Title : Pathogenesis and therapy of spinal and bulbar muscular atrophy (SBMA).

Pub. Date : 2012 Dec

PMID : 22609045






9 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 The cause of SBMA is the expansion of a trinucleotide CAG repeat encoding a polyglutamine tract within the first exon of the androgen receptor (AR) gene. polyglutamine androgen receptor Homo sapiens
2 The cause of SBMA is the expansion of a trinucleotide CAG repeat encoding a polyglutamine tract within the first exon of the androgen receptor (AR) gene. polyglutamine androgen receptor Homo sapiens
3 The cause of SBMA is the expansion of a trinucleotide CAG repeat encoding a polyglutamine tract within the first exon of the androgen receptor (AR) gene. polyglutamine androgen receptor Homo sapiens
4 The ligand-dependent nuclear accumulation of the polyglutamine-expanded AR protein is central to the gender-specific pathogenesis of SBMA, although additional steps, e.g., DNA binding, inter-domain interactions, and post-translational modification of AR, modify toxicity. polyglutamine androgen receptor Homo sapiens
5 The ligand-dependent nuclear accumulation of the polyglutamine-expanded AR protein is central to the gender-specific pathogenesis of SBMA, although additional steps, e.g., DNA binding, inter-domain interactions, and post-translational modification of AR, modify toxicity. polyglutamine androgen receptor Homo sapiens
6 The ligand-dependent nuclear accumulation of the polyglutamine-expanded AR protein is central to the gender-specific pathogenesis of SBMA, although additional steps, e.g., DNA binding, inter-domain interactions, and post-translational modification of AR, modify toxicity. polyglutamine androgen receptor Homo sapiens
7 The interactions with co-regulators are another requisite for the toxic properties of the polyglutamine-expanded AR. polyglutamine androgen receptor Homo sapiens
8 It is also shown that the polyglutamine-expanded AR induces diverse molecular events, such as transcriptional dysregulation, axonal transport disruption, and mitochondrial dysfunction, which play causative roles in the neurodegeneration in SBMA. polyglutamine androgen receptor Homo sapiens
9 It is also shown that the polyglutamine-expanded AR induces diverse molecular events, such as transcriptional dysregulation, axonal transport disruption, and mitochondrial dysfunction, which play causative roles in the neurodegeneration in SBMA. polyglutamine androgen receptor Homo sapiens