1. Zhang, Chunxia, Wang, Meng, Li, Yisi, Zhang, Yi. 2022. Profiling and functional characterization of maternal mRNA translation during mouse maternal-to-zygotic transition. In Science advances, 8, eabj3967. doi:10.1126/sciadv.abj3967. https://pubmed.ncbi.nlm.nih.gov/35108058/
2. Yucel, Esra, Karakus, Ibrahim Serhat, Krolo, Ana, Boztug, Kaan, Baris, Safa. 2020. Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis. In Journal of clinical immunology, 41, 59-65. doi:10.1007/s10875-020-00878-4. https://pubmed.ncbi.nlm.nih.gov/33025377/
3. Dotta, Laura, Baresi, Giulia, Tamassia, Nicola, Porta, Fulvio, Badolato, Raffaele. 2023. Clinical and transcriptomic characteristics of a novel SMARCD2 mutation that disrupts neutrophil maturation and function. In Pediatric blood & cancer, 70, e30671. doi:10.1002/pbc.30671. https://pubmed.ncbi.nlm.nih.gov/37712719/
4. Priam, Pierre, Krasteva, Veneta, Rousseau, Philippe, Sauvageau, Guy, Lessard, Julie A. 2017. SMARCD2 subunit of SWI/SNF chromatin-remodeling complexes mediates granulopoiesis through a CEBPɛ dependent mechanism. In Nature genetics, 49, 753-764. doi:10.1038/ng.3812. https://pubmed.ncbi.nlm.nih.gov/28369034/
5. Witzel, Maximilian, Petersheim, Daniel, Fan, Yanxin, Schäffer, Alejandro A, Klein, Christoph. 2017. Chromatin-remodeling factor SMARCD2 regulates transcriptional networks controlling differentiation of neutrophil granulocytes. In Nature genetics, 49, 742-752. doi:10.1038/ng.3833. https://pubmed.ncbi.nlm.nih.gov/28369036/
6. Kihtir, Zeynep, Çelik, Kıymet, Tayfun Küpesiz, Funda, Ceylaner, Gülay, Bingöl, Ayşen. . Specific Granule Deficiency Due To Novel Homozygote SMARCD2 Variant. In Pediatric allergy, immunology, and pulmonology, 35, 43-46. doi:10.1089/ped.2021.0070. https://pubmed.ncbi.nlm.nih.gov/35320004/
7. Schim van der Loeff, Ina, Sprenkeler, Evelien G G, Tool, Anton T J, Kuijpers, Taco W, Hambleton, Sophie. 2020. Defective neutrophil development and specific granule deficiency caused by a homozygous splice-site mutation in SMARCD2. In The Journal of allergy and clinical immunology, 147, 2381-2385.e2. doi:10.1016/j.jaci.2020.11.025. https://pubmed.ncbi.nlm.nih.gov/33279574/
8. Ibrahim, Abukhiran, Sharathkumar, Anjali, McLaughlin, Heather, Claassen, David, Bhagavathi, Sharathkumar. 2022. Congenital Neutropenia with Specific Granulocyte Deficiency Caused by Novel Double Heterozygous SMARCD2 Mutations. In Hematology reports, 14, 270-275. doi:10.3390/hematolrep14030038. https://pubmed.ncbi.nlm.nih.gov/36135322/
智鼠故事 
