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Eng-King Tan

Showing results (391-400 of 445) with videos related to

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Human Molecular Genetics|August 28, 2015
F-box protein 7 mutations promote protein aggregation in mitochondria and inhibit mitophagyZhi Dong Zhou, Shao Ping Xie, Sushmitha Sathiyamoorthy, et al.
Journal of Parkinson'S Disease|January 24, 2022
Longitudinal Study of SNCA Rep1 Polymorphism on Executive Function in Early Parkinson's DiseaseYi Jayne Tan, Seyed Ehsan Saffari, Yi Zhao, et al.
Human Mutation|February 27, 2010
Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter studyEng-King Tan, Rong Peng, Yik-Ying Teo, et al.
Nature Neuroscience|June 23, 2022
Single-cell transcriptomics and surface epitope detection in human brain epileptic lesions identifies pro-inflammatory signalingPavanish Kumar, Amanda Lim, Sharifah Nur Hazirah, et al.
Parkinsonism & Related Disorders|November 23, 2020
Subjective cognitive Complaints in early Parkinson's disease patients with normal cognition are associated with affective symptomsCong Yang Chua, Matthew Rui En Koh, Nicole Shuang-Yu Chia, et al.
Science Signaling|August 23, 2022
The APP intracellular domain promotes <i>LRRK2</i> expression to enable feed-forward neurodegenerative mechanisms in Parkinson's diseaseZhi-Wei Zhang, Haitao Tu, Mei Jiang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 17, 2005
Alpha-synuclein and Parkinson's disease: implications from the screening of more than 1,900 patientsDaniela Berg, Marc Niwar, Sylvia Maass, et al.
Clinical Genetics|July 1, 2020
Phenotypic bases of NOTCH2NLC GGC expansion positive neuronal intranuclear inclusion disease in a Southeast Asian cohortZhiyong Chen, Zheyu Xu, Qianhui Cheng, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 20, 2026
Ex Vivo LRRK2 Activation in Asian G2385R and R1628P Variant Carriers and Idiopathic Parkinson's DiseaseTzi Shin Toh, Lei Cheng Lit, Shen-Yang Lim, et al.
Molecular Neurodegeneration|June 7, 2020
Utility of plasma Neurofilament light as a diagnostic and prognostic biomarker of the postural instability gait disorder motor subtype in early Parkinson's diseaseAdeline Su Lyn Ng, Yi Jayne Tan, Alisa Cui Wen Yong, et al.
Pageof 45

Showing results (391-400 of 445) with videos related to

Sort By:
Pageof 45
Human Molecular Genetics|August 28, 2015
F-box protein 7 mutations promote protein aggregation in mitochondria and inhibit mitophagyZhi Dong Zhou, Shao Ping Xie, Sushmitha Sathiyamoorthy, et al.
Journal of Parkinson'S Disease|January 24, 2022
Longitudinal Study of SNCA Rep1 Polymorphism on Executive Function in Early Parkinson's DiseaseYi Jayne Tan, Seyed Ehsan Saffari, Yi Zhao, et al.
Human Mutation|February 27, 2010
Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter studyEng-King Tan, Rong Peng, Yik-Ying Teo, et al.
Nature Neuroscience|June 23, 2022
Single-cell transcriptomics and surface epitope detection in human brain epileptic lesions identifies pro-inflammatory signalingPavanish Kumar, Amanda Lim, Sharifah Nur Hazirah, et al.
Parkinsonism & Related Disorders|November 23, 2020
Subjective cognitive Complaints in early Parkinson's disease patients with normal cognition are associated with affective symptomsCong Yang Chua, Matthew Rui En Koh, Nicole Shuang-Yu Chia, et al.
Science Signaling|August 23, 2022
The APP intracellular domain promotes <i>LRRK2</i> expression to enable feed-forward neurodegenerative mechanisms in Parkinson's diseaseZhi-Wei Zhang, Haitao Tu, Mei Jiang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 17, 2005
Alpha-synuclein and Parkinson's disease: implications from the screening of more than 1,900 patientsDaniela Berg, Marc Niwar, Sylvia Maass, et al.
Clinical Genetics|July 1, 2020
Phenotypic bases of NOTCH2NLC GGC expansion positive neuronal intranuclear inclusion disease in a Southeast Asian cohortZhiyong Chen, Zheyu Xu, Qianhui Cheng, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 20, 2026
Ex Vivo LRRK2 Activation in Asian G2385R and R1628P Variant Carriers and Idiopathic Parkinson's DiseaseTzi Shin Toh, Lei Cheng Lit, Shen-Yang Lim, et al.
Molecular Neurodegeneration|June 7, 2020
Utility of plasma Neurofilament light as a diagnostic and prognostic biomarker of the postural instability gait disorder motor subtype in early Parkinson's diseaseAdeline Su Lyn Ng, Yi Jayne Tan, Alisa Cui Wen Yong, et al.
Pageof 45