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Genes|June 24, 2022
Nonalcoholic Fatty Liver Disease in Patients with Inherited and Sporadic Motor Neuron DegenerationBrian Johnson, Angela Kokkinis, Neville Gai, et al.
Neuromuscular Disorders : NMD|September 6, 2016
Quantifying disease activity in fatty-infiltrated skeletal muscle by IDEAL-CPMG in Duchenne muscular dystrophyAmi Mankodi, Courtney A Bishop, Sungyoung Auh, et al.
Molecular and Cellular Biology|December 24, 2008
Regulation of SMN protein stabilityBarrington G Burnett, Eric Muñoz, Animesh Tandon, et al.
Molecular and Cellular Neurosciences|June 23, 2006
The effects of a dominant connexin32 mutant in myelinating Schwann cellsLinda Jo Bone Jeng, Rita J Balice-Gordon, Albee Messing, et al.
Neurology. Clinical Practice|August 14, 2024
Patient-Reported Impact of Symptoms in Spinal and Bulbar Muscular AtrophyAbdullah Alqahtani, Angela Kokkinis, Christine Zizzi, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 11, 2005
Transgenic expression of human connexin32 in myelinating Schwann cells prevents demyelination in connexin32-null miceSteven S Scherer, Yi-Tian Xu, Albee Messing, et al.
Genes & Development|June 20, 2003
Aberrant histone acetylation, altered transcription, and retinal degeneration in a Drosophila model of polyglutamine disease are rescued by CREB-binding proteinJ Paul Taylor, Addis A Taye, Catherine Campbell, et al.
Human Molecular Genetics|March 26, 2003
Aggresomes protect cells by enhancing the degradation of toxic polyglutamine-containing proteinJ Paul Taylor, Fumiaki Tanaka, Jon Robitschek, et al.
Archives of Neurology|June 15, 2007
Safety, tolerability, and pharmacokinetics of high-dose idebenone in patients with Friedreich ataxiaNicholas A Di Prospero, Charlotte J Sumner, Scott R Penzak, et al.
Scientific Reports|June 18, 2016
The polyglutamine-expanded androgen receptor responsible for spinal and bulbar muscular atrophy inhibits the APC/C(Cdh1) ubiquitin ligase complexLaura C Bott, Florian A Salomons, Dragan Maric, et al.
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