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From stem cell to red cell: regulation of erythropoiesis at multiple levels by multiple proteins, RNAs, and chromatin modifications
Abstract
This article reviews the regulation of production of RBCs at several levels. We focus on the regulated expansion of burst-forming unit-erythroid erythroid progenitors by glucocorticoids and other factors that occur during chronic anemia, inflammation, and other conditions of stress. We also highlight the rapid production of RBCs by the coordinated regulation of terminal proliferation and differentiation of committed erythroid colony-forming unit-erythroid progenitors by external signals, such as erythropoietin and adhesion to a fibronectin matrix. We discuss the complex intracellular networks of coordinated gene regulation by transcription factors, chromatin modifiers, and miRNAs that regulate the different stages of erythropoiesis.
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Hematopoietic lineage specification is mediated by the activation of lineage-specific transcription regulators, such as PU.1 and GATA-1.
“Hematopoietic lineage specification is mediated by the activation of lineage-specific transcription regulators, such as PU.1 and GATA-1 (5, 52–54).”
From Histone deacetylase 1 activates PU.1 gene transcription through regulating TAF9 deacetylation and transcription factor IID assembly (2017) · cites this paper as [52]
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Sapolsky, R. M., Romero, L. M., & Munck, A. U. (2000) · Endocrine Reviews · doi:10.1210/edrv.21.1.0389 · Cited by 7,541
High-Resolution Profiling of Histone Methylations in the Human Genome
Barski, A., Cuddapah, S., Cui, K., Roh, T.-Y., Schones, D. E., Wang, Z., Wei, G., Chepelev, I., & Zhao, K. (2007) · Cell · doi:10.1016/j.cell.2007.05.009 · Cited by 6,845
A bivalent chromatin structure marks key developmental genes in embryonic stem cells
Bernstein, B. E., Mikkelsen, T. S., Xie, X., Kamal, M., Huebert, D. J., Cuff, J., Fry, B., Meissner, A., Wernig, M., Plath, K., et al. (2006) · Cell · doi:10.1016/j.cell.2006.02.041 · Cited by 5,361
DNA binding of the glucocorticoid receptor is not essential for survival
Reichardt, H. M., Kaestner, K. H., Tuckermann, J., Kretz, O., Wessely, O., Bock, R., Gass, P., Schmid, W., Herrlich, P., Angel, P., et al. (1998) · Cell · doi:10.1016/s0092-8674(00)81183-6 · Cited by 1,068
Mouse development and cell proliferation in the absence of D-cyclins
Kozar, K., Ciemerych, M. A., Rebel, V. I., Shigematsu, H., Zagozdzon, A., Sicinska, E., Geng, Y., Yu, Q., Bhattacharya, S., Bronson, R. T., et al. (2004) · Cell · doi:10.1016/j.cell.2004.07.025 · Cited by 647
Transcription factors in myeloid development: balancing differentiation with transformation
Rosenbauer, F., & Tenen, D. G. (2007) · Nature Reviews Immunology · doi:10.1038/nri2024 · Cited by 606
Wall, L., deBoer, E., & Grosveld, F. (1988) · Genes & Development · doi:10.1101/gad.2.9.1089 · Cited by 350
The genome-wide dynamics of the binding of Ldb1 complexes during erythroid differentiation
Soler, E., Andrieu-Soler, C., de Boer, E., Bryne, J. C., Thongjuea, S., Stadhouders, R., Palstra, R.-J., Stevens, M., Kockx, C., van IJcken, W., et al. (2010) · Genes & Development · doi:10.1101/gad.551810 · Cited by 245
Pop, R., Shearstone, J. R., Shen, Q., Liu, Y., Hallstrom, K., Koulnis, M., Gribnau, J., & Socolovsky, M. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000484 · Cited by 179
Rb intrinsically promotes erythropoiesis by coupling cell cycle exit with mitochondrial biogenesis
