Lv Liu
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Explore the profile of Lv Liu including associated specialties, affiliations and a list of published articles.
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35
Citations
132
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Recent Articles
1.
Wang C, Chen Y, Huang H, Yuan Z, Dong Y, Jin J, et al.
Mol Med
. 2025 Feb;
31(1):63.
PMID: 39972424
Background: As an endoplasmic reticulum (ER) protein, Reticulum 3 (RTN3) has been reported to play a crucial role in neurodegenerative diseases, lipid metabolism, and chronic kidney disease. The involvement of...
2.
Xun Z, Liu L, Zhang B, Fan L, Zhang L, Zhao H, et al.
Electrophoresis
. 2024 Dec;
45(23-24):2182-2190.
PMID: 39624911
On-line counting of the microparticle/bacteria in the liquid medium has great potential in the food safety and biomedical fields. A new low-cost microfluidic device is proposed for the on-line counting...
3.
Wang C, Chang S, Hu C, Hu Y, Luo H, Liu L, et al.
Mol Med
. 2024 Sep;
30(1):144.
PMID: 39256642
Background: Idiopathic pulmonary fibrosis (IPF) is a special kind of chronic interstitial lung disease with insidious onset. Previous studies have revealed that mutations in ZCCHC8 may lead to IPF. The...
4.
5.
Ji Y, Liu L, Liu Y, Ma Y, Ji Z, Wu X, et al.
Environ Toxicol
. 2024 Mar;
PMID: 38546286
Osteosarcoma predominantly affects adolescents and young adults and is characterized as a malignant bone tumor. In recent decades, substantial advancements have been achieved in both diagnosing and treating osteosarcoma. Resulting...
6.
Gao S, Liu Y, Dong Y, Fan L, Ding Q, Liu L
Front Genet
. 2023 Nov;
14:1205052.
PMID: 38028608
Hereditary spastic paraplegia (HSP) is a progressive upper-motor neurodegenerative disease. Mutations in the gene are associated with autosomal dominant HSP, spastic paraplegia 8 (SPG8). However, due to the small number...
7.
Liu L, Luo H, Sheng Y, Kang X, Peng H, Luo H, et al.
Hereditas
. 2023 Nov;
160(1):37.
PMID: 37978541
Interstitial lung diseases (ILDs), or diffuse pulmonary lung disease, are a subset of lung diseases that primarily affect lung alveoli and the space around interstitial tissue and bronchioles. It clinically...
8.
Dong Y, Zhang Y, Sheng Y, Wang F, Liu L, Fan L
Front Genet
. 2023 Oct;
14:1208540.
PMID: 37881805
Heterozygous mutations in the () gene are one of the causes generating developmental and epileptic encephalopathies. So far, only eleven mutations in the DHDDS gene have been identified. The mutation...
9.
Zhao L, Li W, Liu L, Duan L, Wang L, Yang H, et al.
J Clin Endocrinol Metab
. 2023 Aug;
109(1):e175-e181.
PMID: 37536271
Context: Type B insulin resistance syndrome (TBIRS) is a rare condition, for which effective treatment remains challenging. Objective: This work aimed to summarize the clinical characteristics of TBIRS and explore...
10.
Ji H, Lin Z, Chen C, Xu J, Yu R, Liu L
Genes Dis
. 2023 Jul;
10(3):671-674.
PMID: 37396552
No abstract available.