User profiles for Wei‐Ling Tsou
![]() | Wei-Ling TsouAssistant Professor-Research, Department of Pharmacology Wayne State University School … Verified email at wayne.edu Cited by 1009 |
Nanoplastics impact the zebrafish (Danio rerio) transcriptome: Associated developmental and neurobehavioral consequences
Microplastics (MPs) are a ubiquitous pollutant detected not only in marine and freshwater
bodies, but also in tap and bottled water worldwide. While MPs have been extensively studied, …
bodies, but also in tap and bottled water worldwide. While MPs have been extensively studied, …
An optimal ubiquitin-proteasome pathway in the nervous system: the role of deubiquitinating enzymes
The Ubiquitin-Proteasome Pathway (UPP), which is critical for normal function in the nervous
system and is implicated in various neurological diseases, requires the small modifier …
system and is implicated in various neurological diseases, requires the small modifier …
Ubiquitin-binding site 2 of ataxin-3 prevents its proteasomal degradation by interacting with Rad23
Polyglutamine repeat expansion in ataxin-3 causes neurodegeneration in the most common
dominant ataxia, spinocerebellar ataxia type 3 (SCA3). Since reducing levels of disease …
dominant ataxia, spinocerebellar ataxia type 3 (SCA3). Since reducing levels of disease …
Systematic analysis of the physiological importance of deubiquitinating enzymes
Deubiquitinating enzymes (DUBs) are proteases that control the post-translational modification
of proteins by ubiquitin and in turn regulate diverse cellular pathways. Despite a growing …
of proteins by ubiquitin and in turn regulate diverse cellular pathways. Despite a growing …
Ubiquitination regulates the neuroprotective function of the deubiquitinase ataxin-3 in vivo
Deubiquitinases (DUBs) are proteases that regulate various cellular processes by controlling
protein ubiquitination. Cell-based studies indicate that the regulation of the activity of DUBs …
protein ubiquitination. Cell-based studies indicate that the regulation of the activity of DUBs …
The deubiquitinase ataxin-3 requires Rad23 and DnaJ-1 for its neuroprotective role in Drosophila melanogaster
WL Tsou, M Ouyang, RR Hosking, JR Sutton… - Neurobiology of …, 2015 - Elsevier
Ataxin-3 is a deubiquitinase and polyglutamine (polyQ) disease protein with a protective role
in Drosophila melanogaster models of neurodegeneration. In the fruit fly, wild-type ataxin-3 …
in Drosophila melanogaster models of neurodegeneration. In the fruit fly, wild-type ataxin-3 …
DnaJ-1 and karyopherin α3 suppress degeneration in a new Drosophila model of Spinocerebellar Ataxia Type 6
WL Tsou, RR Hosking, AA Burr… - Human molecular …, 2015 - academic.oup.com
Spinocerebellar ataxia type 6 (SCA6) belongs to the family of CAG/polyglutamine (polyQ)-dependent
neurodegenerative disorders. SCA6 is caused by abnormal expansion in a CAG …
neurodegenerative disorders. SCA6 is caused by abnormal expansion in a CAG …
Using membrane‐targeted green fluorescent protein to monitor neurotoxic protein‐dependent degeneration of Drosophila eyes
AA Burr, WL Tsou, G Ristic… - Journal of neuroscience …, 2014 - Wiley Online Library
Age‐related neurodegeneration has been studied extensively through the use of model
organisms, including the genetically versatile Drosophila melanogaster. Various neurotoxic …
organisms, including the genetically versatile Drosophila melanogaster. Various neurotoxic …
A survey of protein interactions and posttranslational modifications that influence the polyglutamine diseases
The presence and aggregation of misfolded proteins has deleterious effects in the nervous
system. Among the various diseases caused by misfolded proteins is the family of the …
system. Among the various diseases caused by misfolded proteins is the family of the …
Interaction of the polyglutamine protein ataxin-3 with Rad23 regulates toxicity in Drosophila models of Spinocerebellar Ataxia Type 3
Polyglutamine (polyQ) repeat expansion in the deubiquitinase ataxin-3 causes neurodegeneration
in Spinocerebellar Ataxia Type 3 (SCA3), one of nine inherited, incurable diseases …
in Spinocerebellar Ataxia Type 3 (SCA3), one of nine inherited, incurable diseases …