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Identification of Lncrna-Mrna Networks in Hepg2 Cells upon ATP7B Knockout and Copper Accumulation

BACKGROUND: Hepatolenticular degeneration (HLD) is an inherited disorder caused by the mutation in the adenosine triphosphatase copper transporting β gene (ATP7B). W aimed to explore the genetic changes in HLD using bioinformatics analysis. METHODS: The study was conducted in Nepal, in 2019. The GSE...

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Detalles Bibliográficos
Autores principales:	Yan, Yan, Xu, Yin, Chen, Lin, Han, Yongzhu, Yang, Renmin, Hu, Wenbin
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Tehran University of Medical Sciences 2023
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362205/ https://www.ncbi.nlm.nih.gov/pubmed/37484722 http://dx.doi.org/10.18502/ijph.v52i5.12720

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