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Ming-Jen Lee

Showing results (51-60 of 88) with videos related to

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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|November 20, 2015
A single nucleotide TDP-43 mutation within a Taiwanese family: A multifaceted demonYu-Wen Cheng, Ming-Jen Lee, Ta-Fu Chen, et al.
Plos One|November 4, 2015
The Temporal Profiles of Changes in Nerve Excitability Indices in Familial Amyloid PolyneuropathyHsing-Jung Lai, Ya-Wen Chiang, Chih-Chao Yang, et al.
Free Radical Biology & Medicine|December 25, 2012
Increase of oxidative stress by a novel PINK1 mutation, P209AWei-Lin Chien, Tzeng-Ruei Lee, Shih-Ya Hung, et al.
Neurology. Genetics|May 9, 2025
Prevalence and Characteristics of Pathogenic Variants in Taiwanese Patients With Cerebral Small Vessel DiseaseYu-Wen Cheng, Chih-Hao Chen, Ya-Fang Chen, et al.
Parkinsonism & Related Disorders|March 6, 2009
Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutationChun-Hwei Tai, Ruoh-Fan Yen, Chin-Hsien Lin, et al.
Pesticide Biochemistry and Physiology|April 6, 2024
Biophysical mechanisms underlying tefluthrin-induced modulation of gating changes and resurgent current generation in the human Na<sub>v</sub>1.4 channelHsing-Jung Lai, Ming-Jen Lee, Hsin-Wei Yu, et al.
Journal of Alzheimer'S Disease : JAD|February 22, 2011
Clinical phenotype of G206D mutation in the presenilin 1 gene in pathologically confirmed familial Alzheimer's diseaseYa-Ying Wu, Irene Han-Juo Cheng, Chin-Cheng Lee, et al.
Clinical Chemistry|September 18, 2010
The microRNA spectrum in 12 body fluidsJessica A Weber, David H Baxter, Shile Zhang, et al.
Fertility and Sterility|February 6, 2008
Rapid prenatal confirmation of LIT1 hypomethylation using a novel quantitative method (E-Q-PCR) in fetuses with Beckwith-Wiedemann syndrome impressed with ultrasonographyGwo-Chin Ma, Shuenn-Dyh Chang, Yu Chang, et al.
Plos One|January 1, 2015
Soluble AXL: a possible circulating biomarker for neurofibromatosis type 1 related tumor burdenGunnar Johansson, Po-Chun Peng, Po-Yuan Huang, et al.
Pageof 9

Showing results (51-60 of 88) with videos related to

Sort By:
Pageof 9
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|November 20, 2015
A single nucleotide TDP-43 mutation within a Taiwanese family: A multifaceted demonYu-Wen Cheng, Ming-Jen Lee, Ta-Fu Chen, et al.
Plos One|November 4, 2015
The Temporal Profiles of Changes in Nerve Excitability Indices in Familial Amyloid PolyneuropathyHsing-Jung Lai, Ya-Wen Chiang, Chih-Chao Yang, et al.
Free Radical Biology & Medicine|December 25, 2012
Increase of oxidative stress by a novel PINK1 mutation, P209AWei-Lin Chien, Tzeng-Ruei Lee, Shih-Ya Hung, et al.
Neurology. Genetics|May 9, 2025
Prevalence and Characteristics of Pathogenic Variants in Taiwanese Patients With Cerebral Small Vessel DiseaseYu-Wen Cheng, Chih-Hao Chen, Ya-Fang Chen, et al.
Parkinsonism & Related Disorders|March 6, 2009
Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutationChun-Hwei Tai, Ruoh-Fan Yen, Chin-Hsien Lin, et al.
Pesticide Biochemistry and Physiology|April 6, 2024
Biophysical mechanisms underlying tefluthrin-induced modulation of gating changes and resurgent current generation in the human Na<sub>v</sub>1.4 channelHsing-Jung Lai, Ming-Jen Lee, Hsin-Wei Yu, et al.
Journal of Alzheimer'S Disease : JAD|February 22, 2011
Clinical phenotype of G206D mutation in the presenilin 1 gene in pathologically confirmed familial Alzheimer's diseaseYa-Ying Wu, Irene Han-Juo Cheng, Chin-Cheng Lee, et al.
Clinical Chemistry|September 18, 2010
The microRNA spectrum in 12 body fluidsJessica A Weber, David H Baxter, Shile Zhang, et al.
Fertility and Sterility|February 6, 2008
Rapid prenatal confirmation of LIT1 hypomethylation using a novel quantitative method (E-Q-PCR) in fetuses with Beckwith-Wiedemann syndrome impressed with ultrasonographyGwo-Chin Ma, Shuenn-Dyh Chang, Yu Chang, et al.
Plos One|January 1, 2015
Soluble AXL: a possible circulating biomarker for neurofibromatosis type 1 related tumor burdenGunnar Johansson, Po-Chun Peng, Po-Yuan Huang, et al.
Pageof 9