Abstract
Yankun Feng, Binwei Liu, Zhenzhen Lin, Liu Yuanrong, Jin Tan, Jincai Guo, Qun Tang
Abstract
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IARC perspective on oral cancer prevention
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MiR-424/TGIF2-mediated pro-fibrogenic responses in oral submucous fibrosis
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Oral submucous fibrosis in Asian countries
10.1111/jop.12924 · 2020
Drug treatment for oral submucous fibrosis: an update
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Antioxidant treatments in patients with oral submucous fibrosis: a systematic review
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Comparative efficacy of interventions for the management of oral submucous fibrosis: a systematic review and network meta-analysis
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How cells recognize and remove the perforated lysosome
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Molecular mechanisms of macroautophagy, microautophagy, and chaperone-mediated autophagy
10.1272/jnms.jnms.2024_91-102 · 2024
Autophagy genes in biology and disease
10.1038/s41576-022-00562-w · 2023
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crossref
Confidence 100%
ror
Confidence 99%
openalex
Confidence 95%
datacite
Confidence 0%
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Starvation induces rapid degradation of selective autophagy receptors by endosomal microautophagy
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The pro-oxidant adaptor p66SHC promotes B cell mitophagy by disrupting mitochondrial integrity and recruiting LC3-II
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Evaluation of transforming growth factor beta1 gene in oral submucous fibrosis induced in Sprague-Dawley rats by injections of areca nut and pan masala (commercial areca nut product) extracts
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Panax notoginseng saponins inhibit areca nut extract-induced oral submucous fibrosis in vitro
10.1111/jop.12158 · 2014
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[Rat model with oral submucous fibrosis induced by arecoline and mechanical stimulation]
2019
Panax notoginseng saponins improve oral submucous fibrosis by inhibiting the Wnt/β-catenin signal pathway
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Understanding the molecular mechanism associated with reversal of oral submucous fibrosis targeting hydroxylysine aldehyde-derived collagen cross-links
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Epithelial atrophy in oral submucous fibrosis is mediated by copper (II) and arecoline of areca nut
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Role of autophagy and apoptosis in atrophic epithelium in oral submucous fibrosis
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Ginsenoside Rb1 ameliorated bavachin-induced renal fibrosis via suppressing Bip/eIF2alpha/CHOP signaling-mediated EMT
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Panax notoginseng saponins alleviate LPS-induced fibrosis of HK-2 cells by inhibiting the activation of NLRP3 inflammasome and pyroptosis
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Stem-leaf saponins from Panax notoginseng counteract aberrant autophagy and apoptosis in hippocampal neurons of mice with cognitive impairment induced by sleep deprivation
10.1016/j.jgr.2019.01.009 · 2020
Therapeutic implications of targeting autophagy and TGF-beta crosstalk for the treatment of liver fibrosis
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Anti-radiofibrosis effect of dicliptera chinensis polysaccharide on rat dermal fibroblasts via the TGF-β1/Smads/CTGF signaling pathway
10.1016/j.identj.2024.09.024 · 2025
Anti-radiofibrosis effect of dicliptera chinensis polysaccharide on rat dermal fibroblasts via the TGF-β1/Smads/CTGF signaling pathway
10.1016/j.identj.2024.09.024 · doi-reference
Therapeutic implications of targeting autophagy and TGF-beta crosstalk for the treatment of liver fibrosis
10.1016/j.lfs.2023.121894 · doi-reference
Stem-leaf saponins from Panax notoginseng counteract aberrant autophagy and apoptosis in hippocampal neurons of mice with cognitive impairment induced by sleep deprivation
10.1016/j.jgr.2019.01.009 · doi-reference
Panax notoginseng saponins alleviate LPS-induced fibrosis of HK-2 cells by inhibiting the activation of NLRP3 inflammasome and pyroptosis
10.2174/1389201024666230417084507 · doi-reference
Ginsenoside Rb1 ameliorated bavachin-induced renal fibrosis via suppressing Bip/eIF2alpha/CHOP signaling-mediated EMT
10.3389/fphar.2022.872474 · doi-reference
Role of autophagy and apoptosis in atrophic epithelium in oral submucous fibrosis
10.2334/josnusd.19-0170 · doi-reference
Autophagy mediates oral submucous fibrosis
10.3892/etm.2016.3145 · doi-reference
Autophagy in liver diseases: time for translation?
10.1016/j.jhep.2019.01.026 · doi-reference
Epithelial atrophy in oral submucous fibrosis is mediated by copper (II) and arecoline of areca nut
10.1111/jcmm.12622 · doi-reference
Understanding the molecular mechanism associated with reversal of oral submucous fibrosis targeting hydroxylysine aldehyde-derived collagen cross-links
10.4103/jcar.jcar_24_20 · doi-reference
Panax notoginseng saponins improve oral submucous fibrosis by inhibiting the Wnt/β-catenin signal pathway
10.1016/j.oooo.2024.03.011 · doi-reference
Panax notoginseng saponins inhibit areca nut extract-induced oral submucous fibrosis in vitro
10.1111/jop.12158 · doi-reference
Evaluation of transforming growth factor beta1 gene in oral submucous fibrosis induced in Sprague-Dawley rats by injections of areca nut and pan masala (commercial areca nut product) extracts
10.4103/0973-1482.148729 · doi-reference
Characterization of a novel dermal fibrosis model induced by areca nut extract that mimics oral submucous fibrosis
10.1371/journal.pone.0166454 · doi-reference
Analytical methods and biological activities of Panax notoginseng saponins: recent trends
10.1016/j.jep.2019.02.035 · doi-reference
Role of autophagy induced by arecoline in angiogenesis of oral submucous fibrosis
10.1016/j.archoralbio.2019.03.021 · doi-reference
Targeting the senescence-autophagy axis for idiopathic pulmonary fibrosis therapy
10.1016/j.tips.2026.02.007 · doi-reference
Autophagy and renal fibrosis
10.14336/ad.2021.1027 · doi-reference
Autophagy in cardiac pathophysiology: Navigating the complex roles and therapeutic potential in cardiac fibrosis
10.1016/j.lfs.2025.123761 · doi-reference
The pro-oxidant adaptor p66SHC promotes B cell mitophagy by disrupting mitochondrial integrity and recruiting LC3-II
10.1080/15548627.2018.1505153 · doi-reference
Starvation induces rapid degradation of selective autophagy receptors by endosomal microautophagy
10.1083/jcb.201711002 · doi-reference
Autophagy, tissue repair, and fibrosis: a delicate balance
10.1016/j.matbio.2021.01.003 · doi-reference
Autophagy genes in biology and disease
10.1038/s41576-022-00562-w · doi-reference
Molecular mechanisms of macroautophagy, microautophagy, and chaperone-mediated autophagy
10.1272/jnms.jnms.2024_91-102 · doi-reference
How cells recognize and remove the perforated lysosome
10.1080/15548627.2022.2138686 · doi-reference
Comparative efficacy of interventions for the management of oral submucous fibrosis: a systematic review and network meta-analysis
10.3390/jpm12081272 · doi-reference
Antioxidant treatments in patients with oral submucous fibrosis: a systematic review
10.1111/jop.13503 · doi-reference
Drug treatment for oral submucous fibrosis: an update
10.1186/s12903-023-03488-9 · doi-reference
Oral submucous fibrosis in Asian countries
10.1111/jop.12924 · doi-reference
MiR-424/TGIF2-mediated pro-fibrogenic responses in oral submucous fibrosis
10.3390/ijms24065811 · doi-reference
IARC perspective on oral cancer prevention
10.1056/nejmsr2210097 · doi-reference