Publicado 2018
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2142por Izycka-Swieszewska, Ewa, Bien, Ewa, Stefanowicz, Joanna, Szurowska, Edyta, Szutowicz-Zielinska, Ewa, Koczkowska, Magdalena, Sigorski, Dawid, Kloc, Wojciech, Rogowski, Wojciech, Adamkiewicz-Drozynska, Elzbieta“…The present study shows that these tumors are of IDH wild type, PI3K/AKT-activated, having no PTEN and EGFR mutations. …”
Publicado 2018
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2143por Al-Hajri, Aliya, Al-Mughairi, Salim, Somani, Alyma, An, Shu, Liu, Joan, Miserocchi, Anna, McEvoy, Andrew W., Yousry, Tarek, Hoskote, Chandrashekar, Thom, Maria“…It is recognized that IDH mutation negative, low-grade epilepsy associated tumors (LEAT) can show diffuse growth patterns and lack the diagnostic hallmarks of either classical dysembryoplastic neuroepithelial tumors (DNT) or typical ganglioglioma. …”
Publicado 2017
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2144por Fukano, Kazuhiro, Ozawa, Kunio, Kokubu, Masaya, Shimizu, Tetsu, Ito, Shinsaku, Sasaki, Yasuyuki, Nakamura, Akira, Yajima, Shunsuke“…On the basis of these structural features, which have not been identified in the known inositol dehydrogenases, and a phylogenetic analysis of IDH family enzymes, we suggest a novel subfamily of the GFO/IDH/MocA family. …”
Publicado 2018
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2145por Li, Ningning, Zhang, Ying, Sidlauskas, Kastytis, Ellis, Matthew, Evans, Ian, Frankel, Paul, Lau, Joanne, El-Hassan, Tedani, Guglielmi, Loredana, Broni, Jessica, Richard-Loendt, Angela, Brandner, Sebastian“…GPR158 promotes glioma stem cell differentiation and induces apoptosis and is highest expressed in the cerebral cortex and in oligodendrogliomas, lower in IDH mutant astrocytomas and lowest in the most malignant form of glioma, IDH wild-type glioblastoma. …”
Publicado 2018
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2146“…METHOD: A total of 304 adult glioblastoma samples collected after surgical resection were selected for retrospective analysis, and Sanger sequencing was performed to detect IDH and TERT promoter mutations. The methylation of the MGMT promoter was analyzed by pyrosequencing, and MRI‐derived and clinical features were dichotomized into easily acquired variables. …”
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2147por Homma, Taku, Hanashima, Yuya, Maebayashi, Toshiya, Nakanishi, Yoko, Ishige, Toshiyuki, Ohta, Takashi, Yoshino, Atsuo, Hao, Hiroyuki“…Genetically, most glioblastomas do not exhibit the isocitrate dehydrogenase (IDH) 1/2 gene mutation and rarely harbor the 1p/19q co-deletion. …”
Publicado 2019
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2148por Richter, Susan, Gieldon, Laura, Pang, Ying, Peitzsch, Mirko, Huynh, Thanh, Leton, Rocio, Viana, Bruna, Ercolino, Tonino, Mangelis, Anastasios, Rapizzi, Elena, Menschikowski, Mario, Aust, Daniela, Kroiss, Matthias, Beuschlein, Felix, Gudziol, Volker, Timmers, Henri JLM, Lenders, Jacques, Mannelli, Massimo, Cascon, Alberto, Pacak, Karel, Robledo, Mercedes, Eisenhofer, Graeme, Klink, Barbara“…PURPOSE: Metabolic aberrations have been described in neoplasms with mutations in the Krebs cycle genes encoding succinate dehydrogenase (SDH), fumarate hydratase (FH) and isocitrate dehydrogenase (IDH). In turn, accumulation of oncometabolites succinate, fumarate, and 2-hydroxyglutarate can be employed to identify tumors with those mutations. …”
Publicado 2018
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2149por Jaunmuktane, Zane, Capper, David, Jones, David T. W., Schrimpf, Daniel, Sill, Martin, Dutt, Monika, Suraweera, Nirosha, Pfister, Stefan M., von Deimling, Andreas, Brandner, Sebastian“…We report the frequency of IDH mutations in a large cohort of nearly 1550 patients, EGFR amplifications in almost 1900 IDH-wildtype glioblastomas, and histone mutations in 70 adult gliomas. …”
Publicado 2019
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2150“…BACKGROUND: Enasidenib (IDHIFA(®), AG-221) is a first-in-class, targeted inhibitor of mutant IDH2 proteins for treatment of relapsed or refractory acute myeloid leukemia. …”
