1-8 of 8
Belinda K. Singleton
Close
Save search
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Journal Articles

Deletions in the MAL gene result in loss of Mal protein, defining the rare inherited AnWj-negative blood group phenotype

Louise A Tilley, Vanja Karamatic Crew, Tosti J Mankelow, Samah A AlSubhi, Benjamin Jones, Abigail Borowski, Vered Yahalom, Lilach Finkel, Belinda K Singleton, Piers J Walser, Ashley Mark Toye, Timothy J Satchwell, Nicole M Thornton
Journal: Blood
Blood blood.2024025099.
https://doi.org/10.1182/blood.2024025099
Published: 2024
Includes: Supplemental data
Journal Articles

Ex vivo Engineering of Red Blood Cells

Jan Frayne, BsC, PhD, Deborah E Daniels, Jan Frayne, BsC PhD, Timothy J Satchwell, PhD, Joseph Hawksworth, BSc PhD, Belinda K Singleton, Tatyana N Andrienko, PhD, Marieangela C Wilson, Sabine Kupzig, Marjolein Meinders, Ryo Kurita, PhD, Yukio Nakamura, MD PhD, Ivan Ferrer Vicens, PhD MSc, BSc, Rebecca Griffiths, PhD, Nicola Cogan, Kongtana Trakarnsanga, MD PhD, David J. Anstee, PhD FRCPath, Ashley Mark Toye, PhD
Journal: Blood
Blood (2019) 134 (Supplement_1): SCI-5.
https://doi.org/10.1182/blood-2019-121117
Published: 2019
Journal Articles

Mutations in the second zinc finger of human EKLF reduce promoter affinity but give rise to benign and disease phenotypes

Belinda K. Singleton, Winnie Lau, Victoria S. S. Fairweather, Nicholas M. Burton, Marieangela C. Wilson, Steve F. Parsons, Ben M. Richardson, Kongtana Trakarnsanga, R. Leo Brady, David J. Anstee, Jan Frayne
Journal: Blood
Blood (2011) 118 (11): 3137–3145.
https://doi.org/10.1182/blood-2011-04-349985
Published: 2011
Includes: Supplemental data
Journal Articles

A Novel EKLF Mutation in a Patient with Dyserythropoietic Anemia: The First Association of EKLF with Disease in Man.

Belinda K Singleton, Victoria SS Fairweather, Winnie Lau, Stephen F Parsons, Nicholas M Burton, Jan Frayne, R. Leo Brady, David J Anstee
Journal: Blood
Blood (2009) 114 (22): 162.
https://doi.org/10.1182/blood.V114.22.162.162
Published: 2009
Journal Articles

A Novel GATA1 Mutation (Ter414Arg) in a Family with the Rare X-Linked Blood Group Lu(a-b-) Phenotype.

Belinda K Singleton, David Roxby, John Stirling, Frances A Spring, Carolyn Wilson, Joyce Poole, David J Anstee
Journal: Blood
Blood (2009) 114 (22): 1979.
https://doi.org/10.1182/blood.V114.22.1979.1979
Published: 2009
Journal Articles

Mutations in EKLF / KLF1 form the molecular basis of the rare blood group In(Lu) phenotype

Belinda K. Singleton, Nicholas M. Burton, Carole Green, R. Leo Brady, David J. Anstee
Journal: Blood
Blood (2008) 112 (5): 2081–2088.
https://doi.org/10.1182/blood-2008-03-145672
Published: 2008
Includes: Supplemental data
Journal Articles

C1GALT1C1 ( COSMC ) Mutations in Four Individuals with Tn+ Phenotype.

Vanja Karamatic Crew, PhD, Carole Green, FIBMS, Stephen Parsons, PhD, Belinda K. Singleton, PhD, Geoff Daniels, PhD, David J. Anstee, PhD
Journal: Blood
Blood (2007) 110 (11): 1727.
https://doi.org/10.1182/blood.V110.11.1727.1727
Published: 2007
Journal Articles

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

Belinda K. Singleton, Carole A. Green, Neil D. Avent, Peter G. Martin, Elizabeth Smart, Abigail Daka, Edwin G. Narter-Olaga, Linda M. Hawthorne, Geoff Daniels
Journal: Blood
Blood (2000) 95 (1): 12–18.
https://doi.org/10.1182/blood.V95.1.12
Published: 2000