Sankaran, V. G., Orkin, & Walkley, C. R. (2008) · Genes & Development · doi:10.1101/gad.1627208 · Cited by 133
Dynamics of the epigenetic landscape during erythroid differentiation after GATA1 restoration
Wu, W., Cheng, Y., Keller, C. A., Ernst, J., Kumar, S. A., Mishra, T., Morrissey, C., Dorman, C. M., Chen, K.-B., Drautz, D., et al. (2011) · Genome Research · doi:10.1101/gr.125088.111 · Cited by 118
Flagged first, then by citations
Research works printed but not linked: 106
- Palis, 1999, Development of erythroid and myeloid progenitors in the yolk sac and embryo proper of the mouse., Development, 126, 5073, 10.1242/dev.126.22.5073 · DOI
- Elliott, 2008, Erythropoietins: a common mechanism of action., Exp Hematol, 36, 1573, 10.1016/j.exphem.2008.08.003 · DOI
- Fawcett, 1997, Bloom & Fawcett: Concise Histology
- Molineux, 2009, Erythropoiesis and Erythropoietins
- Dolznig, 2006, Erythroid progenitor renewal versus differentiation: genetic evidence for cell autonomous, essential functions of EpoR, Stat5 and the GR., Oncogene, 25, 2890, 10.1038/sj.onc.1209308 · DOI
- Wu, 1995, Generation of committed erythroid BFU-E and CFU-E progenitors does not require erythropoietin or the erythropoietin receptor., Cell, 83, 59, 10.1016/0092-8674(95)90234-1 · DOI
- Kieran, 1996, Thrombopoietin rescues in vitro erythroid colony formation from mouse embryos lacking the erythropoietin receptor., Proc Natl Acad Sci U S A, 93, 9126, 10.1073/pnas.93.17.9126 · DOI
- Lin, 1996, Differential effects of an erythropoietin receptor gene disruption on primitive and definitive erythropoiesis., Genes Dev, 10, 154, 10.1101/gad.10.2.154 · DOI
- Zhang, 2003, Role of Ras signaling in erythroid differentiation of mouse fetal liver cells: functional analysis by a flow cytometry-based novel culture system., Blood, 102, 3938, 10.1182/blood-2003-05-1479 · DOI
- Eshghi, 2007, Alpha4beta1 integrin and erythropoietin mediate temporally distinct steps in erythropoiesis: integrins in red cell development., J Cell Biol, 177, 871, 10.1083/jcb.200702080 · DOI
- Lodish, 2009, Signaling by the erythropoietin receptor., 155, 10.1007/978-3-7643-8698-6_10 · DOI
- Ghaffari, 2006, AKT induces erythroid-cell maturation of JAK2-deficient fetal liver progenitor cells and is required for Epo regulation of erythroid-cell differentiation., Blood, 107, 1888, 10.1182/blood-2005-06-2304 · DOI
- Zhang, 2007, Endogenous K-ras signaling in erythroid differentiation., Cell Cycle, 6, 1970, 10.4161/cc.6.16.4577 · DOI
- Socolovsky, 2001, Ineffective erythropoiesis in Stat5a(−/−)5b(−/−) mice due to decreased survival of early erythroblasts., Blood, 98, 3261, 10.1182/blood.V98.12.3261 · DOI
- Socolovsky, 1999, Fetal anemia and apoptosis of red cell progenitors in Stat5a−/−5b−/− mice: a direct role for Stat5 in Bcl-X(L) induction., Cell, 98, 181, 10.1016/S0092-8674(00)81013-2 · DOI
- Wood, 2009, ID1 promotes expansion and survival of primary erythroid cells and is a target of JAK2V617F-STAT5 signaling., Blood, 114, 1820, 10.1182/blood-2009-02-206573 · DOI
- Zhu, 2008, Hematopoietic-specific Stat5-null mice display microcytic hypochromic anemia associated with reduced transferrin receptor gene expression., Blood, 112, 2071, 10.1182/blood-2007-12-127480 · DOI
- Sathyanarayana, 2008, EPO receptor circuits for primary erythroblast survival., Blood, 111, 5390, 10.1182/blood-2007-10-119743 · DOI
- Cantor, 2002, Transcriptional regulation of erythropoiesis: an affair involving multiple partners., Oncogene, 21, 3368, 10.1038/sj.onc.1205326 · DOI
- Kerenyi, 2010, Networking erythropoiesis., J Exp Med, 207, 2537, 10.1084/jem.20102260 · DOI · Paper page
