1. Song, Tianyu, Zhao, Shuang, Luo, Shanshan, Xie, Liping, Ji, Yong. 2024. SLC44A2 regulates vascular smooth muscle cell phenotypic switching and aortic aneurysm. In The Journal of clinical investigation, 134, . doi:10.1172/JCI173690. https://pubmed.ncbi.nlm.nih.gov/38916960/
2. Tilburg, Julia, Adili, Reheman, Nair, Thankam S, Maracle, Chrissta X, Holinstat, Michael. 2018. Characterization of hemostasis in mice lacking the novel thrombosis susceptibility gene Slc44a2. In Thrombosis research, 171, 155-159. doi:10.1016/j.thromres.2018.09.057. https://pubmed.ncbi.nlm.nih.gov/30312801/
3. Koehl, Bérengère, Vrignaud, Cédric, Mikdar, Mahmoud, Azouzi, Slim, Peyrard, Thierry. 2023. Lack of the human choline transporter-like protein SLC44A2 causes hearing impairment and a rare red blood phenotype. In EMBO molecular medicine, 15, e16320. doi:10.15252/emmm.202216320. https://pubmed.ncbi.nlm.nih.gov/36695047/
4. Zirka, Gaïa, Robert, Philippe, Tilburg, Julia, Morange, Pierre-Emmanuel, Thomas, Grace M. . Impaired adhesion of neutrophils expressing Slc44a2/HNA-3b to VWF protects against NETosis under venous shear rates. In Blood, 137, 2256-2266. doi:10.1182/blood.2020008345. https://pubmed.ncbi.nlm.nih.gov/33556175/
5. Wang, Yufeng, Chen, Xihui, Chen, Qi, Wu, Yuanming, Wang, Li. 2022. SLC44A2 Frequency, a New TaqMan Real-Time Polymerase Chain Reaction Method for HNA-3A/3B Genotyping, and a New Application of Droplet Digital PCR. In Frontiers in genetics, 13, 794285. doi:10.3389/fgene.2022.794285. https://pubmed.ncbi.nlm.nih.gov/35646052/
6. Tilburg, Julia, Coenen, Daniëlle M, Zirka, Gaia, Maracle, Chrissta X, Thomas, Grace M. 2020. SLC44A2 deficient mice have a reduced response in stenosis but not in hypercoagulability driven venous thrombosis. In Journal of thrombosis and haemostasis : JTH, 18, 1714-1727. doi:10.1111/jth.14835. https://pubmed.ncbi.nlm.nih.gov/32297475/
7. Nair, Thankam S, Kommareddi, Pavan K, Galano, Maria M, Elder, James T, Carey, Thomas E. 2016. SLC44A2 single nucleotide polymorphisms, isoforms, and expression: Association with severity of Meniere's disease? In Genomics, 108, 201-208. doi:10.1016/j.ygeno.2016.11.002. https://pubmed.ncbi.nlm.nih.gov/27829169/
8. Chen, Qing, Srivastava, Kshitij, Ardinski, Stefanie C, Schmid, Pirmin, Flegel, Willy A. 2015. Full-length nucleotide sequences of 30 common SLC44A2 alleles encoding human neutrophil antigen-3. In Transfusion, 56, 729-36. doi:10.1111/trf.13300. https://pubmed.ncbi.nlm.nih.gov/26437811/
9. Huvard, Michael J, Schmid, Pirmin, Stroncek, David F, Flegel, Willy A. 2011. Frequencies of SLC44A2 alleles encoding human neutrophil antigen-3 variants in the African American population. In Transfusion, 52, 1106-11. doi:10.1111/j.1537-2995.2011.03396.x. https://pubmed.ncbi.nlm.nih.gov/22040064/
10. Zhi, Liqiang, Feng, Weilou, Liang, Jingqi, Ma, Jianbing, Yao, Shuxin. 2020. The Effect of Common Variants in SLC44A2 on the Contribution to the Risk of Deep Cein Thrombosis after Orthopedic Surgery. In Journal of atherosclerosis and thrombosis, 28, 293-303. doi:10.5551/jat.56333. https://pubmed.ncbi.nlm.nih.gov/32581188/
智鼠故事 
