IndraLab

Statements

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"Spinocerebellar ataxia type-3, also known as Machado-Joseph disease (MJD), is an inherited neurodegenerative disease caused by polyglutamine repeat expansions in the ataxin-3 protein ( Kawaguchi et al[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
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"SCA3 is a neurodegenerative disease caused by CAG repeat expansion in the ataxin-3 gene, resulting in polyQ aggregation."
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"Liu et al. confirmed that ATX-3 is directly related to the occurrence and development of p53-mediated neurodegenerative diseases in zebrafish and type 3 spinal cerebellar ataxia (SCA3) in mouse models[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
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"Machado-Joseph disease (MJD) is a neurodegenerative disease caused by an abnormally expanded polyglutamine tract in the ataxin-3 protein."
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"Spinocerebellar ataxia type 3 (SCA3) is a rare inherited neurodegenerative disease caused by the expansion of a polyglutamine repeat in the protease ataxin-3 (Atx3)."
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"Spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD) is a progressive autosomal dominant neurodegenerative disease caused by abnormal CAG repeats in the exon 10 of ATXN3."
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"This proteotoxic Ataxin 3 underlies the manifestation of the neurodegenerative disorder “Machado Joseph Disease” (MJD) in humans (Durcan and Fon, 2013)."
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"Spinocerebellar ataxia type 3 (SCA3), also known as Machado–Joseph disease, is an autosomal dominant neurodegenerative disorder caused by CAG repeat expansion in exon 10 of ATXN3 [1]."
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"Spinocerebellar ataxia type 3 (SCA3), a neurodegenerative disorder caused by excess CAG repeats in the ATXN3 gene, leads to progressive cerebellar ataxia and other symptoms."
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"The protein ataxin-3 (ATX3) triggers an amyloid-related neurodegenerative disease when its polyglutamine stretch is expanded beyond a critical threshold."
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"CAG-polyglutamine (polyQ) repeat expansions in ATXN3 cause the neurodegenerative disorder spinocerebellar ataxia type 3 (SCA3)."
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"Machado-Joseph disease (MJD) is a dominant neurodegenerative disease caused by an expanded CAG repeat in the ATXN3 gene encoding the ataxin-3 protein."
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"SCA3 or Machado-Joseph disease (MJD) is a dominantly inherited neurodegenerative disease caused by CAG repeat expansion in the ATXN3 gene ( Fan et al., 2014 )."
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"Spinocerebellar ataxia type 3 (SCA3) is an adult-onset neurodegenerative disease caused by a polyglutamine expansion in the ataxin-3 (ATXN3) gene."
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"Spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD) is a neurodegenerative disorder caused by the ATXN3 CAG repeat expansion."
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"SCA3 is a rare neurodegenerative disease caused by ATXN3 gene mutation with expanded CAG repeats ."
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"The most common autosomal dominant ataxia worldwide, spinocerebellar ataxia type 3 (SCA3) is a fatal, progressive neurodegenerative disorder caused by a CAG trinucleotide repeat expansion in the ATXN3 gene."
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"Spinocerebellar ataxia type 3 (SCA3) is an autosomal dominant hereditary neurodegenerative disorder, caused by an abnormal expansion of cytosine-adenine-guanine (CAG) present in the ATXN3 gene, loss or degeneration of Purkinje cells in cerebellum is an important pathological change [1]."
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"Spinocerebellar ataxia type 3 (SCA3) is an uncommon inherited (autosomal dominant) neurodegenerative disorder caused by abnormal accumulation of ataxin-3 protein."
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"Spinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disease caused by a CAG repeat expansion in the ATXN3 gene."
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"Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease, is an autosomal dominant neurodegenerative disorder caused by CAG repeat expansion in exon 10 of ATXN3."
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