Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.

Peripheral androgen receptor gene suppression rescues disease in mouse models of spinal and bulbar muscular atrophy.

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

Androgen receptor abnormality in X-linked spinal and bulbar muscular atrophy.

Spinal and Bulbar Muscular Atrophy Overview.

Muscle expression of mutant androgen receptor accounts for systemic and motor neuron disease phenotypes in spinal and bulbar muscular atrophy.

Protein arginine methyltransferase 6 enhances polyglutamine-expanded androgen receptor function and toxicity in spinal and bulbar muscular atrophy.

Brugada syndrome in spinal and bulbar muscular atrophy.

Swallowing markers in spinal and bulbar muscular atrophy.

Synergic prodegradative activity of Bicalutamide and trehalose on the mutant androgen receptor responsible for spinal and bulbar muscular atrophy.

C(Cdh1) ubiquitin ligase complex.

A novel primer extension method to detect the number of CAG repeats in the androgen receptor gene in families with X-linked spinal and bulbar muscular atrophy.

Antiandrogen flutamide protects male mice from androgen-dependent toxicity in three models of spinal bulbar muscular atrophy.

Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy.

Proteasome-mediated proteolysis of the polyglutamine-expanded androgen receptor is a late event in spinal and bulbar muscular atrophy (SBMA) pathogenesis.

Defects in Neuromuscular Transmission May Underlie Motor Dysfunction in Spinal and Bulbar Muscular Atrophy.

A randomized controlled trial of exercise in spinal and bulbar muscular atrophy.

Distinct acoustic features in spinal and bulbar muscular atrophy patients with laryngospasm.

Endoplasmic reticulum stress in spinal and bulbar muscular atrophy: a potential target for therapy.

Tongue pressure as a novel biomarker of spinal and bulbar muscular atrophy.

Genotype-phenotype correlation in Chinese patients with spinal and bulbar muscular atrophy.

Identification of novel polyglutamine-expanded aggregation species in spinal and bulbar muscular atrophy.

Minor cognitive disturbances in X-linked spinal and bulbar muscular atrophy, Kennedy's disease.

Postural leg tremor in X-linked spinal and bulbar muscular atrophy.

Correlation of clinical and molecular features in spinal bulbar muscular atrophy.

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Peripheral androgen receptor gene suppression rescues disease in mouse models of spinal and bulbar muscular atrophy.

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

Androgen receptor abnormality in X-linked spinal and bulbar muscular atrophy.

Spinal and Bulbar Muscular Atrophy Overview.

Muscle expression of mutant androgen receptor accounts for systemic and motor neuron disease phenotypes in spinal and bulbar muscular atrophy.

Protein arginine methyltransferase 6 enhances polyglutamine-expanded androgen receptor function and toxicity in spinal and bulbar muscular atrophy.

Brugada syndrome in spinal and bulbar muscular atrophy.

Swallowing markers in spinal and bulbar muscular atrophy.

Synergic prodegradative activity of Bicalutamide and trehalose on the mutant androgen receptor responsible for spinal and bulbar muscular atrophy.

C(Cdh1) ubiquitin ligase complex.

A novel primer extension method to detect the number of CAG repeats in the androgen receptor gene in families with X-linked spinal and bulbar muscular atrophy.

Antiandrogen flutamide protects male mice from androgen-dependent toxicity in three models of spinal bulbar muscular atrophy.

Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy.

Proteasome-mediated proteolysis of the polyglutamine-expanded androgen receptor is a late event in spinal and bulbar muscular atrophy (SBMA) pathogenesis.

Defects in Neuromuscular Transmission May Underlie Motor Dysfunction in Spinal and Bulbar Muscular Atrophy.

A randomized controlled trial of exercise in spinal and bulbar muscular atrophy.

Distinct acoustic features in spinal and bulbar muscular atrophy patients with laryngospasm.

Endoplasmic reticulum stress in spinal and bulbar muscular atrophy: a potential target for therapy.

Tongue pressure as a novel biomarker of spinal and bulbar muscular atrophy.

Genotype-phenotype correlation in Chinese patients with spinal and bulbar muscular atrophy.

Identification of novel polyglutamine-expanded aggregation species in spinal and bulbar muscular atrophy.

Minor cognitive disturbances in X-linked spinal and bulbar muscular atrophy, Kennedy's disease.

Postural leg tremor in X-linked spinal and bulbar muscular atrophy.

Correlation of clinical and molecular features in spinal bulbar muscular atrophy.

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.

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