Jing-bin Yan

24/1400 West Beijing Road
Shanghai, 200040, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 11 publications

Dysregulation of RUNX1 isoforms drives mitochondrial defects during neural differentiation in down syndrome.

Dysregulation of RUNX1 isoforms drives mitochondrial defects during neural differentiation in down syndrome.

Journal: Mitochondrion

Published: September 24, 2025

RNA binding protein HuR regulated by OIP5-AS1 may be involved in maternal transcript degradation during the human maternal-to-zygotic transition.

RNA binding protein HuR regulated by OIP5-AS1 may be involved in maternal transcript degradation during the human maternal-to-zygotic transition.

Journal: BMC genomics

Published: November 01, 2024

Missense mutation of c.635 T > C in CAPN3 impairs muscle injury repair in a Limb-Girdel Muscular Dystropy Model.

Missense mutation of c.635 T > C in CAPN3 impairs muscle injury repair in a Limb-Girdel Muscular Dystropy Model.

Journal: Clinical genetics

Published: January 16, 2023

Single-cell RNA sequencing of neural stem cells derived from human trisomic iPSCs reveals the abnormalities during neural differentiation of Down syndrome.

Single-cell RNA sequencing of neural stem cells derived from human trisomic iPSCs reveals the abnormalities during neural differentiation of Down syndrome.

Journal: Frontiers in molecular neuroscience

Published: January 04, 2023

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.

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.

Journal: Cell biology international

Published: January 23, 2020

Dysfunctions of mitochondria in close association with strong perturbation of long noncoding RNAs expression in down syndrome.

Dysfunctions of mitochondria in close association with strong perturbation of long noncoding RNAs expression in down syndrome.

Journal: The international journal of biochemistry & cell biology

Published: December 26, 2016

Identification and functional analysis of long non-coding RNAs in human and mouse early embryos based on single-cell transcriptome data.

Identification and functional analysis of long non-coding RNAs in human and mouse early embryos based on single-cell transcriptome data.

Journal: Oncotarget

Published: January 21, 2016

Detection of fetal epigenetic biomarkers through genome-wide DNA methylation study for non-invasive prenatal diagnosis.

Detection of fetal epigenetic biomarkers through genome-wide DNA methylation study for non-invasive prenatal diagnosis.

Journal: Molecular medicine reports

Published: January 12, 2016

Alteration of gene expression profiling including GPR174 and GNG2 is associated with vasovagal syncope.

Alteration of gene expression profiling including GPR174 and GNG2 is associated with vasovagal syncope.

Journal: Pediatric cardiology

Published: April 30, 2014

Pyrosequencing is an accurate and reliable method for the analysis of heteroplasmy of the A3243G mutation in patients with mitochondrial diabetes.

Pyrosequencing is an accurate and reliable method for the analysis of heteroplasmy of the A3243G mutation in patients with mitochondrial diabetes.

Journal: The Journal of molecular diagnostics : JMD

Published: December 05, 2013

Long-term deregulated human hematopoiesis in goats transplanted in utero with BCR-ABL-transduced lin(-)CD34(+) cord blood cells.

Long-term deregulated human hematopoiesis in goats transplanted in utero with BCR-ABL-transduced lin(-)CD34(+) cord blood cells.

Journal: Cell research

Published: May 01, 2013

Showing 1-11 of 11

Last Updated: 09/26/2026