Xinhui Chen
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Explore the profile of Xinhui Chen including associated specialties, affiliations and a list of published articles.
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58
Citations
526
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Recent Articles
1.
Guo B, Chen X, Chen A, Wang J, Xue W, Wang T, et al.
Nat Commun
. 2025 Feb;
16(1):2046.
PMID: 40016287
Organic memories, with small dimension, fast speed and long retention features, are considered as promising candidates for massive data archiving. In order to satisfy the requirements for ultra-low power and...
2.
Zhao C, Zhang X, Wang H, Qiang H, Liu S, Zhang C, et al.
Int J Mol Sci
. 2025 Jan;
26(2).
PMID: 39859371
Influenza A viruses (IAVs) are highly contagious pathogens that cause zoonotic disease with limited availability of antiviral therapies, presenting ongoing challenges to both public health and the livestock industry. Unveiling...
3.
Dong Q, Wu J, Zhang H, Chen X, Xu X, Chen J, et al.
J Inflamm Res
. 2025 Jan;
18():637-652.
PMID: 39835297
Purpose: Immunometabolism is pivotal in rheumatoid arthritis (RA) pathogenesis, yet the intricacies of its pathological regulatory mechanisms remain poorly understood. This study explores the complex immunometabolic landscape of RA to...
4.
Liu P, Zhang F, Chen X, Zheng X, Chen M, Lin Z, et al.
NPJ Parkinsons Dis
. 2025 Jan;
11(1):21.
PMID: 39833204
Biallelic intronic pentanucleotide repeat expansions, mainly (AAGGG)exp and/or (ACAGG)exp in RFC1, are detected in cerebellar ataxia, neuropathy and vestibular areflexia syndrome, late-onset ataxia, and in a wide disease spectrum including...
5.
Yang D, Huang H, Zeng T, Wang L, Ying C, Chen X, et al.
Parkinsonism Relat Disord
. 2025 Jan;
132:107290.
PMID: 39827654
Background: Primary Familial Brain Calcification (PFBC) can manifest clinically with a complex and heterogeneous array of symptoms, including parkinsonism, dysarthria, and cognitive impairment. However, the distinct presentations of PFBC in...
6.
Chen X, Wang B, Xia H, Wang H, Yang D, Chen M, et al.
Mov Disord
. 2024 Nov;
40(2):315-323.
PMID: 39569876
Background: The pentanucleotide (TTTCA) repeat expansion (exp) insertion, along with the accompanying (TTTTA)exp, causes familial cortical myoclonic tremor with epilepsy (FCMTE). The genotype-phenotype correlations and intergenerational instabilities related to (TTTCA)exp...
7.
Wang H, Wang B, Liao Y, Niu J, Chen M, Chen X, et al.
Eur J Nucl Med Mol Imaging
. 2024 Oct;
52(3):823-835.
PMID: 39438298
Introduction: Progressive supranuclear palsy (PSP) is a neurodegenerative disorder with diverse clinical presentations that are linked to tau pathology. Recently, Subtype and Stage Inference (SuStaIn) algorithm, an innovative data-driven method,...
8.
Chen X, Shi Y, Fu F, Wang L, Yu H, Yang D, et al.
Mov Disord
. 2024 Sep;
39(12):2190-2198.
PMID: 39229657
Background: Primary familial brain calcification (PFBC) is a monogenic disorder characterized by bilateral calcifications in the brain. The genetic basis remains unknown in over half of the PFBC patients, indicating...
9.
Li X, Shi C, Zhou R, Chen X, Xu Q, Zhao C, et al.
J Biomed Mater Res A
. 2024 May;
112(10):1827-1839.
PMID: 38700258
Acute kidney injury (AKI) is a life-threatening disease primarily caused by renal ischemia-reperfusion (I/R) injury, which can result in renal failure. Currently, growth factor therapy is considered a promising and...
10.
Chen X, Zhang F, Shi Y, Wang H, Chen M, Yang D, et al.
Eur J Hum Genet
. 2024 Mar;
33(2):252-257.
PMID: 38467733
Familial cortical myoclonic tremor with epilepsy type 1 (FCMTE1) is caused by (TTTTA)exp(TTTCA)exp repeat expansions in SAMD12, while pure (TTTTA)exp is polymorphic. Our investigation focused on the origin and evolution...