Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: ESCO2[original query] |
---|
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. Journal of medical genetics 2010 Jan 47 (1): 30-7. Vega H, Trainer A H, Gordillo M, Crosier M, Kayserili H, Skovby F, Uzielli M L Giovannucci, Schnur R E, Manouvrier S, Blair E, Hurst J A, Forzano F, Meins M, Simola K O J, Raas-Rothschild A, Hennekam R C M, Jabs E Wa |
Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families. BMC cancer 2019 Apr 19 (1): 313. Shahi Rajendra Bahadur, De Brakeleer Sylvia, Caljon Ben, Pauwels Ingrid, Bonduelle Maryse, Joris Sofie, Fontaine Christel, Vanhoeij Marian, Van Dooren Sonia, Teugels Erik, De Grève Jacqu |
Genetic and Molecular Characterization Revealed the Prognosis Efficiency of Histone Acetylation in Pan-Digestive Cancers. Journal of oncology 2022 4 2022 3938652. Zhang Tao, Wang Bofang, Gu Baohong, Su Fei, Xiang Lin, Liu Le, Li Xuemei, Wang Xueyan, Gao Lei, Chen H |
ESCO2's oncogenic role in human tumors: a pan-cancer analysis and experimental validation. BMC cancer 2024 4 24 (1): 452. Yue Huang, Dapeng Chen, Yi Bai, Yamin Zhang, Zhiwen Zheng, Qingfeng Fu, Bocun Yi, Yuchen Jiang, Zhihong Zhang, Jianqiang Z |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: