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

Year Number of Results
2003 2
2004 5
2005 5
2006 5
2007 1
2008 3
2009 6
2010 5
2011 5
2012 5
2013 9
2014 10
2015 10
2016 8
2017 9
2018 9
2019 3
2020 6
2021 9
2022 14
2023 12
2024 1

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132 results

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Page 1
Uncompensated mitochondrial oxidative stress underlies heart failure in an iPSC-derived model of congenital heart disease.
Xu X, Jin K, Bais AS, Zhu W, Yagi H, Feinstein TN, Nguyen PK, Criscione JD, Liu X, Beutner G, Karunakaran KB, Rao KS, He H, Adams P, Kuo CK, Kostka D, Pryhuber GS, Shiva S, Ganapathiraju MK, Porter GA Jr, Lin JI, Aronow B, Lo CW. Xu X, et al. Among authors: lo cw. Cell Stem Cell. 2022 May 5;29(5):840-855.e7. doi: 10.1016/j.stem.2022.03.003. Epub 2022 Apr 7. Cell Stem Cell. 2022. PMID: 35395180 Free PMC article.
Reply.
Panigrahy A, Lo CW. Panigrahy A, et al. Among authors: lo cw. J Pediatr. 2017 Jun;185:253-254. doi: 10.1016/j.jpeds.2017.02.022. Epub 2017 Mar 7. J Pediatr. 2017. PMID: 28283257 No abstract available.
Cilia and Ciliopathies in Congenital Heart Disease.
Klena NT, Gibbs BC, Lo CW. Klena NT, et al. Among authors: lo cw. Cold Spring Harb Perspect Biol. 2017 Aug 1;9(8):a028266. doi: 10.1101/cshperspect.a028266. Cold Spring Harb Perspect Biol. 2017. PMID: 28159874 Free PMC article. Review.
Diverse application of MRI for mouse phenotyping.
Wu YL, Lo CW. Wu YL, et al. Among authors: lo cw. Birth Defects Res. 2017 Jun 1;109(10):758-770. doi: 10.1002/bdr2.1051. Epub 2017 May 22. Birth Defects Res. 2017. PMID: 28544650 Free PMC article. Review.
Left-right patterning in congenital heart disease beyond heterotaxy.
Gabriel GC, Lo CW. Gabriel GC, et al. Among authors: lo cw. Am J Med Genet C Semin Med Genet. 2020 Mar;184(1):90-96. doi: 10.1002/ajmg.c.31768. Epub 2020 Jan 30. Am J Med Genet C Semin Med Genet. 2020. PMID: 31999049 Free PMC article. Review.
Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genes.
Glessner JT, Ningappa MB, Ngo KA, Zahid M, So J, Higgs BW, Sleiman PMA, Narayanan T, Ranganathan S, March M, Prasadan K, Vaccaro C, Reyes-Mugica M, Velazquez J, Salgado CM, Ebrahimkhani MR, Schmitt L, Rajasundaram D, Paul M, Pellegrino R, Gittes GK, Li D, Wang X, Billings J, Squires R, Ashokkumar C, Sharif K, Kelly D, Dhawan A, Horslen S, Lo CW, Shin D, Subramaniam S, Hakonarson H, Sindhi R. Glessner JT, et al. Among authors: lo cw. J Hepatol. 2023 Dec;79(6):1385-1395. doi: 10.1016/j.jhep.2023.07.039. Epub 2023 Aug 11. J Hepatol. 2023. PMID: 37572794 Free PMC article.
IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans.
Bakey Z, Cabrera OA, Hoefele J, Antony D, Wu K, Stuck MW, Micha D, Eguether T, Smith AO, van der Wel NN, Wagner M, Strittmatter L, Beales PL, Jonassen JA, Thiffault I, Cadieux-Dion M, Boyes L, Sharif S, Tüysüz B, Dunstheimer D, Niessen HWM, Devine W, Lo CW, Mitchison HM, Schmidts M, Pazour GJ. Bakey Z, et al. Among authors: lo cw. PLoS Genet. 2023 Jun 14;19(6):e1010796. doi: 10.1371/journal.pgen.1010796. eCollection 2023 Jun. PLoS Genet. 2023. PMID: 37315079 Free PMC article.
Role of cilia in the pathogenesis of congenital heart disease.
Gabriel GC, Young CB, Lo CW. Gabriel GC, et al. Among authors: lo cw. Semin Cell Dev Biol. 2021 Feb;110:2-10. doi: 10.1016/j.semcdb.2020.04.017. Epub 2020 May 14. Semin Cell Dev Biol. 2021. PMID: 32418658 Free PMC article. Review.
132 results