1. Tuysuz, Beyhan, Uludag Alkaya, Dilek, Geyik, Filiz, Vural, Mehmet, Bilguvar, Kaya. 2022. Biallelic frameshift variants in PHLDB1 cause mild-type osteogenesis imperfecta with regressive spondylometaphyseal changes. In Journal of medical genetics, 60, 819-826. doi:10.1136/jmg-2022-108763. https://pubmed.ncbi.nlm.nih.gov/36543534/
2. Wiley, Mandi M, Khatri, Bhuwan, Joachims, Michelle L, Nordmark, Gunnel, Lessard, Christopher J. 2023. Variants in the DDX6-CXCR5 autoimmune disease risk locus influence the regulatory network in immune cells and salivary gland. In bioRxiv : the preprint server for biology, , . doi:10.1101/2023.10.05.561076. https://pubmed.ncbi.nlm.nih.gov/39071447/
3. Kim, Lyoung Hyo, Kim, Jeong-Hyun, Namgoong, Suhg, Chang, Jong Hee, Shin, Hyoung Doo. 2019. A PHLDB1 variant associated with the nonfunctional pituitary adenoma. In Journal of neuro-oncology, 142, 223-229. doi:10.1007/s11060-018-03082-y. https://pubmed.ncbi.nlm.nih.gov/30868356/
4. Wei, Ying, Wang, Xiaolin, Zhang, Zhe, Cao, Hongxin, Zhao, Xinhan. . Role of Polymorphisms of FAM13A, PHLDB1, and CYP24A1 in Breast Cancer Risk. In Current molecular medicine, 19, 579-588. doi:10.2174/1566524019666190619125109. https://pubmed.ncbi.nlm.nih.gov/31215377/
5. Zhou, Qiong L, Jiang, Zhen Y, Mabardy, Allan S, Chawla, Anil, Czech, Michael P. 2010. A novel pleckstrin homology domain-containing protein enhances insulin-stimulated Akt phosphorylation and GLUT4 translocation in adipocytes. In The Journal of biological chemistry, 285, 27581-9. doi:10.1074/jbc.M110.146886. https://pubmed.ncbi.nlm.nih.gov/20587420/
6. Baskin, Rebekah, Woods, Nicholas T, Mendoza-Fandiño, Gustavo, Egan, Kathleen M, Monteiro, Alvaro N A. 2015. Functional analysis of the 11q23.3 glioma susceptibility locus implicates PHLDB1 and DDX6 in glioma susceptibility. In Scientific reports, 5, 17367. doi:10.1038/srep17367. https://pubmed.ncbi.nlm.nih.gov/26610392/
7. Yang, Bo, Heng, Liang, Du, Shuli, Lang, Hongjun, Li, Shanqu. 2015. Association between RTEL1, PHLDB1, and TREH Polymorphisms and Glioblastoma Risk: A Case-Control Study. In Medical science monitor : international medical journal of experimental and clinical research, 21, 1983-8. doi:10.12659/MSM.893723. https://pubmed.ncbi.nlm.nih.gov/26156397/
8. Feng, Yuan, Su, Yan, Ma, Chunyang, Li, Wenning, Wei, Jiali. 2019. 3'UTR variants of TNS3, PHLDB1, NTN4, and GNG2 genes are associated with IgA nephropathy risk in Chinese Han population. In International immunopharmacology, 71, 295-300. doi:10.1016/j.intimp.2019.03.041. https://pubmed.ncbi.nlm.nih.gov/30928649/
9. Alentorn, Agusti, Labussière, Marianne, Sanson, Marc, Hoang-Xuan, Khê, Idbaih, Ahmed. 2012. [Genetics and brain gliomas]. In Presse medicale (Paris, France : 1983), 42, 806-13. doi:10.1016/j.lpm.2012.05.013. https://pubmed.ncbi.nlm.nih.gov/22789312/
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