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Page 1
Tube morphogenesis: making and shaping biological tubes.
Lubarsky B, Krasnow MA. Lubarsky B, et al. Cell. 2003 Jan 10;112(1):19-28. doi: 10.1016/s0092-8674(02)01283-7. Cell. 2003. PMID: 12526790 Free article. Review.
Requirement for chitin biosynthesis in epithelial tube morphogenesis.
Devine WP, Lubarsky B, Shaw K, Luschnig S, Messina L, Krasnow MA. Devine WP, et al. Among authors: lubarsky b. Proc Natl Acad Sci U S A. 2005 Nov 22;102(47):17014-9. doi: 10.1073/pnas.0506676102. Epub 2005 Nov 15. Proc Natl Acad Sci U S A. 2005. PMID: 16287975 Free PMC article.
Patients with Cystic Fibrosis and a G551D or Homozygous F508del Mutation: Similar Lung Function Decline.
Sawicki GS, McKone EF, Millar SJ, Pasta DJ, Konstan MW, Lubarsky B, Wagener JS. Sawicki GS, et al. Among authors: lubarsky b. Am J Respir Crit Care Med. 2017 Jun 15;195(12):1673-1676. doi: 10.1164/rccm.201608-1678LE. Am J Respir Crit Care Med. 2017. PMID: 28617084 No abstract available.
Assessment of safety and efficacy of long-term treatment with combination lumacaftor and ivacaftor therapy in patients with cystic fibrosis homozygous for the F508del-CFTR mutation (PROGRESS): a phase 3, extension study.
Konstan MW, McKone EF, Moss RB, Marigowda G, Tian S, Waltz D, Huang X, Lubarsky B, Rubin J, Millar SJ, Pasta DJ, Mayer-Hamblett N, Goss CH, Morgan W, Sawicki GS. Konstan MW, et al. Among authors: lubarsky b. Lancet Respir Med. 2017 Feb;5(2):107-118. doi: 10.1016/S2213-2600(16)30427-1. Epub 2016 Dec 21. Lancet Respir Med. 2017. PMID: 28011037 Clinical Trial.
Nutritional Status Improved in Cystic Fibrosis Patients with the G551D Mutation After Treatment with Ivacaftor.
Borowitz D, Lubarsky B, Wilschanski M, Munck A, Gelfond D, Bodewes F, Schwarzenberg SJ. Borowitz D, et al. Among authors: lubarsky b. Dig Dis Sci. 2016 Jan;61(1):198-207. doi: 10.1007/s10620-015-3834-2. Epub 2015 Aug 7. Dig Dis Sci. 2016. PMID: 26250833 Clinical Trial.