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Frontiers in Aging Neuroscience
|
November 30, 2020
Different Perivascular Space Burdens in Idiopathic Rapid Eye Movement Sleep Behavior Disorder and Parkinson's Disease
Xiao-Li Si, Lu-Yan Gu, Zhe Song, et al.
European Journal of Neurology
|
January 25, 2023
Elevated serum anti-Saccharomyces cerevisiae antibody accompanied by gut mycobiota dysbiosis as a biomarker of diagnosis in patients with de novo Parkinson disease
Ying Chen, Li-Ying Zhang, Yi Fang, et al.
Nature Aging
|
August 26, 2025
Mevalonate metabolites boost aged oocyte quality through prenylation of small GTPases
Chuanming Liu, Huidan Zhang, Jialian Mao, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 6, 2021
Apolipoprotein E Genotype Contributes to Motor Progression in Parkinson's Disease
Jia-Li Pu, Chong-Yao Jin, Zhong-Xuan Wang, et al.
Ebiomedicine
|
January 2, 2022
The mitochondrial protease LONP1 maintains oocyte development and survival by suppressing nuclear translocation of AIFM1 in mammals
Xiaoqiang Sheng, Chuanming Liu, Guijun Yan, et al.
European Journal of Neurology
|
September 1, 2022
Different patterns of exosomal α-synuclein between Parkinson's disease and probable rapid eye movement sleep behavior disorder
Yi-Qun Yan, Jia-Li Pu, Ran Zheng, et al.
Nature Aging
|
May 15, 2023
Granulosa cell mevalonate pathway abnormalities contribute to oocyte meiotic defects and aneuploidy
Chuanming Liu, Wu Zuo, Guijun Yan, et al.
Research Square
|
July 23, 2024
Molecular and clinical characterization of a founder mutation causing G6PC3 deficiency
Xin Zhen, Michael Betti, Meltem Ece Kars, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 27, 2024
Molecular and clinical characterization of a founder mutation causing G6PC3 deficiency
Xin Zhen, Michael J Betti, Meltem Ece Kars, et al.
Journal of Clinical Immunology
|
December 4, 2024
Molecular and Clinical Characterization of a Founder Mutation Causing G6PC3 Deficiency
Xin Zhen, Michael J Betti, Meltem Ece Kars, et al.
Page
of 21
Search research articles
Search
Showing results (191-200 of 204) with videos related to
Sort By:
Page
of 21
Frontiers in Aging Neuroscience
|
November 30, 2020
Different Perivascular Space Burdens in Idiopathic Rapid Eye Movement Sleep Behavior Disorder and Parkinson's Disease
Xiao-Li Si, Lu-Yan Gu, Zhe Song, et al.
European Journal of Neurology
|
January 25, 2023
Elevated serum anti-Saccharomyces cerevisiae antibody accompanied by gut mycobiota dysbiosis as a biomarker of diagnosis in patients with de novo Parkinson disease
Ying Chen, Li-Ying Zhang, Yi Fang, et al.
Nature Aging
|
August 26, 2025
Mevalonate metabolites boost aged oocyte quality through prenylation of small GTPases
Chuanming Liu, Huidan Zhang, Jialian Mao, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 6, 2021
Apolipoprotein E Genotype Contributes to Motor Progression in Parkinson's Disease
Jia-Li Pu, Chong-Yao Jin, Zhong-Xuan Wang, et al.
Ebiomedicine
|
January 2, 2022
The mitochondrial protease LONP1 maintains oocyte development and survival by suppressing nuclear translocation of AIFM1 in mammals
Xiaoqiang Sheng, Chuanming Liu, Guijun Yan, et al.
European Journal of Neurology
|
September 1, 2022
Different patterns of exosomal α-synuclein between Parkinson's disease and probable rapid eye movement sleep behavior disorder
Yi-Qun Yan, Jia-Li Pu, Ran Zheng, et al.
Nature Aging
|
May 15, 2023
Granulosa cell mevalonate pathway abnormalities contribute to oocyte meiotic defects and aneuploidy
Chuanming Liu, Wu Zuo, Guijun Yan, et al.
Research Square
|
July 23, 2024
Molecular and clinical characterization of a founder mutation causing G6PC3 deficiency
Xin Zhen, Michael Betti, Meltem Ece Kars, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 27, 2024
Molecular and clinical characterization of a founder mutation causing G6PC3 deficiency
Xin Zhen, Michael J Betti, Meltem Ece Kars, et al.
Journal of Clinical Immunology
|
December 4, 2024
Molecular and Clinical Characterization of a Founder Mutation Causing G6PC3 Deficiency
Xin Zhen, Michael J Betti, Meltem Ece Kars, et al.
Page
of 21