Jiaci Li
Tianjin, China
Last Updated: 09/26/2026
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Found 13 publications
The utility of CNV analysis in identifying the molecular etiology of pediatric epilepsy patients.
Journal: Pediatric research
Published: May 06, 2025
First pathogenic non-coding variant in MMACHC: a functional deletion in the 5'-UTR associated with cobalamin C deficiency.
Journal: Molecular biology reports
Published: November 11, 2024
CTSG polymorphisms in Chinese children with type 1 diabetes mellitus.
Journal: Journal of tropical pediatrics
Published: August 09, 2024
Identification of the synonymous variant c.3141G > A in TNRC6B gene that altered RNA splicing by minigene assay.
Journal: Molecular biology reports
Published: May 13, 2024
Phosphoserine aminotransferase deficiency diagnosed by whole-exome sequencing and LC-MS/MS reanalysis: A case report and review of literature.
Journal: Molecular genetics & genomic medicine
Published: July 25, 2023
Large chromosomal deletions and impaired homologous recombination repairing in HEK293T cells exposed to polychlorinated biphenyl 153.
Journal: PeerJ
Published: April 01, 2021
Modification of COL1A1 in Autologous Adipose Tissue-Derived Progenitor Cells Rescues the Bone Phenotype in a Mouse Model of Osteogenesis Imperfecta.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: September 28, 2020
The synergistic effect of NELL1 and adipose-derived stem cells on promoting bone formation in osteogenesis imperfecta treatment.
Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Published: February 28, 2020
Pretreatment with interleukin 35-engineered mesenchymal stem cells protected against lipopolysaccharide-induced acute lung injury via pulmonary inflammation suppression.
Journal: Inflammopharmacology
Published: October 15, 2019
Last Updated: 09/26/2026