| Year |
Citation |
Score |
| 2024 |
McLean JW, VanHart M, McWilliams MP, Farmer CB, Crossman DK, Cowell RM, Wilson JA, Wilson SM. Analysis of the neuromuscular deficits caused by STAM1 deficiency. Current Research in Neurobiology. 7: 100138. PMID 39280771 DOI: 10.1016/j.crneur.2024.100138 |
0.434 |
|
| 2020 |
Tian T, McLean JW, Wilson JA, Wilson SM. Examination of genetic and pharmacological tools to study the proteasomal deubiquitinating enzyme USP14 in the nervous system. Journal of Neurochemistry. PMID 32901953 DOI: 10.1111/jnc.15180 |
0.42 |
|
| 2018 |
Vaden JH, Tian T, Golf S, McLean JW, Wilson JA, Wilson SM. Chronic overexpression of ubiquitin impairs learning, reduces synaptic plasticity, and enhances GRIA receptor turnover in mice. Journal of Neurochemistry. PMID 30451289 DOI: 10.1111/jnc.14630 |
0.361 |
|
| 2015 |
Watson JA, Bhattacharyya BJ, Vaden JH, Wilson JA, Icyuz M, Howard AD, Phillips E, DeSilva TM, Siegal GP, Bean AJ, King GD, Phillips SE, Miller RJ, Wilson SM. Motor and Sensory Deficits in the teetering Mice Result from Mutation of the ESCRT Component HGS. Plos Genetics. 11: e1005290. PMID 26115514 DOI: 10.1371/Journal.Pgen.1005290 |
0.417 |
|
| 2015 |
Vaden JH, Watson JA, Howard AD, Chen PC, Wilson JA, Wilson SM. Distinct effects of ubiquitin overexpression on NMJ structure and motor performance in mice expressing catalytically inactive USP14. Frontiers in Molecular Neuroscience. 8: 11. PMID 25954152 DOI: 10.3389/Fnmol.2015.00011 |
0.691 |
|
| 2015 |
Vaden JH, Bhattacharyya BJ, Chen PC, Watson JA, Marshall AG, Phillips SE, Wilson JA, King GD, Miller RJ, Wilson SM. Ubiquitin-specific protease 14 regulates c-Jun N-terminal kinase signaling at the neuromuscular junction. Molecular Neurodegeneration. 10: 3. PMID 25575639 DOI: 10.1186/1750-1326-10-3 |
0.646 |
|
| 2014 |
Walters BJ, Hallengren JJ, Theile CS, Ploegh HL, Wilson SM, Dobrunz LE. A catalytic independent function of the deubiquitinating enzyme USP14 regulates hippocampal synaptic short-term plasticity and vesicle number. The Journal of Physiology. 592: 571-86. PMID 24218545 DOI: 10.1113/Jphysiol.2013.266015 |
0.73 |
|
| 2013 |
Marshall AG, Watson JA, Hallengren JJ, Walters BJ, Dobrunz LE, Francillon L, Wilson JA, Phillips SE, Wilson SM. Genetic background alters the severity and onset of neuromuscular disease caused by the loss of ubiquitin-specific protease 14 (usp14). Plos One. 8: e84042. PMID 24358326 DOI: 10.1371/Journal.Pone.0084042 |
0.781 |
|
| 2013 |
Hallengren J, Chen PC, Wilson SM. Neuronal ubiquitin homeostasis. Cell Biochemistry and Biophysics. 67: 67-73. PMID 23686613 DOI: 10.1007/S12013-013-9634-4 |
0.554 |
|
| 2012 |
Jin YN, Chen PC, Watson JA, Walters BJ, Phillips SE, Green K, Schmidt R, Wilson JA, Johnson GV, Roberson ED, Dobrunz LE, Wilson SM. Usp14 deficiency increases tau phosphorylation without altering tau degradation or causing tau-dependent deficits. Plos One. 7: e47884. PMID 23144711 DOI: 10.1371/Journal.Pone.0047884 |
0.757 |
|
| 2012 |
Bhattacharyya BJ, Wilson SM, Jung H, Miller RJ. Altered neurotransmitter release machinery in mice deficient for the deubiquitinating enzyme Usp14. American Journal of Physiology. Cell Physiology. 302: C698-708. PMID 22075695 DOI: 10.1152/ajpcell.00326.2010 |
0.434 |
|
| 2011 |
Chen PC, Bhattacharyya BJ, Hanna J, Minkel H, Wilson JA, Finley D, Miller RJ, Wilson SM. Ubiquitin homeostasis is critical for synaptic development and function. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 17505-13. PMID 22131412 DOI: 10.1523/JNEUROSCI.2922-11.2011 |
0.684 |
|
| 2010 |
Lee BH, Lee MJ, Park S, Oh DC, Elsasser S, Chen PC, Gartner C, Dimova N, Hanna J, Gygi SP, Wilson SM, King RW, Finley D. Enhancement of proteasome activity by a small-molecule inhibitor of USP14. Nature. 467: 179-84. PMID 20829789 DOI: 10.1038/Nature09299 |
0.519 |
|
| 2009 |
Chen PC, Qin LN, Li XM, Walters BJ, Wilson JA, Mei L, Wilson SM. The proteasome-associated deubiquitinating enzyme Usp14 is essential for the maintenance of synaptic ubiquitin levels and the development of neuromuscular junctions. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 10909-19. PMID 19726649 DOI: 10.1523/Jneurosci.2635-09.2009 |
0.74 |
|
| 2009 |
Crimmins S, Sutovsky M, Chen PC, Huffman A, Wheeler C, Swing DA, Roth K, Wilson J, Sutovsky P, Wilson S. Transgenic rescue of ataxia mice reveals a male-specific sterility defect. Developmental Biology. 325: 33-42. PMID 18926813 DOI: 10.1016/J.Ydbio.2008.09.021 |
0.747 |
|
| 2008 |
Qiao L, Hamamichi S, Caldwell KA, Caldwell GA, Yacoubian TA, Wilson S, Xie ZL, Speake LD, Parks R, Crabtree D, Liang Q, Crimmins S, Schneider L, Uchiyama Y, Iwatsubo T, et al. Lysosomal enzyme cathepsin D protects against alpha-synuclein aggregation and toxicity. Molecular Brain. 1: 17. PMID 19021916 DOI: 10.1186/1756-6606-1-17 |
0.72 |
|
| 2006 |
Crimmins S, Jin Y, Wheeler C, Huffman AK, Chapman C, Dobrunz LE, Levey A, Roth KA, Wilson JA, Wilson SM. Transgenic rescue of ataxia mice with neuronal-specific expression of ubiquitin-specific protease 14. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 11423-31. PMID 17079671 DOI: 10.1523/Jneurosci.3600-06.2006 |
0.745 |
|
| 2005 |
Anderson C, Crimmins S, Wilson JA, Korbel GA, Ploegh HL, Wilson SM. Loss of Usp14 results in reduced levels of ubiquitin in ataxia mice. Journal of Neurochemistry. 95: 724-31. PMID 16190881 DOI: 10.1111/J.1471-4159.2005.03409.X |
0.779 |
|
| 2002 |
Wilson SM, Bhattacharyya B, Rachel RA, Coppola V, Tessarollo L, Householder DB, Fletcher CF, Miller RJ, Copeland NG, Jenkins NA. Synaptic defects in ataxia mice result from a mutation in Usp14, encoding a ubiquitin-specific protease. Nature Genetics. 32: 420-5. PMID 12368914 DOI: 10.1038/Ng1006 |
0.517 |
|
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