Results 81 to 90 of about 41,008 (260)
APROXIMACIÓN AL MÉTODO FILOSÓFICO Y LA CREACIÓN CONCEPTUAL
En el presente escrito me propongo mostrar cómo se producen los conceptos desde distintos enfoques filosóficos que encuentran, en ciertos puntos problemáticos y a pesar de sus diferencias irreductibles, zonas de contacto y convergencia entre sí.
Roque Farrán
doaj
This article presents a case study in a secondary school located in a City - Neighborhood of Córdoba Capital whose students are, predominantly, the first generation of families to access, stay, and graduate from secondary school.
Maria Cecilia Bocchio
doaj +1 more source
Immunohistochemistry as a tool for identifying EGFR amplification in CNS tumors
EGFR gene amplification constitutes a diagnostic hallmark for glioblastoma, IDH‐wildtype (GB, IDH‐WT). Herein, we demonstrated that EGFR IHC is a highly specific and sensitive biomarker for identifying EGFR amplification and should be part of the neuropathologist's routine panel of antibodies.
Arnault Tauziède‐Espariat +12 more
wiley +1 more source
This integrated high‐resolution copy number and histomolecular analysis of diffuse hemispheric glioma, H3 G34‐mutant expands the spectrum of associated genetic changes and underscores the presence of universal TP53 abnormalities at copy number, sequence, and protein expression level, with frequent yet largely unrecognized TP53 copy‐neutral loss of ...
Jorge A. Trejo‐Lopez +28 more
wiley +1 more source
We report the clinical and genetic features of an institutional cohort of primary adult gliosarcomas compared to glioblastoma. We performed spatial whole‐transcriptome analysis on glial and sarcomatous regions of four cases to compare gene expression profiles and validated differential protein expression for two markers in tissue sections.
Matthew D. Wood +6 more
wiley +1 more source
Clinical and Genetic Landscape of Glioblastoma, IDH‐Wildtype With FGFR Gene Family Alterations
We analyzed 1076 cases of glioblastoma, IDH‐wildtype (GBM, IDH‐wt) using the C‐CAT genomic database to clarify the clinical and genetic features of FGFR alterations. FGFR::TACC fusions and FGFR1 mutations were identified in distinct subsets and were associated with unique co‐mutation patterns.
Yasuhito Kegoya +9 more
wiley +1 more source

