Hongqiang Du
Overview
Explore the profile of Hongqiang Du including associated specialties, affiliations and a list of published articles.
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Articles
19
Citations
268
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0
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Recent Articles
1.
Zhao R, Zhang Z, Mei S, Sun L, Zhang Q, Lv Q, et al.
J Clin Immunol
. 2025 Feb;
45(1):76.
PMID: 39976696
Deficiency in ELF4, X-linked (DEX) is a newly identified monogenic autoinflammatory disease. Most reported cases are male, leading to the recognition of DEX being primarily limited to male patients. Here...
2.
Olyha S, OConnor S, Kribis M, Bucklin M, Uthaya Kumar D, Tyler P, et al.
J Clin Immunol
. 2024 Jan;
44(2):44.
PMID: 38231408
Defining monogenic drivers of autoinflammatory syndromes elucidates mechanisms of disease in patients with these inborn errors of immunity and can facilitate targeted therapeutic interventions. Here, we describe a cohort of...
3.
Li W, Sun Y, Yu L, Chen R, Gan R, Qiu L, et al.
J Clin Immunol
. 2023 Mar;
43(6):1193-1207.
PMID: 36947335
The dedicator of cytokinesis 2(DOCK2) protein, an atypical guanine nucleotide exchange factor (GEFs), is a member of the DOCKA protein subfamily. DOCK2 protein deficiency is characterized by early-onset lymphopenia, recurrent...
4.
Sun G, Wu M, Lv Q, Yang X, Wu J, Tang W, et al.
J Clin Immunol
. 2023 Feb;
43(5):933-939.
PMID: 36823308
Patients with DEX (deficiency in ELF4, X-linked) were recently reported by our team and others, and cases are very limited worldwide. Our knowledge of this new disease is currently preliminary....
5.
Yang L, Liu P, Du H, Chen R, Zhou B, Li Y, et al.
J Clin Immunol
. 2022 Jul;
42(8):1672-1684.
PMID: 35849269
Purpose: CD81 deficiency is an extremely rare primary immunodeficiency disease characterized by severe and recurrent infections, IgA-related nephropathy, and profound hypogammaglobulinemia. Only one patient has been reported so far, and...
6.
Sun G, Qiu L, Yu L, An Y, Ding Y, Zhou L, et al.
J Clin Immunol
. 2022 Mar;
42(4):798-810.
PMID: 35266071
Monogenic autoinflammatory diseases (mAIDs) are a heterogeneous group of diseases affecting primarily innate immunity, with various genetic causes. Genetic diagnosis of mAIDs can assist in the patient's management and therapy....
7.
Chen J, Wei X, Wang X, Liu T, Zhao Y, Chen L, et al.
Cell Rep
. 2022 Feb;
38(7):110373.
PMID: 35172162
mRNA mA modification is heavily involved in modulation of immune responses. However, its function in antiviral immunity is controversial, and how immune responses regulate mA modification remains elusive. We here...
8.
Du H, Xie L, Li H
Neural Netw
. 2022 Feb;
148:74-84.
PMID: 35104714
Voice conversion has made great progress in the past few years under the studio-quality test scenario in terms of speech quality and speaker similarity. However, in real applications, test speech...
9.
Lv G, Sun G, Wu P, Du X, Zeng T, Wen W, et al.
Pediatr Allergy Immunol
. 2021 Sep;
33(1):e13671.
PMID: 34569645
Background: TYK2 deficiency is a rare primary immunodeficiency disease caused by loss-of-function mutations of TYK2 gene, which is initially proposed as a subset of hyper-IgE syndrome (HIES). However, accumulating evidence...
10.
Du H, Xia H, Liu T, Li Y, Liu J, Xie B, et al.
iScience
. 2021 Mar;
24(3):102169.
PMID: 33665583
Ulcerative colitis (UC) is a chronic inflammatory bowel disease, characterized by relapsing and remitting colon mucosal inflammation. For patients suffering from UC, a higher risk of colon cancer has been...