Cargando…
Novel SOX17 frameshift mutations in endometrial cancer are functionally distinct from recurrent missense mutations
Extensive genomic profiling for endometrioid endometrial carcinoma (EEC) has pointed to genes and pathways important in uterine development as critical mediators of endometrial tumorigenesis. SOX17 is a developmental transcription factor necessary for proper endoderm formation that has been implicat...
Autores principales: | Walker, Christopher J., O'Hern, Matthew J., Serna, Vanida A., Kurita, Takeshi, Miranda, Mario A., Sapp, Caroline E., Mutch, David G., Cohn, David E., Goodfellow, Paul J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5620294/ https://www.ncbi.nlm.nih.gov/pubmed/28978154 http://dx.doi.org/10.18632/oncotarget.20213 |
Ejemplares similares
-
Gene characteristics predicting missense, nonsense and frameshift mutations in tumor samples
por: Gorlov, Ivan P., et al.
Publicado: (2018) -
Ovarian insufficiency and CTNNB1 mutations drive malignant transformation of endometrial hyperplasia with altered PTEN/PI3K activities
por: Terakawa, Jumpei, et al.
Publicado: (2019) -
FGFR2 Point Mutations in 466 Endometrioid Endometrial Tumors: Relationship with MSI, KRAS, PIK3CA, CTNNB1 Mutations and Clinicopathological Features
por: Byron, Sara A., et al.
Publicado: (2012) -
Correction: FGFR2 Point Mutations in 466 Endometrioid Endometrial Tumors: Relationship with MSI, KRAS, PIK3CA, CTNNB1 Mutations and Clinicopathological Features
por: Byron, Sara A., et al.
Publicado: (2012) -
Waardenburg syndrome type II in a Chinese pedigree caused by frameshift mutation in the SOX10 gene
por: Li, Li, et al.
Publicado: (2021)