Aojie J. Cai

No. 1 Xi'an Men Street, West District
Beijing, 100034, China

Last Updated: 09/26/2026

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Found 18 publications

Clinical features and genetic analysis of a child with Christianson syndrome due to variant of SLC9A6 gene

Clinical features and genetic analysis of a child with Christianson syndrome due to variant of SLC9A6 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: June 24, 2025

Clinical phenotypic and genetic analysis of three children with Paroxysmal kinesigenic dyskinesia and Self-limited familial infantile epilepsy caused by PRRT2 gene mutation

Clinical phenotypic and genetic analysis of three children with Paroxysmal kinesigenic dyskinesia and Self-limited familial infantile epilepsy caused by PRRT2 gene mutation

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 15, 2025

Clinical feature and genetic analysis of a case of X-linked alpha-thalassemia mental retardation syndrome neonate caused by ATRX gene variant and literature review

Clinical feature and genetic analysis of a case of X-linked alpha-thalassemia mental retardation syndrome neonate caused by ATRX gene variant and literature review

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 11, 2025

Functional evaluation of a rat model of KCNT1-related epilepsy.

Functional evaluation of a rat model of KCNT1-related epilepsy.

Journal: Epilepsy research
Published: November 06, 2024

Compound heterozygous mutations in the SSPOP gene lead to epilepsy and developmental disorders.

Compound heterozygous mutations in the SSPOP gene lead to epilepsy and developmental disorders.

Journal: Brain : a journal of neurology
Published: October 27, 2024

Focal cortical dysplasia II caused by brain somatic mutation of IRS-1 is associated with ERK signaling pathway activation.

Focal cortical dysplasia II caused by brain somatic mutation of IRS-1 is associated with ERK signaling pathway activation.

Journal: Cerebral cortex (New York, N.Y. : 1991)
Published: March 18, 2024

Neurological function and drug-refractory epilepsy in Sturge-Weber syndrome children: a retrospective analysis.

Neurological function and drug-refractory epilepsy in Sturge-Weber syndrome children: a retrospective analysis.

Journal: European journal of pediatrics
Published: October 06, 2023

Neuroblastoma SH-SY5Y Cell Differentiation to Mature Neuron by AM580 Treatment.

Neuroblastoma SH-SY5Y Cell Differentiation to Mature Neuron by AM580 Treatment.

Journal: Neurochemical research
Published: May 31, 2022

In Vitro Effects of Acitretin on Human Neuronal SH-SY5Y Cells.

In Vitro Effects of Acitretin on Human Neuronal SH-SY5Y Cells.

Journal: Neurochemical research
Published: December 16, 2021

Genetic analysis and identification of novel variations in Chinese patients with pediatric epilepsy by whole-exome sequencing.

Genetic analysis and identification of novel variations in Chinese patients with pediatric epilepsy by whole-exome sequencing.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: December 08, 2021

A novel NAPB splicing mutation identified by Trio-based exome sequencing is associated with early-onset epileptic encephalopathy.

A novel NAPB splicing mutation identified by Trio-based exome sequencing is associated with early-onset epileptic encephalopathy.

Journal: European journal of medical genetics
Published: July 28, 2020

The novel circCLK3/miR-320a/FoxM1 axis promotes cervical cancer progression.

The novel circCLK3/miR-320a/FoxM1 axis promotes cervical cancer progression.

Journal: Cell death & disease
Published: July 22, 2019
Showing 1-12 of 18

Last Updated: 09/26/2026