Yongshun Li
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Explore the profile of Yongshun Li including associated specialties, affiliations and a list of published articles.
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Articles
12
Citations
185
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Recent Articles
1.
Li Y, Liu T, Lai X, Xie H, Tang H, Wu S, et al.
Medicine (Baltimore)
. 2023 Dec;
102(48):e36188.
PMID: 38050301
Cyclophilin D (CypD) is a mitochondrial matrix peptidyl prolidase that regulates the mitochondrial permeability transition pore. Inhibition of CypD was suggested as a therapeutic strategy for acute pancreatitis. Peptide inhibitors...
2.
Liu Q, Li Y, Li W, Zhao J, Qin Z, Yang X, et al.
Sci Rep
. 2022 May;
12(1):7918.
PMID: 35562394
Considering the large-span underground excavation subway station of Qingdao Metro Line 6 of China for analysis, it is necessary to optimize the traditional support system by investigating relevant codes and...
3.
Yao J, Wang Y, Cao C, Song R, Bi D, Zhang H, et al.
Mol Ther Nucleic Acids
. 2021 Jun;
24:986-999.
PMID: 34094716
Gene therapy for curing congenital human diseases is promising, but the feasibility and safety need to be further evaluated. In this study, based on a pig model that carries the...
4.
Zhang Y, Hong Q, Cao C, Yang L, Li Y, Hai T, et al.
Cell Discov
. 2019 Oct;
5:48.
PMID: 31636960
No abstract available.
5.
Li Y, Huang C, Bai Q, Yu J
Biosci Rep
. 2019 Apr;
39(5).
PMID: 30940778
Esophageal cancer is a common digestive tract cancer, which is a serious threat to human health. Ribophorin II (RPN2) is a part of an N-oligosaccharyltransferase complex, which is excessively expressed...
6.
Wang X, Cao C, Li Y, Hai T, Jia Q, Zhang Y, et al.
J Mol Cell Biol
. 2019 Mar;
11(12):1029-1041.
PMID: 30925591
Harlequin ichthyosis (HI) is a severe genetic skin disorder and caused by mutation in the ATP-binding cassette A12 (ABCA12) gene. The retinoid administration has dramatically improved long-term survival of HI,...
7.
Cao C, Zhang Y, Jia Q, Wang X, Zheng Q, Zhang H, et al.
Dis Model Mech
. 2019 Jan;
12(1).
PMID: 30651277
Pigs share many similarities with humans in terms of anatomy, physiology and genetics, and have long been recognized as important experimental animals in biomedical research. Using an N-ethyl-N-nitrosourea (ENU) mutagenesis...
8.
Bai Q, Yu J, Li Y, Ma J, Gou Y
J BUON
. 2018 Dec;
23(5):1439-1447.
PMID: 30570871
Purpose: To study the functioning mode of miR-182 on esophageal squamous cell carcinoma (ESCC) cell growth and metastasis and provide therapeutic targets for ESCC. Methods: miR-182 expression level in ESCC...
9.
Hai T, Guo W, Yao J, Cao C, Luo A, Qi M, et al.
Hum Genet
. 2017 Nov;
136(11-12):1463-1475.
PMID: 29094203
Human Waardenburg syndrome 2A (WS2A) is a dominant hearing loss (HL) syndrome caused by mutations in the microphthalmia-associated transcription factor (MITF) gene. In mouse models with MITF mutations, WS2A is...
10.
Zheng Q, Lin J, Huang J, Zhang H, Zhang R, Zhang X, et al.
Proc Natl Acad Sci U S A
. 2017 Oct;
114(45):E9474-E9482.
PMID: 29078316
Uncoupling protein 1 (UCP1) is localized on the inner mitochondrial membrane and generates heat by uncoupling ATP synthesis from proton transit across the inner membrane. UCP1 is a key element...