1. Trębińska-Stryjewska, Alicja, Wakula, Maciej, Chmielarczyk, Mateusz, Grzybowska, Ewa A. 2023. HAX1: A versatile, intrinsically disordered regulatory protein. In Biochimica et biophysica acta. Molecular cell research, 1870, 119538. doi:10.1016/j.bbamcr.2023.119538. https://pubmed.ncbi.nlm.nih.gov/37454914/
2. Skokowa, Julia, Dale, David C, Touw, Ivo P, Zeidler, Cornelia, Welte, Karl. 2017. Severe congenital neutropenias. In Nature reviews. Disease primers, 3, 17032. doi:10.1038/nrdp.2017.32. https://pubmed.ncbi.nlm.nih.gov/28593997/
3. Jin, Huilin, Huang, Xiaoling, Pan, Qihao, Meng, Xiangqi, Lee, Mong-Hong. 2024. The EIF3H-HAX1 axis increases RAF-MEK-ERK signaling activity to promote colorectal cancer progression. In Nature communications, 15, 2551. doi:10.1038/s41467-024-46521-3. https://pubmed.ncbi.nlm.nih.gov/38514606/
4. Pittermann, Erik, Lachmann, Nico, MacLean, Glenn, Cantz, Tobias, Klusmann, Jan-Henning. 2017. Gene correction of HAX1 reversed Kostmann disease phenotype in patient-specific induced pluripotent stem cells. In Blood advances, 1, 903-914. doi:10.1182/bloodadvances.2016003798. https://pubmed.ncbi.nlm.nih.gov/29296734/
5. Pisani, Cinzia, Onori, Annalisa, Gabanella, Francesca, Passananti, Claudio, Corbi, Nicoletta. 2021. Identification of protein/mRNA network involving the PSORS1 locus gene CCHCR1 and the PSORS4 locus gene HAX1. In Experimental cell research, 399, 112471. doi:10.1016/j.yexcr.2021.112471. https://pubmed.ncbi.nlm.nih.gov/33417922/
6. Balcerak, Anna, Macech-Klicka, Ewelina, Wakula, Maciej, Kudla, Grzegorz, Grzybowska, Ewa A. 2022. The RNA-Binding Landscape of HAX1 Protein Indicates Its Involvement in Translation and Ribosome Assembly. In Cells, 11, . doi:10.3390/cells11192943. https://pubmed.ncbi.nlm.nih.gov/36230905/
7. Doll, Larissa, Aghaallaei, Narges, Dick, Advaita M, Skokowa, Julia, Bajoghli, Baubak. 2021. A zebrafish model for HAX1-associated congenital neutropenia. In Haematologica, 106, 1311-1320. doi:10.3324/haematol.2019.240200. https://pubmed.ncbi.nlm.nih.gov/32327498/