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

Year Number of Results
2002 1
2003 5
2005 4
2006 3
2007 5
2008 2
2009 2
2010 2
2011 2
2012 4
2013 6
2014 5
2015 3
2016 3
2017 4
2018 8
2019 5
2020 3
2021 2
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59 results
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Page 1
Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis.
Magini P, Smits DJ, Vandervore L, Schot R, Columbaro M, Kasteleijn E, van der Ent M, Palombo F, Lequin MH, Dremmen M, de Wit MCY, Severino M, Divizia MT, Striano P, Ordonez-Herrera N, Alhashem A, Al Fares A, Al Ghamdi M, Rolfs A, Bauer P, Demmers J, Verheijen FW, Wilke M, van Slegtenhorst M, van der Spek PJ, Seri M, Jansen AC, Stottmann RW, Hufnagel RB, Hopkin RJ, Aljeaid D, Wiszniewski W, Gawlinski P, Laure-Kamionowska M, Alkuraya FS, Akleh H, Stanley V, Musaev D, Gleeson JG, Zaki MS, Brunetti-Pierri N, Cappuccio G, Davidov B, Basel-Salmon L, Bazak L, Shahar NR, Bertoli-Avella A, Mirzaa GM, Dobyns WB, Pippucci T, Fornerod M, Mancini GMS. Magini P, et al. Among authors: columbaro m. Am J Hum Genet. 2019 Oct 3;105(4):689-705. doi: 10.1016/j.ajhg.2019.08.006. Epub 2019 Sep 5. Am J Hum Genet. 2019. PMID: 31495489 Free PMC article.
Inducing cancer indolence by targeting mitochondrial Complex I is potentiated by blocking macrophage-mediated adaptive responses.
Kurelac I, Iommarini L, Vatrinet R, Amato LB, De Luise M, Leone G, Girolimetti G, Umesh Ganesh N, Bridgeman VL, Ombrato L, Columbaro M, Ragazzi M, Gibellini L, Sollazzo M, Feichtinger RG, Vidali S, Baldassarre M, Foriel S, Vidone M, Cossarizza A, Grifoni D, Kofler B, Malanchi I, Porcelli AM, Gasparre G. Kurelac I, et al. Among authors: columbaro m. Nat Commun. 2019 Feb 22;10(1):903. doi: 10.1038/s41467-019-08839-1. Nat Commun. 2019. PMID: 30796225 Free PMC article.
Lamins and bone disorders: current understanding and perspectives.
Gargiuli C, Schena E, Mattioli E, Columbaro M, D'Apice MR, Novelli G, Greggi T, Lattanzi G. Gargiuli C, et al. Among authors: columbaro m. Oncotarget. 2018 Apr 27;9(32):22817-22831. doi: 10.18632/oncotarget.25071. eCollection 2018 Apr 27. Oncotarget. 2018. PMID: 29854317 Free PMC article. Review.
Samp1 Mislocalization in Emery-Dreifuss Muscular Dystrophy.
Mattioli E, Columbaro M, Jafferali MH, Schena E, Hallberg E, Lattanzi G. Mattioli E, et al. Among authors: columbaro m. Cells. 2018 Oct 15;7(10):170. doi: 10.3390/cells7100170. Cells. 2018. PMID: 30326651 Free PMC article.
Laminopathies: a chromatin affair.
Maraldi NM, Lattanzi G, Capanni C, Columbaro M, Mattioli E, Sabatelli P, Squarzoni S, Manzoli FA. Maraldi NM, et al. Among authors: columbaro m. Adv Enzyme Regul. 2006;46:33-49. doi: 10.1016/j.advenzreg.2006.01.001. Epub 2006 Jul 18. Adv Enzyme Regul. 2006. PMID: 16857244 Review. No abstract available.
Altered adipocyte differentiation and unbalanced autophagy in type 2 Familial Partial Lipodystrophy: an in vitro and in vivo study of adipose tissue browning.
Pellegrini C, Columbaro M, Schena E, Prencipe S, Andrenacci D, Iozzo P, Angela Guzzardi M, Capanni C, Mattioli E, Loi M, Araujo-Vilar D, Squarzoni S, Cinti S, Morselli P, Giorgetti A, Zanotti L, Gambineri A, Lattanzi G. Pellegrini C, et al. Among authors: columbaro m. Exp Mol Med. 2019 Aug 2;51(8):1-17. doi: 10.1038/s12276-019-0289-0. Exp Mol Med. 2019. PMID: 31375660 Free PMC article.
59 results
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