Yingying Shi
No. 7 Weiwu Road
Zhengzhou, 450003, China
Zhengzhou, 450003, China
Last Updated: 09/26/2026
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Found 15 publications
De novo Mutation Enables NOTCH3ECD Aggregation and Mitochondrial Dysfunction via Interactions with BAX and BCL-2.
Journal: Journal of Alzheimer's disease : JAD
Published: January 10, 2022
Changes in the Morphology, Number, and Protein Levels of Plasma Exosomes in CADASIL Patients.
Journal: Journal of Alzheimer's disease : JAD
Published: March 22, 2021
Genotype-phenotype correlations of heterozygous HTRA1-related cerebral small vessel disease: case report and systematic review.
Journal: Neurogenetics
Published: December 24, 2020
A Novel Mutation Outside of the EGFr Encoding Exons of NOTCH3 Gene in a Chinese with CADASIL.
Journal: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association
Published: May 25, 2020
Changes in the Morphology, Number, and Pathological Protein Levels of Plasma Exosomes May Help Diagnose Alzheimer's Disease.
Journal: Journal of Alzheimer's disease : JAD
Published: December 30, 2019
A Pilot Study of Urinary Exosomes in Alzheimer's Disease.
Journal: Neuro-degenerative diseases
Published: October 31, 2019
Clinical Features of 4 Novel NOTCH3 Mutations of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy in China.
Journal: Medical science monitor basic research
Published: September 27, 2019
Probable Novel PSEN1 Gln222Leu Mutation in a Chinese Family with Early-Onset Alzheimer's Disease.
Journal: Current Alzheimer research
Published: April 22, 2019
Gene mutations in a Han Chinese Alzheimer's disease cohort.
Journal: Brain and behavior
Published: May 29, 2018
A novel SETX gene mutation associated with Juvenile amyotrophic lateral sclerosis.
Journal: Brain and behavior
Published: March 07, 2018
CADASIL with clinical manifestations of baldness, lumbago and Parkinson's symptoms
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: December 01, 2017
A novel SYNE1 gene mutation in a Chinese family of Emery-Dreifuss muscular dystrophy-like.
Journal: BMC medical genetics
Published: October 27, 2016
Last Updated: 09/26/2026