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2151por Bello, Natalie A., Schwartz, Joseph E., Kronish, Ian M., Oparil, Suzanne, Anstey, D. Edmund, Wei, Ying, Cheung, Ying Kuen K., Muntner, Paul, Shimbo, Daichi“…METHODS AND RESULTS: We analyzed data from 316 community‐dwelling adults not taking antihypertensive medication from the IDH (Improving the Detection of Hypertension) study who performed HBPM for 14 days. …”
Publicado 2018
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2152por Rey, Veronica, Menendez, Sofia T., Estupiñan, Oscar, Rodriguez, Aida, Santos, Laura, Tornin, Juan, Martinez-Cruzado, Lucia, Castillo, David, Ordoñez, Gonzalo R., Costilla, Serafin, Alvarez-Fernandez, Carlos, Astudillo, Aurora, Braña, Alejandro, Rodriguez, Rene“…Different mutations in Isocitrate Dehydrogenase-1 (IDH1), Isocitrate Dehydrogenase-2 (IDH2), and Tumor Supressor P53 (TP53) and deletion of Cyclin Dependent Kinase Inhibitor 2A (CDKN2A) were detected both in cell lines and tumor samples. …”
Publicado 2019
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2153“…In patients with GBM from the CGGA database, a higher RELB expression level was associated with a shorter survival time, a mesenchymal subtype and IDH1 wild-type gliomas. Kaplan-Meier survival analysis, survival nomograms and Cox analysis demonstrated an independent prognostic value for RELB expression. …”
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2154“…Large-scale whole-exome sequencing of AML patients has revealed the presence of mutations, translocations or duplications in several epigenetic effectors such as DNMT3, MLL, ASXL1, and TET2, often times co-occuring with mutations in metabolic enzymes such as IDH1 and IDH2. These mutations often result in impaired enzymatic activity which leads to an altered epigenetic landscape through dysregulation of chromatin modifications such as DNA methylation, histone acetylation and methylation. …”
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2155“…Molecular testing performed on the tumor showed no alterations in the IDH1, IDH2, EGFR, or BRAF genes by sequencing, intact 1p/19q by FISH, and a novel BCR-NTRK2 fusion transcript by reverse transcription and anchored multiplex PCR. …”
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2156por Han, Ming-Zhi, Wang, Shuai, Zhao, Wen-Bo, Ni, Shi-Lei, Yang, Ning, Kong, Yang, Huang, Bin, Chen, An-Jing, Li, Xin-Gang, Wang, Jian, Wang, Dong-Hai“…FINDINGS: HVEM was found to be elevated in aggressive gliomas, particularly in the mesenchymal and isocitrate dehydrogenase (IDH) wild-type molecular subtypes of GBM. HVEM(high) tumours tended to be associated with amplification of EGFR and loss of PTEN, while HVEM(low) tumours harbored mutations in IDH1 (93%). …”
Publicado 2019
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2157por Pekova, Barbora, Dvorakova, Sarka, Sykorova, Vlasta, Vacinova, Gabriela, Vaclavikova, Eliska, Moravcova, Jitka, Katra, Rami, Vlcek, Petr, Sykorova, Pavla, Kodetova, Daniela, Vcelak, Josef, Bendlova, Bela“…DNA from samples was used for next-generation sequencing to identify mutations in the following genes: HRAS, KRAS, NRAS, BRAF, IDH1, CHEK2, PPM1D, EIF1AX, EZH1 and for capillary sequencing in case of the TERT promoter. …”
Publicado 2019
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2158por Shang, Wen-Hui, Han, Jia-Run, Yan, Jia-Nan, Du, Yi-Nan, Xu, Yun-Sheng, Xue, Chang-Feng, Zhang, Tie-Tao, Wu, Hai-Tao, Zhu, Bei-Wei“…However, TGFBI had no correlation with gonad index (GI) or protein content. 6PGD, IDH, multifunctional protein ADE2 isoform X3, and ALDH were shown to interact with each other and might play key roles in changing the condition factor of S. nudus gonads.…”
Publicado 2019
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2159“…OBJECTIVE: To report a rare case of cervical intradural disc herniation (IDH) with Brown-Séquard syndrome and to review the related literature. …”
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2160“…Defining molecular markers for diffuse gliomas are IDH1/IDH2 mutations, 1p/19q codeletion and mutations in histone H3 genes. …”
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