- Bauer, 2011, Update on fetal hemoglobin gene regulation in hemoglobinopathies., Curr Opin Pediatr, 23, 1, 10.1097/MOP.0b013e3283420fd0 · DOI
- Gilliland, 2004, The molecular basis of leukemia., Hematology Am Soc Hematol Educ Program, 80, 10.1182/asheducation-2004.1.80 · DOI
- Tijssen, 2011, Genome-wide analysis of simultaneous GATA1/2, RUNX1, FLI1, and SCL binding in megakaryocytes identifies hematopoietic regulators., Dev Cell, 20, 597, 10.1016/j.devcel.2011.04.008 · DOI
- Bresnick, 2005, Developmental control via GATA factor interplay at chromatin domains., J Cell Physiol, 205, 1, 10.1002/jcp.20393 · DOI
- Fujiwara, 2009, Discovering hematopoietic mechanisms through genome-wide analysis of GATA factor chromatin occupancy., Mol Cell, 36, 667, 10.1016/j.molcel.2009.11.001 · DOI
- Yu, 2009, Insights into GATA-1-mediated gene activation versus repression via genome-wide chromatin occupancy analysis., Mol Cell, 36, 682, 10.1016/j.molcel.2009.11.002 · DOI
- Heintzman, 2007, The gateway to transcription: identifying, characterizing and understanding promoters in the eukaryotic genome., Cell Mol Life Sci, 64, 386, 10.1007/s00018-006-6295-0 · DOI
- Cui, 2009, Chromatin signatures in multipotent human hematopoietic stem cells indicate the fate of bivalent genes during differentiation., Cell Stem Cell, 4, 80, 10.1016/j.stem.2008.11.011 · DOI
- Cheng, 2009, Erythroid GATA1 function revealed by genome-wide analysis of transcription factor occupancy, histone modifications, and mRNA expression., Genome Res, 19, 2172, 10.1101/gr.098921.109 · DOI · Paper page
- Kassouf, 2010, Genome-wide identification of TAL1's functional targets: insights into its mechanisms of action in primary erythroid cells., Genome Res, 20, 1064, 10.1101/gr.104935.110 · DOI
- Tripic, 2009, SCL and associated proteins distinguish active from repressive GATA transcription factor complexes., Blood, 113, 2191, 10.1182/blood-2008-07-169417 · DOI
- Miller, 1993, A novel, erythroid cell-specific murine transcription factor that binds to the CACCC element and is related to the Kruppel family of nuclear proteins., Mol Cell Biol, 13, 2776, 10.1128/MCB.13.5.2776 · DOI
- Tallack, 2010, A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cells., Genome Res, 20, 1052, 10.1101/gr.106575.110 · DOI
- Jackson, 1993, Visualization of focal sites of transcription within human nuclei., EMBO J, 12, 1059, 10.1002/j.1460-2075.1993.tb05747.x · DOI
- Schoenfelder, 2010, Preferential associations between co-regulated genes reveal a transcriptional interactome in erythroid cells., Nat Genet, 42, 53, 10.1038/ng.496 · DOI
- Capron, 2011, LYL-1 deficiency induces a stress erythropoiesis., Exp Hematol, 39, 629, 10.1016/j.exphem.2011.02.014 · DOI
- Maeda, 2009, LRF is an essential downstream target of GATA1 in erythroid development and regulates BIM-dependent apoptosis., Dev Cell, 17, 527, 10.1016/j.devcel.2009.09.005 · DOI
- Guenther, 2007, A chromatin landmark and transcription initiation at most promoters in human cells., Cell, 130, 77, 10.1016/j.cell.2007.05.042 · DOI
- Muse, 2007, RNA polymerase is poised for activation across the genome., Nat Genet, 39, 1507, 10.1038/ng.2007.21 · DOI
- Zeitlinger, 2007, RNA polymerase stalling at developmental control genes in the Drosophila melanogaster embryo., Nat Genet, 39, 1512, 10.1038/ng.2007.26 · DOI
- Sawado, 2003, The beta-globin locus control region (LCR) functions primarily by enhancing the transition from transcription initiation to elongation., Genes Dev, 17, 1009, 10.1101/gad.1072303 · DOI
- Monteiro, 2011, The gata1/pu.1 lineage fate paradigm varies between blood populations and is modulated by tif1gamma., EMBO J, 30, 1093, 10.1038/emboj.2011.34 · DOI
