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2. Floriot, Sandrine, Bellutti, Laura, Castille, Johan, Vilotte, Jean-Luc, Livera, Gabriel. 2022. CEP250 is Required for Maintaining Centrosome Cohesion in the Germline and Fertility in Male Mice. In Frontiers in cell and developmental biology, 9, 754054. doi:10.3389/fcell.2021.754054. https://pubmed.ncbi.nlm.nih.gov/35127699/
3. Kang, Minjin, Kim, Jung Ah, Song, Mee Hyun, Gee, Heon Yung, Jung, Jinsei. 2023. Novel Variant in CEP250 Causes Protein Mislocalization and Leads to Nonsyndromic Autosomal Recessive Type of Progressive Hearing Loss. In Cells, 12, . doi:10.3390/cells12182328. https://pubmed.ncbi.nlm.nih.gov/37759551/
4. Abu-Diab, Alaa, Gopalakrishnan, Prakadeeswari, Matsevich, Chen, Sharon, Dror, Khateb, Samer. . Homozygous Knockout of Cep250 Leads to a Relatively Late-Onset Retinal Degeneration and Sensorineural Hearing Loss in Mice. In Translational vision science & technology, 12, 3. doi:10.1167/tvst.12.3.3. https://pubmed.ncbi.nlm.nih.gov/36857066/
5. Chen, Chong, Rong, Yu, Zhuang, Youyuan, Qu, Jia, Liu, Xinting. 2023. RNA-Seq Analysis Reveals an Essential Role of the cGMP-PKG-MAPK Pathways in Retinal Degeneration Caused by Cep250 Deficiency. In International journal of molecular sciences, 24, . doi:10.3390/ijms24108843. https://pubmed.ncbi.nlm.nih.gov/37240188/
6. Zeng, Lu, Fan, Xiude, Wang, Xiaoyun, Han, Qunying, Liu, Zhengwen. 2020. Involvement of NEK2 and its interaction with NDC80 and CEP250 in hepatocellular carcinoma. In BMC medical genomics, 13, 158. doi:10.1186/s12920-020-00812-y. https://pubmed.ncbi.nlm.nih.gov/33109182/
7. Giordano, Guido, Cipolletta, Giampiero, Mellone, Agostino, Costa, Maria Claudia, Pancione, Massimo. 2024. Altered centriolar cohesion by CEP250 and appendages impact outcome of patients with pancreatic cancer. In Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 24, 899-908. doi:10.1016/j.pan.2024.06.010. https://pubmed.ncbi.nlm.nih.gov/38942662/
8. Xiang, Mingfei, Wang, Yu, Jiao, Yuying, Cao, Yunxia, Zhu, Fuxi. 2024. A homozygous loss-of-function mutation in CEP250 is associated with acephalic spermatozoa syndrome in humans. In Andrology, , . doi:10.1111/andr.13827. https://pubmed.ncbi.nlm.nih.gov/39726222/
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