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

Year Number of Results
1979 1
1993 1
2000 1
2002 1
2005 3
2006 3
2008 4
2009 3
2010 5
2011 3
2012 2
2014 1
2015 3
2017 2
2018 3
2019 4
2020 6
2021 2
2022 7
2023 4
2024 0

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PubMed for id: 157570

53 results

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Page 1
Symmetric control of sister chromatid cohesion establishment.
Zhang J, Li L, Miao Y, Liu X, Sun H, Jiang M, Li X, Li Z, Liu C, Liu B, Xu X, Cao Q, Hou W, Chen C, Lou H. Zhang J, et al. Nucleic Acids Res. 2023 Jun 9;51(10):4760-4773. doi: 10.1093/nar/gkad146. Nucleic Acids Res. 2023. PMID: 36912084 Free PMC article.
The replicative helicase MCM recruits cohesin acetyltransferase ESCO2 to mediate centromeric sister chromatid cohesion.
Ivanov MP, Ladurner R, Poser I, Beveridge R, Rampler E, Hudecz O, Novatchkova M, Hériché JK, Wutz G, van der Lelij P, Kreidl E, Hutchins JR, Axelsson-Ekker H, Ellenberg J, Hyman AA, Mechtler K, Peters JM. Ivanov MP, et al. EMBO J. 2018 Aug 1;37(15):e97150. doi: 10.15252/embj.201797150. Epub 2018 Jun 21. EMBO J. 2018. PMID: 29930102 Free PMC article.
A child with Roberts syndrome.
Abbas R, Waqar S, Ahmad TM, Irfan Waheed KA, Sultan T, Qureshi AU. Abbas R, et al. J Coll Physicians Surg Pak. 2011 Jul;21(7):431-3. J Coll Physicians Surg Pak. 2011. PMID: 21777535
ESCO2 Spectrum Disorder.
Vega H, Gordillo M, Jabs EW. Vega H, et al. 2006 Apr 18 [updated 2020 Mar 26]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2006 Apr 18 [updated 2020 Mar 26]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301332 Free Books & Documents. Review.
Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome.
Vega H, Trainer AH, Gordillo M, Crosier M, Kayserili H, Skovby F, Uzielli ML, Schnur RE, Manouvrier S, Blair E, Hurst JA, Forzano F, Meins M, Simola KO, Raas-Rothschild A, Hennekam RC, Jabs EW. Vega H, et al. J Med Genet. 2010 Jan;47(1):30-7. doi: 10.1136/jmg.2009.068395. Epub 2009 Jul 1. J Med Genet. 2010. PMID: 19574259
The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity.
Gordillo M, Vega H, Trainer AH, Hou F, Sakai N, Luque R, Kayserili H, Basaran S, Skovby F, Hennekam RC, Uzielli ML, Schnur RE, Manouvrier S, Chang S, Blair E, Hurst JA, Forzano F, Meins M, Simola KO, Raas-Rothschild A, Schultz RA, McDaniel LD, Ozono K, Inui K, Zou H, Jabs EW. Gordillo M, et al. Hum Mol Genet. 2008 Jul 15;17(14):2172-80. doi: 10.1093/hmg/ddn116. Epub 2008 Apr 14. Hum Mol Genet. 2008. PMID: 18411254
53 results