2022
DOI: 10.1007/s00383-022-05202-2
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Differential expression profiling of onco and tumor-suppressor genes from major-signaling pathways in Wilms’ tumor

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Cited by 3 publications
(2 citation statements)
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“…WT2 gene (Wilms' Tumor 2 gene) is located on chromosome 11p15. The abnormal regulation of chromosome 11p15.5 is related to Beckwith-Widemann syndrome (macrosomia, macroglossia, hemihypertrophy, omphalocele, visceromegaly, Wilms' tumor) [65,66]. We must note that most cases of Wilms' tumor do not exhibit mutations of the above-mentioned genes [67].…”
Section: Nephroblastoma or Wilms' Tumor (Wt)mentioning
confidence: 99%
“…WT2 gene (Wilms' Tumor 2 gene) is located on chromosome 11p15. The abnormal regulation of chromosome 11p15.5 is related to Beckwith-Widemann syndrome (macrosomia, macroglossia, hemihypertrophy, omphalocele, visceromegaly, Wilms' tumor) [65,66]. We must note that most cases of Wilms' tumor do not exhibit mutations of the above-mentioned genes [67].…”
Section: Nephroblastoma or Wilms' Tumor (Wt)mentioning
confidence: 99%
“…FGFR3 is also downregulated in WT [ 66 ]; however, in pediatric CNS tumors, opposite FGFR3 expression profiles are observed. In NB, high expression levels are associated with worse overall survival and event-free survival (EFS) [ 67 ].…”
Section: Protein Kinases In Pediatric Oncology and Their Association ...mentioning
confidence: 99%