Zhengfeng Xu
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Explore the profile of Zhengfeng Xu including associated specialties, affiliations and a list of published articles.
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Articles
114
Citations
980
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Recent Articles
1.
Shen J, Wang Q, Huang Q, Ying X, Wang Z, Xu Z, et al.
J Cell Biochem
. 2025 Jan;
126(1):e30702.
PMID: 39835731
tRNA-derived fragments (tRFs) are a newly recognized class of small noncoding RNAs (sncRNAs) that play significant roles in various diseases. The Wnt pathway plays a key role in various physiological...
2.
Zhu S, Xie P, Yang Y, Wang Y, Zhang C, Zhang Y, et al.
Nat Struct Mol Biol
. 2025 Jan;
32(2):381-392.
PMID: 39820605
Up to an estimated 10% of women experience miscarriage in their lifetimes. Embryonic aneuploidy is a leading cause for miscarriage, infertility and congenital defects. Here we identify variants of ELL3,...
3.
Tan J, Huang M, Ji X, Liu A, Qiao F, Zhang C, et al.
BMC Pediatr
. 2025 Jan;
25(1):18.
PMID: 39789493
Background: Chromosomal inversions are underappreciated causes of rare diseases given their detection, resolution, and clinical interpretation remain challenging. Heterozygous mutations in the MEIS2 gene cause an autosomal dominant syndrome characterized...
4.
Yang C, Chi X, Wang Y, Zhang C, Zhou R, Jia X, et al.
J Int Med Res
. 2024 Dec;
52(12):3000605241301879.
PMID: 39648848
Objective: This study aimed to analyse the causes of foetal mild-to-moderate isolated ventriculomegaly (IVM) and to evaluate the prognosis of neurological development in surviving children in different subgroups. Methods: We...
5.
Tan J, Tan J, Jiang Z, Shao B, Wang Y, Zhang J, et al.
Clin Chem Lab Med
. 2024 Nov;
63(3):535-544.
PMID: 39560290
Objectives: Expanded carrier screening (ECS) is a preventive genetic test that enables couples to know their risk of having a child affected by certain monogenetic diseases. This study aimed to...
6.
Tan J, Jin S, Huang L, Shao B, Wang Y, Wang Y, et al.
Heliyon
. 2024 Oct;
10(19):e38222.
PMID: 39386847
Molecular genetic analysis of the cytochrome P450 family 21 subfamily A member 2 () gene is challenging owing to the highly homologous with its pseudogene. A reliable approach for the...
7.
Liang D, Lin Y, Luo C, Li H, Hu P, Xu Z
Mol Genet Genomic Med
. 2024 Jun;
12(6):e2479.
PMID: 38860502
Background: As a screening method, inaccuracies in noninvasive prenatal screening (NIPS) exist, which are often attributable to biological factors. One such factor is the history of transplantation. However, there are...
8.
Wang Y, Sun Y, Meng L, He Q, Zhao J, Zhou R, et al.
Clin Transl Med
. 2024 May;
14(5):e1706.
PMID: 38797938
No abstract available.
9.
Zhang Z, Hong D, Ma D, Yang P, Zhang J, Wang X, et al.
Mol Neurobiol
. 2024 May;
61(12):10645-10655.
PMID: 38767836
Duchenne muscular dystrophy (DMD), a lethal X-linked recessive genetic disease, is characterized by progressive muscle wasting which will lead to premature death by cardiorespiratory complications in their late twenties. And...
10.
Huang M, Zhang Q, Jiao J, Shi J, Xu Y, Zhang C, et al.
J Transl Med
. 2024 May;
22(1):451.
PMID: 38741136
Background: Facioscapulohumeral muscular dystrophy (FSHD) is a high-prevalence autosomal dominant neuromuscular disease characterized by significant clinical and genetic heterogeneity. Genetic diagnosis of FSHD remains a challenge because it cannot be...