Publications by authors named "Jingbin Yan"

Claim this Profile
D
Dysregulation of RUNX1 isoforms drives mitochondrial defects during neural differentiation in down syndrome.
Yan-Na Liu, Qin Cai, Ke-Yi Li, Wen-Xiu Li, Guang He, Jing-Bin Yan

Mitochondrion· December 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
RNA binding protein HuR regulated by OIP5-AS1 may be involved in maternal transcript degradation during the human maternal-to-zygotic transition.
Yan-Na Liu, Ke-Yi Li, Hao Wei, Wen-Xiu Li, Yue-Hua Zhang, Jing-Bin Yan

BMC Genomics· July 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Improved non-singular fast terminal sliding mode PMSM control strategy.
Jingbin Yan, Haoxuan Hu

PLoS One· July 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Early-life gut microbiota in food allergic children and its impact on the development of allergic disease.
Xiumei Yan, Jingbin Yan, Qiangwei Xiang, Huan Dai, Yinghui Wang

Ital J Pediatr· November 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical features and underlying mechanisms of KAT6B disease in a Chinese boy.
Xiaoang Sun, Xiaona Luo, Longlong Lin, Simei Wang, Chunmei Wang, Jingbin Yan

Mol Genet Genomic Med· September 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Missense mutation of c.635 T > C in CAPN3 impairs muscle injury repair in a Limb-Girdel Muscular Dystropy Model.
Hou-Shi Ma, Xiu-Li Gong, Wen-Xiu Li, Qin Cai, Yan-Wen Chen, Jing-Bin Yan

Clin Genet· June 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Single-cell RNA sequencing of neural stem cells derived from human trisomic iPSCs reveals the abnormalities during neural differentiation of Down syndrome.
Jia-Jun Qiu, Yan-Na Liu, Hao Wei, Fanyi Zeng, Jing-Bin Yan

Front Mol Neurosci· June 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
RUNX1 Upregulation Causes Mitochondrial Dysfunction via Regulating the PI3K-Akt Pathway in iPSC from Patients with Down Syndrome.
Yanna Liu, Yuehua Zhang, Zhaorui Ren, Fanyi Zeng, Jingbin Yan

Mol Cells· April 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Segawa syndrome caused by gene mutation and its mechanism.
Yilin Wang, Chunmei Wang, Meiyan Liu, Wuhen Xu, Simei Wang, Jingbin Yan

Front Genet· December 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Induced pluripotent stem cells (SHCDNi006-A cells) isolated from the peripheral blood mononuclear cells of a five-month-old Chinese girl with the heterozygous missense mutation (c.2800 G>A) in the KCNT1 gene.
Xiaona Luo, Yilin Wang, Fang Yuan, Longlong Lin, Anqi Wang, Jingbin Yan

Stem Cell Res· July 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical Study of 8 Cases of Gene Mutation-Related Neurological Diseases and Their Mechanisms.
Xiaona Luo, Xiaoang Sun, Yilin Wang, Longlong Lin, Fang Yuan, Meiyan Liu, Jingbin Yan

Front Cell Dev Biol· March 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
RNA editing regulates lncRNA splicing in human early embryo development.
Jiajun Qiu, Xiao Ma, Fanyi Zeng, Jingbin Yan

PLoS Comput Biol· December 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mechanisms of Congenital Myasthenia Caused by Three Mutations in the Gene.
Xiaona Luo, Chunmei Wang, Longlong Lin, Fang Yuan, Simei Wang, Jingbin Yan

Front Pediatr· November 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genome-wide hypermethylation is closely associated with abnormal expression of genes involved in neural development in induced pluripotent stem cells derived from a Down syndrome mouse model.
Jiao-Jiao Xi, Guan-Heng Yang, Yan-Na Liu, Jia-Jun Qiu, Xiu-Li Gong, Jing-Bin Yan

Cell Biol Int· July 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Cis-acting: A pattern of lncRNAs for gene regulation in induced pluripotent stem cells from patients with Down syndrome determined by integrative analysis of lncRNA and mRNA profiling data.
Wenbo Ma, Yanna Liu, Houshi Ma, Zhaorui Ren, Jingbin Yan

Exp Ther Med· July 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[Genome-wide analysis of aberrant DNA methylation patterns in iPSCs derived from patients with Down syndrome].
Wenbo Ma, Yanna Liu, Jingbin Yan

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· June 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Generation and characterization of the induced pluripotent stem cell line SHCDNi004-A from a ten-year-old Chinese boy with X-linked mental retardation in IL1RAPL1 deficiency.
Fang Yuan, Simei Wang, Yilin Wang, Anqi Wang, Chao Wang, Jie Yang, Jingbin Yan

Stem Cell Res· May 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Fructooligosaccharides protect against OVA-induced food allergy in mice by regulating the Th17/Treg cell balance using tryptophan metabolites.
Xiumei Yan, Jingbin Yan, Qiangwei Xiang, Fanyan Wang, Huan Dai

Food Funct· April 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Induced pluripotent stem cells (SHCDNi002-A cells) isolated from the peripheral blood mononuclear cells of a 1-year-old Chinese girl with mediator complex subunit 12-related syndrome.
Yilin Wang, Fang Yuan, Anqi Wang, Chao Wang, Longlong Lin, Jingbin Yan

Stem Cell Res· July 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Generation of an induced pluripotent stem cell line (SHCDNi003-A) from a one-year-old Chinese Han infant with Allan-Herndon-Dudley syndrome.
Anqi Wang, Jiaming Xi, Fang Yuan, Yilin Wang, Simei Wang, Jie Yang, Jingbin Yan

Stem Cell Res· July 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
De Novo Mutation of m.3243A>G together with m.16093T>C Associated with Atypical Clinical Features in a Pedigree with MIDD Syndrome.
Zhixin Jiang, Yinan Zhang, Jingbin Yan, Fengwen Li, Xinqian Geng, Yanmei Feng

J Diabetes Res· January 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Recent Progress on Genetic Diagnosis and Therapy for β-Thalassemia in China and Around the World.
Jingzhi Zhang, Jingbin Yan, Fanyi Zeng

Hum Gene Ther· February 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Protective effect of baicalin on the small intestine in rats with food allergy.
Xiumei Yan, Jingbin Yan, Kaiyu Huang, Tongtong Pan, Zhang Xu

Life Sci· December 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Dysfunctions of mitochondria in close association with strong perturbation of long noncoding RNAs expression in down syndrome.
Jia-Jun Qiu, Yan-Na Liu, Zhao-Rui Ren, Jing-Bin Yan

Int J Biochem Cell Biol· November 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Detection of fetal epigenetic biomarkers through genome-wide DNA methylation study for non-invasive prenatal diagnosis.
Hong-Dan Wang, Lin Liu, Hui-Ru Zhao, Qiao-Fang Hou, Jing-Bin Yan

Mol Med Rep· June 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis