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

Year Number of Results
2002 3
2003 7
2004 4
2005 3
2006 9
2007 4
2008 6
2009 10
2010 10
2011 8
2012 13
2013 9
2014 7
2015 12
2016 13
2017 10
2018 14
2019 12
2020 12
2021 15
2022 13
2023 20
2024 5

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194 results

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Page 1
Zebrafish as an animal model for biomedical research.
Choi TY, Choi TI, Lee YR, Choe SK, Kim CH. Choi TY, et al. Among authors: kim ch. Exp Mol Med. 2021 Mar;53(3):310-317. doi: 10.1038/s12276-021-00571-5. Epub 2021 Mar 1. Exp Mol Med. 2021. PMID: 33649498 Free PMC article. Review.
Editorial: Zebrafish as a model for human congenital disorders.
Kumar M, Kim CH, Singla N. Kumar M, et al. Among authors: kim ch. Front Cell Dev Biol. 2023 Jun 20;11:1235580. doi: 10.3389/fcell.2023.1235580. eCollection 2023. Front Cell Dev Biol. 2023. PMID: 37408532 Free PMC article. No abstract available.
IFT46 gene promoter-driven ciliopathy disease model in zebrafish.
Lee MS, Han HJ, Choi TI, Lee KH, Baasankhuu A, Kim HT, Kim CH. Lee MS, et al. Among authors: kim ch. Front Cell Dev Biol. 2023 Jun 8;11:1200599. doi: 10.3389/fcell.2023.1200599. eCollection 2023. Front Cell Dev Biol. 2023. PMID: 37363725 Free PMC article.
Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X-linked intellectual disability.
Lee YR, Thomas MG, Roychaudhury A, Skinner C, Maconachie G, Crosier M, Horak H, Constantinescu CS, Choi TI, Kyung JJ, Wang T, Ku B, Chodirker BN, Hammer MF, Gottlob I, Norton WHJ, Chudley AE, Schwartz CE, Kim CH. Lee YR, et al. Among authors: kim ch. Res Sq [Preprint]. 2023 Mar 20:rs.3.rs-2683050. doi: 10.21203/rs.3.rs-2683050/v1. Res Sq. 2023. PMID: 36993381 Free PMC article. Preprint.
A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome.
Ben-Mahmoud A, Kishikawa S, Gupta V, Leach NT, Shen Y, Moldovan O, Goel H, Hopper B, Ranguin K, Gruchy N, Maas SM, Lacassie Y, Kim SH, Kim WY, Quade BJ, Morton CC, Kim CH, Layman LC, Kim HG. Ben-Mahmoud A, et al. Among authors: kim ch. Sci Rep. 2023 Aug 10;13(1):12984. doi: 10.1038/s41598-023-40037-4. Sci Rep. 2023. PMID: 37563198 Free PMC article.
Variants in ZFX are associated with an X-linked neurodevelopmental disorder with recurrent facial gestalt.
Shepherdson JL, Hutchison K, Don DW, McGillivray G, Choi TI, Allan CA, Amor DJ, Banka S, Basel DG, Buch LD, Carere DA, Carroll R, Clayton-Smith J, Crawford A, Dunø M, Faivre L, Gilfillan CP, Gold NB, Gripp KW, Hobson E, Holtz AM, Innes AM, Isidor B, Jackson A, Katsonis P, Amel Riazat Kesh L; Genomics England Research Consortium; Küry S, Lecoquierre F, Lockhart P, Maraval J, Matsumoto N, McCarrier J, McCarthy J, Miyake N, Moey LH, Németh AH, Østergaard E, Patel R, Pope K, Posey JE, Schnur RE, Shaw M, Stolerman E, Taylor JP, Wadman E, Wakeling E, White SM, Wong LC, Lupski JR, Lichtarge O, Corbett MA, Gecz J, Nicolet CM, Farnham PJ, Kim CH, Shinawi M. Shepherdson JL, et al. Among authors: kim ch. Am J Hum Genet. 2024 Mar 7;111(3):487-508. doi: 10.1016/j.ajhg.2024.01.007. Epub 2024 Feb 6. Am J Hum Genet. 2024. PMID: 38325380
194 results