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Xiao-Hui Xie

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Recent Articles
1.
Yang J, Gu H, Yuan Z, Xie X, Yang Y, Tan Z
BMC Med Genomics . 2024 May; 17(1):136. PMID: 38773541
Background: Bosma arhinia microphthalmia syndrome (BAMS; MIM603457) is a rare genetic disorder, predominantly autosomal dominant. It is a multi-system developmental disorder characterized by severe hypoplasia of the nose and eyes,...
2.
Zhang C, Wang J, Xie X
Ther Apher Dial . 2023 Oct; 28(2):297-304. PMID: 37873732
Introduction: The study aimed to explore feasibility and effect of hospital-community online management on the medication management of elderly peritoneal dialysis (PD) patients with end-stage renal disease (ESRD) during COVID-19....
3.
Li Q, Zhang T, Meng J, Wang L, Hua Q, Xie X, et al.
Behav Brain Res . 2023 Sep; 455:114660. PMID: 37690701
Abnormal hemispheric specialization and inter-hemispheric interactions may contribute to the pathogenesis of general anxiety disorder (GAD). The current study investigated these abnormalities in GAD patients based on the two analytic...
4.
Xie X, Jiang M, Xiong Z, Huang X
Dis Markers . 2022 Oct; 2022:2594091. PMID: 36188428
The transplacental transfer of maternal antibodies to the fetus is a critical mechanism for infant protection and perinatal disease. Hemolytic disease of the fetus and newborn (HDFN) is a representative...
5.
Gu H, Yuan Z, Xie X, Yang Y, Tan Z
J Hum Genet . 2022 Jun; 67(10):573-577. PMID: 35691949
Heterotaxy syndrome is a very rare congenital disease, which is caused by the disorder of left-right asymmetry during visceral development. However, pathogenic genetic lesions are found in less than 20%...
6.
Xu Q, Liu Z, Zhu Z, Fan Y, Chen R, Xie X, et al.
Bioengineered . 2021 Nov; 12(2):12179-12190. PMID: 34783299
Growth factor receptor bound protein 7 (GRB7) plays an important role in regulating the growth and metastasis of ovarian cancer. Angiogenesis is the basis for the growth, invasion, and metastasis...
7.
Yuan Z, Xie X, Gu H, Zhang W, Hu Y, Yang Y, et al.
Front Cardiovasc Med . 2021 Sep; 8:708033. PMID: 34485408
This study aims to identify genetic lesions in patients with congenital heart disease (CHD) with or without other phenotypes. In this study, over 400 patients were recruited and several novel...
8.
Xie X, Tang J, Liu Z, Peng S, Yuan Z, Gu H, et al.
Front Neurosci . 2021 Aug; 15:697167. PMID: 34335171
Charcot neuroarthropathy is a systemic disease with pathological changes in the musculoskeletal system, which leads to fractures, dislocations, and deformities involving multiple bones and joints, particularly those of the feet....
9.
Yao Y, Zhang Y, Xie X, Chen L, Zhu F, Zhou M
Curr Med Sci . 2020 Aug; 40(4):795-800. PMID: 32862392
Non-Herlitz junctional epidermolysis bullosa (JEB-nH), an autosomal recessive bullous genodermatosis, is characterized by generalized skin blistering from birth onward, dental anomalies, universal alopecia and nail dystrophy. The underlying defect is...
10.
Wang T, Xie X, Li K, Deng Y, Chen H
Curr Med Sci . 2018 Aug; 38(3):443-448. PMID: 30074210
This study was designed to analyze the effect of the mitochondrial respiratory pathways of Candida albicans (C. albicans) on the biofilm formation. The 2, 3-bis (2-methoxy- 4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT) reduction assay...