1. Li, Fei, Dai, Yun, Xu, Hao, Lv, Mengqin, Ma, Xiangyi. 2019. XPNPEP2 is associated with lymph node metastasis in prostate cancer patients. In Scientific reports, 9, 10078. doi:10.1038/s41598-019-45245-5. https://pubmed.ncbi.nlm.nih.gov/31296901/
2. Cheng, Teng, Wei, Rui, Jiang, Guiying, Li, Fei, Xi, Ling. . XPNPEP2 is overexpressed in cervical cancer and promotes cervical cancer metastasis. In Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 39, 1010428317717122. doi:10.1177/1010428317717122. https://pubmed.ncbi.nlm.nih.gov/28670957/
3. Cilia La Corte, Amy L, Carter, Angela M, Rice, Gillian I, Grant, Peter J, Hooper, Nigel M. 2011. A functional XPNPEP2 promoter haplotype leads to reduced plasma aminopeptidase P and increased risk of ACE inhibitor-induced angioedema. In Human mutation, 32, 1326-31. doi:10.1002/humu.21579. https://pubmed.ncbi.nlm.nih.gov/21898657/
4. Woodard-Grice, Alencia V, Lucisano, Amelia C, Byrd, James B, Simmons, William H, Brown, Nancy J. . Sex-dependent and race-dependent association of XPNPEP2 C-2399A polymorphism with angiotensin-converting enzyme inhibitor-associated angioedema. In Pharmacogenetics and genomics, 20, 532-6. doi:10.1097/FPC.0b013e32833d3acb. https://pubmed.ncbi.nlm.nih.gov/20625347/
5. Illés, Anett, Pikó, Henriett, Árvai, Kristóf, Lakatos, Péter, Beke, Artúr. 2024. Screening of premature ovarian insufficiency associated genes in Hungarian patients with next generation sequencing. In BMC medical genomics, 17, 98. doi:10.1186/s12920-024-01873-z. https://pubmed.ncbi.nlm.nih.gov/38649916/
6. Duan, Qing Ling, Nikpoor, Borzoo, Dube, Marie-Pierre, Adam, Albert, Rouleau, Guy A. 2005. A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitors. In American journal of human genetics, 77, 617-26. doi:. https://pubmed.ncbi.nlm.nih.gov/16175507/
7. Jedidi, Ines, Ouchari, Mouna, Yin, Qinan. 2018. Sex chromosomes-linked single-gene disorders involved in human infertility. In European journal of medical genetics, 62, 103560. doi:10.1016/j.ejmg.2018.10.012. https://pubmed.ncbi.nlm.nih.gov/31402110/
8. Prueitt, R L, Ross, J L, Zinn, A R. . Physical mapping of nine Xq translocation breakpoints and identification of XPNPEP2 as a premature ovarian failure candidate gene. In Cytogenetics and cell genetics, 89, 44-50. doi:. https://pubmed.ncbi.nlm.nih.gov/10894934/
9. Sprinkle, T J, Stone, A A, Venema, R C, Caldwell, C, Ryan, J W. . Assignment of the membrane-bound human aminopeptidase P gene (XPNPEP2) to chromosome Xq25. In Genomics, 50, 114-6. doi:. https://pubmed.ncbi.nlm.nih.gov/9628831/