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Results by year

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

Year Number of Results
1979 2
1980 1
1981 2
1983 2
1984 1
1986 1
1988 1
1989 1
1991 2
1992 1
1996 1
1997 2
1999 1
2000 2
2001 2
2002 6
2003 1
2004 4
2005 3
2006 3
2007 8
2008 10
2009 12
2010 9
2011 4
2012 7
2013 18
2014 14
2015 7
2016 9
2017 10
2018 16
2019 11
2020 21
2021 16
2022 15
2023 4
2024 6

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Article attribute

Article type

Publication date

PubMed for id: 870646

215 results

Results by year

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Page 1
Practical guide for the diagnosis and management of primary ciliary dyskinesia.
Takeuchi K, Abo M, Date H, Gotoh S, Kamijo A, Kaneko T, Keicho N, Kodama S, Koinuma G, Kondo M, Masuda S, Mori E, Morimoto K, Nagao M, Nakano A, Nakatani K, Nishida N, Nishikido T, Ohara H, Okinaka Y, Sakaida H, Shiraishi K, Suzaki I, Tojima I, Tsunemi Y, Kainuma K, Ota N, Takeno S, Fujieda S. Takeuchi K, et al. Auris Nasus Larynx. 2024 Jun;51(3):553-568. doi: 10.1016/j.anl.2024.02.001. Epub 2024 Mar 27. Auris Nasus Larynx. 2024. PMID: 38537559 Free article. Review.
Lentiviral expression of wild-type LAMA3A restores cell adhesion in airway basal cells from children with epidermolysis bullosa.
Lau CH, Rouhani MJ, Maughan EF, Orr JC, Kolluri KK, Pearce DR, Haughey EK, Sutton L, Flatau S, Balboa PL, Bageta ML, O'Callaghan C, Smith CM, Janes SM, Hewitt R, Petrof G, Martinez AE, McGrath JA, Butler CR, Hynds RE. Lau CH, et al. Mol Ther. 2024 May 1;32(5):1497-1509. doi: 10.1016/j.ymthe.2024.02.032. Epub 2024 Feb 29. Mol Ther. 2024. PMID: 38429928 Free article.
Skewed X-chromosome inactivation drives the proportion of DNAAF6-defective airway motile cilia and variable expressivity in primary ciliary dyskinesia.
Thomas L, Cuisset L, Papon JF, Tamalet A, Pin I, Abou Taam R, Faucon C, Montantin G, Tissier S, Duquesnoy P, Dastot-Le Moal F, Copin B, Carion N, Louis B, Chantot-Bastaraud S, Siffroi JP, Mitri R, Coste A, Escudier E, Thouvenin G, Amselem S, Legendre M. Thomas L, et al. J Med Genet. 2024 May 21;61(6):595-604. doi: 10.1136/jmg-2023-109700. J Med Genet. 2024. PMID: 38408845
Pathogenic variants in CLXN encoding the outer dynein arm docking-associated calcium-binding protein calaxin cause primary ciliary dyskinesia.
Hjeij R, Aprea I, Poeta M, Nöthe-Menchen T, Bracht D, Raidt J, Honecker BI, Dougherty GW, Olbrich H, Schwartz O, Keller U, Nüsse H, Diderich KEM, Vogelberg C, Santamaria F, Omran H. Hjeij R, et al. Genet Med. 2023 May;25(5):100798. doi: 10.1016/j.gim.2023.100798. Epub 2023 Jan 31. Genet Med. 2023. PMID: 36727596 Free article.
215 results