Jizhen Zou

Beijing, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 23 publications

Comparison of efficacy of exosomes derived from human umbilical cord blood mesenchymal stem cells in treating mouse acute lung injury via different routes.

Comparison of efficacy of exosomes derived from human umbilical cord blood mesenchymal stem cells in treating mouse acute lung injury via different routes.

Journal: Frontiers in pediatrics

Published: January 15, 2025

Maternal Myo-Inositol Deficiency Involved Autophagy Impairment by PI3K/Akt/mTOR Signaling in Neural Tube Defects During Pregnancy.

Maternal Myo-Inositol Deficiency Involved Autophagy Impairment by PI3K/Akt/mTOR Signaling in Neural Tube Defects During Pregnancy.

Journal: Molecular neurobiology

Published: August 26, 2024

Establishment and validation of a predictive nomogram for the risk of premalignant lesions in children with choledochal cyst.

Establishment and validation of a predictive nomogram for the risk of premalignant lesions in children with choledochal cyst.

Journal: Frontiers in pediatrics

Published: November 26, 2022

Loss-of-Function of p21-Activated Kinase 2 Links BMP Signaling to Neural Tube Patterning Defects.

Loss-of-Function of p21-Activated Kinase 2 Links BMP Signaling to Neural Tube Patterning Defects.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: July 13, 2022

A mosaic karyotype of 45,X/46,X,psu idic(Y)(q12) in a ten-year-old boy: integrating high-throughput sequencing with cytogenetic technique for precise diagnosis and genetic counselling.

A mosaic karyotype of 45,X/46,X,psu idic(Y)(q12) in a ten-year-old boy: integrating high-throughput sequencing with cytogenetic technique for precise diagnosis and genetic counselling.

Journal: BMC pediatrics

Published: January 23, 2022

Antisense oligonucleotides targeting the SMN2 promoter region enhance SMN2 expression in spinal muscular atrophy cell lines and mouse model.

Antisense oligonucleotides targeting the SMN2 promoter region enhance SMN2 expression in spinal muscular atrophy cell lines and mouse model.

Journal: Human molecular genetics

Published: September 22, 2021

Low folate concentration impacts mismatch repair deficiency in neural tube defects.

Low folate concentration impacts mismatch repair deficiency in neural tube defects.

Journal: Epigenomics

Published: November 27, 2019

Association between rare variants in specific functional pathways and human neural tube defects multiple subphenotypes.

Association between rare variants in specific functional pathways and human neural tube defects multiple subphenotypes.

Journal: Neural development

Published: November 08, 2019

Sporadic Hirschsprung Disease: Mutational Spectrum and Novel Candidate Genes Revealed by Next-generation Sequencing.

Sporadic Hirschsprung Disease: Mutational Spectrum and Novel Candidate Genes Revealed by Next-generation Sequencing.

Journal: Scientific reports

Published: April 28, 2017

Quantitative Measurement of PARD3 Copy Number Variations in Human Neural Tube Defects.

Quantitative Measurement of PARD3 Copy Number Variations in Human Neural Tube Defects.

Journal: Cellular and molecular neurobiology

Published: March 01, 2017

Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation.

Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation.

Journal: Human mutation

Published: May 11, 2016

Deregulation of the planar cell polarity genes CELSR3 and FZD3 in Hirschsprung disease.

Deregulation of the planar cell polarity genes CELSR3 and FZD3 in Hirschsprung disease.

Journal: Experimental and molecular pathology

Published: May 08, 2016

Showing 1-12 of 23

Last Updated: 09/26/2026