Comparing the two leading erythroid lines BEL-A and HUDEP-2 von Daniels, Deborah E., Downes, Damien J., Ferrer-Vicens, Ivan, Ferguson, Daniel C. J., Singleton, Belinda K., Wilson, Marieangela C., Trakarnsanga, Kongtana, Kurita, Ryo, Nakamura, Yukio, Anstee, David J., Frayne, Jan

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Erratum to: Comparing the two leading erythroid lines BEL-A and HUDEP-2 von Daniels, Deborah E, Downes, Damien J, Ferrer-Vicens, Ivan, Ferguson, Daniel C J, Singleton, Belinda K, Wilson, Marieangela C, Trakarnsanga, Kongtana, Kurita, Ryo, Nakamura, Yukio, Anstee, David J, Frayne, Jan

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Disruption of the tumour-associated EMP3 enhances erythroid proliferation and causes the MAM-negative phenotype von Thornton, Nicole, Karamatic Crew, Vanja, Tilley, Louise, Green, Carole A., Tay, Chwen Ling, Griffiths, Rebecca E., Singleton, Belinda K., Spring, Frances, Walser, Piers, Alattar, Abdul Ghani, Jones, Benjamin, Laundy, Rosalind, Storry, Jill R., Möller, Mattias, Wall, Lorna, Charlewood, Richard, Westhoff, Connie M., Lomas-Francis, Christine, Yahalom, Vered, Feick, Ute, Seltsam, Axel, Mayer, Beate, Olsson, Martin L., Anstee, David J.

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Induction of adult levels of β-globin in human erythroid cells that intrinsically express embryonic or fetal globin by transduction with KLF1 and BCL11A-XL von Trakarnsanga, Kongtana, Wilson, Marieangela C, Lau, Winnie, Singleton, Belinda K, Parsons, Steve F, Sakuntanaga, Punthita, Kurita, Ryo, Nakamura, Yukio, Anstee, David J, Frayne, Jan

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Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype von Singleton, Belinda K., Burton, Nicholas M., Green, Carole, Brady, R.Leo, Anstee, David J.

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Characterization and evolutionary origin of novel C2H2 zinc finger protein (ZNF648) required for both erythroid and megakaryocyte differentiation in humans von Ferguson, Daniel C.J., Mokim, Juraidah Haji, Meinders, Marjolein, Moody, Edmund R.R., Williams, Tom A., Cooke, Sarah, Trakarnsanga, Kongtana, Daniels, Deborah E., Ferrer-Vicens, Ivan, Shoemark, Deborah, Tipgomut, Chartsiam, Macinnes, Katherine A., Wilson, Marieangela C., Singleton, Belinda K., Frayne, Jan

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Mutations in the second zinc finger of human EKLF reduce promoter affinity but give rise to benign and disease phenotypes von Singleton, Belinda K., Lau, Winnie, Fairweather, Victoria S.S., Burton, Nicholas M., Wilson, Marieangela C., Parsons, Steve F., Richardson, Ben M., Trakarnsanga, Kongtana, Brady, R. Leo, Anstee, David J., Frayne, Jan

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Blood group type A secretors are associated with a higher risk of COVID‐19 cardiovascular disease complications von Mankelow, Tosti J., Singleton, Belinda K., Moura, Pedro L., Stevens‐Hernandez, Christian J., Cogan, Nicola M., Gyorffy, Gyongyver, Kupzig, Sabine, Nichols, Luned, Asby, Claire, Pooley, Jennifer, Ruffino, Gabriella, Hosseini, Faroakh, Moghaddas, Fiona, Attwood, Marie, Noel, Alan, Cooper, Alex, Arnold, David T., Hamilton, Fergus, Hyams, Catherine, Finn, Adam, Toye, Ashley M., Anstee, David J.

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Autophagy facilitates organelle clearance during differentiation of human erythroblasts: Evidence for a role for ATG4 paralogs during autophagosome maturation von Betin, Virginie M.S., Singleton, Belinda K., Parsons, Stephen F., Anstee, David J., Lane, Jon D.

