Benchang S. Li
Xi'an, China
Last Updated: 09/26/2026
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Found 18 publications
Aptamer-targeted hybrid nanoparticles based on human exosomes and LXR agonist-loaded liposomes for enhanced anti-AML therapy.
Journal: Nucleosides, nucleotides & nucleic acids
Published: March 19, 2026
Visualizing NEK9 in action: aptamer-based fluorescent probes for real-time live-cell imaging.
Journal: Nucleosides, nucleotides & nucleic acids
Published: September 10, 2025
Inhibition of osteogenic differentiation of mouse bone marrow mesenchymal stem cells and maxillary expansion osteogenesis by cytoskeleton-associated protein 4 knockout
Journal: Zhonghua kou qiang yi xue za zhi = Zhonghua kouqiang yixue zazhi = Chinese journal of stomatology
Published: April 23, 2025
Clinical features and genetic analysis of a child with Congenital disorder of glycosylation due to novel variants of COG6 gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: November 11, 2024
Clinical phenotype, genetic characteristics, and creation of immortalized cell lines for patients from a pedigree affected with Hunter syndrome
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 03, 2024
Insights From a Novel Splicing Variant and Recurrent Arginine Variants in the CHD3 Gene Causing Snijders Blok-Campeau Syndrome.
Journal: American journal of medical genetics. Part A
Published: June 16, 2024
Correction to: Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review.
Journal: Journal of applied genetics
Published: March 25, 2024
Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review.
Journal: Journal of applied genetics
Published: January 23, 2024
A Novel Frameshift Variant of the ELF4 Gene in a Patient with Autoinflammatory Disease: Clinical Features, Transcriptomic Profiling and Functional Studies.
Journal: Journal of clinical immunology
Published: December 07, 2023
A Novel Homozygous Deletion Including Exon 1 of FA2H Gene Causes Spastic Paraplegia-35: Genetic and Lipidomics Analysis of the Patients.
Journal: Pediatric neurology
Published: August 14, 2023
Establishment of a novel human induced pluripotent stem cell line (SIPDi001-A) with compound heterozygous mutations in the UBR7 gene from a Li-Campeau syndrome patient.
Journal: Stem cell research
Published: May 25, 2023
Novel maternal duplication of 6p22.3-p25.3 with subtelomeric 6p25.3 deletion: new clinical findings and genotype-phenotype correlations.
Journal: Molecular cytogenetics
Published: March 30, 2023
Last Updated: 09/26/2026