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Blood|August 5, 2016
A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemiaDaniel A Lichtenstein, Andrew W Crispin, Anoop K Sendamarai, et al.Science Signaling|April 16, 2015
The mTORC1/4E-BP pathway coordinates hemoglobin production with L-leucine availabilityJacky Chung, Daniel E Bauer, Alireza Ghamari, et al.Nature Genetics|June 30, 2009
Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type IIKlaus Schwarz, Achille Iolascon, Fatima Verissimo, et al.Blood|January 24, 2013
Glucose metabolism impacts the spatiotemporal onset and magnitude of HSC induction in vivoJames M Harris, Virginie Esain, Gregory M Frechette, et al.Nature|March 3, 2006
Mitoferrin is essential for erythroid iron assimilationGeorge C Shaw, John J Cope, Liangtao Li, et al.Elife|May 30, 2017
Erythropoietin signaling regulates heme biosynthesisJacky Chung, Johannes G Wittig, Alireza Ghamari, et al.Science (New York, N.Y.)|May 13, 2017
Restored iron transport by a small molecule promotes absorption and hemoglobinization in animalsAnthony S Grillo, Anna M SantaMaria, Martin D Kafina, et al.American Journal of Human Genetics|January 10, 2012
ABCB6 mutations cause ocular colobomaLejin Wang, Lejing Wang, Fei He, et al.Blood|September 20, 2015
Hematopoietic stem cells develop in the absence of endothelial cadherin 5 expressionHeidi Anderson, Taylor C Patch, Pavankumar N G Reddy, et al.Cell Metabolism|February 19, 2013
Snx3 regulates recycling of the transferrin receptor and iron assimilationCaiyong Chen, Daniel Garcia-Santos, Yuichi Ishikawa, et al.Pageof 8