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Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach von Waye, John S, Riemer, Cathy, Gallivan, Monica V E, Kollia, Panagoula, Galanello, Renzo, Perseu, Lucia, Anstee, David J, Faustino, Paula, Harteveld, Cornelis L, Hoyer, James D, Peterson, Kenneth R, Giordano, Piero C, Stojiljkovic, Maja, Schrijver, Iris, Thein, Swee Lay, Gibbons, Richard J, Jarvis, Martin, Hardison, Ross C, Maglott, Donna, Francina, Alain, Borg, Joseph, Wada, Takahito, Basak, A Nazli, Giardine, Belinda, Pavlovic, Sonja, Costa, Flavia C, Papadopoulos, Petros, Old, John, Philipsen, Sjaak, Menzel, Stephan, Higgs, Douglas R, Radmilovic, Milena, Wajcman, Henri, Patrinos, George P, Fedosyuk, Halyna, Georgitsi, Marianthi, Traeger-Synodinos, Jan, Papadakis, Manoussos N, Joly, Philippe, Papachatzopoulou, Adamantia, Tully, Ray, Miller, Webb, Zukic, Branka, Felice, Alex E, Kanavakis, Emmanuel, Singleton, Belinda K, Wiemann, Claudia, Moradkhani, Kamran, Satta, Stefania, Clark, Barnaby, Chui, David H K

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Blood group phenotypes resulting from mutations in erythroid transcription factors von Singleton, Belinda K, Frayne, Jan, Anstee, David J

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A novel GATA1 mutation (Stop414Arg) in a family with the rare X‐linked blood group Lu(a‐b‐) phenotype and mild macrothrombocytic thrombocytopenia von Singleton, Belinda K., Roxby, David J., Stirling, John W., Spring, Frances A., Wilson, Carolyn, Poole, Joyce, Anstee, David J.

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New mutations in C1GALT1C1 in individuals with Tn positive phenotype von Karamatic Crew, Vanja, Singleton, Belinda K., Green, Carole, Parsons, Stephen F., Daniels, Geoff, Anstee, David J.

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Clustered DNA damage leads to complex genetic changes in irradiated human cells von SINGLETON, Belinda K, GRIFFIN, Carol S, THACKER, John

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Characterization and evolutionary origin of novel C2H2 zinc finger protein (ZNF648) required for both erythroid and megakaryocyt differentiation in humans von Ferguson, Daniel C. J., Mokim, Juraidah Haji, Meinders, Marjolein, Moody, Edmund R. R., Williams, Tom A., Cooke, Sarah, Trakarnsanga, Kongtana, Daniels, Deborah E., Ferrer-Vicens, Ivan, Shoemark, Deborah, Tipgomut, Chartsiam, Macinnes, Katherine A., Wilson, Marieangela C., Singleton, Belinda K., Frayne, Jan

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McLeod syndrome resulting from a novel XK mutation von Singleton, Belinda K., Green, Carole A., Renaud, Susanne, Fuhr, Peter, Poole, Joyce, Daniels, Geoff L.

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Ex vivo Engineering of Red Blood Cells von Frayne, Jan, Daniels, Deborah E, Frayne, Jan, Satchwell, Timothy J, Hawksworth, Joseph, Singleton, Belinda K, Andrienko, Tatyana N, Wilson, Marieangela C, Kupzig, Sabine, Meinders, Marjolein, Kurita, Ryo, Nakamura, Yukio, Ferrer Vicens, Ivan, Griffiths, Rebecca, Cogan, Nicola, Trakarnsanga, Kongtana, Anstee, David J., Toye, Ashley Mark

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Characterization and evolutionary origin of novel C 2 H 2 zinc finger protein (ZNF648) required for both erythroid and megakaryocyte differentiation in humans von Ferguson, Daniel C J, Mokim, Juraidah Haji, Meinders, Marjolein, Moody, Edmund R R, Williams, Tom A, Cooke, Sarah, Trakarnsanga, Kongtana, Daniels, Deborah E, Ferrer-Vicens, Ivan, Shoemark, Deborah, Tipgomut, Chartsiam, Macinnes, Katherine A, Wilson, Marieangela C, Singleton, Belinda K, Frayne, Jan

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The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the Rh D-negative blood group phenotype von SINGLETON, B. K, GREEN, C. A, AVENT, N. D, MARTIN, P. G, SMART, E, DAKA, A, NARTER-OLAGA, E. G, HAWTHORNE, L. M, DANIELS, G

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A novel GATA 1 mutation ( S top414 A rg) in a family with the rare X ‐linked blood group L u(a‐b‐) phenotype and mild macrothrombocytic thrombocytopenia von Singleton, Belinda K., Roxby, David J., Stirling, John W., Spring, Frances A., Wilson, Carolyn, Poole, Joyce, Anstee, David J.

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