Pages that link to "Q28250966"
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The following pages link to Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p (Q28250966):
Displaying 50 items.
- Nuclear localization of the spinocerebellar ataxia type 7 protein, ataxin-7 (Q22003756) (← links)
- Cloning and mapping of ZNF231, a novel brain-specific gene encoding neuronal double zinc finger protein whose expression is enhanced in a neurodegenerative disorder, multiple system atrophy (MSA) (Q22007950) (← links)
- The presynaptic cytomatrix protein Bassoon: sequence and chromosomal localization of the human BSN gene (Q22010021) (← links)
- Spinocerebellar ataxia type 6 mutation alters P-type calcium channel function (Q22253850) (← links)
- Characterization of C14orf4, a novel intronless human gene containing a polyglutamine repeat, mapped to the ARVD1 critical region (Q24290561) (← links)
- USP7, a ubiquitin-specific protease, interacts with ataxin-1, the SCA1 gene product (Q24300683) (← links)
- A human HAP1 homologue. Cloning, expression, and interaction with huntingtin (Q24316147) (← links)
- Functional architecture of atrophins (Q24323171) (← links)
- Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals (Q24324374) (← links)
- Abnormal gene product identified in hereditary dentatorubral–pallidoluysian atrophy (DRPLA) brain (Q24324461) (← links)
- Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10 (Q24534014) (← links)
- Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations (Q24539225) (← links)
- Simple tandem DNA repeats and human genetic disease (Q24561717) (← links)
- Molecular cloning of a full-length cDNA for dentatorubral-pallidoluysian atrophy and regional expressions of the expanded alleles in the CNS (Q24671945) (← links)
- The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2 (Q24672255) (← links)
- Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1 (Q24675962) (← links)
- The localization and interactions of huntingtin (Q24676589) (← links)
- Molecular pathology of dentatorubral-pallidoluysian atrophy (Q24676632) (← links)
- Mouse models of polyglutamine diseases: review and data table. Part I (Q26853025) (← links)
- Isolation and characterization of novel CAG repeat containing genes expressed in human brain (Q28138069) (← links)
- Aberrant interactions of transcriptional repressor proteins with the Huntington's disease gene product, huntingtin (Q28141695) (← links)
- Genomic structure and alternative splicing of the insulin receptor tyrosine kinase substrate of 53-kDa protein (Q28190085) (← links)
- HnRNP A1 and A/B interaction with PABPN1 in oculopharyngeal muscular dystrophy (Q28204171) (← links)
- Cytochrome c oxidase subunit Vb interacts with human androgen receptor: a potential mechanism for neurotoxicity in spinobulbar muscular atrophy (Q28206942) (← links)
- CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1 (Q28235526) (← links)
- The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family (Q28240104) (← links)
- Dentatorubral pallidoluysian atrophy (DRPLA) protein is cleaved by caspase-3 during apoptosis (Q28253849) (← links)
- Interaction of huntingtin-associated protein with dynactin P150Glued (Q28260988) (← links)
- Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo (Q28279878) (← links)
- Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA) (Q28306588) (← links)
- Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form (Q28509836) (← links)
- Machado Joseph disease maps to the same region of chromosome 14 as the spinocerebellar ataxia type 3 locus (Q30495377) (← links)
- Single cell analysis of CAG repeat in brains of dentatorubral-pallidoluysian atrophy (DRPLA). (Q30725562) (← links)
- CAG-encoded polyglutamine length polymorphism in the human genome (Q33285435) (← links)
- HAP1 can sequester a subset of TBP in cytoplasmic inclusions via specific interaction with the conserved TBP(CORE). (Q33299019) (← links)
- Differential diagnosis of Parkinson's disease (Q33545288) (← links)
- Allele distribution of a highly polymorphic repeat on chromosome 12 in patients with symptoms of chorea and ataxia (Q33677166) (← links)
- Meiotic instability associated with the CAGR1 trinucleotide repeat at 13q13. (Q33678843) (← links)
- Characterisation of the unstable expanded CAG repeat in the MJD1 gene in four Brazilian families of Portuguese descent with Machado-Joseph disease (Q33682673) (← links)
- Familial psychiatric presentation of Huntington's disease (Q33683204) (← links)
- The relationship between (CAG)n repeat number and age of onset in a family with dentatorubral-pallidoluysian atrophy (DRPLA): diagnostic implications of confirmatory and predictive testing (Q33683245) (← links)
- Diagnosis of inherited metabolic disorders affecting the nervous system (Q33734674) (← links)
- Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutation (Q33735577) (← links)
- Oligonucleotide-based strategies to combat polyglutamine diseases (Q33791247) (← links)
- Structure based molecular inhibition of Caspase-8 for treatment of multi-neurodegenerative diseases using known natural compounds (Q33803242) (← links)
- Tissue transglutaminase: a possible role in neurodegenerative diseases (Q33881855) (← links)
- Nuclear accumulation of truncated atrophin-1 fragments in a transgenic mouse model of DRPLA. (Q33890266) (← links)
- Identification of alternative splicing of spinocerebellar ataxia type 2 gene. (Q33943155) (← links)
- Histone deacetylase inhibitors reduce polyglutamine toxicity (Q33953013) (← links)
- The complex clinical and genetic classification of inherited ataxias. I. Dominant ataxias (Q33998074) (← links)