Shuizi Ding
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Explore the profile of Shuizi Ding including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
288
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0
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Recent Articles
1.
Wang R, Yang D, Tu C, Lei C, Ding S, Guo T, et al.
Front Med
. 2023 Jun;
17(5):957-971.
PMID: 37314648
Primary ciliary dyskinesia (PCD) is a congenital, motile ciliopathy with pleiotropic symptoms. Although nearly 50 causative genes have been identified, they only account for approximately 70% of definitive PCD cases....
2.
Lei C, Ge H, Ding S, Zhou X, Yang B, Yang D, et al.
J Infect
. 2023 Mar;
86(4):e81-e83.
PMID: 36871871
No abstract available.
3.
Ahangari F, Price N, Malik S, Chioccioli M, Barnthaler T, Adams T, et al.
JCI Insight
. 2023 Jan;
8(4).
PMID: 36626225
Idiopathic pulmonary fibrosis (IPF) is a progressive and ultimately fatal disease. Recent findings have shown a marked metabolic reprogramming associated with changes in mitochondrial homeostasis and autophagy during pulmonary fibrosis....
4.
Chioccioli M, Roy S, Newell R, Pestano L, Dickinson B, Rigby K, et al.
EBioMedicine
. 2022 Oct;
85:104304.
PMID: 36265417
Background: MicroRNAs are non-coding RNAs that negatively regulate gene networks. Previously, we reported that systemically delivered miR-29 mimic MRG-201 reduced fibrosis in animal models, supporting the consideration of miR-29-based therapies...
5.
Ahangari F, Becker C, Foster D, Chioccioli M, Nelson M, Beke K, et al.
Am J Respir Crit Care Med
. 2022 Aug;
206(12):1463-1479.
PMID: 35998281
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, and often fatal disorder. Two U.S. Food and Drug Administration-approved antifibrotic drugs, nintedanib and pirfenidone, slow the rate of decline in lung...
6.
Liu Y, Lei C, Wang R, Yang D, Yang B, Xu Y, et al.
Front Genet
. 2022 Jul;
13:940292.
PMID: 35873463
Whole-exome sequencing (WES) based copy number variation (CNV) analysis has been reported to improve the diagnostic rate in rare genetic diseases. In this study, we aim to find the disease-associated...
7.
Xu Y, Yang B, Lei C, Yang D, Ding S, Lu C, et al.
Pharmgenomics Pers Med
. 2022 Apr;
15:341-350.
PMID: 35449766
Primary ciliary dyskinesia (PCD) is a rare genetic disease caused by mutations of genes coding motile-cilia-related proteins. variants can cause PCD via disrupting the assembling of inner dynein and dynein...
8.
Lei C, Zhou X, Ding S, Xu Y, Yang B, Guo W, et al.
Front Med (Lausanne)
. 2022 Feb;
9:819425.
PMID: 35155502
Background: spp. has been well-recognized as an important cause of community-acquired pneumonia. Current community-acquired pneumonia guidelines recommended covering the treatment of because of the high mortality associated with inadequate antibiotic...
9.
Lei C, Yang D, Wang R, Ding S, Wang L, Guo T, et al.
J Hum Genet
. 2021 Nov;
67(4):197-201.
PMID: 34815526
Objective: Primary ciliary dyskinesia (PCD) is a heterogeneous disease characterized by the failure of mucociliary clearance. Dynein regulatory complex subunit 1 (DRC1) variants can cause PCD by disrupting the nexin...
10.
Wang S, Ding S, Luo H, Chai X
Int J Gen Med
. 2021 May;
14:1829-1841.
PMID: 34012289
Background: Sepsis is a life-threatening multiple-organ dysfunction caused by dysregulation of host response to severe infection. Liver failure is a validated independent predictor of mortality. Accurate and rapid assessment of...