(Q24316105)

GOA release 2020-03-11

Ataxin 1

1 reference

K(lysine) acetyltransferase 5

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Harry T Orr

12

0 references

Huda Zoghbi

object named as

Huda Y Zoghbi

9

0 references

J. Michael Andresen

11

object named as

J Michael Andresen

0 references

author name string

Heliane G Serra

1

0 references

Lisa Duvick

2

0 references

Tao Zu

3

0 references

Kerri Carlson

4

0 references

Sam Stevens

5

0 references

Nathan Jorgensen

6

0 references

Alana Lysholm

7

0 references

Eric Burright

8

0 references

H Brent Clark

Electron microscopic analysis of postnatal histogenesis in the cerebellar cortex of staggerer mutant mice

10

0 references

language of work or name

English

0 references

publication date

17 November 2006

0 references

published in

Cell

0 references

volume

127

0 references

issue

4

0 references

page(s)

697-708

0 references

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Deficient cerebellar long-term depression and impaired motor learning in mGluR1 mutant mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Early dendritic development of Purkinje cells in the rat cerebellum. A light and electron microscopic study using axonal tracing in 'in vitro' slices

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

The AXH domain of Ataxin-1 mediates neurodegeneration through its interaction with Gfi-1/Senseless proteins

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

The AXH module: an independently folded domain common to ataxin-1 and HBP1

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Progressive atrophy of cerebellar Purkinje cell dendrites during aging of the heterozygous staggerer mouse (Rora(+/sg)).

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

The cells and molecules that make a cerebellum.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Prominent expression of nuclear hormone receptor ROR alpha in Purkinje cells from early development

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Mutation of the E6-AP ubiquitin ligase reduces nuclear inclusion frequency while accelerating polyglutamine-induced pathology in SCA1 mice.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Interaction between mutant ataxin-1 and PQBP-1 affects transcription and cell death

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

A long CAG repeat in the mouse Sca1 locus replicates SCA1 features and reveals the impact of protein solubility on selective neurodegeneration.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Serine 776 of ataxin-1 is critical for polyglutamine-induced disease in SCA1 transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

RORalpha coordinates reciprocal signaling in cerebellar development through sonic hedgehog and calcium-dependent pathways

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Orphan nuclear receptor ROR alpha-deficient mice display the cerebellar defects of staggerer.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Postnatal cerebellar cells from staggerer mutant mice express embryonic cell surface characteristic

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Identification of genes that modify ataxin-1-induced neurodegeneration.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Ataxia and epileptic seizures in mice lacking type 1 inositol 1,4,5-trisphosphate receptor.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Disruption of the nuclear hormone receptor RORalpha in staggerer mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Polyglutamine expansion down-regulates specific neuronal genes before pathologic changes in SCA1.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Spectrin mutations cause spinocerebellar ataxia type 5.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Controlling nuclear receptors: the circular logic of cofactor cycles

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Ataxin 1, a SCA1 neurodegenerative disorder protein, is functionally linked to the silencing mediator of retinoid and thyroid hormone receptors

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Ataxia and altered dendritic calcium signaling in mice carrying a targeted null mutation of the calbindin D28k gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

staggerer phenotype in retinoid-related orphan receptor alpha-deficient mice.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Tip60 is a nuclear hormone receptor coactivator

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

The co-repressor hairless protects RORalpha orphan nuclear receptor from proteasome-mediated degradation

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

The structure of the AXH domain of spinocerebellar ataxin-1

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

The spinocerebellar ataxia type 1 protein, ataxin-1, has RNA-binding activity that is inversely affected by the length of its polyglutamine tract

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Over-expression of inducible HSP70 chaperone suppresses neuropathology and improves motor function in SCA1 mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Cloning and developmental expression analysis of the murine homolog of the spinocerebellar ataxia type 1 gene (Sca1).

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Gene profiling links SCA1 pathophysiology to glutamate signaling in Purkinje cells of transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Spinocerebellar ataxia type 1--modeling the pathogenesis of a polyglutamine neurodegenerative disorder in transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Toxic proteins in neurodegenerative disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

mGluR1 in cerebellar Purkinje cells essential for long-term depression, synapse elimination, and motor coordination

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Glutamine repeats and neurodegeneration

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Immunohistochemical characterization of the orphan nuclear receptor ROR alpha in the mouse nervous system.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Amino acids in a region of ataxin-1 outside of the polyglutamine tract influence the course of disease in SCA1 transgenic mice.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Purkinje cell expression of a mutant allele of SCA1 in transgenic mice leads to disparate effects on motor behaviors, followed by a progressive cerebellar dysfunction and histological alterations.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Recovery from polyglutamine-induced neurodegeneration in conditional SCA1 transgenic mice.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

Climbing fiber activation of EAAT4 transporters and kainate receptors in cerebellar Purkinje cells

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2006.09.036

7 January 2021