- Bai, 2010, TIF1gamma controls erythroid cell fate by regulating transcription elongation., Cell, 142, 133, 10.1016/j.cell.2010.05.028 · DOI
- Suganuma, 2011, Signals and combinatorial functions of histone modifications., Annu Rev Biochem, 80, 473, 10.1146/annurev-biochem-061809-175347 · DOI
- Talbert, 2010, Histone variants: ancient wrap artists of the epigenome., Nat Rev Mol Cell Biol, 11, 264, 10.1038/nrm2861 · DOI
- Schubeler, 2004, The histone modification pattern of active genes revealed through genome-wide chromatin analysis of a higher eukaryote., Genes Dev, 18, 1263, 10.1101/gad.1198204 · DOI
- Feng, 2010, Early mammalian erythropoiesis requires the Dot1L methyltransferase., Blood, 116, 4483, 10.1182/blood-2010-03-276501 · DOI
- Orford, 2008, Differential H3K4 methylation identifies developmentally poised hematopoietic genes., Dev Cell, 14, 798, 10.1016/j.devcel.2008.04.002 · DOI
- Wong, 2011, Gene induction and repression during terminal erythropoiesis are mediated by distinct epigenetic changes., Blood, 118, e128, 10.1182/blood-2011-03-341404 · DOI · Paper page
- Kinross, 2006, E2f4 regulates fetal erythropoiesis through the promotion of cellular proliferation., Blood, 108, 886, 10.1182/blood-2005-09-008656 · DOI
- Sankaran, 2010, Advances in the understanding of haemoglobin switching., Br J Haematol, 149, 181, 10.1111/j.1365-2141.2010.08105.x · DOI
- Muir, 1958, Erythropoiesis: an electron microscopical study., Q J Exp Physiol Cogn Med Sci, 43, 106
- Ji, 2011, Formation of mammalian erythrocytes: chromatin condensation and enucleation., Trends Cell Biol, 21, 409, 10.1016/j.tcb.2011.04.003 · DOI
- Palis, 2010, Primitive erythropoiesis in the mammalian embryo., Int J Dev Biol, 54, 1011, 10.1387/ijdb.093056jp · DOI
- Jayapal, 2010, Down-regulation of Myc is essential for terminal erythroid maturation., J Biol Chem, 285, 40252, 10.1074/jbc.M110.181073 · DOI
- Fujieda, 2005, A putative role for histone deacetylase in the differentiation of human erythroid cells., Int J Oncol, 27, 743
- Popova, 2009, Chromatin condensation in terminally differentiating mouse erythroblasts does not involve special architectural proteins but depends on histone deacetylation., Chromosome Res, 17, 47, 10.1007/s10577-008-9005-y · DOI
- Ji, 2010, Histone deacetylase 2 is required for chromatin condensation and subsequent enucleation of cultured mouse fetal erythroblasts., Haematologica, 95, 2013, 10.3324/haematol.2010.029827 · DOI
- Bartel, 2009, MicroRNAs: target recognition and regulatory functions., Cell, 136, 215, 10.1016/j.cell.2009.01.002 · DOI · Paper page
- Guo, 2010, Mammalian microRNAs predominantly act to decrease target mRNA levels., Nature, 466, 835, 10.1038/nature09267 · DOI · Paper page
- Lu, 2008, MicroRNA-mediated control of cell fate in megakaryocyte-erythrocyte progenitors., Dev Cell, 14, 843, 10.1016/j.devcel.2008.03.012 · DOI · Paper page
- Felli, 2005, MicroRNAs 221 and 222 inhibit normal erythropoiesis and erythroleukemic cell growth via kit receptor down-modulation., Proc Natl Acad Sci U S A, 102, 18081, 10.1073/pnas.0506216102 · DOI · Paper page
- Wang, 2008, MicroRNA miR-24 inhibits erythropoiesis by targeting activin type I receptor ALK4., Blood, 111, 588, 10.1182/blood-2007-05-092718 · DOI
- Felli, 2009, MicroRNA 223-dependent expression of LMO2 regulates normal erythropoiesis., Haematologica, 94, 479, 10.3324/haematol.2008.002345 · DOI
- Dore, 2008, A GATA-1-regulated microRNA locus essential for erythropoiesis., Proc Natl Acad Sci U S A, 105, 3333, 10.1073/pnas.0712312105 · DOI · Paper page
