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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1995 1
1997 1
1999 1
2000 2
2001 3
2002 3
2009 2
2010 3
2011 2
2012 7
2013 3
2014 7
2015 6
2016 8
2017 8
2018 8
2019 9
2020 9
2021 15
2022 2
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93 results
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Page 1
p53 is a central regulator driving neurodegeneration caused by C9orf72 poly(PR).
Maor-Nof M, Shipony Z, Lopez-Gonzalez R, Nakayama L, Zhang YJ, Couthouis J, Blum JA, Castruita PA, Linares GR, Ruan K, Ramaswami G, Simon DJ, Nof A, Santana M, Han K, Sinnott-Armstrong N, Bassik MC, Geschwind DH, Tessier-Lavigne M, Attardi LD, Lloyd TE, Ichida JK, Gao FB, Greenleaf WJ, Yokoyama JS, Petrucelli L, Gitler AD. Maor-Nof M, et al. Among authors: lloyd te. Cell. 2021 Feb 4;184(3):689-708.e20. doi: 10.1016/j.cell.2020.12.025. Epub 2021 Jan 21. Cell. 2021. PMID: 33482083
Stress Granule Assembly Disrupts Nucleocytoplasmic Transport.
Zhang K, Daigle JG, Cunningham KM, Coyne AN, Ruan K, Grima JC, Bowen KE, Wadhwa H, Yang P, Rigo F, Taylor JP, Gitler AD, Rothstein JD, Lloyd TE. Zhang K, et al. Among authors: lloyd te. Cell. 2018 May 3;173(4):958-971.e17. doi: 10.1016/j.cell.2018.03.025. Epub 2018 Apr 5. Cell. 2018. PMID: 29628143 Free PMC article.
Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study.
Pipis M, Feely SME, Polke JM, Skorupinska M, Perez L, Shy RR, Laura M, Morrow JM, Moroni I, Pisciotta C, Taroni F, Vujovic D, Lloyd TE, Acsadi G, Yum SW, Lewis RA, Finkel RS, Herrmann DN, Day JW, Li J, Saporta M, Sadjadi R, Walk D, Burns J, Muntoni F, Ramchandren S, Horvath R, Johnson NE, Züchner S, Pareyson D, Scherer SS, Rossor AM, Shy ME, Reilly MM; Inherited Neuropathies Consortium - Rare Disease Clinical Research Network (INC-RDCRN). Pipis M, et al. Among authors: lloyd te. Brain. 2020 Dec 1;143(12):3589-3602. doi: 10.1093/brain/awaa323. Brain. 2020. PMID: 33415332 Free PMC article.
The C9orf72 repeat expansion disrupts nucleocytoplasmic transport.
Zhang K, Donnelly CJ, Haeusler AR, Grima JC, Machamer JB, Steinwald P, Daley EL, Miller SJ, Cunningham KM, Vidensky S, Gupta S, Thomas MA, Hong I, Chiu SL, Huganir RL, Ostrow LW, Matunis MJ, Wang J, Sattler R, Lloyd TE, Rothstein JD. Zhang K, et al. Among authors: lloyd te. Nature. 2015 Sep 3;525(7567):56-61. doi: 10.1038/nature14973. Epub 2015 Aug 26. Nature. 2015. PMID: 26308891 Free PMC article.
Secondary Causes of Myositis.
Berth SH, Lloyd TE. Berth SH, et al. Among authors: lloyd te. Curr Treat Options Neurol. 2020;22(11):38. doi: 10.1007/s11940-020-00646-0. Epub 2020 Oct 6. Curr Treat Options Neurol. 2020. PMID: 33041620 Free PMC article. Review.
Nucleocytoplasmic transport in C9orf72-mediated ALS/FTD.
Zhang K, Grima JC, Rothstein JD, Lloyd TE. Zhang K, et al. Among authors: lloyd te. Nucleus. 2016 Apr 25;7(2):132-7. doi: 10.1080/19491034.2016.1172152. Epub 2016 Apr 26. Nucleus. 2016. PMID: 27116041 Free PMC article. Review.
New Developments in the Genetics of Inclusion Body Myositis.
Britson KA, Yang SY, Lloyd TE. Britson KA, et al. Among authors: lloyd te. Curr Rheumatol Rep. 2018 Apr 2;20(5):26. doi: 10.1007/s11926-018-0738-0. Curr Rheumatol Rep. 2018. PMID: 29611059 Free PMC article. Review.
Drosophila models of neurologic disease.
Wu MN, Lloyd TE. Wu MN, et al. Among authors: lloyd te. Exp Neurol. 2015 Dec;274(Pt A):1-3. doi: 10.1016/j.expneurol.2015.10.004. Exp Neurol. 2015. PMID: 26566006 No abstract available.
93 results