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

Year Number of Results
1965 1
1971 1
1978 1
1991 1
1992 1
1999 1
2000 1
2001 1
2009 5
2010 3
2011 7
2012 2
2013 1
2014 6
2015 3
2016 5
2017 6
2018 5
2019 4
2020 6
2021 2
2022 5
2023 3
2024 1

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69 results

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Page 1
The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis.
Weiss K, Lazar HP, Kurolap A, Martinez AF, Paperna T, Cohen L, Smeland MF, Whalen S, Heide S, Keren B, Terhal P, Irving M, Takaku M, Roberts JD, Petrovich RM, Schrier Vergano SA, Kenney A, Hove H, DeChene E, Quinonez SC, Colin E, Ziegler A, Rumple M, Jain M, Monteil D, Roeder ER, Nugent K, van Haeringen A, Gambello M, Santani A, Medne L, Krock B, Skraban CM, Zackai EH, Dubbs HA, Smol T, Ghoumid J, Parker MJ, Wright M, Turnpenny P, Clayton-Smith J, Metcalfe K, Kurumizaka H, Gelb BD, Baris Feldman H, Campeau PM, Muenke M, Wade PA, Lachlan K. Weiss K, et al. Among authors: takaku m. Genet Med. 2020 Feb;22(2):389-397. doi: 10.1038/s41436-019-0612-0. Epub 2019 Aug 7. Genet Med. 2020. PMID: 31388190 Free PMC article.
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
Snijders Blok L, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, Nowak CB, Douglas J, Swoboda KJ, Steeves MA, Sahai I, Stumpel CTRM, Stegmann APA, Wheeler P, Willing M, Fiala E, Kochhar A, Gibson WT, Cohen ASA, Agbahovbe R, Innes AM, Au PYB, Rankin J, Anderson IJ, Skinner SA, Louie RJ, Warren HE, Afenjar A, Keren B, Nava C, Buratti J, Isapof A, Rodriguez D, Lewandowski R, Propst J, van Essen T, Choi M, Lee S, Chae JH, Price S, Schnur RE, Douglas G, Wentzensen IM, Zweier C, Reis A, Bialer MG, Moore C, Koopmans M, Brilstra EH, Monroe GR, van Gassen KLI, van Binsbergen E, Newbury-Ecob R, Bownass L, Bader I, Mayr JA, Wortmann SB, Jakielski KJ, Strand EA, Kloth K, Bierhals T; DDD study; Roberts JD, Petrovich RM, Machida S, Kurumizaka H, Lelieveld S, Pfundt R, Jansen S, Deriziotis P, Faivre L, Thevenon J, Assoum M, Shriberg L, Kleefstra T, Brunner HG, Wade PA, Fisher SE, Campeau PM. Snijders Blok L, et al. Among authors: takaku m. Nat Commun. 2018 Nov 5;9(1):4619. doi: 10.1038/s41467-018-06014-6. Nat Commun. 2018. PMID: 30397230 Free PMC article.
ATAC-seq Optimization for Cancer Epigenetics Research.
Cooper M, Ray A, Bhattacharya A, Dhasarathy A, Takaku M. Cooper M, et al. Among authors: takaku m. J Vis Exp. 2022 Jun 30;(184):10.3791/64242. doi: 10.3791/64242. J Vis Exp. 2022. PMID: 35848835 Free PMC article.
P4HTM: A Novel Downstream Target of GATA3 in Breast Cancer.
DiDonna SC, Nagornyuk A, Adhikari N, Takada M, Takaku M. DiDonna SC, et al. Among authors: takaku m. Res Sq [Preprint]. 2023 Feb 28:rs.3.rs-2622989. doi: 10.21203/rs.3.rs-2622989/v1. Res Sq. 2023. PMID: 36909571 Free PMC article. Preprint.
Holliday junction-binding activity of human SPF45.
Horikoshi N, Morozumi Y, Takaku M, Takizawa Y, Kurumizaka H. Horikoshi N, et al. Among authors: takaku m. Genes Cells. 2010 Apr 1;15(4):373-83. doi: 10.1111/j.1365-2443.2010.01383.x. Epub 2010 Mar 4. Genes Cells. 2010. PMID: 20236180 Free article.
69 results