LRRK 2 gene mutations in the pathophysiology of the ROCO domain and therapeutic targets for Parkinson’s disease: a review

por Chen, Meng-Ling, Wu, Ruey-Meei
Publicado 2018

Homozygous mutation of the LRRK2 ROC domain as a novel genetic model of parkinsonism

por Chen, Meng-Ling, Wu, Ruey-Meei
Publicado 2022

Mutational Analysis of Angiogenin Gene in Parkinson's Disease

por Chen, Meng-Ling, Wu, Ruey-Meei, Tai, Chun-Hwei, Lin, Chin-Hsien
Publicado 2014

Novel variant Pro143Ala in HTRA2 contributes to Parkinson’s disease by inducing hyperphosphorylation of HTRA2 protein in mitochondria

por Lin, Chin-Hsien, Chen, Meng-Ling, Chen, Grace Shiahuy, Tai, Chun-Hwei, Wu, Ruey-Meei
Publicado 2011

A clinical and genetic study of early‐onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next‐generation sequencing

por Lin, Chin‐Hsien, Chen, Pei‐Lung, Tai, Chun‐Hwei, Lin, Hang‐I, Chen, Chih‐Shan, Chen, Meng‐Ling, Wu, Ruey‐Meei
Publicado 2019

Cuticular competing endogenous RNAs regulate insecticide penetration and resistance in a major agricultural pest

por Meng, Li-Wei, Yuan, Guo-Rui, Chen, Meng-Ling, Zheng, Li-Sha, Dou, Wei, Peng, Yu, Bai, Wen-Jie, Li, Zhen-Yu, Vontas, John, Wang, Jin-Jun
Publicado 2023

Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy

por Lin, Chin-Hsien, Tsai, Pei-I, Lin, Han-Yi, Hattori, Nobutaka, Funayama, Manabu, Jeon, Beomseok, Sato, Kota, Abe, Koji, Mukai, Yohei, Takahashi, Yuji, Li, Yuanzhe, Nishioka, Kenya, Yoshino, Hiroyo, Daida, Kensuke, Chen, Meng-Ling, Cheng, Jay, Huang, Cheng-Yen, Tzeng, Shiou-Ru, Wu, Yen-Sheng, Lai, Hsing-Jung, Tsai, Hsin-Hsi, Yen, Ruoh-Fang, Lee, Ni-Chung, Lo, Wen-Chun, Hung, Yu-Chien, Chan, Chih-Chiang, Ke, Yi-Ci, Chao, Chi-Chao, Hsieh, Sung-Tsang, Farrer, Matthew, Wu, Ruey-Meei
Publicado 2020