1. Chen, Xue, Wang, Xiaoguang, Jiang, Chao, Sheng, Xunlun, Zhao, Chen. . IFT52 as a Novel Candidate for Ciliopathies Involving Retinal Degeneration. In Investigative ophthalmology & visual science, 59, 4581-4589. doi:10.1167/iovs.17-23351. https://pubmed.ncbi.nlm.nih.gov/30242358/
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3. Ishida, Yamato, Tasaki, Koshi, Katoh, Yohei, Nakayama, Kazuhisa. 2022. Molecular basis underlying the ciliary defects caused by IFT52 variations found in skeletal ciliopathies. In Molecular biology of the cell, 33, ar83. doi:10.1091/mbc.E22-05-0188. https://pubmed.ncbi.nlm.nih.gov/35704471/
4. Dupont, Marie Alice, Humbert, Camille, Huber, Céline, Saunier, Sophie, Delous, Marion. . Human IFT52 mutations uncover a novel role for the protein in microtubule dynamics and centrosome cohesion. In Human molecular genetics, 28, 2720-2737. doi:10.1093/hmg/ddz091. https://pubmed.ncbi.nlm.nih.gov/31042281/
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7. Lucker, Ben F, Miller, Mark S, Dziedzic, Slawomir A, Blackmarr, Philip T, Cole, Douglas G. 2010. Direct interactions of intraflagellar transport complex B proteins IFT88, IFT52, and IFT46. In The Journal of biological chemistry, 285, 21508-18. doi:10.1074/jbc.M110.106997. https://pubmed.ncbi.nlm.nih.gov/20435895/
8. Udupa, Prajna, Shrikondawar, Akshaykumar Nanaji, Ranjan, Akash, Ghosh, Debasish Kumar. 2023. Assessing type I collagen expression and quality in cellular models of osteogenesis imperfecta. In Clinical genetics, 105, 329-334. doi:10.1111/cge.14463. https://pubmed.ncbi.nlm.nih.gov/38014644/
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