2023
DOI: 10.1016/j.thromres.2022.11.013
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Targeted DNA sequencing to identify genetic aberrations in glioblastoma that underlie venous thromboembolism; a cohort study

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Cited by 5 publications
(2 citation statements)
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“…There is evidence that several uncommon hereditary diseases, such as tuberous sclerosis and neurofibromatosis types 1 and 2, are becoming more common. 26…”
Section: Family Historymentioning
confidence: 99%
“…There is evidence that several uncommon hereditary diseases, such as tuberous sclerosis and neurofibromatosis types 1 and 2, are becoming more common. 26…”
Section: Family Historymentioning
confidence: 99%
“…Activation of the Epidermal Growth Factor Receptor (EGFR), through genomic amplifications or mutations, was reported to be positively correlated with F3 expression in GBM [13]. A significant positive association between the amplification status of the EGFR locus in GBM and the presence of histologically detectable intra-tumoral thrombosis was suggested by Furuta et al [14]; however, the link between VTE and the presence of EGFR amplifications in GBM nevertheless remains uncertain [15,16]. In addition to specific genomic alterations, chromosomal instability also activates innate immune pathways, potentially leading to F3 expression in human tumors [17].…”
Section: Introductionmentioning
confidence: 99%