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LiYing Cui

Showing results (261-270 of 323) with videos related to

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Neurobiology of Aging|May 8, 2021
Authors' reply: Four novel optineurin mutations in patients with sporadic amyotrophic lateral sclerosis in Mainland ChinaLu Yang, Yanfei Cheng, Xinmiao Jia, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 19, 2021
Association of apolipoprotein E ε4 allele and amyotrophic lateral sclerosis in Chinese populationDi He, Liang Shang, Qing Liu, et al.
Journal of Medical Genetics|September 12, 2019
Single-molecule optical mapping enables quantitative measurement of D4Z4 repeats in facioscapulohumeral muscular dystrophy (FSHD)Yi Dai, Pidong Li, Zhiqiang Wang, et al.
Current Alzheimer Research|June 9, 2021
Clinical Phenotype and Mutation Spectrum of Alzheimer's Disease with Causative Genetic Mutation in a Chinese CohortChenhui Mao, Jie Li, Liling Dong, et al.
Scientific Data|February 7, 2025
An EEG dataset for interictal epileptiform discharge with spatial distribution informationNan Lin, Mengxuan Zheng, Lian Li, et al.
Orphanet Journal of Rare Diseases|November 8, 2022
Mutation spectrum of chinese amyotrophic lateral sclerosis patients with frontotemporal dementiaXunzhe Yang, Xiaohai Sun, Qing Liu, et al.
Neurobiology of Aging|April 28, 2018
Genetic analysis of TIA1 gene in Chinese patients with amyotrophic lateral sclerosisKang Zhang, Qing Liu, Dongchao Shen, et al.
ACS Applied Materials & Interfaces|February 7, 2012
Patterning organic/inorganic hybrid Bragg stacks by integrating one-dimensional photonic crystals and macrocavities through photolithography: toward tunable colorful patterns as highly selective sensorsZhanhua Wang, Junhu Zhang, Jing Xie, et al.
Clinical Neurology and Neurosurgery|April 22, 2021
A longitudinal observation of brain structure between AD and FTLDJie Li, Yong Fan, Bo Hou, et al.
Medcomm|September 12, 2024
Loss-of-function variants in RNA binding motif protein X-linked induce neuronal defects contributing to amyotrophic lateral sclerosis pathogenesisDi He, Xinyi He, Dongchao Shen, et al.
Pageof 33

Showing results (261-270 of 323) with videos related to

Sort By:
Pageof 33
Neurobiology of Aging|May 8, 2021
Authors' reply: Four novel optineurin mutations in patients with sporadic amyotrophic lateral sclerosis in Mainland ChinaLu Yang, Yanfei Cheng, Xinmiao Jia, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 19, 2021
Association of apolipoprotein E ε4 allele and amyotrophic lateral sclerosis in Chinese populationDi He, Liang Shang, Qing Liu, et al.
Journal of Medical Genetics|September 12, 2019
Single-molecule optical mapping enables quantitative measurement of D4Z4 repeats in facioscapulohumeral muscular dystrophy (FSHD)Yi Dai, Pidong Li, Zhiqiang Wang, et al.
Current Alzheimer Research|June 9, 2021
Clinical Phenotype and Mutation Spectrum of Alzheimer's Disease with Causative Genetic Mutation in a Chinese CohortChenhui Mao, Jie Li, Liling Dong, et al.
Scientific Data|February 7, 2025
An EEG dataset for interictal epileptiform discharge with spatial distribution informationNan Lin, Mengxuan Zheng, Lian Li, et al.
Orphanet Journal of Rare Diseases|November 8, 2022
Mutation spectrum of chinese amyotrophic lateral sclerosis patients with frontotemporal dementiaXunzhe Yang, Xiaohai Sun, Qing Liu, et al.
Neurobiology of Aging|April 28, 2018
Genetic analysis of TIA1 gene in Chinese patients with amyotrophic lateral sclerosisKang Zhang, Qing Liu, Dongchao Shen, et al.
ACS Applied Materials & Interfaces|February 7, 2012
Patterning organic/inorganic hybrid Bragg stacks by integrating one-dimensional photonic crystals and macrocavities through photolithography: toward tunable colorful patterns as highly selective sensorsZhanhua Wang, Junhu Zhang, Jing Xie, et al.
Clinical Neurology and Neurosurgery|April 22, 2021
A longitudinal observation of brain structure between AD and FTLDJie Li, Yong Fan, Bo Hou, et al.
Medcomm|September 12, 2024
Loss-of-function variants in RNA binding motif protein X-linked induce neuronal defects contributing to amyotrophic lateral sclerosis pathogenesisDi He, Xinyi He, Dongchao Shen, et al.
Pageof 33