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  1. 2581
    “…METHODS: We evaluated four patients from the GLAD study (mean age 39years; 2 female, 3 AA IDH-mutant, 1 GBM IDH-wildtype) who underwent MRS at baseline and following eight weeks of KDT. …”
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  2. 2582
  3. 2583
    “…A multivariable prediction model was developed as follows: Y(ME) = 0.672 + 0.513X(Grade) + 0.380X(SVZ) + 0.439X(MGMT) + 0.320X(IDH) + 0.333X(1p/19q). The R-square value of goodness of fit was 0.780. …”
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  4. 2584
  5. 2585
    “…High risk scores were associated with an age of > 40, wild-type IDH1, a WHO grade of III, an unmethylated MGMT promoter, and 1p/19q non-codeletion. …”
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  6. 2586
    “…METHODS: We applied immunohistochemistry in tumor tissue sections of 18 high-grade glioma (HGG) patients (4 anaplastic astrocytoma, IDH-wildtype WHO-III; 14 glioblastomas (GBM), IDH-wildtype WHO-IV) in order to assess and quantify leucocytes (CD45) and macrophages (CD68, CD163) within the tumor core, infiltration zone and perivascular spaces. …”
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  7. 2587
    “…Correlation analysis showed that HOXD10 expression was significantly related to IDH1 status. Univariate analysis revealed that low HOXD10 expression, complete surgical resection, postoperative radiotherapy, postoperative temozolomide chemotherapy and IDH1 mutation were all beneficial prognostic factors. …”
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  8. 2588
  9. 2589
    “…A detailed determination was successful for IDH 1/2 mutation in 99.4% of cases, for 1p/19q codeletion in 97.4% of cases, for TERT mutation in 98.9% of cases, and for MGMT promoter methylation in 99.1% of cases. …”
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  10. 2590
    “…Expression of tRFdb-3012a/b was correlated with IDH mutant status and MGMT promoter mutation in gliomas, and tRFdb-3012a/b and ts-23 tended to be highly expressed in patients with the IDH mutant. …”
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  11. 2591
    “…The following molecular markers were analyzed: EGFR amplification, TERT promoter mutation, CDKN2A/B homozygous loss, chromosome 7 + /10- aneuploidy, MGMT methylation, IDH mutation, ATRX loss, p53 mutation and 1p19q codeletion. …”
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  12. 2592
  13. 2593
    “…BACKGROUND: Gliomas with FGFR3::TACC3 fusion mainly occur in adults, display pathological features of glioblastomas (GB) and are usually classified as glioblastoma, IDH-wildtype. However, cases demonstrating pathological features of low-grade glioma (LGG) lead to difficulties in classification and clinical management. …”
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  14. 2594
  15. 2595
    Publicado 2013
    Tabla de Contenidos: “…Condiciones sociales de la población indígena e inversión federal en los 125 municipios con menor IDH / Jesús Mena Vázquez -- Cap. 5. Incidencia delictiva en los 125 municipios más marginados del país / Juan Pablo Aguirre Quezada.…”
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  16. 2596
    por Guo, Xu, Wang, Gang
    Publicado 2023
    “…BACKGROUND: Glioma is the most common primary intracranial malignancy in clinical practice, and in particular, IDH‐wildtype glioblastoma has the worst prognosis. …”
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  17. 2597
    por Aggarwal, Surinder K.
    Publicado 1998
    “…In an attempt to elucidate its mechanism(s) of action, liver and kidney tissues from normal and CDDP treated (1.8 mg/kg) dogs were evaluated for changes in various dehydrogenases [MDH, SDH, β-HBDH, IDH and G-6-PDH] and nonspecific lipase enzymes. …”
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  18. 2598
    por Cardaci, Simone, Ciriolo, Maria Rosa
    Publicado 2012
    “…In the last ten years, a causal role in carcinogenesis has been documented for inherited and acquired alterations in three TCA cycle enzymes, succinate dehydrogenase (SDH), fumarate hydratase (FH), and isocitrate dehydrogenase (IDH), pointing towards metabolic alterations as the underlying hallmark of cancer. …”
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  19. 2599
    “…Protein structure modeling showed that somatic mutations in IDH2, RASGEF1B, and MSH4 can affect protein structures.…”
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  20. 2600
    “…Third, genetic disruptions directly within the core epigenetic machinery, exemplified by the recently identified mutations within isocitrate dehydrogenase genes IDH1/2 and variant histone genes H3.3/H3F3A. These constitute the ‘good, the bad and the ugly’ of epigenetic mechanisms in cancer.…”
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