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Chaodong Wang

Showing results (71-80 of 100) with videos related to

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Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|May 24, 2024
Heterogeneous blood-brain barrier dysfunction in cerebral small vessel diseasesYunqing Ying, Yingying Li, Tingyan Yao, et al.
Molecular Immunology|July 17, 2012
Immune-related GTPase Irgm1 exacerbates experimental auto-immune encephalomyelitis by promoting the disruption of blood-brain barrier and blood-cerebrospinal fluid barrierChaodong Wang, Caihong Wang, Haiyan Dong, et al.
Parkinsonism & Related Disorders|June 18, 2021
A novel FBXO7-R345P mutation in a Chinese family with autosomal recessive parkinsonian-pyramidal syndromeZhanjun Wang, Yang Song, Wenjia Zhu, et al.
Scientific Reports|May 22, 2013
IRGM1 regulates oxidized LDL uptake by macrophage via actin-dependent receptor internalization during atherosclerosisFucan Xia, Rui Li, Chaodong Wang, et al.
Neurobiology of Aging|October 8, 2013
Clinical profiles of Parkinson's disease associated with common leucine-rich repeat kinase 2 and glucocerebrosidase genetic variants in Chinese individualsChaodong Wang, Yanning Cai, Zhuqin Gu, et al.
Neurology. Genetics|December 16, 2022
Heterozygous <i>HTRA1</i> Mutations Cause Cerebral Small Vessel Diseases: Genetic, Clinical, and Pathologic Findings From 3 Chinese PedigreesTingyan Yao, Junge Zhu, Xiao Wu, et al.
Parkinsonism & Related Disorders|June 5, 2012
Penetrance of LRRK2 G2385R and R1628P is modified by common PD-associated genetic variantsChaodong Wang, Yanning Cai, Zheng Zheng, et al.
Journal of Alzheimer'S Disease : JAD|March 1, 2019
Diagnostic Approach of Early-Onset Dementia with Negative Family History: Implications from Two Cases of Early-Onset Alzheimer's Disease with De Novo PSEN1 MutationJia Liu, Qianqian Wang, Donglai Jing, et al.
Brain : a Journal of Neurology|January 10, 2023
Decreased water exchange rate across blood-brain barrier in hereditary cerebral small vessel diseaseYingying Li, Yunqing Ying, Tingyan Yao, et al.
Neuroscience Letters|March 22, 2021
Autosomal recessive spastic ataxia of Charlevoix-Saguenay caused by novel mutations in SACS gene: A report of two Chinese familiesZhanjun Wang, Yang Song, Xianling Wang, et al.
Pageof 10

Showing results (71-80 of 100) with videos related to

Sort By:
Pageof 10
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|May 24, 2024
Heterogeneous blood-brain barrier dysfunction in cerebral small vessel diseasesYunqing Ying, Yingying Li, Tingyan Yao, et al.
Molecular Immunology|July 17, 2012
Immune-related GTPase Irgm1 exacerbates experimental auto-immune encephalomyelitis by promoting the disruption of blood-brain barrier and blood-cerebrospinal fluid barrierChaodong Wang, Caihong Wang, Haiyan Dong, et al.
Parkinsonism & Related Disorders|June 18, 2021
A novel FBXO7-R345P mutation in a Chinese family with autosomal recessive parkinsonian-pyramidal syndromeZhanjun Wang, Yang Song, Wenjia Zhu, et al.
Scientific Reports|May 22, 2013
IRGM1 regulates oxidized LDL uptake by macrophage via actin-dependent receptor internalization during atherosclerosisFucan Xia, Rui Li, Chaodong Wang, et al.
Neurobiology of Aging|October 8, 2013
Clinical profiles of Parkinson's disease associated with common leucine-rich repeat kinase 2 and glucocerebrosidase genetic variants in Chinese individualsChaodong Wang, Yanning Cai, Zhuqin Gu, et al.
Neurology. Genetics|December 16, 2022
Heterozygous <i>HTRA1</i> Mutations Cause Cerebral Small Vessel Diseases: Genetic, Clinical, and Pathologic Findings From 3 Chinese PedigreesTingyan Yao, Junge Zhu, Xiao Wu, et al.
Parkinsonism & Related Disorders|June 5, 2012
Penetrance of LRRK2 G2385R and R1628P is modified by common PD-associated genetic variantsChaodong Wang, Yanning Cai, Zheng Zheng, et al.
Journal of Alzheimer'S Disease : JAD|March 1, 2019
Diagnostic Approach of Early-Onset Dementia with Negative Family History: Implications from Two Cases of Early-Onset Alzheimer's Disease with De Novo PSEN1 MutationJia Liu, Qianqian Wang, Donglai Jing, et al.
Brain : a Journal of Neurology|January 10, 2023
Decreased water exchange rate across blood-brain barrier in hereditary cerebral small vessel diseaseYingying Li, Yunqing Ying, Tingyan Yao, et al.
Neuroscience Letters|March 22, 2021
Autosomal recessive spastic ataxia of Charlevoix-Saguenay caused by novel mutations in SACS gene: A report of two Chinese familiesZhanjun Wang, Yang Song, Xianling Wang, et al.
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