Please use this identifier to cite or link to this item:
https://hdl.handle.net/10356/142251
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Huo, Jianxin | en_US |
dc.contributor.author | Xu, Shengli | en_US |
dc.contributor.author | Lam, Kong-Peng | en_US |
dc.date.accessioned | 2020-06-18T01:22:47Z | - |
dc.date.available | 2020-06-18T01:22:47Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | Huo, J., Xu, S., & Lam, K.-P. (2019). FAIM : an antagonist of Fas-killing and beyond. Cells, 8(6), 541-. doi:10.3390/cells8060541 | en_US |
dc.identifier.issn | 2073-4409 | en_US |
dc.identifier.uri | https://hdl.handle.net/10356/142251 | - |
dc.description.abstract | Fas Apoptosis Inhibitory Molecule (FAIM) is an anti-apoptotic protein that is up-regulated in B cell receptor (BCR)-activated B cells and confers upon them resistance to Fas-mediated cell death. Faim has two alternatively spliced isoforms, with the short isoform ubiquitously expressed in various tissues and the long isoform mainly found in the nervous tissues. FAIM is evolutionarily conserved but does not share any significant primary sequence homology with any known protein. The function of FAIM has been extensively studied in the past 20 years, with its primary role being ascribed to be anti-apoptotic. In addition, several other functions of FAIM were also discovered in different physiological and pathological conditions, such as cell growth, metabolism, Alzheimer’s disease and tumorigenesis. However, the detailed molecular mechanisms underlying FAIM’s role in these conditions remain unknown. In this review, we summarize comprehensively the functions of FAIM in these different contexts and discuss its potential as a diagnostic, prognostic or therapeutic target. | en_US |
dc.description.sponsorship | ASTAR (Agency for Sci., Tech. and Research, S’pore) | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Cells | en_US |
dc.rights | © 2019 The Author(s). Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). | en_US |
dc.subject | Science::Biological sciences | en_US |
dc.title | FAIM : an antagonist of Fas-killing and beyond | en_US |
dc.type | Journal Article | en |
dc.contributor.school | School of Biological Sciences | en_US |
dc.contributor.organization | Bioprocessing Technology Institute, A*STAR | en_US |
dc.identifier.doi | 10.3390/cells8060541 | - |
dc.description.version | Published version | en_US |
dc.identifier.pmid | 31167518 | - |
dc.identifier.issue | 6 | en_US |
dc.identifier.volume | 8 | en_US |
dc.subject.keywords | FAIM | en_US |
dc.subject.keywords | B Cells | en_US |
item.grantfulltext | open | - |
item.fulltext | With Fulltext | - |
Appears in Collections: | SBS Journal Articles |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
FAIM An Antagonist of Fas-Killing and Beyond.pdf | 833.36 kB | Adobe PDF | ![]() View/Open |
SCOPUSTM
Citations
20
8
Updated on Mar 26, 2023
Web of ScienceTM
Citations
20
10
Updated on Apr 1, 2023
Page view(s)
198
Updated on Apr 1, 2023
Download(s) 50
28
Updated on Apr 1, 2023
Google ScholarTM
Check
Altmetric
Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.