Bocheng Xu
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Explore the profile of Bocheng Xu including associated specialties, affiliations and a list of published articles.
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Articles
39
Citations
326
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Recent Articles
1.
Fu L, Zheng X, Luo J, Zhang Y, Gao X, Jin L, et al.
Int J Antimicrob Agents
. 2024 Nov;
64(6):107371.
PMID: 39486466
Objectives: Skin injuries and infections are an inevitable part of daily human life, particularly with chronic wounds, becoming an increasing socioeconomic burden. In treating skin infections and promoting wound healing,...
2.
Tan Y, Tian H, Xiao Y, Xu B, Wang H, Yang M, et al.
Int J Legal Med
. 2024 Sep;
139(1):77-85.
PMID: 39325160
Whole exome sequencing (WES) is widely used in clinical diagnosis. Before obtaining an accurate diagnosis, it is essential to conduct sample identity testing and paternity testing on trio samples. Currently,...
3.
Xu B, Wang L, Yang C, Yan R, Zhang P, Jin M, et al.
J Adv Res
. 2024 Jan;
67():301-315.
PMID: 38266820
Introduction: The design of precision antimicrobials aims to personalize the treatment of drug-resistant bacterial infections and avoid host microbiota dysbiosis. Objectives: This study aimed to propose an efficient de novo...
4.
Li F, Xu B, Lu Z, Chen J, Fu Y, Huang J, et al.
Small
. 2024 Jan;
20(25):e2311101.
PMID: 38234132
Developing novel substances to synergize with nanozymes is a challenging yet indispensable task to enable the nanozyme-based therapeutics to tackle individual variations in tumor physicochemical properties. The advancement of machine...
5.
Wang P, Liao H, Wang Q, Xie H, Xu B, Xiang Q, et al.
Clin Genet
. 2024 Jan;
105(5):549-554.
PMID: 38225536
Congenital hyperinsulinism (CHI; OMIM: 256450) is characterized by persistent insulin secretion despite severe hypoglycemia. The most common causes are variants in the ATP-binding cassette subfamily C member 8(ABCC8) and potassium...
6.
Hu T, Liu L, Wang H, Yang M, Xu B, Xie H, et al.
J Genet Genomics
. 2024 Jan;
51(5):543-553.
PMID: 38181896
Noncompaction of the ventricular myocardium (NVM), the third most diagnosed cardiomyopathy, is characterized by prominent trabeculae and intratrabecular recesses. However, the genetic etiology of 40%-60% of NVM cases remains unknown....
7.
Chen J, Xiang Q, Xiao X, Xu B, Xie H, Wang H, et al.
Mol Genet Genomic Med
. 2023 Nov;
12(1):e2303.
PMID: 37930140
Background: Congenital talipes equinovarus (CTEV) is a rotational foot deformity that affects muscles, bones, connective tissue, and vascular or neurological tissues. The etiology of CTEV is complex and unclear, involving...
8.
He T, Sun H, Xu B, Qu H, Cai X, Zhou H, et al.
Front Neurol
. 2023 Oct;
14:1228218.
PMID: 37789895
Pontocerebellar hypoplasia type 8(PCH8) is a rare neurodegenerative disorder, reportedly caused by pathogenic variants of the in autosomal recessive inheritance, and variants have also been implicated in other diseases, and...
9.
Xu B, Shaoyong W, Wang L, Yang C, Chen T, Jiang X, et al.
Sci Adv
. 2023 Sep;
9(39):eadf8782.
PMID: 37774026
Specifically targeted antimicrobial peptides (STAMPs) are novel alternatives to antibiotics, whereas the development of STAMPs for colonic infections is hindered by limited de novo design efficiency and colonic bioavailability. In...
10.
He T, Yao Q, Xu B, Yang M, Jiang J, Xiang Q, et al.
Mol Genet Genomic Med
. 2023 Jul;
11(11):e2253.
PMID: 37489051
Background: The L1 cell adhesion molecule (L1CAM, OMIM 308840) gene is primarily expressed in the nervous system and encodes the L1 adhesion molecule protein. Variations in L1CAM cause a wide...