Title : Viral delivery of miR-196a ameliorates the SBMA phenotype via the silencing of CELF2.

Pub. Date : 2012 Jul

PMID : 22660636






4 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Spinal and bulbar muscular atrophy (SBMA) is an inherited neurodegenerative disorder caused by the expansion of the polyglutamine (polyQ) tract of the androgen receptor (AR-polyQ). polyglutamine androgen receptor Homo sapiens
2 Spinal and bulbar muscular atrophy (SBMA) is an inherited neurodegenerative disorder caused by the expansion of the polyglutamine (polyQ) tract of the androgen receptor (AR-polyQ). polyglutamine androgen receptor Homo sapiens
3 Spinal and bulbar muscular atrophy (SBMA) is an inherited neurodegenerative disorder caused by the expansion of the polyglutamine (polyQ) tract of the androgen receptor (AR-polyQ). polyglutamine androgen receptor Homo sapiens
4 Spinal and bulbar muscular atrophy (SBMA) is an inherited neurodegenerative disorder caused by the expansion of the polyglutamine (polyQ) tract of the androgen receptor (AR-polyQ). polyglutamine androgen receptor Homo sapiens