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

Year Number of Results
2003 1
2004 5
2006 2
2007 1
2008 2
2010 1
2011 4
2012 2
2013 7
2014 4
2015 2
2016 1
2019 3
2020 2
2021 2
2022 2
2023 4
2024 1

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44 results

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Page 1
Epithelial zonation along the mouse and human small intestine defines five discrete metabolic domains.
Zwick RK, Kasparek P, Palikuqi B, Viragova S, Weichselbaum L, McGinnis CS, McKinley KL, Rathnayake A, Vaka D, Nguyen V, Trentesaux C, Reyes E, Gupta AR, Gartner ZJ, Locksley RM, Gardner JM, Itzkovitz S, Boffelli D, Klein OD. Zwick RK, et al. Among authors: boffelli d. bioRxiv [Preprint]. 2023 Sep 22:2023.09.20.558726. doi: 10.1101/2023.09.20.558726. bioRxiv. 2023. PMID: 37790430 Free PMC article. Updated. Preprint.
Comparative genomics at the vertebrate extremes.
Boffelli D, Nobrega MA, Rubin EM. Boffelli D, et al. Nat Rev Genet. 2004 Jun;5(6):456-65. doi: 10.1038/nrg1350. Nat Rev Genet. 2004. PMID: 15153998 Review. No abstract available.
Epithelial zonation along the mouse and human small intestine defines five discrete metabolic domains.
Zwick RK, Kasparek P, Palikuqi B, Viragova S, Weichselbaum L, McGinnis CS, McKinley KL, Rathnayake A, Vaka D, Nguyen V, Trentesaux C, Reyes E, Gupta AR, Gartner ZJ, Locksley RM, Gardner JM, Itzkovitz S, Boffelli D, Klein OD. Zwick RK, et al. Among authors: boffelli d. Nat Cell Biol. 2024 Feb;26(2):250-262. doi: 10.1038/s41556-023-01337-z. Epub 2024 Feb 6. Nat Cell Biol. 2024. PMID: 38321203
Patterning and folding of intestinal villi by active mesenchymal dewetting.
Huycke TR, Miyazaki H, Häkkinen TJ, Srivastava V, Barruet E, McGinnis CS, Kalantari A, Cornwall-Scoones J, Vaka D, Zhu Q, Jo H, DeGrado WF, Thomson M, Garikipati K, Boffelli D, Klein OD, Gartner ZJ. Huycke TR, et al. Among authors: boffelli d. bioRxiv [Preprint]. 2023 Aug 15:2023.06.25.546328. doi: 10.1101/2023.06.25.546328. bioRxiv. 2023. PMID: 37425793 Free PMC article. Preprint.
Towards a reference genome that captures global genetic diversity.
Wong KHY, Ma W, Wei CY, Yeh EC, Lin WJ, Wang EHF, Su JP, Hsieh FJ, Kao HJ, Chen HH, Chow SK, Young E, Chu C, Poon A, Yang CF, Lin DS, Hu YF, Wu JY, Lee NC, Hwu WL, Boffelli D, Martin D, Xiao M, Kwok PY. Wong KHY, et al. Among authors: boffelli d. Nat Commun. 2020 Oct 30;11(1):5482. doi: 10.1038/s41467-020-19311-w. Nat Commun. 2020. PMID: 33127893 Free PMC article.
Application of full-genome analysis to diagnose rare monogenic disorders.
Shieh JT, Penon-Portmann M, Wong KHY, Levy-Sakin M, Verghese M, Slavotinek A, Gallagher RC, Mendelsohn BA, Tenney J, Beleford D, Perry H, Chow SK, Sharo AG, Brenner SE, Qi Z, Yu J, Klein OD, Martin D, Kwok PY, Boffelli D. Shieh JT, et al. Among authors: boffelli d. NPJ Genom Med. 2021 Sep 23;6(1):77. doi: 10.1038/s41525-021-00241-5. NPJ Genom Med. 2021. PMID: 34556655 Free PMC article.
44 results