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Science Bulletin
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November 7, 2025
Interactions between rare and common variant genetic risks in determining telomere length
Shiyu Zhang, Lu Li, Zheng Wang, et al.
Cell & Bioscience
|
February 24, 2026
NOTCH2NLC GGC repeat expansions cause retinal neurodegeneration in neuronal intranuclear inclusion disease mouse model
Haibo Li, Ying Jiang, Lusi Zhang, et al.
Frontiers in Aging Neuroscience
|
February 27, 2023
Genetic and clinical analysis of <i>TP73</i> gene in amyotrophic lateral sclerosis patients from Chinese mainland
Xuxiong Tang, Yanchun Yuan, Zhen Liu, et al.
Gut Microbes
|
March 28, 2024
Integrated analysis of gut metabolome, microbiome, and brain function reveal the role of gut-brain axis in longevity
Bin Jiao, Ziyu Ouyang, Qianqian Liu, et al.
Gene
|
April 21, 2022
The association between LIN28A gene rare variants and Parkinson's disease in Chinese population
Xiurong Huang, Yuwen Zhao, Hongxu Pan, et al.
Cell & Bioscience
|
October 7, 2025
HnRNP M expression rescues neurodegeneration in neuronal intranuclear inclusion disease mouse model by restoring dysregulated RNA splicing and transcription
Yongcheng Pan, Yangping Li, Ying Jiang, et al.
Frontiers in Cellular Neuroscience
|
July 29, 2015
Contra-Directional Expression of Serum Homocysteine and Uric Acid as Important Biomarkers of Multiple System Atrophy Severity: A Cross-Sectional Study
Dan Chen, Xiaobo Wei, Jing Zou, et al.
Frontiers in Aging Neuroscience
|
November 26, 2020
Association of Genes Involved in the Metabolic Pathways of Amyloid-β and Tau Proteins With Sporadic Late-Onset Alzheimer's Disease in the Southern Han Chinese Population
Xuewen Xiao, Bin Jiao, Xinxin Liao, et al.
Stem Cell Research
|
September 7, 2019
Generation of an induced pluripotent stem cell line (XHCSUi001-A) from urine cells of a patient with spinocerebellar ataxia type 3
Lang He, Wei Ye, Zhao Chen, et al.
Molecular Psychiatry
|
June 20, 2018
A presenilin-1 mutation causes Alzheimer disease without affecting Notch signaling
Shuting Zhang, Fang Cai, Yili Wu, et al.
Page
of 52
Search research articles
Search
Showing results (241-250 of 514) with videos related to
Sort By:
Page
of 52
Science Bulletin
|
November 7, 2025
Interactions between rare and common variant genetic risks in determining telomere length
Shiyu Zhang, Lu Li, Zheng Wang, et al.
Cell & Bioscience
|
February 24, 2026
NOTCH2NLC GGC repeat expansions cause retinal neurodegeneration in neuronal intranuclear inclusion disease mouse model
Haibo Li, Ying Jiang, Lusi Zhang, et al.
Frontiers in Aging Neuroscience
|
February 27, 2023
Genetic and clinical analysis of <i>TP73</i> gene in amyotrophic lateral sclerosis patients from Chinese mainland
Xuxiong Tang, Yanchun Yuan, Zhen Liu, et al.
Gut Microbes
|
March 28, 2024
Integrated analysis of gut metabolome, microbiome, and brain function reveal the role of gut-brain axis in longevity
Bin Jiao, Ziyu Ouyang, Qianqian Liu, et al.
Gene
|
April 21, 2022
The association between LIN28A gene rare variants and Parkinson's disease in Chinese population
Xiurong Huang, Yuwen Zhao, Hongxu Pan, et al.
Cell & Bioscience
|
October 7, 2025
HnRNP M expression rescues neurodegeneration in neuronal intranuclear inclusion disease mouse model by restoring dysregulated RNA splicing and transcription
Yongcheng Pan, Yangping Li, Ying Jiang, et al.
Frontiers in Cellular Neuroscience
|
July 29, 2015
Contra-Directional Expression of Serum Homocysteine and Uric Acid as Important Biomarkers of Multiple System Atrophy Severity: A Cross-Sectional Study
Dan Chen, Xiaobo Wei, Jing Zou, et al.
Frontiers in Aging Neuroscience
|
November 26, 2020
Association of Genes Involved in the Metabolic Pathways of Amyloid-β and Tau Proteins With Sporadic Late-Onset Alzheimer's Disease in the Southern Han Chinese Population
Xuewen Xiao, Bin Jiao, Xinxin Liao, et al.
Stem Cell Research
|
September 7, 2019
Generation of an induced pluripotent stem cell line (XHCSUi001-A) from urine cells of a patient with spinocerebellar ataxia type 3
Lang He, Wei Ye, Zhao Chen, et al.
Molecular Psychiatry
|
June 20, 2018
A presenilin-1 mutation causes Alzheimer disease without affecting Notch signaling
Shuting Zhang, Fang Cai, Yili Wu, et al.
Page
of 52