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HAX1 deletion impairs BCR internalization and leads to delayed BCR-mediated apoptosis
Cellular & Molecular Immunology Open Access 13 April 2015
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Dong F, Dale DC, Bonilla MA, Freedman M, Fasth A, Neijens HJ et al. Mutations in the granulocyte colony-stimulating factor receptor gene in patients with severe congenital neutropenia. Leukemia 1997; 11: 120–125.
Druhan LJ, Ai J, Massullo P, Kindwall-Keller T, Ranalli MA, Avalos BR . Novel mechanism of G-CSF refractoriness in patients with severe congenital neutropenia. Blood 2005; 105: 584–591.
Freedman MH, Bonilla MA, Fier C, Bolyard AA, Scarlata D, Boxer LA et al. Myelodysplasia syndrome and acute myeloid leukemia in patients with congenital neutropenia receiving G-CSF therapy. Blood 2000; 96: 429–436.
Dale DC, Person RE, Bolyard AA, Aprikyan AG, Bos C, Bonilla MA et al. Mutation in the gene encoding neutrophil elastase in congenital and cyclic neutropenia. Blood 2000; 96: 2317–2322.
Cassinat B, Bellanne-Chantelot C, Notz-Carrere A, Menot ML, Vaury C, Micheau M et al. Screening for G-CSF receptor mutations in patients with secondary myeloid or lymphoid transformation of severe congenital neutropenia. A report from the French Neutropenia Register. Leukemia 2004; 18: 1553–1555.
Germeshausen M, Ballmaier M, Schulze H, Welte K, Flohr T, Beiske K et al. Granulocyte colony-stimulating factor receptor mutations in a patient with acute lymphoblastic leukemia secondary to severe congenital neutropenia. Blood 2001; 97: 829–831.
Poncz M, Solowiejczyk D, Harpel B, Mory Y, Schwartz E, Surrey S . Construction of human gene libraries from small amounts of peripheral blood. Analysis of beta-like globin. Hemoglobin 1982; 6: 27–36.
Bellanne-Chantelot C, Clauin S, Leblanc T, Cassinat B, Rodrigues-Lima F, Beaufils S et al. Mutations in the ELA2 gene correlate with more severe expression of neutropenia: a study of 81 patients from French Neutropenia Register. Blood 2004; 103: 4119–4125.
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Yetgin, S., Germeshausen, M., Touw, I. et al. Acute lymphoblastic leukemia in a patient with congenital neutropenia without G-CSF-R and ELA2 mutations. Leukemia 19, 1710–1711 (2005). https://doi.org/10.1038/sj.leu.2403850
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DOI: https://doi.org/10.1038/sj.leu.2403850
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