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

Year Number of Results
2002 4
2003 6
2004 7
2005 5
2006 5
2007 3
2008 13
2009 9
2010 11
2011 14
2012 9
2013 19
2014 17
2015 18
2016 17
2017 21
2018 20
2019 23
2020 22
2021 15
2022 16
2023 17
2024 4

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273 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: kurumizaka h. 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: kurumizaka h. Nat Commun. 2018 Nov 5;9(1):4619. doi: 10.1038/s41467-018-06014-6. Nat Commun. 2018. PMID: 30397230 Free PMC article.
Transcription through the nucleosome.
Kujirai T, Kurumizaka H. Kujirai T, et al. Among authors: kurumizaka h. Curr Opin Struct Biol. 2020 Apr;61:42-49. doi: 10.1016/j.sbi.2019.10.007. Epub 2019 Nov 29. Curr Opin Struct Biol. 2020. PMID: 31790919 Free article. Review.
Structural perspectives on transcription in chromatin.
Sekine SI, Ehara H, Kujirai T, Kurumizaka H. Sekine SI, et al. Among authors: kurumizaka h. Trends Cell Biol. 2024 Mar;34(3):211-224. doi: 10.1016/j.tcb.2023.07.011. Epub 2023 Aug 16. Trends Cell Biol. 2024. PMID: 37596139 Review.
Structural diversity of the nucleosome.
Koyama M, Kurumizaka H. Koyama M, et al. Among authors: kurumizaka h. J Biochem. 2018 Feb 1;163(2):85-95. doi: 10.1093/jb/mvx081. J Biochem. 2018. PMID: 29161414 Review.
Chromatin structure related to oncogenesis.
Matsumoto S, Horikoshi N, Takizawa Y, Kurumizaka H. Matsumoto S, et al. Among authors: kurumizaka h. Cancer Sci. 2023 Aug;114(8):3068-3075. doi: 10.1111/cas.15850. Epub 2023 May 23. Cancer Sci. 2023. PMID: 37218420 Free PMC article. Review.
Nucleosome organization and chromatin dynamics in telomeres.
Ichikawa Y, Nishimura Y, Kurumizaka H, Shimizu M. Ichikawa Y, et al. Among authors: kurumizaka h. Biomol Concepts. 2015 Mar;6(1):67-75. doi: 10.1515/bmc-2014-0035. Biomol Concepts. 2015. PMID: 25720088 Free article. Review.
273 results