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Neurogenetics Branch,
National Institute of Neurological Disorders and Stroke,
Neurogenetics Branch, National Institute of Neurological Disorders and Stroke
Laura C. Bott has not added Biography.
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Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia.
JAMA neurology May, 2015 | Pubmed ID: 25751282
Insulinlike growth factor (IGF)-1 administration ameliorates disease manifestations in a mouse model of spinal and bulbar muscular atrophy.
Molecular medicine (Cambridge, Mass.) Dec, 2012 | Pubmed ID: 22952056
Muscle matters in Kennedy's disease.
Neuron Apr, 2014 | Pubmed ID: 24742452
Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeat.
Neuromuscular disorders : NMD Nov, 2014 | Pubmed ID: 25047668
The ubiquitin-proteasome system in neurodegenerative diseases: precipitating factor, yet part of the solution.
Frontiers in molecular neuroscience , 2014 | Pubmed ID: 25132814
MiR-298 Counteracts Mutant Androgen Receptor Toxicity in Spinal and Bulbar Muscular Atrophy.
Molecular therapy : the journal of the American Society of Gene Therapy 05, 2016 | Pubmed ID: 26755334
A small-molecule Nrf1 and Nrf2 activator mitigates polyglutamine toxicity in spinal and bulbar muscular atrophy.
Human molecular genetics 05, 2016 | Pubmed ID: 26962150
The polyglutamine-expanded androgen receptor has increased DNA binding and reduced transcriptional activity.
Biochemistry and biophysics reports Sep, 2015 | Pubmed ID: 29124176
National Institutes of Health
Northwestern University
Naemeh Pourshafie1,
Philip R. Lee2,
Ke-lian Chen1,
George G. Harmison1,
Laura C. Bott1,3,
Kenneth H. Fischbeck1,
Carlo Rinaldi1,4
1Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health,
2Section on Nervous System Development and Plasticity, The Eunice Kennedy Shriver National Institute of Child and Human Development, National Institutes of Health,
3Department of Molecular Biosciences, Rice Institute for Biomedical Research, Northwestern University,
4Department of Physiology, Anatomy and Genetics, University of Oxford
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