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

Year Number of Results
1983 1
1985 1
2001 1
2002 1
2004 3
2005 3
2006 5
2007 2
2008 4
2009 3
2010 5
2011 4
2012 6
2013 8
2014 10
2015 22
2016 18
2017 25
2018 13
2019 4
2020 7
2021 5
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131 results
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Page 1
Clinical and translational advances in esophageal squamous cell carcinoma.
Reichenbach ZW, Murray MG, Saxena R, Farkas D, Karassik EG, Klochkova A, Patel K, Tice C, Hall TM, Gang J, Parkman HP, Ward SJ, Tétreault MP, Whelan KA. Reichenbach ZW, et al. Among authors: tetreault mp. Adv Cancer Res. 2019;144:95-135. doi: 10.1016/bs.acr.2019.05.004. Epub 2019 Jun 10. Adv Cancer Res. 2019. PMID: 31349905 Review.
XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia.
Hoch NC, Hanzlikova H, Rulten SL, Tétreault M, Komulainen E, Ju L, Hornyak P, Zeng Z, Gittens W, Rey SA, Staras K, Mancini GM, McKinnon PJ, Wang ZQ, Wagner JD; Care4Rare Canada Consortium, Yoon G, Caldecott KW. Hoch NC, et al. Among authors: tetreault m. Nature. 2017 Jan 5;541(7635):87-91. doi: 10.1038/nature20790. Epub 2016 Dec 21. Nature. 2017. PMID: 28002403 Free PMC article.
Epineural optogenetic activation of nociceptors initiates and amplifies inflammation.
Michoud F, Seehus C, Schönle P, Brun N, Taub D, Zhang Z, Jain A, Furfaro I, Akouissi O, Moon R, Meier P, Galan K, Doyle B, Tetreault M, Talbot S, Browne LE, Huang Q, Woolf CJ, Lacour SP. Michoud F, et al. Among authors: tetreault m. Nat Biotechnol. 2021 Feb;39(2):179-185. doi: 10.1038/s41587-020-0673-2. Epub 2020 Sep 21. Nat Biotechnol. 2021. PMID: 32958958 Free PMC article.
A Molecular Diagnosis of LGMDR1 Established by RNA Sequencing.
Nicolau S, Choquet K, Bareke E, Shao YH, Brais B, O'Ferrall EK, Tétreault M, Karamchandani J. Nicolau S, et al. Among authors: tetreault m. Can J Neurol Sci. 2021 Mar;48(2):293-296. doi: 10.1017/cjn.2020.141. Epub 2020 Jul 10. Can J Neurol Sci. 2021. PMID: 32646536 No abstract available.
Krüppel-like factors in cancer.
Tetreault MP, Yang Y, Katz JP. Tetreault MP, et al. Nat Rev Cancer. 2013 Oct;13(10):701-13. doi: 10.1038/nrc3582. Nat Rev Cancer. 2013. PMID: 24060862 Review.
Homozygous pathogenic variant in BRAT1 associated with nonprogressive cerebellar ataxia.
Mahjoub A, Cihlarova Z, Tétreault M, MacNeil L, Sondheimer N, Caldecott KW, Hanzlikova H, Yoon G; Care4Rare Canada Consortium. Mahjoub A, et al. Among authors: tetreault m. Neurol Genet. 2019 Sep 4;5(5):e359. doi: 10.1212/NXG.0000000000000359. eCollection 2019 Oct. Neurol Genet. 2019. PMID: 31742228 Free PMC article.
Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy.
Gauquelin L, Hartley T, Tarnopolsky M, Dyment DA, Brais B, Geraghty MT, Tétreault M, Ahmed S, Rojas S, Choquet K, Majewski J, Bernier F, Innes AM, Rouleau G, Suchowersky O, Boycott KM, Yoon G. Gauquelin L, et al. Among authors: tetreault m. Mov Disord Clin Pract. 2020 Sep 29;7(8):940-949. doi: 10.1002/mdc3.13086. eCollection 2020 Nov. Mov Disord Clin Pract. 2020. PMID: 33163565
131 results
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