1. Liang, Chunyang, Wang, Yibing, Murota, Yukiko, Siomi, Mikiko C, Liu, Qinghua. 2015. TAF11 Assembles the RISC Loading Complex to Enhance RNAi Efficiency. In Molecular cell, 59, 807-18. doi:10.1016/j.molcel.2015.07.006. https://pubmed.ncbi.nlm.nih.gov/26257286/
2. Robinson, M M, Yatherajam, G, Ranallo, R T, Paule, M R, Stargell, L A. . Mapping and functional characterization of the TAF11 interaction with TFIIA. In Molecular and cellular biology, 25, 945-57. doi:. https://pubmed.ncbi.nlm.nih.gov/15657423/
3. Gupta, Kapil, Watson, Aleksandra A, Baptista, Tiago, Tora, Làszlò, Berger, Imre. 2017. Architecture of TAF11/TAF13/TBP complex suggests novel regulation properties of general transcription factor TFIID. In eLife, 6, . doi:10.7554/eLife.30395. https://pubmed.ncbi.nlm.nih.gov/29111974/
4. Tremblay, Deanna C, Alexander, Graham, Moseley, Shawn, Chadwick, Brian P. 2010. Expression, tandem repeat copy number variation and stability of four macrosatellite arrays in the human genome. In BMC genomics, 11, 632. doi:10.1186/1471-2164-11-632. https://pubmed.ncbi.nlm.nih.gov/21078170/
5. Liu, Muqiu, Jiang, Zhihao, Liu, Min, Du, Qun, Dong, Yan. 2024. SLAMF1 as a novel molecule mediating the causal association between rheumatoid arthritis and interstitial lung disease: A Mendelian randomization study combined with transcriptomics and in vivo validation. In International immunopharmacology, 142, 113082. doi:10.1016/j.intimp.2024.113082. https://pubmed.ncbi.nlm.nih.gov/39260308/
6. Tawamie, Hasan, Martianov, Igor, Wohlfahrt, Natalie, Colombo, Roberto, Abou Jamra, Rami. . Hypomorphic Pathogenic Variants in TAF13 Are Associated with Autosomal-Recessive Intellectual Disability and Microcephaly. In American journal of human genetics, 100, 555-561. doi:10.1016/j.ajhg.2017.01.032. https://pubmed.ncbi.nlm.nih.gov/28257693/
7. Balog, Judit, Miller, Dan, Sanchez-Curtailles, Elena, Tapscott, Stephen J, van der Maarel, Silvère M. 2011. Epigenetic regulation of the X-chromosomal macrosatellite repeat encoding for the cancer/testis gene CT47. In European journal of human genetics : EJHG, 20, 185-91. doi:10.1038/ejhg.2011.150. https://pubmed.ncbi.nlm.nih.gov/21811308/