Homozygosity Enhances Severity in Spinocerebellar Ataxia Type 3-Reference-Cited by-同舟云学术

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Homozygosity Enhances Severity in Spinocerebellar Ataxia Type 3

Published:2008-04 Issue:4 Volume:38 Page:296-299
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Carvalho Daniel R.,La Rocque-Ferreira Alessandra,Rizzo Isabela M.,Imamura Erica U.,Speck-Martins Carlos E.

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health

Reference14 articles.

1. Epidemiology and clinical aspects of Machado-Joseph disease;Sequeiros;Adv Neurol,1993

2. Dominantly inherited ataxias: lessons learned from Machado-Joseph disease/spinocerebellar ataxia type 3;Paulson;Semin Neurol,2007

3. Correlation between CAG repeat length and clinical features in Machado-Joseph disease;Maciel;Am J Hum Genet,1995

4. Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease;Takiyama;Hum Mol Genet,1995

5. Homozygous inheritance of the Machado-Joseph disease gene;Lang;Ann Neurol,1994

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1. Polyglutamine disorders: Pathogenesis and potential drug interventions;Life Sciences;2024-05

2. The deubiquitinase function of ataxin-3 and its role in the pathogenesis of Machado-Joseph disease and other diseases;Biochemical Journal;2024-03-18

3. Disease-associated oligodendrocyte signatures are spatiotemporally dysregulated in spinocerebellar ataxia type 3;Frontiers in Neuroscience;2023-02-15

4. Novel Machado-Joseph disease-modifying genes and pathways identified by whole-exome sequencing;Neurobiology of Disease;2022-01

5. MiRNA-Mediated Knockdown of ATXN3 Alleviates Molecular Disease Hallmarks in a Mouse Model for Spinocerebellar Ataxia Type 3;Nucleic Acid Therapeutics;2021-12-07

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