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Home All issues Volume 29 / No 2 (Février 2013) Med Sci (Paris), 29 2 (2013) 124-126 References
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Issue
Med Sci (Paris)
Volume 29, Number 2, Février 2013
Page(s) 124 - 126
Section Nouvelles
DOI https://doi.org/10.1051/medsci/2013292003
Published online 28 February 2013
  1. Chen R, Davydov EV, Sirota M, Butte AJ. Non-synonymous synonymous coding SNPs show similar likelihood, effect size of human disease association. PLoS One 2010 ; 5 : e13574. [CrossRef] [PubMed] [Google Scholar]
  2. Cartegni L, Chew SL, Krainer AR. Listening to silence and understanding nonsense: exonic mutations that affect splicing. Nat Rev Genet 2002 ; 3 : 285–298. [CrossRef] [PubMed] [Google Scholar]
  3. Nackley AG, Shabalina SA, Tchivileva IE, et al. Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure. Science 2006 ; 314 : 1930–1933. [CrossRef] [PubMed] [Google Scholar]
  4. Shen LX, Basilion JP, Stanton VP. Single-nucleotide polymorphisms can cause different structural folds of mRNA. Proc Natl Acad Sci USA 1999 ; 96 : 7871–7876. [CrossRef] [Google Scholar]
  5. Kimchi-Sarfaty C, Oh JM, Kim IW, et al. A «Silent» polymorphism in the MDR1 gene changes substrate specificity. Science 2007 ; 315 : 525–528. [CrossRef] [PubMed] [Google Scholar]
  6. Hunt R, Sauna ZE, Ambudkar SV, et al. Silent (synonymous) SNP: should we care about them? Methods Mol Biol 2009 ; 578 : 23–39. [CrossRef] [PubMed] [Google Scholar]
  7. Sauna ZE, Kimchi-Sarfaty C. Understanding the contribution of synonymous mutations to human disease. Nat Rev Genet 2011 ; 12 : 683–691. [CrossRef] [PubMed] [Google Scholar]
  8. Mocellin S, Verdi D, Pooley KA, et al. Telomerase reverse transcriptase locus polymorphisms and cancer risk: a field synopsis and meta-analysis. J Natl Cancer Inst 2012 ; 104 : 840–854. [CrossRef] [PubMed] [Google Scholar]
  9. Brest P, Lapaquette P, Souidi M, et al. A synonymous variant in IRGM alters a binding site for miR-196 and causes deregulation of IRGM-dependent xenophagy in Crohn’s disease. Nat Genet 2011 ; 43 : 242–245. [CrossRef] [PubMed] [Google Scholar]
  10. Ho PA, Kopecky KJ, Alonzo TA, et al. Prognostic implications of the IDH1 synonymous SNP rs11554137 in pediatric and adult AML: a report from the Children’s Oncology Group and SWOG. Blood 2011 ; 118 : 4561–4566. [CrossRef] [PubMed] [Google Scholar]
  11. Jordan B. Chroniques génomiques. The sound of silence. Med Sci (Paris) 2012 ; 28 : 435–437. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  12. Londoño-Vallejo A. Un Nobel centenaire célèbre télomères et télomérase. Med Sci (Paris) 2009 ; 25 : 973–976. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  13. Glasser AL, Pierre Lapaquette P, Darfeuille-Michaud A. Altération de l’autophagie chez les patients atteints de maladie de Crohn : une porte ouverte pour des bactéries invasives ? Med Sci (Paris) 2009 ; 25 : 349–351. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]

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