DOIAbstract
SummaryPolyglutamine expansion diseases are triggered by the accumulation of toxic proteins. A new study reports that RNA molecules containing long CAG repeats can also be toxic to neurons and may play a significant role in pathogenesis
SummaryPolyglutamine expansion diseases are triggered by the accumulation of toxic proteins. A new study reports that RNA molecules containing long CAG repeats can also be toxic to neurons and may play a significant role in pathogenesis
Nine dominantly inherited neurodegenerative diseases are caused by expansion of a CAG repeat encodin...
The causes of neuronal death in neurodegenerative diseases are multifaceted, but an emerging theme i...
The number of neurodegenerative diseases resulting from repeat expansion has increased extraordinari...
SummaryPolyglutamine expansion diseases are triggered by the accumulation of toxic proteins. A new s...
A substantial body of evidence supports the identity of polyglutamine as the pathogenic agent in a v...
Polyglutamine expansion causes neurodegeneration by altering the neuronal differentiation progra
Polyglutamine diseases are a family of nine neurodegenerative disorders caused by expansion in diffe...
Polyglutamine (polyQ) disorders constitute a family of devastating, dominantly inherited neurodegene...
The polyglutamine diseases are caused by an expansion of a CAG repeat sequence. This group of late-...
A substantial body of evidence supports the identity of polyglutamine as the pathogenic agent in a v...
A substantial body of evidence supports the identity of polyglutamine as the pathogenic agent in a v...
Nine genetic diseases arise from expansion of CAG repeats in seemingly unrelated genes. They are ref...
Abstract In Huntington's disease and other polyglutamine (polyQ) disorders, mutant proteins con...
Spinocerebellar ataxia type 3 (SCA3) is one of nine human nucleotide repeat expansion diseases due t...
Polyglutamine diseases are neurodegenerative disorders caused by expansion of polyglutamine tracts i...
Nine dominantly inherited neurodegenerative diseases are caused by expansion of a CAG repeat encodin...
The causes of neuronal death in neurodegenerative diseases are multifaceted, but an emerging theme i...
The number of neurodegenerative diseases resulting from repeat expansion has increased extraordinari...
SummaryPolyglutamine expansion diseases are triggered by the accumulation of toxic proteins. A new s...
A substantial body of evidence supports the identity of polyglutamine as the pathogenic agent in a v...
Polyglutamine expansion causes neurodegeneration by altering the neuronal differentiation progra
Polyglutamine diseases are a family of nine neurodegenerative disorders caused by expansion in diffe...
Polyglutamine (polyQ) disorders constitute a family of devastating, dominantly inherited neurodegene...
The polyglutamine diseases are caused by an expansion of a CAG repeat sequence. This group of late-...
A substantial body of evidence supports the identity of polyglutamine as the pathogenic agent in a v...
A substantial body of evidence supports the identity of polyglutamine as the pathogenic agent in a v...
Nine genetic diseases arise from expansion of CAG repeats in seemingly unrelated genes. They are ref...
Abstract In Huntington's disease and other polyglutamine (polyQ) disorders, mutant proteins con...
Spinocerebellar ataxia type 3 (SCA3) is one of nine human nucleotide repeat expansion diseases due t...
Polyglutamine diseases are neurodegenerative disorders caused by expansion of polyglutamine tracts i...
Nine dominantly inherited neurodegenerative diseases are caused by expansion of a CAG repeat encodin...
The causes of neuronal death in neurodegenerative diseases are multifaceted, but an emerging theme i...
The number of neurodegenerative diseases resulting from repeat expansion has increased extraordinari...
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