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Neurogenetics Branch,
National Institute of Neurological Disorders and Stroke,
Neurogenetics Branch, National Institute of Neurological Disorders and Stroke
Ke-lian Chen has not added Biography.
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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
Stem cell-derived motor neurons from spinal and bulbar muscular atrophy patients.
Neurobiology of disease Oct, 2014 | Pubmed ID: 24925468
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
Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia.
JAMA neurology May, 2015 | Pubmed ID: 25751282
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 novel mutation in in a Malian family with spastic paraplegia and sensory loss.
Annals of clinical and translational neurology 04, 2017 | Pubmed ID: 28382308
National Institutes of Health
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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