SCA1-phosphorylation, a regulator of Ataxin-1 function and pathogenesis. - Wikidata - wikimedia - TriplyDB

SCA1-phosphorylation, a regulator of Ataxin-1 function and pathogenesis.

SCA1-phosphorylation, a regulator of Ataxin-1 function and pathogenesis.

http://www.wikidata.org/entity/Q38005302

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Beyond the glutamine expansion: influence of posttranslational modifications of ataxin-1 in the pathogenesis of spinocerebellar ataxia type 1 Oligonucleotide-based strategies to combat polyglutamine diseases.Consensus Paper: Cerebellar Development.RNA toxicity in polyglutamine disorders: concepts, models, and progress of research Kaleidoscopic protein-protein interactions in the life and death of ataxin-1: new strategies against protein aggregation.Chaperones in Polyglutamine Aggregation: Beyond the Q-Stretch.The autosomal dominant spinocerebellar ataxias: emerging mechanistic themes suggest pervasive Purkinje cell vulnerability.Allele-selective suppression of mutant genes in polyglutamine diseases.Progressive impairment of cerebellar mGluR signalling and its therapeutic potential for cerebellar ataxia in spinocerebellar ataxia type 1 model mice.Arabidopsis MSL10 has a regulated cell death signaling activity that is separable from its mechanosensitive ion channel activity.Purkinje Cell Signaling Deficits in Animal Models of Ataxia.Roles of Post-translational Modifications in Spinocerebellar Ataxias

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P2860

SCA1-phosphorylation, a regulator of Ataxin-1 function and pathogenesis.

http://www.wikidata.org/entity/Q38005302

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SCA1-phosphorylation, a regulator of Ataxin-1 function and pathogenesis.

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SCA1-phosphorylation, a regulator of Ataxin-1 function and pathogenesis.

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SCA1-phosphorylation, a regulator of Ataxin-1 function and pathogenesis.

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J.PNEUROBIO.2012.04.003

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Progress in Neurobiology

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SCA1-phosphorylation, a regulator of Ataxin-1 function and pathogenesis.

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Harry T Orr

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P2860

Identification of a self-association region within the SCA1 gene product, ataxin-1

U2AF-homology motif interactions are required for alternative splicing regulation by SPF45

RNA association and nucleocytoplasmic shuttling by ataxin-1

A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration

Boat, an AXH domain protein, suppresses the cytotoxicity of mutant ataxin-1.

miR-19, miR-101 and miR-130 co-regulate ATXN1 levels to potentially modulate SCA1 pathogenesis

Opposing effects of polyglutamine expansion on native protein complexes contribute to SCA1

Phosphorylation of S776 and 14-3-3 binding modulate ataxin-1 interaction with splicing factors

Mice lacking ataxin-1 display learning deficits and decreased hippocampal paired-pulse facilitation

Interaction of Akt-phosphorylated ataxin-1 with 14-3-3 mediates neurodegeneration in spinocerebellar ataxia type 1.

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179-185

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scholarly article

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10.1016/J.PNEUROBIO.2012.04.003

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3

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2012-04-16T00:00:00Z

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22531670

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phosphorylation

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3408849

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