References
- Westman JS, Benktander J, Storry JR, et al. Identification of the molecular and genetic basis of PX2, a glycosphingolipid blood group antigen lacking on globoside-deficient erythrocytes. J Biol Chem 2015;290:18505–18.
- Storry JR, Castilho L, Chen Q, et al. International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Terminology: report of the Seoul and London meetings. ISBT Sci Ser 2016;11:118–22.
- Storry JR, Banch Clausen F, Castilho L, et al. International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Terminology: report of the Dubai, Copenhagen and Toronto meetings. Vox Sang, in press (Epub ahead of print 12 Nov 2018, doi: 10.1111/vox.12717).
- Teneberg S, Lönnroth I, Torres Lopez JF, et al. Molecular mimicry in the recognition of glycosphingolipids by Gal alpha 3 Gal beta 4 GlcNAc beta-binding Clostridium difficile toxin A, human natural anti alpha-galactosyl IgG and the monoclonal antibody Gal-13: characterization of a binding-active human glycosphingolipid, non-identical with the animal receptor. Glycobiology 1996;6:599–609.
- Toivonen S, Aitio O, Renkonen O. Alpha 2,3-sialylation of terminal GalNAc beta 1-3Gal determinants by ST3Gal II reveals the multifunctionality of the enzyme. The resulting Neu5Ac alpha 2-3GalNAc linkage is resistant to sialidases from Newcastle disease virus and Streptococcus pneumoniae. J Biol Chem 2001;276:37141–8.
- Möller M, Jöud M, Storry JR, Olsson ML. Erythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project. Blood Adv 2016;1:240–9.
- Westman JS, Hellberg Å, Peyrard T, et al. P1/P2 genotyping of known and novel null alleles in the P1PK and GLOB histo-blood group systems. Transfusion 2013;53(11 Suppl 2):2928– 39.
- Hellberg Å, Westman JS, Olsson ML. An update on the GLOB blood group system and collection. Immunohematology 2013;29:19–24.
- Ricci Hagman J, Hult AK, Westman JS, et al. Multiple miscarriages in two sisters of Thai origin with the rare Pk phenotype caused by a novel nonsense mutation at the B3GALNT1 locus. Transfus Med, in press (Epub ahead of print 6 June 2018, doi: 10.1111/tme.12544).