...NF1, KMT2D, and GRIN2A. No significant correlations were found between TMB and age, neuro-invasion (p = 0.125), and tumo...
...NF1) was compared between women with a primary breast cancer (PBC) and SBC who underwent multigene panel testing at a si...
...NF1, MAX, SDHA, and SDHD). We report the expected prevalence of germline mutations in Korean PPGL patients. NGS is a use...
...NF1, TERT promoter, and BRAF V600E mutations. Median OS from HGG diagnosis was 23.4 months, and median OS following ECM ...
...NF1 (p < 0.01), KRAS (p < 0.01), and TP53 (p < 0.001) were significantly associated with gender. This work revealed the ...
Neurofibromatosis type 1 is a genetic disorder associated with cognitive deficits, learning disabilities and behavioral ...
...NF1(n = 3), TP53(n = 4) and EGFR(n = 5). However, by phylogenetic analysis, there were no protein-coding mutations as re...
...NF1, and KRAS and SOS1 in the MAPK pathway; between PSPH and SHMT2 in serine biosynthesis; between AKT3 and TSC2 in the ...
...NF1, CDKN2B, KMT2D, GLI1, ATM, TERT, PI3KCA, NOTCH1, MAP2K4, ERBB4, ARID1A, TSC2, and TNFAIP3. At least 1 targetable GA ...
...NF1) were most common in patients with situ recurrent GBM, while mutations in the MUC family and TP53 pathway (MUC16, CH...
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