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Mutant fibroblast growth factor receptor 3 induces intracellular signaling and cellular transformation in a cell type- and mutation-specific manner.

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Oncogene2009PMID 19749790PMC2789045stubpubmedProvenance
Source
PubMed
Retrieved
Sep 8, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Run
ING-CIVIC-20260908-000001
Published

Abstract

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Linked entities

Linked entities (5)

How each link was made (MeSH, dictionary, registry reference, curation…) and whether it has been validated. Candidate links are not counted in entity statistics.

Validated 5

Curated evidence

Evidence citing this paper (2)

civicProvenance
Source
CIViC — Clinical Interpretation of Variants in Cancer
Dataset
CIViC evidence items
Version
civic-2026-09-08
Retrieved
Sep 8, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Evidence
expert curation
License
CC0 1.0
PMID
19749790
Run
ING-CIVIC-20260908-000001
Open at source
CuratedShowing 1–2 of 2 evidence items · levels, directions and significance as curated at the source; each row links to its CIViC record.
TherapyCancerTypeLevelDirection · significanceRating (1–5)StatusEvidenceSource
FGFR3 Y373C1
(oncogenic)Malignant Bladder NeoplasmALIASOncogenicDSupports Oncogenicity3accepted
EID8880

Using site-directed mutagenesis, the authors investigated the phenotypic and signaling consequences of three FGFR3 mutations, S249C, Y373C (in the paper described as Y375C), and K652E, in immortalized… (full text at CIViC)

PMID 19749790 · di Martino et al., 2009 · Open in CIViC

civic
FGFR3 S249C1
(oncogenic)Transitional Cell CarcinomaOncogenicDSupports Oncogenicity3accepted
EID8855

Compared to controls (empty vector, FGFR3 wildtype, and S249C-Kinase dead cell lines), stable expression of S249C in NIH-3T3 cells resulted in a transformed spindle-like morphology, a 3-fold prolifera… (full text at CIViC)

PMID 19749790 · di Martino et al., 2009 · Open in CIViC

civic