Cep135-KO 基因敲除小鼠

1. Yang, Guangrun, Zhou, Jiafu, Guo, Zhong, Zhang, Dapeng, Wen, Haitao. 2023. miR-26b Targets CEP135 Gene to Regulate Nasopharyngeal Carcinoma Proliferation and Migration by NF-κB Pathway. In Molecular biotechnology, 65, 1857-1868. doi:10.1007/s12033-023-00691-5. https://pubmed.ncbi.nlm.nih.gov/36820950/

2. Shaheen, Ranad, Maddirevula, Sateesh, Ewida, Nour, Walsh, Christopher, Alkuraya, Fowzan S. 2018. Genomic and phenotypic delineation of congenital microcephaly. In Genetics in medicine : official journal of the American College of Medical Genetics, 21, 545-552. doi:10.1038/s41436-018-0140-3. https://pubmed.ncbi.nlm.nih.gov/30214071/

3. Inanç, Burcu, Pütz, Monika, Lalor, Pierce, Gergely, Fanni, Morrison, Ciaran G. 2013. Abnormal centrosomal structure and duplication in Cep135-deficient vertebrate cells. In Molecular biology of the cell, 24, 2645-54. doi:10.1091/mbc.E13-03-0149. https://pubmed.ncbi.nlm.nih.gov/23864714/

4. Derkac, Irmante, Januleviciene, Ingrida, Sepetiene, Ramune, Valiauga, Rasa, Velickiene, Dzilda. 2018. The Association of CEP135 rs4865047 and NPY2R rs1902491 Single Nucleotide Polymorphisms (SNPs) with Rapid Progression of Proliferative Diabetic Retinopathy in Patients with Type 1 Diabetes Mellitus. In Medical science monitor : international medical journal of experimental and clinical research, 24, 8891-8898. doi:10.12659/MSM.909803. https://pubmed.ncbi.nlm.nih.gov/30531682/

5. Sha, Yan-Wei, Xu, Xiaohui, Mei, Li-Bin, He, Xiao-Qin, Li, Lin. 2017. A homozygous CEP135 mutation is associated with multiple morphological abnormalities of the sperm flagella (MMAF). In Gene, 633, 48-53. doi:10.1016/j.gene.2017.08.033. https://pubmed.ncbi.nlm.nih.gov/28866084/

6. Nerakh, Gayatri, Mounika, K, Geeta, K, Nalluri, Hima Bindu. 2021. CEP135 associated primary microcephaly-A rare presentation in early second trimester. In European journal of medical genetics, 64, 104233. doi:10.1016/j.ejmg.2021.104233. https://pubmed.ncbi.nlm.nih.gov/33933664/

7. Hussain, Muhammad Sajid, Baig, Shahid Mahmood, Neumann, Sascha, Noegel, Angelika Anna, Nürnberg, Peter. 2012. A truncating mutation of CEP135 causes primary microcephaly and disturbed centrosomal function. In American journal of human genetics, 90, 871-8. doi:10.1016/j.ajhg.2012.03.016. https://pubmed.ncbi.nlm.nih.gov/22521416/

8. Mkrtchyan, Garik V, Veviorskiy, Alexander, Izumchenko, Evgeny, Zhavoronkov, Alex, Scheibye-Knudsen, Morten. 2022. High-confidence cancer patient stratification through multiomics investigation of DNA repair disorders. In Cell death & disease, 13, 999. doi:10.1038/s41419-022-05437-w. https://pubmed.ncbi.nlm.nih.gov/36435816/

9. Bayless, Brian A, Giddings, Thomas H, Winey, Mark, Pearson, Chad G. 2012. Bld10/Cep135 stabilizes basal bodies to resist cilia-generated forces. In Molecular biology of the cell, 23, 4820-32. doi:10.1091/mbc.E12-08-0577. https://pubmed.ncbi.nlm.nih.gov/23115304/

10. Rasool, Sajida, Baig, Jamshaid Mahmood, Moawia, Abubakar, Nürnberg, Peter, Hussain, Muhammad Sajid. 2020. An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan. In Molecular genetics & genomic medicine, 8, e1408. doi:10.1002/mgg3.1408. https://pubmed.ncbi.nlm.nih.gov/32677750/