1. Li, Ting, Wu, Yao, Chen, Wei-Cheng, Sheng, Wei, Huang, Guo-Ying. 2022. Functional analysis of HECA variants identified in congenital heart disease in the Chinese population. In Journal of clinical laboratory analysis, 36, e24649. doi:10.1002/jcla.24649. https://pubmed.ncbi.nlm.nih.gov/35949005/
2. Marečková, Magda, Garcia-Alonso, Luz, Moullet, Marie, Zondervan, Krina T, Vento-Tormo, Roser. 2024. An integrated single-cell reference atlas of the human endometrium. In Nature genetics, 56, 1925-1937. doi:10.1038/s41588-024-01873-w. https://pubmed.ncbi.nlm.nih.gov/39198675/
3. Dowejko, Albert, Bauer, Richard, Bauer, Karin, Müller-Richter, Urs D A, Reichert, Torsten E. 2011. The human HECA interacts with cyclins and CDKs to antagonize Wnt-mediated proliferation and chemoresistance of head and neck cancer cells. In Experimental cell research, 318, 489-99. doi:10.1016/j.yexcr.2011.11.004. https://pubmed.ncbi.nlm.nih.gov/22100912/
4. Rojas, Clemencia M, Ham, Jong Hyun, Deng, Wen-Ling, Doyle, Jeff J, Collmer, Alan. 2002. HecA, a member of a class of adhesins produced by diverse pathogenic bacteria, contributes to the attachment, aggregation, epidermal cell killing, and virulence phenotypes of Erwinia chrysanthemi EC16 on Nicotiana clevelandii seedlings. In Proceedings of the National Academy of Sciences of the United States of America, 99, 13142-7. doi:. https://pubmed.ncbi.nlm.nih.gov/12271135/
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