My Bibliography

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Birdsall V, Kirwan K, Zhu M, Imoto Y, Wilson SM, Watanabe S, Waites CL. Axonal transport of Hrs is activity dependent and facilitates synaptic vesicle protein degradation. Life Sci Alliance. 2022 Oct;5(10). doi: 10.26508/lsa.202000745. Print 2022 Oct. PubMed PMID: 35636965; PubMed Central PMCID: PMC9152131.

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McLean JW, Wilson JA, Tian T, Watson JA, VanHart M, Bean AJ, Scherer SS, Crossman DK, Ubogu E, Wilson SM. Disruption of Endosomal Sorting in Schwann Cells Leads to Defective Myelination and Endosomal Abnormalities Observed in Charcot-Marie-Tooth Disease. J Neurosci. 2022 Jun 22;42(25):5085-5101. doi: 10.1523/JNEUROSCI.2481-21.2022. Epub 2022 May 19. PubMed PMID: 35589390; PubMed Central PMCID: PMC9233440.

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Tian T, McLean JW, Wilson JA, Wilson SM. Examination of genetic and pharmacological tools to study the proteasomal deubiquitinating enzyme ubiquitin-specific protease 14 in the nervous system. J Neurochem. 2021 Feb;156(3):309-323. doi: 10.1111/jnc.15180. Epub 2020 Sep 30. PubMed PMID: 32901953; PubMed Central PMCID: PMC8489120.

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Vaden JH, Tian T, Golf S, McLean JW, Wilson JA, Wilson SM. Chronic over-expression of ubiquitin impairs learning, reduces synaptic plasticity, and enhances GRIA receptor turnover in mice. J Neurochem. 2019 Feb;148(3):386-399. doi: 10.1111/jnc.14630. Epub 2018 Dec 10. PubMed PMID: 30451289.

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Kiprowska MJ, Stepanova A, Todaro DR, Galkin A, Haas A, Wilson SM, Figueiredo-Pereira ME. Neurotoxic mechanisms by which the USP14 inhibitor IU1 depletes ubiquitinated proteins and Tau in rat cerebral cortical neurons: Relevance to Alzheimer's disease. Biochim Biophys Acta Mol Basis Dis. 2017 Jun;1863(6):1157-1170. doi: 10.1016/j.bbadis.2017.03.017. Epub 2017 Apr 1. PubMed PMID: 28372990; PubMed Central PMCID: PMC5549686.

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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 Genet. 2015 Jun;11(6):e1005290. doi: 10.1371/journal.pgen.1005290. eCollection 2015 Jun. PubMed PMID: 26115514; PubMed Central PMCID: PMC4482608.

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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. Front Mol Neurosci. 2015;8:11. doi: 10.3389/fnmol.2015.00011. eCollection 2015. PubMed PMID: 25954152; PubMed Central PMCID: PMC4407586.

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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. Mol Neurodegener. 2015 Jan 10;10:3. doi: 10.1186/1750-1326-10-3. PubMed PMID: 25575639; PubMed Central PMCID: PMC4417291.

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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. J Physiol. 2014 Feb 15;592(4):571-86. doi: 10.1113/jphysiol.2013.266015. Epub 2013 Nov 11. PubMed PMID: 24218545; PubMed Central PMCID: PMC3934702.

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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. 2013;8(12):e84042. doi: 10.1371/journal.pone.0084042. eCollection 2013. PubMed PMID: 24358326; PubMed Central PMCID: PMC3865287.

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Jarome TJ, Kwapis JL, Hallengren JJ, Wilson SM, Helmstetter FJ. The ubiquitin-specific protease 14 (USP14) is a critical regulator of long-term memory formation. Learn Mem. 2013 Dec 16;21(1):9-13. doi: 10.1101/lm.032771.113. PubMed PMID: 24344179; PubMed Central PMCID: PMC3867711.

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Hallengren J, Chen PC, Wilson SM. Neuronal ubiquitin homeostasis. Cell Biochem Biophys. 2013 Sep;67(1):67-73. doi: 10.1007/s12013-013-9634-4. Review. PubMed PMID: 23686613; PubMed Central PMCID: PMC3758786.

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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. 2012;7(10):e47884. doi: 10.1371/journal.pone.0047884. Epub 2012 Oct 29. PubMed PMID: 23144711; PubMed Central PMCID: PMC3483306.

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Bhattacharyya BJ, Wilson SM, Jung H, Miller RJ. Altered neurotransmitter release machinery in mice deficient for the deubiquitinating enzyme Usp14. Am J Physiol Cell Physiol. 2012 Feb 15;302(4):C698-708. doi: 10.1152/ajpcell.00326.2010. Epub 2011 Nov 9. PubMed PMID: 22075695; PubMed Central PMCID: PMC3287356.

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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. J Neurosci. 2011 Nov 30;31(48):17505-13. doi: 10.1523/JNEUROSCI.2922-11.2011. PubMed PMID: 22131412; PubMed Central PMCID: PMC3253363.

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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. 2010 Sep 9;467(7312):179-84. doi: 10.1038/nature09299. PubMed PMID: 20829789; PubMed Central PMCID: PMC2939003.

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Lappe-Siefke C, Loebrich S, Hevers W, Waidmann OB, Schweizer M, Fehr S, Fritschy JM, Dikic I, Eilers J, Wilson SM, Kneussel M. The ataxia (axJ) mutation causes abnormal GABAA receptor turnover in mice. PLoS Genet. 2009 Sep;5(9):e1000631. doi: 10.1371/journal.pgen.1000631. Epub 2009 Sep 4. PubMed PMID: 19759851; PubMed Central PMCID: PMC2744266.

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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. J Neurosci. 2009 Sep 2;29(35):10909-19. doi: 10.1523/JNEUROSCI.2635-09.2009. PubMed PMID: 19726649; PubMed Central PMCID: PMC2766780.

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Cartier AE, Djakovic SN, Salehi A, Wilson SM, Masliah E, Patrick GN. Regulation of synaptic structure by ubiquitin C-terminal hydrolase L1. J Neurosci. 2009 Jun 17;29(24):7857-68. doi: 10.1523/JNEUROSCI.1817-09.2009. PubMed PMID: 19535597; PubMed Central PMCID: PMC2748938.

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Ye T, Fu D, Warren WS. Nonlinear absorption microscopy. Photochem Photobiol. 2009 May-Jun;85(3):631-45. doi: 10.1111/j.1751-1097.2008.00514.x. Epub 2009 Jan 23. Review. PubMed PMID: 19170931; PubMed Central PMCID: PMC7341902.

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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. Dev Biol. 2009 Jan 1;325(1):33-42. doi: 10.1016/j.ydbio.2008.09.021. Epub 2008 Sep 27. PubMed PMID: 18926813; PubMed Central PMCID: PMC2651617.

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Walters BJ, Campbell SL, Chen PC, Taylor AP, Schroeder DG, Dobrunz LE, Artavanis-Tsakonas K, Ploegh HL, Wilson JA, Cox GA, Wilson SM. Differential effects of Usp14 and Uch-L1 on the ubiquitin proteasome system and synaptic activity. Mol Cell Neurosci. 2008 Dec;39(4):539-48. doi: 10.1016/j.mcn.2008.07.028. Epub 2008 Aug 15. PubMed PMID: 18771733; PubMed Central PMCID: PMC2734958.

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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, Zhou Y, Peng L, Lu Y, Standaert DG, Walls KC, Shacka JJ, Roth KA, Zhang J. Lysosomal enzyme cathepsin D protects against alpha-synuclein aggregation and toxicity. Mol Brain. 2008 Nov 21;1:17. doi: 10.1186/1756-6606-1-17. PubMed PMID: 19021916; PubMed Central PMCID: PMC2600785.

