Comparing the two leading erythroid lines BEL-A and HUDEP-2
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
Published in Haematologica (Roma) (01.08.2020)
Published in Haematologica (Roma) (01.08.2020)
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Erratum to: Comparing the two leading erythroid lines BEL-A and HUDEP-2
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
Published in Haematologica (Roma) (01.01.2024)
Published in Haematologica (Roma) (01.01.2024)
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Disruption of the tumour-associated EMP3 enhances erythroid proliferation and causes the MAM-negative phenotype
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.
Published in Nature communications (16.07.2020)
Published in Nature communications (16.07.2020)
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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
Trakarnsanga, Kongtana, Wilson, Marieangela C, Lau, Winnie, Singleton, Belinda K, Parsons, Steve F, Sakuntanaga, Punthita, Kurita, Ryo, Nakamura, Yukio, Anstee, David J, Frayne, Jan
Published in Haematologica (Roma) (01.11.2014)
Published in Haematologica (Roma) (01.11.2014)
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Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype
Singleton, Belinda K., Burton, Nicholas M., Green, Carole, Brady, R.Leo, Anstee, David J.
Published in Blood (01.09.2008)
Published in Blood (01.09.2008)
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Characterization and evolutionary origin of novel C2H2 zinc finger protein (ZNF648) required for both erythroid and megakaryocyte differentiation in humans
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
Published in Haematologica (Roma) (01.11.2021)
Published in Haematologica (Roma) (01.11.2021)
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Mutations in the second zinc finger of human EKLF reduce promoter affinity but give rise to benign and disease phenotypes
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
Published in Blood (15.09.2011)
Published in Blood (15.09.2011)
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Blood group type A secretors are associated with a higher risk of COVID‐19 cardiovascular disease complications
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.
Published in EJHaem (01.05.2021)
Published in EJHaem (01.05.2021)
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Deletions in the MAL gene result in loss of Mal protein, defining the rare inherited AnWj-negative blood group phenotype
Tilley, Louise A., Karamatic Crew, Vanja, Mankelow, Tosti J., AlSubhi, Samah A., Jones, Benjamin, Borowski, Abigail, Yahalom, Vered, Finkel, Lilach, Singleton, Belinda K., Walser, Piers J., Toye, Ashley M., Satchwell, Timothy J., Thornton, Nicole M.
Published in Blood (16.08.2024)
Published in Blood (16.08.2024)
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Autophagy facilitates organelle clearance during differentiation of human erythroblasts: Evidence for a role for ATG4 paralogs during autophagosome maturation
Betin, Virginie M.S., Singleton, Belinda K., Parsons, Stephen F., Anstee, David J., Lane, Jon D.
Published in Autophagy (01.06.2013)
Published in Autophagy (01.06.2013)
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Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach
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
Published in Nature genetics (01.04.2011)
Published in Nature genetics (01.04.2011)
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Blood group phenotypes resulting from mutations in erythroid transcription factors
Singleton, Belinda K, Frayne, Jan, Anstee, David J
Published in Current opinion in hematology (01.11.2012)
Published in Current opinion in hematology (01.11.2012)
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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
Singleton, Belinda K., Roxby, David J., Stirling, John W., Spring, Frances A., Wilson, Carolyn, Poole, Joyce, Anstee, David J.
Published in British journal of haematology (01.04.2013)
Published in British journal of haematology (01.04.2013)
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New mutations in C1GALT1C1 in individuals with Tn positive phenotype
Karamatic Crew, Vanja, Singleton, Belinda K., Green, Carole, Parsons, Stephen F., Daniels, Geoff, Anstee, David J.
Published in British journal of haematology (01.08.2008)
Published in British journal of haematology (01.08.2008)
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Clustered DNA damage leads to complex genetic changes in irradiated human cells
SINGLETON, Belinda K, GRIFFIN, Carol S, THACKER, John
Published in Cancer research (Chicago, Ill.) (01.11.2002)
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Published in Cancer research (Chicago, Ill.) (01.11.2002)
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McLeod syndrome resulting from a novel XK mutation
Singleton, Belinda K., Green, Carole A., Renaud, Susanne, Fuhr, Peter, Poole, Joyce, Daniels, Geoff L.
Published in British journal of haematology (01.08.2003)
Published in British journal of haematology (01.08.2003)
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Combined immunodeficiency associated with increased apoptosis of lymphocytes and radiosensitivity of fibroblasts
PEAKE, J, WAUGH, A, MALAISE, E. P, FISCHER, A, HIVROZ, C, JEGGO, P. A, LE DEIST, F, PRIESTLEY, A, RIEUX-LAUCAT, F, FORAY, N, CAPULAS, E, SINGLETON, B. K, DE VILLARTAY, J.-P, CANT, A
Published in Cancer research (Chicago, Ill.) (15.07.1999)
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Published in Cancer research (Chicago, Ill.) (15.07.1999)
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Ex vivo Engineering of Red Blood Cells
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
Published in Blood (13.11.2019)
Published in Blood (13.11.2019)
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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
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
Published in Haematologica (Roma) (01.11.2021)
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Published in Haematologica (Roma) (01.11.2021)
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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
Singleton, Belinda K., Roxby, David J., Stirling, John W., Spring, Frances A., Wilson, Carolyn, Poole, Joyce, Anstee, David J.
Published in British journal of haematology (01.04.2013)
Published in British journal of haematology (01.04.2013)
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