- Pase, 2009, miR-451 regulates zebrafish erythroid maturation in vivo via its target gata2., Blood, 113, 1794, 10.1182/blood-2008-05-155812 · DOI
- Fu, 2009, Mir-144 selectively regulates embryonic alpha-hemoglobin synthesis during primitive erythropoiesis., Blood, 113, 1340, 10.1182/blood-2008-08-174854 · DOI
- Patrick, 2010, Defective erythroid differentiation in miR-451 mutant mice mediated by 14-3-3zeta., Genes Dev, 24, 1614, 10.1101/gad.1942810 · DOI
- Rasmussen, 2010, The miR-144/451 locus is required for erythroid homeostasis., J Exp Med, 207, 1351, 10.1084/jem.20100458 · DOI · Paper page
- Yu, 2010, miR-451 protects against erythroid oxidant stress by repressing 14-3-3zeta., Genes Dev, 24, 1620, 10.1101/gad.1942110 · DOI
- Sankaran, 2011, MicroRNA-15a and -16-1 act via MYB to elevate fetal hemoglobin expression in human trisomy 13., Proc Natl Acad Sci U S A, 108, 1519, 10.1073/pnas.1018384108 · DOI
- Zhang, 2011, miR-191 regulates mouse erythroblast enucleation by down-regulating Riok3 and Mxi1., Genes Dev, 25, 119, 10.1101/gad.1998711 · DOI
- Huarte, 2010, A large intergenic noncoding RNA induced by p53 mediates global gene repression in the p53 response., Cell, 142, 409, 10.1016/j.cell.2010.06.040 · DOI · Paper page
- Loewer, 2010, Large intergenic non-coding RNA-RoR modulates reprogramming of human induced pluripotent stem cells., Nat Genet, 42, 1113, 10.1038/ng.710 · DOI
- Harandi, 2010, Murine erythroid short-term radioprotection requires a BMP4-dependent, self-renewing population of stress erythroid progenitors., J Clin Invest, 120, 4507, 10.1172/JCI41291 · DOI
- McCulloch, 1964, Spleen-colony formation in anemic mice of genotype Ww., Science, 144, 844, 10.1126/science.144.3620.844 · DOI
- Hara, 1976, Erthropoietic precursors in mice with phenylhydrazine-induced anemia., Am J Hematol, 1, 453, 10.1002/ajh.2830010410 · DOI
- Kreja, 1985, On the role of the spleen in Friend virus (F-MuLV-P) erythroleukemia., Exp Hematol, 13, 623
- Slaper-Cortenbach, 1987, Different stimulative effects of human bone marrow and fetal liver stromal cells on erythropoiesis in long-term culture., Blood, 69, 135, 10.1182/blood.V69.1.135.bloodjournal691135 · DOI
- Yanai, 1989, Spleen stromal cell lines selectively support erythroid colony formation., Blood, 74, 2391, 10.1182/blood.V74.7.2391.2391 · DOI
- Ohneda, 1990, Microenvironment created by stromal cells is essential for a rapid expansion of erythroid cells in mouse fetal liver., Development, 110, 379, 10.1242/dev.110.2.379 · DOI
- Flygare, 2007, Diamond-Blackfan anemia: erythropoiesis lost in translation., Blood, 109, 3152, 10.1182/blood-2006-09-001222 · DOI
- Vlachos, 2008, Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference., Br J Haematol, 142, 859, 10.1111/j.1365-2141.2008.07269.x · DOI
- Bauer, 1999, The glucocorticoid receptor is required for stress erythropoiesis., Genes Dev, 13, 2996, 10.1101/gad.13.22.2996 · DOI
- Ganguli, 2002, The p53 tumour suppressor inhibits glucocorticoid-induced proliferation of erythroid progenitors., EMBO Rep, 3, 569, 10.1093/embo-reports/kvf114 · DOI
- von Lindern, 1999, The glucocorticoid receptor cooperates with the erythropoietin receptor and c-Kit to enhance and sustain proliferation of erythroid progenitors in vitro., Blood, 94, 550, 10.1182/blood.V94.2.550 · DOI
- Flygare, 2011, HIF-1alpha synergizes with glucocorticoids to promote BFU-E progenitor self-renewal., Blood, 117, 3435, 10.1182/blood-2010-07-295550 · DOI
