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[HTML][HTML] Partial loss of ataxin-1 function contributes to transcriptional dysregulation in spinocerebellar ataxia type 1 pathogenesis

J Crespo-Barreto, JD Fryer, CA Shaw, HT Orr… - PLoS …, 2010 - journals.plos.org
Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative disease
caused by expansion of a CAG repeat that encodes a polyglutamine tract in ATAXIN1 …
被引用次数：145 相关文章

Partial Loss of Ataxin-1 Function Contributes to Transcriptional Dysregulation in Spinocerebellar Ataxia Type 1 Pathogenesis

J Crespo-Barreto, JD Fryer, CA Shaw, HT Orr… - PLoS …, 2010 - search.proquest.com
Abstract Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative
disease caused by expansion of a CAG repeat that encodes a polyglutamine tract in …

Partial loss of ataxin-1 function contributes to transcriptional dysregulation in spinocerebellar ataxia type 1 pathogenesis.

J Crespo-Barreto, JD Fryer, CA Shaw, HT Orr… - Plos Genetics, 2010 - europepmc.org
Abstract Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative
disease caused by expansion of a CAG repeat that encodes a polyglutamine tract in …

Partial loss of Ataxin-1 function contributes to transcriptional dysregulation in spinocerebellar ataxia type 1 pathogenesis

J Crespo-Barreto, JD Fryer, CA Shaw, HT Orr… - PLoS …, 2010 - go.gale.com
Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative disease
caused by expansion of a CAG repeat that encodes a polyglutamine tract in ATAXIN1 …
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[PDF][PDF] Partial Loss of Ataxin-1 Function Contributes to Transcriptional Dysregulation in

J Crespo-Barreto, JD Fryer, CA Shaw, HT Orr… - 2010 - pdfs.semanticscholar.org
Abstract Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative
disease caused by expansion of a CAG repeat that encodes a polyglutamine tract in …
[HTML] nih.gov

[HTML][HTML] Partial Loss of Ataxin-1 Function Contributes to Transcriptional Dysregulation in Spinocerebellar Ataxia Type 1 Pathogenesis

J Crespo-Barreto, JD Fryer, CA Shaw, HT Orr… - PLoS …, 2010 - ncbi.nlm.nih.gov
Abstract Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative
disease caused by expansion of a CAG repeat that encodes a polyglutamine tract in …

Partial Loss of Ataxin-1 Function Contributes to Transcriptional Dysregulation in Spinocerebellar Ataxia Type 1 Pathogenesis.

J Crespo-Barreto, JD Fryer, CA Shaw, HT Orr… - PLoS …, 2010 - search.ebscohost.com
Abstract Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative
disease caused by expansion of a CAG repeat that encodes a polyglutamine tract in …
[PDF] cyberleninka.org

[PDF][PDF] Partial Loss of Ataxin-1 Function Contributes to Transcriptional Dysregulation in

J Crespo-Barreto, JD Fryer, CA Shaw, HT Orr… - 2010 - cyberleninka.org
Abstract Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative
disease caused by expansion of a CAG repeat that encodes a polyglutamine tract in …

Partial loss of ataxin-1 function contributes to transcriptional dysregulation in spinocerebellar ataxia type 1 pathogenesis

J Crespo-Barreto, JD Fryer, CA Shaw… - PLoS …, 2010 - pubmed.ncbi.nlm.nih.gov
Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative disease
caused by expansion of a CAG repeat that encodes a polyglutamine tract in ATAXIN1 …

Partial loss of ataxin-1 function contributes to transcriptional dysregulation in spinocerebellar ataxia type 1 pathogenesis

J Crespo-Barreto, JD Fryer, CA Shaw… - PLoS …, 2010 - mayoclinic.elsevierpure.com
Abstract Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative
disease caused by expansion of a CAG repeat that encodes a polyglutamine tract in …