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Huaying Cai

Showing results (1-10 of 30) with videos related to

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Frontiers in Cellular and Infection Microbiology|January 29, 2026
Integrating microbial genomics and neurotranscriptomics to understand the impact of probiotic strains on neurological healthXiaolan Jin, Huaying Cai, Zhengwei Li
Neural Regeneration Research|October 16, 2014
Acrylamide inhibits nerve sprouting induced by botulinum toxin type AHong Jiang, Yi Xiang, Xingyue Hu, et al.
Aging|August 16, 2021
Inhibition of endoplasmic reticulum stress reverses synaptic plasticity deficits in striatum of DYT1 dystonia miceHuaying Cai, Linhui Ni, Xingyue Hu, et al.
Human Mutation|May 14, 2026
Decoding Pathogenic Mutational Landscapes in Alzheimer's Disease Through Integrated TranscriptomicsWan Ma, Fenfang Zhou, Huaying Cai, et al.
Open Medicine (Warsaw, Poland)|November 15, 2018
Guillain-Barré Syndrome and Low Back Pain: Two Cases and Literature ReviewXianjun Ding, Hong Jiang, Xingyue Hu, et al.
Pharmaceuticals (Basel, Switzerland)|July 30, 2025
Correction: Fu et al. C16 Peptide and Ang-1 Improve Functional Disability and Pathological Changes in an Alzheimer's Disease Model Associated with Vascular Dysfunction. <i>Pharmaceuticals</i> 2022, <i>15</i>, 471Xiaoxiao Fu, Jing Wang, Huaying Cai, et al.
Pharmaceuticals (Basel, Switzerland)|April 23, 2022
C16 Peptide and Ang-1 Improve Functional Disability and Pathological Changes in an Alzheimer's Disease Model Associated with Vascular DysfunctionXiaoxiao Fu, Jing Wang, Huaying Cai, et al.
Reviews in Cardiovascular Medicine|May 9, 2019
Pitfalls in the diagnosis and initial management of acute cerebral venous thrombosisHuaying Cai, Xiaobin Ye, Weiliang Zheng, et al.
Artificial Intelligence in Medicine|March 8, 2020
Gait characteristics and clinical relevance of hereditary spinocerebellar ataxia on deep learningLuya Jin, Wen Lv, Guocan Han, et al.
Rinsho Shinkeigaku = Clinical Neurology|June 20, 2014
[Familial progressive external opthalmoplegia, parkinsonism and polyneuropathy associated with POLG1 mutation]Masako Mukai, Keizo Sugaya, Shiro Matsubara, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Frontiers in Cellular and Infection Microbiology|January 29, 2026
Integrating microbial genomics and neurotranscriptomics to understand the impact of probiotic strains on neurological healthXiaolan Jin, Huaying Cai, Zhengwei Li
Neural Regeneration Research|October 16, 2014
Acrylamide inhibits nerve sprouting induced by botulinum toxin type AHong Jiang, Yi Xiang, Xingyue Hu, et al.
Aging|August 16, 2021
Inhibition of endoplasmic reticulum stress reverses synaptic plasticity deficits in striatum of DYT1 dystonia miceHuaying Cai, Linhui Ni, Xingyue Hu, et al.
Human Mutation|May 14, 2026
Decoding Pathogenic Mutational Landscapes in Alzheimer's Disease Through Integrated TranscriptomicsWan Ma, Fenfang Zhou, Huaying Cai, et al.
Open Medicine (Warsaw, Poland)|November 15, 2018
Guillain-Barré Syndrome and Low Back Pain: Two Cases and Literature ReviewXianjun Ding, Hong Jiang, Xingyue Hu, et al.
Pharmaceuticals (Basel, Switzerland)|July 30, 2025
Correction: Fu et al. C16 Peptide and Ang-1 Improve Functional Disability and Pathological Changes in an Alzheimer's Disease Model Associated with Vascular Dysfunction. <i>Pharmaceuticals</i> 2022, <i>15</i>, 471Xiaoxiao Fu, Jing Wang, Huaying Cai, et al.
Pharmaceuticals (Basel, Switzerland)|April 23, 2022
C16 Peptide and Ang-1 Improve Functional Disability and Pathological Changes in an Alzheimer's Disease Model Associated with Vascular DysfunctionXiaoxiao Fu, Jing Wang, Huaying Cai, et al.
Reviews in Cardiovascular Medicine|May 9, 2019
Pitfalls in the diagnosis and initial management of acute cerebral venous thrombosisHuaying Cai, Xiaobin Ye, Weiliang Zheng, et al.
Artificial Intelligence in Medicine|March 8, 2020
Gait characteristics and clinical relevance of hereditary spinocerebellar ataxia on deep learningLuya Jin, Wen Lv, Guocan Han, et al.
Rinsho Shinkeigaku = Clinical Neurology|June 20, 2014
[Familial progressive external opthalmoplegia, parkinsonism and polyneuropathy associated with POLG1 mutation]Masako Mukai, Keizo Sugaya, Shiro Matsubara, et al.
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