Pages that link to "Q22254111"
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The following pages link to A novel protein with RNA-binding motifs interacts with ataxin-2 (Q22254111):
Displaying 50 items.
- RNA binding fox-1 homolog 1 (Q21106557) (← links)
- ataxin 2 (Q21171902) (← links)
- Chronic cocaine-regulated epigenomic changes in mouse nucleus accumbens. (Q21999524) (← links)
- Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human (Q24290184) (← links)
- Cloning and characterization of a family of proteins associated with Mpl (Q24292135) (← links)
- A negative coregulator for the human ER (Q24292390) (← links)
- Ataxin-2 and its Drosophila homolog, ATX2, physically assemble with polyribosomes (Q24296835) (← links)
- Ataxin-2 interacts with the DEAD/H-box RNA helicase DDX6 and interferes with P-bodies and stress granules (Q24301077) (← links)
- Ataxin-2 and huntingtin interact with endophilin-A complexes to function in plastin-associated pathways (Q24317006) (← links)
- An integrative approach to gain insights into the cellular function of human ataxin-2 (Q24338666) (← links)
- Homologues of the Caenorhabditis elegans Fox-1 protein are neuronal splicing regulators in mammals (Q24537300) (← links)
- A Drosophila homolog of the polyglutamine disease gene SCA2 is a dosage-sensitive regulator of actin filament formation (Q24543178) (← links)
- Tissue-specific splicing regulator Fox-1 induces exon skipping by interfering E complex formation on the downstream intron of human F1gamma gene (Q24565018) (← links)
- Structure and function of the C-terminal PABC domain of human poly(A)-binding protein (Q24635302) (← links)
- Identification of neuronal nuclei (NeuN) as Fox-3, a new member of the Fox-1 gene family of splicing factors (Q24652281) (← links)
- Tissue-dependent isoforms of mammalian Fox-1 homologs are associated with tissue-specific splicing activities (Q24792095) (← links)
- The splicing regulatory element, UGCAUG, is phylogenetically and spatially conserved in introns that flank tissue-specific alternative exons (Q24801957) (← links)
- Cell biology of spinocerebellar ataxia (Q26829511) (← links)
- Orchestration of neurodevelopmental programs by RBFOX1: implications for autism spectrum disorder (Q26853067) (← links)
- RNA protein interaction in neurons (Q27001674) (← links)
- Ataxin-2 regulates RGS8 translation in a new BAC-SCA2 transgenic mouse model (Q27311213) (← links)
- Essential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development (Q27320880) (← links)
- The structure of the AXH domain of spinocerebellar ataxin-1 (Q27642446) (← links)
- Motor Dysfunctions and Neuropathology in Mouse Models of Spinocerebellar Ataxia Type 2: A Comprehensive Review (Q28076174) (← links)
- The promise and perils of HDAC inhibitors in neurodegeneration (Q28087539) (← links)
- Interaction between mutant ataxin-1 and PQBP-1 affects transcription and cell death (Q28204152) (← links)
- The splicing regulator Rbfox2 is required for both cerebellar development and mature motor function (Q28510582) (← links)
- NeuN/Rbfox3 Nuclear and Cytoplasmic Isoforms Differentially Regulate Alternative Splicing and Nonsense-Mediated Decay of Rbfox2 (Q28594228) (← links)
- Fox-3 and PSF interact to activate neural cell-specific alternative splicing (Q28595064) (← links)
- Fox-2 mediates epithelial cell-specific fibroblast growth factor receptor 2 exon choice (Q28768535) (← links)
- Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT (Q30350558) (← links)
- Therapeutic prospects for spinocerebellar ataxia type 2 and 3. (Q30410969) (← links)
- Trypanosome MKT1 and the RNA-binding protein ZC3H11: interactions and potential roles in post-transcriptional regulatory networks (Q30439959) (← links)
- Role of the cytoplasmic isoform of RBFOX1/A2BP1 in establishing the architecture of the developing cerebral cortex (Q30670360) (← links)
- Systems biology analysis of Drosophila in vivo screen data elucidates core networks for DNA damage repair in SCA1. (Q30687417) (← links)
- Identification and expression of the gene for human ataxin-2-related protein on chromosome 16. (Q30892767) (← links)
- The ortholog of human ataxin-2 is essential for early embryonic patterning in C. elegans (Q30986380) (← links)
- Dissociated fear and spatial learning in mice with deficiency of ataxin-2 (Q33484172) (← links)
- Genetic variance in the spinocerebellar ataxia type 2 (ATXN2) gene in children with severe early onset obesity (Q33519049) (← links)
- Autoregulation of Fox protein expression to produce dominant negative splicing factors (Q33611623) (← links)
- Mutant huntingtin impairs Ku70-mediated DNA repair (Q33840010) (← links)
- DrosophilaAtaxin 2-binding protein 1 marks an intermediate step in the molecular differentiation of female germline cysts (Q34107589) (← links)
- Interaction of expanded polyglutamine stretches with nuclear transcription factors leads to aberrant transcriptional regulation in polyglutamine diseases (Q34158010) (← links)
- Evaluation of A2BP1 as an obesity gene (Q34237671) (← links)
- FOX-2 dependent splicing of ataxin-2 transcript is affected by ataxin-1 overexpression (Q34292752) (← links)
- ETS1 regulates the expression of ATXN2. (Q34390181) (← links)
- Tissue-specific functional networks for prioritizing phenotype and disease genes (Q34426375) (← links)
- PQBP-1 (Np/PQ): a polyglutamine tract-binding and nuclear inclusion-forming protein (Q34446581) (← links)
- Fox-2 splicing factor binds to a conserved intron motif to promote inclusion of protein 4.1R alternative exon 16. (Q34502131) (← links)
- Caenorhabditis elegans atx-2 promotes germline proliferation and the oocyte fate (Q34569891) (← links)