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Advances in Experimental Medicine and Biology
|
February 11, 2018
Gene Therapies for Polyglutamine Diseases
Carlos A Matos, Vítor Carmona, Udaya-Geetha Vijayakumar, et al.
The Journal of Cell Biology
|
February 17, 2016
Ataxin-3 phosphorylation decreases neuronal defects in spinocerebellar ataxia type 3 models
Carlos A Matos, Clévio Nóbrega, Susana R Louros, et al.
Human Molecular Genetics
|
September 17, 2018
Cordycepin activates autophagy through AMPK phosphorylation to reduce abnormalities in Machado-Joseph disease models
Adriana Marcelo, Filipa Brito, Sara Carmo-Silva, et al.
Biochimica Et Biophysica Acta
|
June 16, 2015
SUMOylation of the brain-predominant Ataxin-3 isoform modulates its interaction with p97
Bruno Almeida, Isabel A Abreu, Carlos A Matos, et al.
BMC Research Notes
|
April 12, 2020
The cholesterol 24-hydroxylase activates autophagy and decreases mutant huntingtin build-up in a neuroblastoma culture model of Huntington's disease
Clévio Nóbrega, André Conceição, Rafael G Costa, et al.
Acta Neuropathologica
|
June 15, 2019
Restoring brain cholesterol turnover improves autophagy and has therapeutic potential in mouse models of spinocerebellar ataxia
Clévio Nóbrega, Liliana Mendonça, Adriana Marcelo, et al.
Cell Death & Disease
|
November 30, 2021
Autophagy in Spinocerebellar ataxia type 2, a dysregulated pathway, and a target for therapy
Adriana Marcelo, Inês T Afonso, Ricardo Afonso-Reis, et al.
Cell Death & Disease
|
November 10, 2025
Molecular hallmarks of neurodegeneration in polyglutamine spinocerebellar ataxias
Clévio Nóbrega, Adriana Marcelo, Ana Teresa Rajado, et al.
Brain : a Journal of Neurology
|
December 13, 2022
The stress granule protein G3BP1 alleviates spinocerebellar ataxia-associated deficits
Rebekah Koppenol, André Conceição, Inês T Afonso, et al.
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of 2
Search research articles
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Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Advances in Experimental Medicine and Biology
|
February 11, 2018
Gene Therapies for Polyglutamine Diseases
Carlos A Matos, Vítor Carmona, Udaya-Geetha Vijayakumar, et al.
The Journal of Cell Biology
|
February 17, 2016
Ataxin-3 phosphorylation decreases neuronal defects in spinocerebellar ataxia type 3 models
Carlos A Matos, Clévio Nóbrega, Susana R Louros, et al.
Human Molecular Genetics
|
September 17, 2018
Cordycepin activates autophagy through AMPK phosphorylation to reduce abnormalities in Machado-Joseph disease models
Adriana Marcelo, Filipa Brito, Sara Carmo-Silva, et al.
Biochimica Et Biophysica Acta
|
June 16, 2015
SUMOylation of the brain-predominant Ataxin-3 isoform modulates its interaction with p97
Bruno Almeida, Isabel A Abreu, Carlos A Matos, et al.
BMC Research Notes
|
April 12, 2020
The cholesterol 24-hydroxylase activates autophagy and decreases mutant huntingtin build-up in a neuroblastoma culture model of Huntington's disease
Clévio Nóbrega, André Conceição, Rafael G Costa, et al.
Acta Neuropathologica
|
June 15, 2019
Restoring brain cholesterol turnover improves autophagy and has therapeutic potential in mouse models of spinocerebellar ataxia
Clévio Nóbrega, Liliana Mendonça, Adriana Marcelo, et al.
Cell Death & Disease
|
November 30, 2021
Autophagy in Spinocerebellar ataxia type 2, a dysregulated pathway, and a target for therapy
Adriana Marcelo, Inês T Afonso, Ricardo Afonso-Reis, et al.
Cell Death & Disease
|
November 10, 2025
Molecular hallmarks of neurodegeneration in polyglutamine spinocerebellar ataxias
Clévio Nóbrega, Adriana Marcelo, Ana Teresa Rajado, et al.
Brain : a Journal of Neurology
|
December 13, 2022
The stress granule protein G3BP1 alleviates spinocerebellar ataxia-associated deficits
Rebekah Koppenol, André Conceição, Inês T Afonso, et al.
Page
of 2