Results 31 to 40 of about 58,205 (308)

Single-center, observational study of AML/MDS-EB with IDH1/2 mutations: genetic profile, immunophenotypes, mutational kinetics and outcomes

open access: yesHematology, 2023
Objective IDH1/2 mutations, intervening in epigenetic procedures, are frequently encountered in acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS).
Vasiliki Papadopoulou   +6 more
doaj   +1 more source

TET2 inhibits differentiation of embryonic stem cells but does not overcome methylation-induced gene silencing [PDF]

open access: yes, 2014
TET2 is a methylcytosine dioxygenase that is frequently mutated in myeloid malignancies, notably myelodysplasia and acute myeloid leukemia. TET2 catalyses the conversion of 5′-methylcytosine to 5′-hydroxymethylcytosine within DNA and has been implicated ...
Chevassut, Timothy   +2 more
core   +3 more sources

Molecular and Genetic Determinants of Glioma Cell Invasion. [PDF]

open access: yes, 2017
A diffusely invasive nature is a major obstacle in treating a malignant brain tumor, "diffuse glioma", which prevents neurooncologists from surgically removing the tumor cells even in combination with chemotherapy and radiation.
Kato, Yoichiro   +4 more
core   +2 more sources

Favorable role of IDH1/2 mutations aided with MGMT promoter gene methylation in the outcome of patients with malignant glioma

open access: yesFuture Science OA, 2021
Aim: The implications of molecular biomarkers IDH1/2 mutations and MGMT gene promoter methylation were evaluated for prognostic outcome of glioma patients. Materials & methods: Glioma cases were analyzed for IDH1/2 mutations and MGMT promoter methylation
Arshad A Pandith   +13 more
doaj   +1 more source

Predictive MGMT status in a homogeneous cohort of IDH wildtype glioblastoma patients [PDF]

open access: yes, 2019
Methylation of the O(6)-Methylguanine-DNA methyltransferase (MGMT) promoter is predictive for treatment response in glioblastoma patients. However, precise predictive cutoff values to distinguish "MGMT methylated" from "MGMT unmethylated" patients remain
Hempt, Claudia   +12 more
core   +1 more source

The diagnostic value of lower glucose consumption for IDH1 mutated gliomas on FDG-PET

open access: yesBMC Cancer, 2021
Background Non-invasive diagnosis of IDH1 mutation for gliomas has great clinical significance, and PET has natural advantage to detect metabolism, as IDH mutated gliomas share lower glucose consumption. Methods Clinical data of patients with gliomas and
Feng-Min Liu   +9 more
doaj   +1 more source

IDH1 Non-Canonical Mutations and Survival in Patients with Glioma

open access: yesDiagnostics, 2021
Background: Non-canonical mutations of the isocitrate dehydrogenase (IDH) genes have been described in about 20–25% and 5–12% of patients with WHO grade II and III gliomas, respectively.
Enrico Franceschi   +10 more
doaj   +1 more source

NIMG-42LOWER BRAIN NETWORK EFFICIENCY IN IDH1 WILD TYPE (IDH-WT) MALIGNANT ASTROCYTOMA COMPARED TO IDH1 MUTANT (IDH1-M) [PDF]

open access: yesNeuro-Oncology, 2015
We previously demonstrated that patients with IDH1-WT compared to IDH1-M malignant astrocytoma exhibited worse cognitive function. We hypothesized that this is due to greater lesion momentum that may preclude compensatory brain reorganization. Therefore, in the present study, we examined the structural connectome of patients with IDH1-M and -WT tumors ...
Shelli Kesler   +4 more
openaire   +1 more source

TET2, ASXL1, IDH1, and IDH2 Single Nucleotide Polymorphisms in Turkish Patients with Chronic Myeloproliferative Neoplasms

open access: yesTurkish Journal of Hematology, 2017
We aimed to determine the genotype distribution, allele frequency, and prognostic impact of IDH1/2, TET2, and ASXL1 single nucleotide polymorphisms (SNPs) in myeloproliferative neoplasms (MPNs).
Nur Soyer   +7 more
doaj   +1 more source

Optimizing survival outcomes with post-remission therapy in acute myeloid leukemia. [PDF]

open access: yes, 2019
Optimization of post-remission therapies to maintain complete remission and prevent relapse is a major challenge in treating patients with acute myeloid leukemia (AML).
Chan, Steven M   +4 more
core   +1 more source

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