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Current Opinion in Neurology|July 14, 2020
Recent therapeutic prospects for Machado-Joseph diseaseMaria do Carmo Costa
Cell Research|July 24, 2013
New hope for therapy in neurodegenerative diseasesMaria do Carmo Costa, Henry L Paulson
Progress in Neurobiology|December 3, 2011
Toward understanding Machado-Joseph diseaseMaria do Carmo Costa, Henry L Paulson
Journal of Human Genetics|August 9, 2002
Identification of three novel polymorphisms in the MJD1 gene and study of their frequency in the Portuguese populationMaria do Carmo Costa, Jorge Sequeiros, Patrícia Maciel
Frontiers in Molecular Neuroscience|May 1, 2023
Regional and age-dependent changes in ubiquitination in cellular and mouse models of spinocerebellar ataxia type 3Haiyang Luo, Sokol V Todi, Henry L Paulson, et al.
Biorxiv : the Preprint Server for Biology|March 9, 2023
Regional and age-dependent changes in ubiquitination in cellular and mouse models of Spinocerebellar ataxia type 3Haiyang Luo, Sokol V Todi, Henry L Paulson, et al.
Journal of Molecular Neuroscience : MN|July 10, 2019
Selection of Reference Genes for Normalization of Gene Expression Data in Blood of Machado-Joseph Disease/Spinocerebellar Ataxia Type 3 (MJD/SCA3) SubjectsAna F Ferreira, Mafalda Raposo, João Vasconcelos, et al.
Journal of Human Genetics|December 24, 2005
The CAG repeat at the Huntington disease gene in the Portuguese population: insights into its dynamics and to the origin of the mutationMaria do Carmo Costa, Paula Magalhães, Laura Guimarães, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 9, 2011
Early changes in cerebellar physiology accompany motor dysfunction in the polyglutamine disease spinocerebellar ataxia type 3Vikram G Shakkottai, Maria do Carmo Costa, James M Dell'Orco, et al.
Biochimica Et Biophysica Acta|July 20, 2010
Absence of ataxin-3 leads to cytoskeletal disorganization and increased cell deathAna-João Rodrigues, Maria do Carmo Costa, Teresa-Luísa Silva, et al.
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