ESCO2 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "ESCO2" in English language version.

Last modified: 18:15:32, 8 August 2026 (UTC)

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Vega H, Waisfisz Q, Gordillo M, Sakai N, Yanagihara I, Yamada M, et al. (May 2005). "Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion". Nature Genetics. 37 (5): 468–470. doi:10.1038/ng1548. PMID 15821733. S2CID 22948986.
Hou F, Zou H (August 2005). "Two human orthologues of Eco1/Ctf7 acetyltransferases are both required for proper sister-chromatid cohesion". Molecular Biology of the Cell. 16 (8): 3908–3918. doi:10.1091/mbc.E04-12-1063. PMC 1182326. PMID 15958495.
Gordillo M, Vega H, Trainer AH, Hou F, Sakai N, Luque R, et al. (July 2008). "The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity". Human Molecular Genetics. 17 (14): 2172–2180. doi:10.1093/hmg/ddn116. PMID 18411254.
Kantaputra PN, Dejkhamron P, Intachai W, Ngamphiw C, Kawasaki K, Ohazama A, et al. (January 2021). "Juberg-Hayward syndrome is a cohesinopathy, caused by mutation in ESCO2". European Journal of Orthodontics. 43 (1): 45–50. doi:10.1093/ejo/cjaa023. PMID 32255174.

Vega H, Waisfisz Q, Gordillo M, Sakai N, Yanagihara I, Yamada M, et al. (May 2005). "Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion". Nature Genetics. 37 (5): 468–470. doi:10.1038/ng1548. PMID 15821733. S2CID 22948986.
Hou F, Zou H (August 2005). "Two human orthologues of Eco1/Ctf7 acetyltransferases are both required for proper sister-chromatid cohesion". Molecular Biology of the Cell. 16 (8): 3908–3918. doi:10.1091/mbc.E04-12-1063. PMC 1182326. PMID 15958495.
Gordillo M, Vega H, Trainer AH, Hou F, Sakai N, Luque R, et al. (July 2008). "The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity". Human Molecular Genetics. 17 (14): 2172–2180. doi:10.1093/hmg/ddn116. PMID 18411254.
Kantaputra PN, Dejkhamron P, Intachai W, Ngamphiw C, Kawasaki K, Ohazama A, et al. (January 2021). "Juberg-Hayward syndrome is a cohesinopathy, caused by mutation in ESCO2". European Journal of Orthodontics. 43 (1): 45–50. doi:10.1093/ejo/cjaa023. PMID 32255174.

Vega H, Waisfisz Q, Gordillo M, Sakai N, Yanagihara I, Yamada M, et al. (May 2005). "Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion". Nature Genetics. 37 (5): 468–470. doi:10.1038/ng1548. PMID 15821733. S2CID 22948986.