» Authors » Xiaoyong Zheng

Xiaoyong Zheng

Explore the profile of Xiaoyong Zheng including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 28
Citations 260
Followers 0
Related Specialties
Top 10 Co-Authors
Published In
Affiliations
Soon will be listed here.
Recent Articles
1.
Feng S, Feng Z, Wei Y, Zheng X, Deng Z, Liao Z, et al.
Cell Mol Life Sci . 2024 Jun; 81(1):260. PMID: 38878096
The pathological advancement of osteoporosis is caused by the uneven development of bone marrow-derived mesenchymal stem cells (BMSCs) in terms of osteogenesis and adipogenesis. While the role of EEF1B2 in...
2.
Liao Z, Zheng X, Li H, Deng Z, Feng S, Tan H, et al.
FASEB J . 2024 May; 38(9):e23657. PMID: 38713087
The pathogenesis of osteoporosis (OP) is closely associated with the disrupted balance between osteogenesis and adipogenesis in bone marrow-derived mesenchymal stem cells (BMSCs). We analyzed published single-cell RNA sequencing (scRNA-seq)...
3.
Jia K, Zeng M, Zheng X, Xie H, Yang L, Xie Y, et al.
Hamostaseologie . 2023 Dec; 43(6):e1. PMID: 38096836
No abstract available.
4.
Deng Z, Rong S, Gan L, Wang F, Bao L, Cai F, et al.
iScience . 2023 Aug; 26(8):107200. PMID: 37554462
Human epiphyseal development has been mainly investigated through radiological and histological approaches, uncovering few details of cellular temporal genetic alternations. Using single-cell RNA sequencing, we investigated the dynamic transcriptome changes...
5.
Jia K, Zeng M, Zheng X, Xie H, Yang L, Xie Y, et al.
Hamostaseologie . 2023 Jul; 43(6):426-431. PMID: 37516116
Objective:  Our study aimed to analyze the phenotype and genotype of a pedigree with inherited dysfibrinogenemia, and preliminarily elucidate the probable pathogenesis. Methods:  The one-stage clotting method was used to...
6.
Zheng X, Chen Y, Wen M, Jin Y, Zeng M, Jia K, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi . 2023 Feb; 40(3):276-281. PMID: 36854400
Objective: To retrospectively analyze the clinical phenotypes and genetic variants in two Chinese pedigrees affected with Hereditary hypofibrinemia (IFD) and explore their molecular pathogenesis. Methods: Two probands and their pedigree...
7.
Jiang S, Chen Y, Xie H, Liu M, Zheng X, Wang M
Hamostaseologie . 2022 Dec; 43(2):142-145. PMID: 36481867
Background:  Hereditary coagulation factor XII (FXII) deficiency is an autosomal recessive disorder. At present, the contribution of severe FXII deficiency to the development of thromboembolism is still undetermined. There are...
8.
Zheng X, Ma Y, Bai Y, Huang T, Lv X, Deng J, et al.
Front Immunol . 2022 Nov; 13:984480. PMID: 36389763
The incidence and mortality of colorectal cancer (CRC) are increasing year by year. The accurate classification of CRC can realize the purpose of personalized and precise treatment for patients. The...
9.
Liao Z, Jin Y, Chu Y, Wu H, Li X, Deng Z, et al.
Commun Biol . 2022 Apr; 5(1):324. PMID: 35388143
Alcohol-induced osteonecrosis of the femoral head (ONFH) is a disabling disease with a high incidence and elusive pathogenesis. Here, we used single-cell RNA sequencing to explore the transcriptomic landscape of...
10.
Lian W, Jin H, Cao J, Zhang X, Zhu T, Zhao S, et al.
Cancer Cell Int . 2020 Apr; 20:105. PMID: 32256214
Background: Tumor progression and distant metastasis are the main causes of deaths in colorectal cancer (CRC) patients, and the molecular mechanisms in CRC metastasis have not been completely discovered. Methods:...