Jianlan Peng
Overview
Explore the profile of Jianlan Peng including associated specialties, affiliations and a list of published articles.
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Articles
8
Citations
294
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0
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Recent Articles
1.
Peng J, Liu C, Mo M, Huang Y, Lu Y, Xiao M, et al.
Int J Biol Macromol
. 2024 Nov;
283(Pt 2):137746.
PMID: 39551312
Nanozymes have become promising alternative antibacterial agents for bacteria-infected wounds. In this study, fucoidan-confined gold nanoparticles (Fuc@AuNPs) are developed by in situ reduction, and stabilized by sulfate groups of fucoidan....
2.
Peng J, Li S, Ti H
Int J Nanomedicine
. 2024 Jun;
19:5895-5930.
PMID: 38895146
Low immunogenicity of tumors poses a challenge in the development of effective tumor immunotherapy. However, emerging evidence suggests that certain therapeutic approaches, such as chemotherapy, radiotherapy, and phototherapy, can induce...
3.
Wang W, Ou Z, Peng J, Wang N, Zhou Y
BMC Musculoskelet Disord
. 2022 Dec;
23(1):1123.
PMID: 36550476
Background: Through the bioinformatics analysis to screen out the potential chromatin regulators (CRs) under the immune infiltration of osteoarthritis (OA), thus providing some theoretical support for future studies of epigenetic...
4.
Wang W, Ou Z, Peng J, Zhou Y, Wang N
Ann Transl Med
. 2022 Nov;
10(20):1116.
PMID: 36388797
Background: Osteoarthritis (OA) is a common clinical disease caused by a variety of factors, including genetic variants. Although genome-wide association studies (GWAS) have been performed to elucidate the genetic basis...
5.
Wiszniewski W, Lewis R, Stockton D, Peng J, Mardon G, Chen R, et al.
Hum Genet
. 2010 Dec;
129(3):319-27.
PMID: 21153841
Leber congenital amaurosis (LCA) is a clinically and genetically heterogeneous retinal dystrophy. The causes of LCA have been unraveled partially at the molecular level. At least 14 genes have been...
6.
Li Y, Wang H, Peng J, Gibbs R, Lewis R, Lupski J, et al.
Invest Ophthalmol Vis Sci
. 2008 Oct;
50(3):1336-43.
PMID: 18936139
Purpose: The purpose of this study was to perform a comprehensive survey of all known Leber congenital amaurosis (LCA) genes and loci in a collection of 37 consanguineous LCA families...
7.
Srivatsan A, Han Y, Peng J, Tehranchi A, Gibbs R, Wang J, et al.
PLoS Genet
. 2008 Aug;
4(8):e1000139.
PMID: 18670626
Whole-genome sequencing is a powerful technique for obtaining the reference sequence information of multiple organisms. Its use can be dramatically expanded to rapidly identify genomic variations, which can be linked...
8.
Ware S, Peng J, Zhu L, Fernbach S, Colicos S, Casey B, et al.
Am J Hum Genet
. 2003 Dec;
74(1):93-105.
PMID: 14681828
Mutations in the zinc finger transcription factor ZIC3 cause X-linked heterotaxy and have also been identified in patients with isolated congenital heart disease (CHD). To determine the relative contribution of...