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[HTML][HTML] Loss of the Spinocerebellar Ataxia type 3 disease protein ATXN3 alters transcription of multiple signal transduction pathways

L Zeng, D Zhang, HS McLoughlin, AJ Zalon… - PLoS …, 2018 - journals.plos.org
Spinocerebellar ataxia type 3 (SCA3) is a dominantly inherited neurodegenerative disorder
caused by a polyglutamine-encoding CAG repeat expansion in the ATXN3 gene which …
被引用次数：30 相关文章

Loss of the Spinocerebellar Ataxia type 3 disease protein ATXN3 alters transcription of multiple signal transduction pathways

L Zeng, D Zhang, HS McLoughlin, AJ Zalon, L Aravind… - PLoS ONE, 2018 - go.gale.com
Spinocerebellar ataxia type 3 (SCA3) is a dominantly inherited neurodegenerative disorder
caused by a polyglutamine-encoding CAG repeat expansion in the ATXN3 gene which …

Loss of the Spinocerebellar Ataxia type 3 disease protein ATXN3 alters transcription of multiple signal transduction pathways.

L Zeng, D Zhang, HS McLoughlin, AJ Zalon… - PLoS …, 2018 - search.ebscohost.com
Abstract Spinocerebellar ataxia type 3 (SCA3) is a dominantly inherited neurodegenerative
disorder caused by a polyglutamine-encoding CAG repeat expansion in the ATXN3 gene …

Loss of the Spinocerebellar Ataxia type 3 disease protein ATXN3 alters transcription of multiple signal transduction pathways.

L Zeng, D Zhang, HS McLoughlin, AJ Zalon, L Aravind… - Plos one, 2018 - europepmc.org
Abstract Spinocerebellar ataxia type 3 (SCA3) is a dominantly inherited neurodegenerative
disorder caused by a polyglutamine-encoding CAG repeat expansion in the ATXN3 gene …
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[HTML][HTML] Loss of the Spinocerebellar Ataxia type 3 disease protein ATXN3 alters transcription of multiple signal transduction pathways

L Zeng, D Zhang, HS McLoughlin, AJ Zalon, L Aravind… - PLoS ONE, 2018 - ncbi.nlm.nih.gov
Abstract Spinocerebellar ataxia type 3 (SCA3) is a dominantly inherited neurodegenerative
disorder caused by a polyglutamine-encoding CAG repeat expansion in the ATXN3 gene …

Loss of the Spinocerebellar Ataxia type 3 disease protein ATXN3 alters transcription of multiple signal transduction pathways

L Zeng, D Zhang, HS McLoughlin, AJ Zalon… - PloS …, 2018 - pubmed.ncbi.nlm.nih.gov
Spinocerebellar ataxia type 3 (SCA3) is a dominantly inherited neurodegenerative disorder
caused by a polyglutamine-encoding CAG repeat expansion in the ATXN3 gene which …
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[PDF][PDF] Loss of the Spinocerebellar Ataxia type 3 disease protein ATXN3 alters transcription of multiple signal transduction pathways

L Zeng, D Zhang, HS McLoughlin, AJ Zalon… - PLoS …, 2018 - pdfs.semanticscholar.org
Abstract Spinocerebellar ataxia type 3 (SCA3) is a dominantly inherited neurodegenerative
disorder caused by a polyglutamine-encoding CAG repeat expansion in the ATXN3 gene …

[引用][C] Loss of the Spinocerebellar Ataxia type 3 disease protein ATXN3 alters transcription of multiple signal transduction pathways

L Zeng, D Zhang, HS McLoughlin, AJ Zalon… - PLoS …, 2018 - ui.adsabs.harvard.edu
Loss of the Spinocerebellar Ataxia type 3 disease protein ATXN3 alters transcription of
multiple signal transduction pathways - NASA/ADS Now on home page ads icon ads …

Loss of the Spinocerebellar Ataxia type 3 disease protein ATXN3 alters transcription of multiple signal transduction pathways.

L Zeng, D Zhang, HS McLoughlin, AJ Zalon, L Aravind… - Plos one, 2018 - europepmc.org
Abstract Spinocerebellar ataxia type 3 (SCA3) is a dominantly inherited neurodegenerative
disorder caused by a polyglutamine-encoding CAG repeat expansion in the ATXN3 gene …