1. Kalayinia, Samira, Mahdavi, Mohammad, Houshmand, Golnaz, Pourirahim, Maryam, Maleki, Majid. 2022. Novel homozygous stop-gain pathogenic variant of PPP1R13L gene leads to arrhythmogenic cardiomyopathy. In BMC cardiovascular disorders, 22, 359. doi:10.1186/s12872-022-02802-7. https://pubmed.ncbi.nlm.nih.gov/35933355/
2. Yin, Jiaoyang, Wang, Chunhong, Vogel, Ulla, Sun, Zhenxiang, Du, Shuai. 2023. Common variants of pro-inflammatory gene IL1B and interactions with PPP1R13L and POLR1G in relation to lung cancer among Northeast Chinese. In Scientific reports, 13, 7352. doi:10.1038/s41598-023-34069-z. https://pubmed.ncbi.nlm.nih.gov/37147350/
3. Robinson, H K, Zaklyazminskaya, E, Povolotskaya, I, Turner, C L, Ellard, S. 2020. Biallelic variants in PPP1R13L cause paediatric dilated cardiomyopathy. In Clinical genetics, 98, 331-340. doi:10.1111/cge.13812. https://pubmed.ncbi.nlm.nih.gov/32666529/
4. Zhang, Hongchao, Zhang, Guopei, Zhang, Jingyue, Yang, Jinghua, Lu, Xiaobo. 2022. Transcription factor SP1 and oncoprotein PPP1R13L regulate nicotine-induced epithelial-mesenchymal transition in lung adenocarcinoma via a feedback loop. In Biochemical pharmacology, 206, 115344. doi:10.1016/j.bcp.2022.115344. https://pubmed.ncbi.nlm.nih.gov/36372331/
5. Falik-Zaccai, Tzipora C, Barsheshet, Yiftah, Mandel, Hanna, Bitterman-Deutsch, Ora, Avni, Orly. . Sequence variation in PPP1R13L results in a novel form of cardio-cutaneous syndrome. In EMBO molecular medicine, 9, 319-336. doi:10.15252/emmm.201606523. https://pubmed.ncbi.nlm.nih.gov/28069640/
6. Laska, Magdalena J, Vogel, Ulla B, Jensen, Uffe B, Nexø, Bjørn A. 2010. p53 and PPP1R13L (alias iASPP or RAI) form a feedback loop to regulate genotoxic stress responses. In Biochimica et biophysica acta, 1800, 1231-40. doi:10.1016/j.bbagen.2010.09.002. https://pubmed.ncbi.nlm.nih.gov/20840860/
7. Toonen, Joseph, Liang, Lina, Sidjanin, Duska J. 2012. Waved with open eyelids 2 (woe2) is a novel spontaneous mouse mutation in the protein phosphatase 1, regulatory (inhibitor) subunit 13 like (Ppp1r13l) gene. In BMC genetics, 13, 76. doi:10.1186/1471-2156-13-76. https://pubmed.ncbi.nlm.nih.gov/22928477/
8. Coudert, Alicia, Thevenon, Julien, Testard, Quentin, Coutton, Charles, Le Tanno, Pauline. 2024. An Extended Phenotype of PPP1R13L Cardiocutaneous Syndrome. In American journal of medical genetics. Part A, , e63932. doi:10.1002/ajmg.a.63932. https://pubmed.ncbi.nlm.nih.gov/39579152/
智鼠故事 
