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Lidangzhi Mo

Observed name: Mo, Lidangzhi
ORCID: 0000-0001-6563-9962
Observed ORCID: 0000-0001-6563-9962
OpenAlex ID: A5071749636
Aberrant activation of TGF-β1 induces high bone turnover via Rho GTPases-mediated cytoskeletal remodeling in Camurati-Engelmann disease
2022 · Qi Chen, Yan Yao, et al. · Frontiers in Endocrinology · 11
Hedgehog pathway is negatively regulated during the development of Drosophila melanogaster PheRS-m (Drosophila homologs gene of human FARS2) mutants
2022 · Lidangzhi Mo, Rui Li, et al. · Human Cell · 8
Insights From a Novel Splicing Variant and Recurrent Arginine Variants in the CHD3 Gene Causing Snijders Blok–Campeau Syndrome
2024 · Xiaoling Tie, Fengyu Che, et al. · American Journal of Medical Genetics Part A · 3
Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review
2024 · Fengyu Che, Chenhao Li, et al. · Journal of Applied Genetics · 3
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A Novel Homozygous Deletion Including Exon 1 of FA2H Gene Causes Spastic Paraplegia-35: Genetic and Lipidomics Analysis of the Patients
2024 · Lidangzhi Mo, Xiaoling Tie, et al. · Pediatric Neurology · 3
Aptamer-targeted hybrid nanoparticles based on human exosomes and LXR agonist-loaded liposomes for enhanced anti-AML therapy
2026 · Liyu Zhang, Ying Yang, et al. · Nucleosides Nucleotides & Nucleic Acids · 2
Correction to: Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review
2024 · Fengyu Che, Chenhao Li, et al. · Journal of Applied Genetics · 1
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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
2023 · Benchang Li, Yafei Zhou, et al. · Stem Cell Research · 1
Deep Learning-Based Detection of Facial Dysmorphic Features for Rare Genetic Disorders in Pediatric Populations
2026 · Fengyu Che, Tianwei Lin, et al. · Preprints.org
Aptamer-targeted hybrid nanoparticles based on human exosomes and LXR agonist-loaded liposomes for enhanced anti-AML therapy
2026 · Zhang, Liyu, Yang, Ying, et al. · Figshare
Visualizing NEK9 in action: aptamer-based fluorescent probes for real-time live-cell imaging
2025 · Liyu Zhang, Ying Yang, et al. · Nucleosides Nucleotides & Nucleic Acids
[Clinical features and genetic analysis of a child with Congenital disorder of glycosylation due to novel variants of COG6 gene].
2024 · Liyu Zhang, Ying Yang, et al. · PubMed
[Clinical phenotype, genetic characteristics, and creation of immortalized cell lines for patients from a pedigree affected with Hunter syndrome].
2024 · Benchang Li, Fengyu Che, et al. · PubMed
Works count: 14
Citation count: 32
H-index: 3
I10-index: 1
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