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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.

Coiled-coil domain containing 19

NESG1, nasopharyngeal epithelium specific protein 1
Top mentioned proteins: p21, Inactive, CdS, TRAF2, E2F1
Papers on NESG1
Proteomic features of potential tumor suppressor NESG1 in nasopharyngeal carcinoma.
Fang et al., Guangzhou, China. In Proteomics, 2012
We previously defined the recently revised NESG1 gene as a potential tumor suppressor in nasopharyngeal carcinoma (NPC).
Decreased expression of updated NESG1 in nasopharyngeal carcinoma: its potential role and preliminarily functional mechanism.
Fang et al., China. In Int J Cancer, 2011
Decreased expression of NESG1 is associated with nasopharyngeal carcinoma.
[Construction of a lentiviral vector containing human NESG1 gene and its expression in 293FT cells].
Fang et al., Guangzhou, China. In Nan Fang Yi Ke Da Xue Xue Bao, 2011
OBJECTIVE: To construct a lentiviral vector carrying human NESG1-EGFP gene and observe its expression in 293FT cells.
Potential tumor suppressor NESG1 as an unfavorable prognosis factor in nasopharyngeal carcinoma.
Fang et al., Guangzhou, China. In Plos One, 2010
Decreased NESG1 expression is an unfavorable prognostic factor for nasopharyngeal carcinoma.
Proteomic profiling of glucocorticoid-exposed myogenic cells: Time series assessment of protein translocation and transcription of inactive mRNAs.
Hathout et al., Washington, D.C., United States. In Proteome Sci, 2008
Quantitative fluorography identified 16 2D gel spots showing rapid changes in translation; five of these were identified by MS/MS (pyruvate kinase, annexin A6 isoform A and isoform B, nasopharyngeal epithelium specific protein 1, and isoform 2 of Replication factor C subunit 1), and all showed the 5' terminal oligopyrimidine motifs associated with mRNA sequestration to and from inactive mRNA pools.
Molecular cloning of a novel tissue-specific gene from human nasopharyngeal epithelium.
Cao et al., Changsha, China. In Gene, 1999
The cDNA fragment of the gene, termed NESG1, was originally isolated by mRNA differential display, and was not homologous to any of the known genes in the database.
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