Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
6 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
XUTs are a class of Xrn1-sensitive antisense regulatory non-coding RNA in yeast.
Nature. 2011 Jun 22;475(7354):114-7. doi: 10.1038/nature10118.
Nature. 2011.
PMID: 21697827
CIRCUS: a package for Circos display of structural genome variations from paired-end and mate-pair sequencing data.
Naquin D, d'Aubenton-Carafa Y, Thermes C, Silvain M.
Naquin D, et al. Among authors: silvain m.
BMC Bioinformatics. 2014 Jun 18;15:198. doi: 10.1186/1471-2105-15-198.
BMC Bioinformatics. 2014.
PMID: 24938393
Free PMC article.
Item in Clipboard
Replication landscape of the human genome.
Petryk N, Kahli M, d'Aubenton-Carafa Y, Jaszczyszyn Y, Shen Y, Silvain M, Thermes C, Chen CL, Hyrien O.
Petryk N, et al. Among authors: silvain m.
Nat Commun. 2016 Jan 11;7:10208. doi: 10.1038/ncomms10208.
Nat Commun. 2016.
PMID: 26751768
Free PMC article.
Item in Clipboard
ssb gene duplication restores the viability of ΔholC and ΔholD Escherichia coli mutants.
Duigou S, Silvain M, Viguera E, Michel B.
Duigou S, et al. Among authors: silvain m.
PLoS Genet. 2014 Oct 16;10(10):e1004719. doi: 10.1371/journal.pgen.1004719. eCollection 2014 Oct.
PLoS Genet. 2014.
PMID: 25329071
Free PMC article.
Item in Clipboard
DNA Physical Properties and Nucleosome Positions Are Major Determinants of HIV-1 Integrase Selectivity.
Naughtin M, Haftek-Terreau Z, Xavier J, Meyer S, Silvain M, Jaszczyszyn Y, Levy N, Miele V, Benleulmi MS, Ruff M, Parissi V, Vaillant C, Lavigne M.
Naughtin M, et al. Among authors: silvain m.
PLoS One. 2015 Jun 15;10(6):e0129427. doi: 10.1371/journal.pone.0129427. eCollection 2015.
PLoS One. 2015.
PMID: 26075397
Free PMC article.
Item in Clipboard
Anderson's disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalities.
Silvain M, Bligny D, Aparicio T, Laforêt P, Grodet A, Peretti N, Ménard D, Djouadi F, Jardel C, Bégué JM, Walker F, Schmitz J, Lachaux A, Aggerbeck LP, Samson-Bouma ME.
Silvain M, et al.
Clin Genet. 2008 Dec;74(6):546-52. doi: 10.1111/j.1399-0004.2008.01069.x. Epub 2008 Sep 11.
Clin Genet. 2008.
PMID: 18786134
Item in Clipboard
Cite
Cite