Cargando…
Down‐regulation of MYH10 driven by chromosome 17p13.1 deletion promotes hepatocellular carcinoma metastasis through activation of the EGFR pathway
Somatic copy number alterations (CNAs) are a genomic hallmark of cancers. Among them, the chromosome 17p13.1 deletions are recurrent in hepatocellular carcinoma (HCC). Here, utilizing an integrative omics analysis, we screened out a novel tumour suppressor gene within 17p13.1, myosin heavy chain 10...
Autores principales: | Jin, Qian, Cheng, Min, Xia, Xia, Han, Yuqing, Zhang, Jing, Cao, Pengbo, Zhou, Gangqiao |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8650048/ https://www.ncbi.nlm.nih.gov/pubmed/34738311 http://dx.doi.org/10.1111/jcmm.17036 |
Ejemplares similares
-
Acute myeloid leukemia with inv(16)(p13.1q22) and deletion of the 5’MYH11/3’CBFB gene fusion: a report of two cases and literature review
por: Lv, Lili, et al.
Publicado: (2020) -
Prenatal Diagnosis of 17p13.1p13.3 Duplication
por: Kiiski, Kirsi, et al.
Publicado: (2012) -
A Case of Acute Myeloid Leukemia With inv(16)(p13.1q22);CBFB-MYH11 Presenting With Faggot Cells
por: Kim, Jung-Ah, et al.
Publicado: (2021) -
Generating endogenous Myh11-driven Cre mice for sex-independent gene deletion in smooth muscle cells
por: Zhao, Yang, et al.
Publicado: (2023) -
Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment
por: Pettigrew, Kerry A., et al.
Publicado: (2015)