- Kolbus, 2003, Cooperative signaling between cytokine receptors and the glucocorticoid receptor in the expansion of erythroid progenitors: molecular analysis by expression profiling., Blood, 102, 3136, 10.1182/blood-2003-03-0923 · DOI
- Wessely, 1997, The glucocorticoid receptor is a key regulator of the decision between self-renewal and differentiation in erythroid progenitors., EMBO J, 16, 267, 10.1093/emboj/16.2.267 · DOI
- Chou, 2010, Fetal liver hepatic progenitors are supportive stromal cells for hematopoietic stem cells., Proc Natl Acad Sci U S A, 107, 7799, 10.1073/pnas.1003586107 · DOI
- Broudy, 1996, Interaction of stem cell factor and its receptor c-kit mediates lodgment and acute expansion of hematopoietic cells in the murine spleen., Blood, 88, 75, 10.1182/blood.V88.1.75.75 · DOI
- Huddleston, 2003, Functional p85alpha gene is required for normal murine fetal erythropoiesis., Blood, 102, 142, 10.1182/blood-2002-10-3245 · DOI
- Bakker, 2007, Differential regulation of Foxo3a target genes in erythropoiesis., Mol Cell Biol, 27, 3839, 10.1128/MCB.01662-06 · DOI
- Munugalavadla, 2005, Repression of c-kit and its downstream substrates by GATA-1 inhibits cell proliferation during erythroid maturation., Mol Cell Biol, 25, 6747, 10.1128/MCB.25.15.6747-6759.2005 · DOI
- Hegde, 2007, An intronic sequence mutated in flexed-tail mice regulates splicing of Smad5., Mamm Genome, 18, 852, 10.1007/s00335-007-9074-9 · DOI
- Lenox, 2005, BMP4 and Madh5 regulate the erythroid response to acute anemia., Blood, 105, 2741, 10.1182/blood-2004-02-0703 · DOI
- Subramanian, 2008, Friend virus utilizes the BMP4-dependent stress erythropoiesis pathway to induce erythroleukemia., J Virol, 82, 382, 10.1128/JVI.02487-06 · DOI
- Singbrant, 2010, Canonical BMP signaling is dispensable for hematopoietic stem cell function in both adult and fetal liver hematopoiesis, but essential to preserve colon architecture., Blood, 115, 4689, 10.1182/blood-2009-05-220988 · DOI
- Singbrant, 2006, Smad5 is dispensable for adult murine hematopoiesis., Blood, 108, 3707, 10.1182/blood-2006-02-003384 · DOI
- Wu, 2010, Hypoxia regulates BMP4 expression in the murine spleen during the recovery from acute anemia., PLoS One, 5, e11303, 10.1371/journal.pone.0011303 · DOI
- Millot, 2010, Erythropoietin stimulates spleen BMP4-dependent stress erythropoiesis and partially corrects anemia in a mouse model of generalized inflammation., Blood, 116, 6072, 10.1182/blood-2010-04-281840 · DOI
- Perry, 2009, Maintenance of the BMP4-dependent stress erythropoiesis pathway in the murine spleen requires hedgehog signaling., Blood, 113, 911, 10.1182/blood-2008-03-147892 · DOI
- Lugus, 2007, GATA2 functions at multiple steps in hemangioblast development and differentiation., Development, 134, 393, 10.1242/dev.02731 · DOI
- Fuchs, 2002, Inhibition of Smad5 in human hematopoietic progenitors blocks erythroid differentiation induced by BMP4., Blood Cells Mol Dis, 28, 221, 10.1006/bcmd.2002.0487 · DOI
- Perry, 2007, BMP4, SCF, and hypoxia cooperatively regulate the expansion of murine stress erythroid progenitors., Blood, 109, 4494, 10.1182/blood-2006-04-016154 · DOI
- Sankaran, 2010, Reversing the hemoglobin switch., N Engl J Med, 363, 2258, 10.1056/NEJMcibr1010767 · DOI
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Metadata
- Authors
- Hattangadi, S. M., Wong, P., Zhang, L., Flygare, J., & Lodish, H. F.
- Affiliations
- Whitehead Institute for Biomedical Research, Cambridge, MA;
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2011-12-08
- Volume
- 118
- Issue
- 24
- Pages
- 6258-6268
- ISSN
- 0006-4971
- 1528-0020
- Cited by
- 423
- References
- 11
- Language
- en
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