Qing-He Xing
Overview
Explore the profile of Qing-He Xing including associated specialties, affiliations and a list of published articles.
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Articles
25
Citations
266
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0
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Recent Articles
1.
Wang L, Yu B, Peng Y, Mou K, Zhan Y, Wang Y, et al.
Innovation (Camb)
. 2025 Feb;
6(2):100773.
PMID: 39991480
Pharmacogenomic landscapes and related databases are important for identifying the biomarkers of drug response and toxicity. However, these data are still lacking for the Chinese population. In this study, we...
2.
Ding J, Chi H, Qiu Y, Wang R, Yang J, She H, et al.
Biochim Biophys Acta Mol Basis Dis
. 2024 Dec;
1871(3):167624.
PMID: 39705897
Background: Ubiquitin-specific protease 53 (USP53) deficiency is associated with familial intrahepatic cholestasis in which serum gamma-glutamyl transferase (GGT) activity is relatively low. However, how USP53 deficiency contributes to cholestasis is...
3.
Cheng Y, Zhang Y, Wei B, Chen L, Xing Q, Wang J
Gastroenterol Rep (Oxf)
. 2024 Jan;
12:goad073.
PMID: 38283825
No abstract available.
4.
Zhao J, Qiu Y, Wang L, Li Z, Xie X, Lu Y, et al.
J Mol Diagn
. 2023 Feb;
25(4):227-233.
PMID: 36739965
Δ-3-oxosteroid 5β-reductase (AKR1D1) deficiency presents with neonatal cholestasis and liver failure in early infancy and features high levels of 3-oxo-Δ-bile acids in urine. Genetic analysis is needed for definitive diagnosis,...
5.
Qiu Y, Wang L, Huang M, Lian M, Wang F, Gong Y, et al.
J Cell Physiol
. 2022 May;
237(6):2713-2723.
PMID: 35621037
TMEM67 (mecklin or MKS3) locates in the transition zone of cilia. Dysfunction of TMEM67 disrupts cilia-related signaling and leads to developmental defects of multiple organs in humans. Typical autosomal recessive...
6.
Wang L, Qiu Y, Xu H, Zhu J, Li S, Ouyang W, et al.
Liver Int
. 2021 Nov;
42(2):402-411.
PMID: 34811877
Background & Aims: Biallelic pathogenic variants in MYO5B cause microvillus inclusion disease (MVID), or familial intrahepatic cholestasis (FIC). The reported FIC patients are scarce and so the genotype-phenotype correlation has...
7.
Luan W, Hao C, Li J, Wei Q, Gong J, Qiu Y, et al.
J Med Genet
. 2020 Aug;
58(8):514-525.
PMID: 32737136
Background: For many children with intrahepatic cholestasis and high-serum gamma-glutamyl transferase (GGT) activity, a genetic aetiology of hepatobiliary disease remains undefined. We sought to identify novel genes mutated in children...
8.
Zhang J, Liu L, Gong J, Hao C, Qiu Y, Lu Y, et al.
Hum Mutat
. 2019 Nov;
41(2):502-511.
PMID: 31696999
To assess the spectrum of pediatric clinical phenotypes in TJP2 disease, we reviewed records of our seven patients in whom intrahepatic cholestasis was associated with biallelic TJP2 variants (13; 12...
9.
Wang Y, Sun S, Qiu Y, Xing Q, Lu W
BMC Med Genet
. 2018 Aug;
19(1):139.
PMID: 30086703
Background: Branchio-oto-renal (BOR) syndrome is a dominant autosomal disorder characterized by phenotypes such as hearing loss, branchial fistulae, preauricular pits, and renal abnormalities. EYA1, the human homolog of the Drosophila...
10.
Chen S, Zhang L, Yang F, Yang L, Yang Y, Chen Z, et al.
Basic Clin Pharmacol Toxicol
. 2018 Mar;
123(3):308-313.
PMID: 29575644
Genetic risk factors could cause cutaneous adverse drug reactions (cADRs) in patients after treatment with clarithromycin. This study explored the association of HLA class I genes with clarithromycin-cADRs in Han...