Laura C. Bott

Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia.

Insulinlike growth factor (IGF)-1 administration ameliorates disease manifestations in a mouse model of spinal and bulbar muscular atrophy.

Muscle matters in Kennedy's disease.

Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeat.

The ubiquitin-proteasome system in neurodegenerative diseases: precipitating factor, yet part of the solution.

MiR-298 Counteracts Mutant Androgen Receptor Toxicity in Spinal and Bulbar Muscular Atrophy.

A small-molecule Nrf1 and Nrf2 activator mitigates polyglutamine toxicity in spinal and bulbar muscular atrophy.

The polyglutamine-expanded androgen receptor has increased DNA binding and reduced transcriptional activity.