1. Cassetta, Luca, Fragkogianni, Stamatina, Sims, Andrew H, Smith, Harriet O, Pollard, Jeffrey W. 2019. Human Tumor-Associated Macrophage and Monocyte Transcriptional Landscapes Reveal Cancer-Specific Reprogramming, Biomarkers, and Therapeutic Targets. In Cancer cell, 35, 588-602.e10. doi:10.1016/j.ccell.2019.02.009. https://pubmed.ncbi.nlm.nih.gov/30930117/
2. Li, Sensen, Jiang, Longfeng, Yang, Yanbing, Deng, Xiaozhao, Li, Yaojun. 2020. Siglec1 enhances inflammation through miR-1260-dependent degradation of IκBα in COPD. In Experimental and molecular pathology, 113, 104398. doi:10.1016/j.yexmp.2020.104398. https://pubmed.ncbi.nlm.nih.gov/32007531/
3. Graf, Manuel, von Stuckrad, Sae Lim, Uruha, Akinori, Schneider, Udo, Rose, Thomas. . SIGLEC1 enables straightforward assessment of type I interferon activity in idiopathic inflammatory myopathies. In RMD open, 8, . doi:10.1136/rmdopen-2021-001934. https://pubmed.ncbi.nlm.nih.gov/35177553/
4. Prather, Randall S, Rowland, Raymond R R, Ewen, Catherine, Egen, Tina, Green, Jonathan A. 2013. An intact sialoadhesin (Sn/SIGLEC1/CD169) is not required for attachment/internalization of the porcine reproductive and respiratory syndrome virus. In Journal of virology, 87, 9538-46. doi:10.1128/JVI.00177-13. https://pubmed.ncbi.nlm.nih.gov/23785195/
5. Singh, Rohit, Choi, Beom K. 2019. Siglec1-expressing subcapsular sinus macrophages provide soil for melanoma lymph node metastasis. In eLife, 8, . doi:10.7554/eLife.48916. https://pubmed.ncbi.nlm.nih.gov/31872800/
6. Chen, Jia, Yang, Xichao, Huang, Yumin, Wu, Zhenbiao, Feng, Yuan. 2024. Knockdown of SIGLEC1 inhibits osteogenic differentiation to alleviate ankylosing spondylitis progression by suppressing the TGF-β1/SMAD signaling pathway. In Naunyn-Schmiedeberg's archives of pharmacology, , . doi:10.1007/s00210-024-03456-2. https://pubmed.ncbi.nlm.nih.gov/39305328/
7. Souza de Lima, Dhemerson, Nunes, Vinicius C L, Ogusku, Mauricio M, Pontillo, Alessandra, Alencar, Bruna de Cunha. 2017. Polymorphisms in SIGLEC1 contribute to susceptibility to pulmonary active tuberculosis possibly through the modulation of IL-1ß. In Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases, 55, 313-317. doi:10.1016/j.meegid.2017.09.031. https://pubmed.ncbi.nlm.nih.gov/28964857/
8. Gao, Qi, Yang, Yunlong, Luo, Yizhuo, Zheng, Zezhong, Zhang, Guihong. 2022. Adaptation of African swine fever virus to porcine kidney cells stably expressing CD163 and Siglec1. In Frontiers in immunology, 13, 1015224. doi:10.3389/fimmu.2022.1015224. https://pubmed.ncbi.nlm.nih.gov/36389805/
9. Rajagopala, Seesandra V, Strickland, Britton A, Pakala, Suman B, Turner, Justin H, Das, Suman R. 2023. Mucosal Gene Expression in Response to SARS-CoV-2 Is Associated with Viral Load. In Journal of virology, 97, e0147822. doi:10.1128/jvi.01478-22. https://pubmed.ncbi.nlm.nih.gov/36656015/
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