1. Zhu, Jiamei, Zhang, Ting, Jiang, Juan, Xia, Nan, Chen, Youguo. 2024. Genetic variation perspective reveals potential drug targets for subtypes of endometrial cancer. In Scientific reports, 14, 28180. doi:10.1038/s41598-024-78689-5. https://pubmed.ncbi.nlm.nih.gov/39548148/
2. Sopha, Pattarawut, Kadokura, Hiroshi, Yamamoto, Yo-hei, Tsuru, Akio, Kohno, Kenji. 2012. A novel mammalian ER-located J-protein, DNAJB14, can accelerate ERAD of misfolded membrane proteins. In Cell structure and function, 37, 177-87. doi:. https://pubmed.ncbi.nlm.nih.gov/23018488/
3. Li, Kai, Jiang, Qiang, Bai, Xue, Ruan, Mei-Yu, Cai, Shi-Qing. 2016. Tetrameric Assembly of K+ Channels Requires ER-Located Chaperone Proteins. In Molecular cell, 65, 52-65. doi:10.1016/j.molcel.2016.10.027. https://pubmed.ncbi.nlm.nih.gov/27916661/
4. Wang, Geqiang, Li, Yongji, Liu, Jiaxing, Cai, Weixin, Li, Xiaodong. 2024. Heat shock protein-related diagnostic signature and molecular subtypes in ankylosing spondylitis: new pathogenesis insights. In International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group, 41, 2336149. doi:10.1080/02656736.2024.2336149. https://pubmed.ncbi.nlm.nih.gov/38679420/
5. Purificação, Aline Dias da, Debbas, Victor, Tanaka, Leonardo Yuji, Laurindo, Francisco Rafael Martins, Oliveira, Percillia Victoria Santos. 2023. DNAJB12 and DNJB14 are non-redundant Hsp40 redox chaperones involved in endoplasmic reticulum protein reflux. In Biochimica et biophysica acta. General subjects, 1868, 130502. doi:10.1016/j.bbagen.2023.130502. https://pubmed.ncbi.nlm.nih.gov/37925033/
6. Goodwin, Edward C, Motamedi, Nasim, Lipovsky, Alex, Fernández-Busnadiego, Rubén, DiMaio, Daniel. 2014. Expression of DNAJB12 or DNAJB14 causes coordinate invasion of the nucleus by membranes associated with a novel nuclear pore structure. In PloS one, 9, e94322. doi:10.1371/journal.pone.0094322. https://pubmed.ncbi.nlm.nih.gov/24732912/
7. Ravindran, Madhu Sudhan, Engelke, Martin F, Verhey, Kristen J, Tsai, Billy. 2017. Exploiting the kinesin-1 molecular motor to generate a virus membrane penetration site. In Nature communications, 8, 15496. doi:10.1038/ncomms15496. https://pubmed.ncbi.nlm.nih.gov/28537258/