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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. J Neurosci. 2006 Nov 1;26(44):11423-31. doi: 10.1523/JNEUROSCI.3600-06.2006. PubMed PMID: 17079671; PubMed Central PMCID: PMC6674543.

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Anderson C, Crimmins S, Wilson JA, Korbel GA, Ploegh HL, Wilson SM. Loss of Usp14 results in reduced levels of ubiquitin in ataxia mice. J Neurochem. 2005 Nov;95(3):724-31. doi: 10.1111/j.1471-4159.2005.03409.x. Epub 2005 Sep 29. PubMed PMID: 16190881.

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Miller RJ, Wilson SM. Neurological disease: UPS stops delivering!. Trends Pharmacol Sci. 2003 Jan;24(1):18-23. doi: 10.1016/s0165-6147(02)00011-1. Review. PubMed PMID: 12498726.

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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. Nat Genet. 2002 Nov;32(3):420-5. doi: 10.1038/ng1006. Epub 2002 Oct 7. PubMed PMID: 12368914.

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Hector RE, Nykamp KR, Dheur S, Anderson JT, Non PJ, Urbinati CR, Wilson SM, Minvielle-Sebastia L, Swanson MS. Dual requirement for yeast hnRNP Nab2p in mRNA poly(A) tail length control and nuclear export. EMBO J. 2002 Apr 2;21(7):1800-10. doi: 10.1093/emboj/21.7.1800. PubMed PMID: 11927564; PubMed Central PMCID: PMC125947.

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Wilson SM, Householder DB, Coppola V, Tessarollo L, Fritzsch B, Lee EC, Goss D, Carlson GA, Copeland NG, Jenkins NA. Mutations in Cdh23 cause nonsyndromic hearing loss in waltzer mice. Genomics. 2001 Jun 1;74(2):228-33. doi: 10.1006/geno.2001.6554. PubMed PMID: 11386759.

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Wilson SM, Toth PT, Oh SB, Gillard SE, Volsen S, Ren D, Philipson LH, Lee EC, Fletcher CF, Tessarollo L, Copeland NG, Jenkins NA, Miller RJ. The status of voltage-dependent calcium channels in alpha 1E knock-out mice. J Neurosci. 2000 Dec 1;20(23):8566-71. doi: 10.1523/JNEUROSCI.20-23-08566.2000. PubMed PMID: 11102459; PubMed Central PMCID: PMC6773068.

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Wilson SM, Yip R, Swing DA, O'Sullivan TN, Zhang Y, Novak EK, Swank RT, Russell LB, Copeland NG, Jenkins NA. A mutation in Rab27a causes the vesicle transport defects observed in ashen mice. Proc Natl Acad Sci U S A. 2000 Jul 5;97(14):7933-8. doi: 10.1073/pnas.140212797. PubMed PMID: 10859366; PubMed Central PMCID: PMC16648.

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Conrad NK, Wilson SM, Steinmetz EJ, Patturajan M, Brow DA, Swanson MS, Corden JL. A yeast heterogeneous nuclear ribonucleoprotein complex associated with RNA polymerase II. Genetics. 2000 Feb;154(2):557-71. doi: 10.1093/genetics/154.2.557. PubMed PMID: 10655211; PubMed Central PMCID: PMC1460961.

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Wilson SM, Datar KV, Paddy MR, Swedlow JR, Swanson MS. Characterization of nuclear polyadenylated RNA-binding proteins in Saccharomyces cerevisiae. J Cell Biol. 1994 Dec;127(5):1173-84. doi: 10.1083/jcb.127.5.1173. PubMed PMID: 7962083; PubMed Central PMCID: PMC2120247.

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Anderson JT, Wilson SM, Datar KV, Swanson MS. NAB2: a yeast nuclear polyadenylated RNA-binding protein essential for cell viability. Mol Cell Biol. 1993 May;13(5):2730-41. doi: 10.1128/mcb.13.5.2730-2741.1993. PubMed PMID: 8474438; PubMed Central PMCID: PMC359649.