Title : Transcriptional activation of TFEB/ZKSCAN3 target genes underlies enhanced autophagy in spinobulbar muscular atrophy.

Pub. Date : 2014 Mar 1

PMID : 24150846






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Spinobulbar muscular atrophy (SBMA) is an inherited neuromuscular disorder caused by the expansion of a CAG repeat encoding a polyglutamine tract in exon 1 of the androgen receptor (AR) gene. polyglutamine androgen receptor Mus musculus
2 Spinobulbar muscular atrophy (SBMA) is an inherited neuromuscular disorder caused by the expansion of a CAG repeat encoding a polyglutamine tract in exon 1 of the androgen receptor (AR) gene. polyglutamine androgen receptor Mus musculus