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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2011 | 1 |
2013 | 2 |
2015 | 1 |
2016 | 1 |
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Mitochondrial Dysfunction Induces Senescence with a Distinct Secretory Phenotype.
Cell Metab. 2016 Feb 9;23(2):303-14. doi: 10.1016/j.cmet.2015.11.011. Epub 2015 Dec 10.
Cell Metab. 2016.
PMID: 26686024
Free PMC article.
Towards understanding region-specificity of triplet repeat diseases: coupled immunohistology and mass spectrometry imaging.
Platt V, Lee DY, Canaria CA, Frankel K, Bernstein S, McMurray CT.
Platt V, et al.
Methods Mol Biol. 2013;1010:213-30. doi: 10.1007/978-1-62703-411-1_14.
Methods Mol Biol. 2013.
PMID: 23754228
Free PMC article.
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A brief history of triplet repeat diseases.
Budworth H, McMurray CT.
Budworth H, et al.
Methods Mol Biol. 2013;1010:3-17. doi: 10.1007/978-1-62703-411-1_1.
Methods Mol Biol. 2013.
PMID: 23754215
Free PMC article.
Review.
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The DNA repair endonuclease XPG interacts directly and functionally with the WRN helicase defective in Werner syndrome.
Trego KS, Chernikova SB, Davalos AR, Perry JJ, Finger LD, Ng C, Tsai MS, Yannone SM, Tainer JA, Campisi J, Cooper PK.
Trego KS, et al.
Cell Cycle. 2011 Jun 15;10(12):1998-2007. doi: 10.4161/cc.10.12.15878. Epub 2011 Jun 15.
Cell Cycle. 2011.
PMID: 21558802
Free PMC article.
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