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Neurobiology of Disease, ISSN 0969-9961, 2008, Volume 31, Issue 1, pp. 89 - 101
Journal Article
Journal Article
Neuropharmacology, ISSN 0028-3908, 12/2015, Volume 99, pp. 308 - 317
Journal Article
Neuropharmacology, ISSN 0028-3908, 07/2013, Volume 70, pp. 1 - 11
Journal Article
Neurobiology of Disease, ISSN 0969-9961, 2009, Volume 37, Issue 2, pp. 284 - 293
Abstract Spinocerebellar ataxia type 3 (SCA3), or Machado–Joseph disease (MJD), is caused by the expansion of a polyglutamine repeat in the ataxin-3 protein.... 
Neurology | Polyglutamine | SCA3 | CAG repeat instability | MJD | Spinocerebellar ataxia type 3 | Intranuclear inclusion bodies | Late onset | Machado–Joseph disease | Transgenic mouse model | Machado-Joseph disease | EXPANDED POLYGLUTAMINE | AMPA NEUROTOXICITY | NEURONAL LOSS | NEUROSCIENCES | CEREBELLAR-ATAXIA | MACHADO-JOSEPH-DISEASE | IN-VIVO | INTERGENERATIONAL INSTABILITY | INTRANUCLEAR INCLUSIONS | DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY | HUNTINGTONS-DISEASE | Ataxin-3 | Gene Expression - genetics | Machado-Joseph Disease - metabolism | Trinucleotide Repeats - genetics | Brain - metabolism | Nuclear Proteins - genetics | Disease Models, Animal | Genetic Predisposition to Disease - genetics | Brain - physiopathology | Intranuclear Inclusion Bodies - genetics | Rats | Mice, Transgenic | Sex Characteristics | Transcription Factors - genetics | Mutation - genetics | Disease Progression | Intranuclear Inclusion Bodies - pathology | Chromosomal Instability - genetics | Movement Disorders - metabolism | Animals | Movement Disorders - physiopathology | Age of Onset | Brain - pathology | Machado-Joseph Disease - physiopathology | Mice | Movement Disorders - genetics | Intranuclear Inclusion Bodies - metabolism | Machado-Joseph Disease - genetics | Disease transmission | Neurons | Analysis | Spinocerebellar ataxia | Medical genetics | Genetic aspects | Models | Genetic engineering
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 05/2019, Volume 28, Issue 9, pp. 1463 - 1473
Abstract Spinocerebellar ataxia type 3 (SCA3) is caused by the expansion of CAG repeats in the ATXN3 gene leading to an elongated polyglutamine tract in the... 
NUCLEAR-LOCALIZATION | PROTEIN | SCA3 | BIOCHEMISTRY & MOLECULAR BIOLOGY | MACHADO-JOSEPH-DISEASE | MOUSE MODEL | GENETICS & HEREDITY | NEURODEGENERATION | EXPRESSION | MOTOR DYSFUNCTION | CONDITIONAL MODEL | TRANSGENIC MICE | Index Medicus
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 07/2007, Volume 27, Issue 28, pp. 7418 - 7428
Spinocerebellar ataxia type 3 (SCA3) is an autosomal dominantly inherited neurodegenerative disorder caused by the expansion of a CAG repeat in the MJD1 gene... 
Spinocerebellar ataxia type 3 (SCA3) | Mouse model | Nuclear localization | Polyglutamine diseases | Neurodegenerative diseases | Machado-Joseph disease (MJD) | mouse model | spinocerebellar ataxia type 3 ( SCA3) | EXPANDED CAG REPEAT | MUTANT HUNTINGTIN | NEUROSCIENCES | CELL-DEATH | NEURONAL INTRANUCLEAR INCLUSIONS | neurodegenerative diseases | MACHADO-JOSEPH-DISEASE | nuclear localization | FUNCTIONAL-ANALYSIS | polyglutamine diseases | BODY FORMATION | HUNTINGTONS-DISEASE | TRANSGENIC MICE | Trinucleotide Repeats | Ataxin-3 | Machado-Joseph Disease - metabolism | Peptides - genetics | Ubiquitin - metabolism | Machado-Joseph Disease - mortality | Motor Activity | Tissue Distribution | Machado-Joseph Disease - complications | Cell Nucleus - metabolism | Inclusion Bodies - metabolism | Nuclear Proteins - genetics | Mental Disorders - etiology | Repressor Proteins - metabolism | Exploratory Behavior | Back - abnormalities | Repressor Proteins - genetics | Mice, Transgenic | Nuclear Proteins - metabolism | Machado-Joseph Disease - psychology | Nerve Tissue Proteins - genetics | Immunohistochemistry - methods | Nerve Tissue Proteins - metabolism | Phenotype | Animals | Staining and Labeling | Mice | Tremor - etiology | Nerve Degeneration - etiology | spinocerebellar ataxia type 3 (SCA3) | Machado–Joseph disease (MJD)
Journal Article
Molecular Therapy, ISSN 1525-0016, 04/2017, Volume 25, Issue 4, pp. 1038 - 1055
Journal Article
Neurobiology of Disease, ISSN 0969-9961, 2015, Volume 73, pp. 174 - 188
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2018, Volume 13, Issue 8, pp. e0201794 - e0201794
Journal Article