Juping Du
Overview
Explore the profile of Juping Du including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
25
Citations
1220
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Wang N, Yang Y, Tian X, Fu H, Chen S, Du J, et al.
Orphanet J Rare Dis
. 2025 Feb;
20(1):66.
PMID: 39934873
Background: Gitelman syndrome (GS) is an inherited renal tubular disorder characterized by hypokalemic alkalosis and hypomagnesemia, due to biallelic pathogenic variants in the solute carrier family 12 member 3 (SLC12A3)...
2.
Chen S, Zhao W, Du J, Chen S, Li J, Shen B, et al.
BMC Genomics
. 2024 Sep;
25(1):899.
PMID: 39350019
Background: Recombination signal-binding protein for immunoglobulin kappa J region (RBPJ) is a transcriptional regulator that plays an important role in maintaining immune homeostasis. This study aimed to estimate the expression...
3.
Chen S, Xu G, Zhao Z, Du J, Shen B, Li C
BMC Med Genomics
. 2024 Apr;
17(1):108.
PMID: 38671472
Background: Alport syndrome (AS) is characterised by haematuria, proteinuria, a gradual decline in kidney function, hearing loss, and eye abnormalities. The disease is caused by mutations in COL4An (n = ...
4.
Kang H, Lv H, Tung T, Ma D, Wang Z, Du J, et al.
Asian J Surg
. 2023 Aug;
47(1):201-207.
PMID: 37574361
Background: Invasive lung adenocarcinoma (LUAD) patients with the micropapillary (MPP) component tend to have extremely poor prognosis. To optimize clinical outcomes, a better understanding of specific concurrent gene alterations and...
5.
Du J, Zheng L, Chen S, Wang N, Pu X, Yu D, et al.
Front Immunol
. 2022 Nov;
13:950144.
PMID: 36439145
Nuclear-factor, interleukin 3 regulated (NFIL3) is an immune regulator that plays an essential role in autoimmune diseases. However, the relationship between rheumatoid arthritis (RA) and NFIL3 remains largely unknown. In...
6.
Chen S, Du J, Jiang H, Zhao W, Wang N, Ying A, et al.
Front Mol Neurosci
. 2022 Nov;
15:1019974.
PMID: 36438189
Objectives: Autosomal recessive inherited ataxia with oculomotor apraxia type 2 (AOA2), caused by gene mutations, is characterized by early-onset, progressive cerebellar ataxia, peripheral neuropathy, oculomotor apraxia and elevated serum α-fetoprotein...
7.
Tian X, Zheng J, Mou W, Lu G, Chen S, Du J, et al.
Front Pharmacol
. 2022 Aug;
13:939542.
PMID: 35935823
Pancreatic adenocarcinoma (PAAD) is one of the most aggressive and fatal gastrointestinal malignancies with high morbidity and mortality worldwide. Accumulating evidence has revealed the clinical significance of the interaction between...
8.
Zhu X, Wang J, Du J, Chen S, Chen S, Li J, et al.
Infect Drug Resist
. 2022 Apr;
15:1857-1870.
PMID: 35450115
Objective: Abnormal liver function and liver injury related to COVID-19 during hospitalization has received widespread attention. However, the long-term observation of patients' liver functions after discharge has not been investigated....
9.
Yu D, Du J, Pu X, Zheng L, Chen S, Wang N, et al.
Front Cell Infect Microbiol
. 2022 Feb;
11:763507.
PMID: 35145919
The relationship among the gut microbiome, global fecal metabolites and rheumatoid arthritis (RA) has not been systematically evaluated. In this study, we performed 16S rDNA sequencing and liquid chromatography-tandem mass...
10.
Wang N, Zheng Y, Zhang L, Tian X, Fang Y, Qi M, et al.
Front Genet
. 2022 Feb;
12:811833.
PMID: 35111204
Primary coenzyme Q10 deficiency-6 (COQ10D6), as a rare autosomal recessive disease caused by mutations, is characterized by progressive infantile-onset nephrotic syndrome resulting in end-stage renal failure and sensorineural hearing loss....