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447 results
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Single-cell absolute contact probability detection reveals chromosomes are organized by multiple low-frequency yet specific interactions.
Cattoni DI, Cardozo Gizzi AM, Georgieva M, Di Stefano M, Valeri A, Chamousset D, Houbron C, Déjardin S, Fiche JB, González I, Chang JM, Sexton T, Marti-Renom MA, Bantignies F, Cavalli G, Nollmann M. Cattoni DI, et al. Among authors: di stefano m. Nat Commun. 2017 Nov 24;8(1):1753. doi: 10.1038/s41467-017-01962-x. Nat Commun. 2017. PMID: 29170434 Free PMC article.
Restraint-based three-dimensional modeling of genomes and genomic domains.
Serra F, Di Stefano M, Spill YG, Cuartero Y, Goodstadt M, Baù D, Marti-Renom MA. Serra F, et al. Among authors: di stefano m. FEBS Lett. 2015 Oct 7;589(20 Pt A):2987-95. doi: 10.1016/j.febslet.2015.05.012. Epub 2015 May 14. FEBS Lett. 2015. PMID: 25980604 Review.
The elusive quest for RNA knots.
Burton AS, Di Stefano M, Lehman N, Orland H, Micheletti C. Burton AS, et al. Among authors: di stefano m. RNA Biol. 2016;13(2):134-9. doi: 10.1080/15476286.2015.1132069. RNA Biol. 2016. PMID: 26828280 Free PMC article.
Absence of knots in known RNA structures.
Micheletti C, Di Stefano M, Orland H. Micheletti C, et al. Among authors: di stefano m. Proc Natl Acad Sci U S A. 2015 Feb 17;112(7):2052-7. doi: 10.1073/pnas.1418445112. Epub 2015 Feb 2. Proc Natl Acad Sci U S A. 2015. PMID: 25646433 Free PMC article.
Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.
Albagha OM, Wani SE, Visconti MR, Alonso N, Goodman K, Brandi ML, Cundy T, Chung PY, Dargie R, Devogelaer JP, Falchetti A, Fraser WD, Gennari L, Gianfrancesco F, Hooper MJ, Van Hul W, Isaia G, Nicholson GC, Nuti R, Papapoulos S, Montes Jdel P, Ratajczak T, Rea SL, Rendina D, Gonzalez-Sarmiento R, Di Stefano M, Ward LC, Walsh JP, Ralston SH; Genetic Determinants of Paget's Disease (GDPD) Consortium. Albagha OM, et al. Among authors: di stefano m. Nat Genet. 2011 May 29;43(7):685-9. doi: 10.1038/ng.845. Nat Genet. 2011. PMID: 21623375
Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.
Albagha OM, Visconti MR, Alonso N, Langston AL, Cundy T, Dargie R, Dunlop MG, Fraser WD, Hooper MJ, Isaia G, Nicholson GC, del Pino Montes J, Gonzalez-Sarmiento R, di Stefano M, Tenesa A, Walsh JP, Ralston SH. Albagha OM, et al. Among authors: di stefano m. Nat Genet. 2010 Jun;42(6):520-4. doi: 10.1038/ng.562. Epub 2010 May 2. Nat Genet. 2010. PMID: 20436471 Free PMC article.
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