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

Year Number of Results
2009 5
2010 7
2011 4
2012 11
2013 15
2014 22
2015 11
2016 16
2017 11
2018 13
2019 9
2020 1
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106 results
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Page 1
Inner lumen proteins stabilize doublet microtubules in cilia and flagella.
Owa M, Uchihashi T, Yanagisawa HA, Yamano T, Iguchi H, Fukuzawa H, Wakabayashi KI, Ando T, Kikkawa M. Owa M, et al. Nat Commun. 2019 Mar 8;10(1):1143. doi: 10.1038/s41467-019-09051-x. Nat Commun. 2019. PMID: 30850601 Free PMC article.
Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES).
Leung GKC, Mak CCY, Fung JLF, Wong WHS, Tsang MHY, Yu MHC, Pei SLC, Yeung KS, Mok GTK, Lee CP, Hui APW, Tang MHY, Chan KYK, Liu APY, Yang W, Sham PC, Kan ASY, Chung BHY. Leung GKC, et al. BMC Med Genomics. 2018 Oct 25;11(1):93. doi: 10.1186/s12920-018-0409-z. BMC Med Genomics. 2018. PMID: 30359267 Free PMC article.
Genomic profiling supports the diagnosis of primary ciliary dyskinesia and reveals novel candidate genes and genetic variants.
Andjelkovic M, Minic P, Vreca M, Stojiljkovic M, Skakic A, Sovtic A, Rodic M, Skodric-Trifunovic V, Maric N, Visekruna J, Spasovski V, Pavlovic S. Andjelkovic M, et al. PLoS One. 2018 Oct 9;13(10):e0205422. doi: 10.1371/journal.pone.0205422. eCollection 2018. PLoS One. 2018. PMID: 30300419 Free PMC article.
Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects.
Loges NT, Antony D, Maver A, Deardorff MA, Güleç EY, Gezdirici A, Nöthe-Menchen T, Höben IM, Jelten L, Frank D, Werner C, Tebbe J, Wu K, Goldmuntz E, Čuturilo G, Krock B, Ritter A, Hjeij R, Bakey Z, Pennekamp P, Dworniczak B, Brunner H, Peterlin B, Tanidir C, Olbrich H, Omran H, Schmidts M. Loges NT, et al. Am J Hum Genet. 2018 Dec 6;103(6):995-1008. doi: 10.1016/j.ajhg.2018.10.020. Epub 2018 Nov 21. Am J Hum Genet. 2018. PMID: 30471718 Free PMC article.
Mutations in Outer Dynein Arm Heavy Chain DNAH9 Cause Motile Cilia Defects and Situs Inversus.
Fassad MR, Shoemark A, Legendre M, Hirst RA, Koll F, le Borgne P, Louis B, Daudvohra F, Patel MP, Thomas L, Dixon M, Burgoyne T, Hayes J, Nicholson AG, Cullup T, Jenkins L, Carr SB, Aurora P, Lemullois M, Aubusson-Fleury A, Papon JF, O'Callaghan C, Amselem S, Hogg C, Escudier E, Tassin AM, Mitchison HM. Fassad MR, et al. Am J Hum Genet. 2018 Dec 6;103(6):984-994. doi: 10.1016/j.ajhg.2018.10.016. Epub 2018 Nov 21. Am J Hum Genet. 2018. PMID: 30471717 Free PMC article.
Clinical and Genetic Analysis of Children with Kartagener Syndrome.
Pereira R, Barbosa T, Gales L, Oliveira E, Santos R, Oliveira J, Sousa M. Pereira R, et al. Cells. 2019 Aug 15;8(8):900. doi: 10.3390/cells8080900. Cells. 2019. PMID: 31443223 Free PMC article.
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