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R24DK094746

Funded outputs count: 7
Funder award ID: R24DK094746
OpenAlex ID: G2604589674
Alternative start codon selection shapes mitochondrial function and rare human diseases
2025 · Jimmy Ly, Matteo Di Bernardo, et al. · Molecular Cell · 8
Mutations in the iron-sulfur cluster biogenesis protein HSCB cause congenital sideroblastic anemia
2020 · Andrew Crispin, Chaoshe Guo, et al. · Journal of Clinical Investigation · 32
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On-chip recapitulation of clinical bone marrow toxicities and patient-specific pathophysiology
2020 · David B. Chou, Viktoras Frismantas, et al. · Nature Biomedical Engineering · 295
Prognostic Mutations in Myelodysplastic Syndrome after Stem-Cell Transplantation
2017 · R. Coleman Lindsley, Wael Saber, et al. · New England Journal of Medicine · 772
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Physiologic Expression of Sf3b1 K700E Causes Impaired Erythropoiesis, Aberrant Splicing, and Sensitivity to Therapeutic Spliceosome Modulation
2016 · Esther A. Obeng, Ryan J. Chappell, et al. · Cancer Cell · 379
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Pediatric aplastic anemia and refractory cytopenia: A retrospective analysis assessing outcomes and histomorphologic predictors
2015 · Craig M. Forester, Sarah E. Sartain, et al. · American Journal of Hematology · 28
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Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity
2014 · M. Y. Zhang, S. B. Keel, et al. · Haematologica · 122
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