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Proceedings of the National Academy of Sciences of the United States of America|April 10, 2007
Network of coregulated spliceosome components revealed by zebrafish mutant in recycling factor p110Nikolaus S Trede, Jan Medenbach, Andrey Damianov, et al.The Journal of Biological Chemistry|August 16, 2017
Reductions in the mitochondrial ABC transporter Abcb10 affect the transcriptional profile of heme biosynthesis genesAlexandra Seguin, Naoko Takahashi-Makise, Yvette Y Yien, et al.The Journal of Clinical Investigation|July 8, 2020
Mutations in the iron-sulfur cluster biogenesis protein HSCB cause congenital sideroblastic anemiaAndrew Crispin, Chaoshe Guo, Caiyong Chen, et al.Genome Research|May 5, 2012
Mutation mapping and identification by whole-genome sequencingIgnaty Leshchiner, Kristen Alexa, Peter Kelsey, et al.Nature|August 20, 2005
Deficiency of glutaredoxin 5 reveals Fe-S clusters are required for vertebrate haem synthesisRebecca A Wingert, Jenna L Galloway, Bruce Barut, et al.Developmental Biology|September 11, 2012
Teleost growth factor independence (gfi) genes differentially regulate successive waves of hematopoiesisJeffrey D Cooney, Gordon J Hildick-Smith, Ebrahim Shafizadeh, et al.The Journal of Biological Chemistry|June 11, 2020
The mitochondrial metal transporters mitoferrin1 and mitoferrin2 are required for liver regeneration and cell proliferation in miceAlexandra Seguin, Xuan Jia, Aubree M Earl, et al.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.Pageof 8