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Baojiang Wang

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Articles 26
Citations 339
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Recent Articles
1.
Bao Y, Wu W, Lin J, Yang Y, Lin S, Su J, et al.
Mol Med . 2025 Mar; 31(1):96. PMID: 40075271
X-linked Alport syndrome (XLAS) caused by X-linked COL4A5 gene mutation is a hereditary disease that affects mainly the kidney. XLAS patients, especially males whose single copy of the COL4A5 gene...
2.
Wang B, Qin Y, Chen Y, Zheng X, Chen Y, Zhao J, et al.
Brain Behav Immun Health . 2025 Jan; 43():100929. PMID: 39810796
Purpose: Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder increasingly recognized for its strong association with chronic inflammation. Adipose tissue functions as an endocrine organ and can secrete inflammatory...
3.
Chen Y, Wang B, Lai W, Chen Y, Pan R, Tang Z, et al.
Front Neurosci . 2022 Oct; 16:990040. PMID: 36188472
Traditional Chinese herbal medicine aiming at nourishing formed a distinctive school of thought in history to achieve anti-aging and longevity. In the formula Gancao nourishing (GCNY) decoction, all of the...
4.
Chen Y, Wang B, Chen Y, Wu Q, Lai W, Wei L, et al.
Front Immunol . 2022 Jun; 13:888612. PMID: 35720292
HAPLN1 maintains aggregation and the binding activity of extracellular matrix (ECM) molecules (such as hyaluronic acid and proteoglycan) to stabilize the macromolecular structure of the ECM. An increase in HAPLN1...
5.
Wang B, Qin Y, Wu Q, Li X, Xie D, Zhao Z, et al.
Front Immunol . 2022 Apr; 13:818518. PMID: 35422816
Autism spectrum disorder (ASD) is a complex pervasive neurodevelopmental disorder and neuroinflammation may contribute to the pathogenesis of ASD. However, the exact mechanisms of abnormal release of proinflammatory mediators in...
6.
Chen Y, Chen Y, Zhao L, He H, Wei L, Lai W, et al.
J Inflamm Res . 2021 Nov; 14:5501-5511. PMID: 34737599
Purpose: Inflamm-aging is a novel-concept in rheumatoid arthritis (RA) with accelerating aging process. We try to find a correlation between serum albumin/globulin (A/G) ratio and clinical biochemical parameters, incidence of...
7.
Li X, Lai L, Su J, Chen S, Lin S, Wang B, et al.
J Diabetes Investig . 2021 May; 12(11):2062-2070. PMID: 33979016
Aims/introduction: Emerging evidence suggests that expression quantitative trait loci (eQTLs) are more likely to associate with complex diseases. Transient receptor potential cation channel subfamily M member 5 (TRPM5) is a...
8.
Li X, Su J, Zheng K, Lin S, Chen S, Wang B, et al.
Nagoya J Med Sci . 2020 Dec; 82(4):703-709. PMID: 33311801
Estrogen has an important role in regulating glucose homeostasis, and existing evidence indicates that it might be involved in the development of hyperglycemia in pregnancy. It mediates its effect through...
9.
Li X, Su J, Chen S, Lin S, Zheng X, Wang B, et al.
BMC Res Notes . 2020 Feb; 13(1):102. PMID: 32093765
Objective: The arachidonate 5-lipoxygenase (ALOX5) pathway has been investigated in diverse chronic inflammatory diseases including metabolic disorders. Recently, the ALOX5 polymorphism rs4987105 was identified to confer susceptibility to type 2...
10.
Li S, Duan S, Qin Y, Lin S, Zheng K, Li X, et al.
Transl Vis Sci Technol . 2019 Jul; 8(4):3. PMID: 31316863
Purpose: Leber's hereditary optic neuropathy (LHON) is a mitochondrial DNA (mtDNA)-associated, maternally inherited eye disease. Mutation heteroplasmy level is one of the leading causes to trigger LHON manifestation. In this...