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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 2

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Publication date

PubMed for id: 870646

211 results

Results by year

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Page 1
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.
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.
Airway Disease in Children with Primary Ciliary Dyskinesia: Impact of Ciliary Ultrastructure Defect and Genotype.
Kinghorn B, Rosenfeld M, Sullivan E, Onchiri F, Ferkol TW, Sagel SD, Dell SD, Milla C, Shapiro AJ, Sullivan KM, Zariwala MA, Pittman JE, Mollica F, Tiddens HAWM, Kemner-van de Corput M, Knowles MR, Davis SD, Leigh MW. Kinghorn B, et al. Ann Am Thorac Soc. 2023 Apr;20(4):539-547. doi: 10.1513/AnnalsATS.202206-524OC. Ann Am Thorac Soc. 2023. PMID: 36442147 Free PMC article.
[Sinusitis, otitis media and diffuse bronchiectasis in both lungs].
Zhou WJ, Zhao XY, Liu YP, Zheng SY, Xu KF, Tian XL. Zhou WJ, et al. Zhonghua Jie He He Hu Xi Za Zhi. 2022 Nov 12;45(11):1117-1120. doi: 10.3760/cma.j.cn112147-20220518-00424. Zhonghua Jie He He Hu Xi Za Zhi. 2022. PMID: 36344229 Chinese.
Biallelic DAW1 variants cause a motile ciliopathy characterized by laterality defects and subtle ciliary beating abnormalities.
Leslie JS, Hjeij R, Vivante A, Bearce EA, Dyer L, Wang J, Rawlins L, Kennedy J, Ubeyratna N, Fasham J, Irons ZH, Craig SB, Koenig J, George S, Pode-Shakked B, Bolkier Y, Barel O, Mane S, Frederiksen KK, Wenger O, Scott E, Cross HE, Lorentzen E, Norris DP, Anikster Y, Omran H, Grimes DT, Crosby AH, Baple EL. Leslie JS, et al. Genet Med. 2022 Nov;24(11):2249-2261. doi: 10.1016/j.gim.2022.07.019. Epub 2022 Sep 8. Genet Med. 2022. PMID: 36074124 Free PMC article.
211 results