Resultados de procura - Ho Yin Edwin Chan
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Drosophila models of human neurodegenerative disease por Ho Yin Edwin Chan, Nancy M. Bonini
Publicado 2000Revisão -
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Isorhynchophylline, a natural alkaloid, promotes the degradation of alpha-synuclein in neuronal cells via inducing autophagy por Jiahong Lu, Jieqiong Tan, Siva Sundara Kumar Durairajan, Liang‐Feng Liu, Zhuohua Zhang, Long Ma, Han‐Ming Shen, Ho Yin Edwin Chan, Min Li
Publicado 2012Artigo -
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Nuclear retention of full-length HTT RNA is mediated by splicing factors MBNL1 and U2AF65 por Xin Sun, Pan P. Li, Shanshan Zhu, Rachael Cohen, Leonard O. Marque, Christopher A. Ross, Stefan M. Pulst, Ho Yin Edwin Chan, Russell L. Margolis, Dobrila D. Rudnicki
Publicado 2015Artigo -
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Chronic alcohol metabolism results in <scp>DNA</scp> repair infidelity and cell cycle‐induced senescence in neurons por Jacquelyne Ka‐Li Sun, Deng Wu, Genper Chi‐Ngai Wong, Tsun Ming Lau, Meigui Yang, Ronald P. Hart, Kin Ming Kwan, Ho Yin Edwin Chan, Hei‐Man Chow
Publicado 2023Artigo -
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Intrinsically cell-penetrating multivalent and multitargeting ligands for myotonic dystrophy type 1 por Ju‐Yeon Lee, Yugang Bai, Ullas V. Chembazhi, Shaohong Peng, Kevin Yum, Long M. Luu, Lauren D. Hagler, Julio F. Serrano, Ho Yin Edwin Chan, Auinash Kalsotra, Steven C. Zimmerman
Publicado 2019Artigo -
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Targeting Toxic RNAs that Cause Myotonic Dystrophy Type 1 (DM1) with a Bisamidinium Inhibitor por Chun‐Ho Wong, Lien Nguyen, Jessie Peh, Long M. Luu, Jeannette S. Sanchez, Stacie L. Richardson, Tiziano Tuccinardi, Ho Tsoi, Wood Yee Chan, Ho Yin Edwin Chan, Anne M. Baranger, Paul J. Hergenrother, Steven C. Zimmerman
Publicado 2014Artigo -
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Pharmacologically reversible zonation-dependent endothelial cell transcriptomic changes with neurodegenerative disease associations in the aged brain por Lei Zhao, Zhongqi Li, Joaquim S. L. Vong, Xinyi Chen, H. M. Lai, Leo Y. C. Yan, Junzhe Huang, Samuel K. H. Sy, Xiao Yu Tian, Yü Huang, Ho Yin Edwin Chan, Hon‐Cheong So, Wai‐Lung Ng, Yamei Tang, Wei‐Jye Lin, Vincent Mok, Ho Ko
Publicado 2020Artigo -
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A novel missense mutation in<i>CCDC88C</i>activates the JNK pathway and causes a dominant form of spinocerebellar ataxia por Ho Tsoi, Allen Chi-Shing Yu, Zhefan Stephen Chen, Nelson K N Ng, Anne Chan, Liz Y. P. Yuen, Jill Abrigo, Suk Ying Tsang, Stephen Kwok‐Wing Tsui, Tony M F Tong, Ivan F. M. Lo, Stephen T.S. Lam, Vincent Mok, Ka Sing Wong, Jacky Chi Ki Ngo, Kwok‐Fai Lau, Ting‐Fung Chan, Ho Yin Edwin Chan
Publicado 2014Artigo
Ferramentas de procura:
Materias Relacionadas
Biology
Cell biology
Gene
Genetics
Biochemistry
Medicine
RNA
Disease
Molecular biology
Apoptosis
Chemistry
Neuroscience
Internal medicine
Neurodegeneration
Nucleus
Pathology
RNA-binding protein
Allele
Autophagy
Biophysics
Cell
Cell nucleus
DNA
Drosophila melanogaster
Function (biology)
Messenger RNA
Mutant
Myotonic dystrophy
Nuclear export signal
PI3K/AKT/mTOR pathway