International Society of Blood Transfusion. Red Cell immunogenetics and blood group terminology. Available from https://www.isbtweb.org/isbt-working-parties/rcibgt.html. Accessed 18 February 2022.International Society of Blood TransfusionAvailable from https://www.isbtweb.org/isbt-working-parties/rcibgt.html. Accessed 18 February 2022.Search in Google Scholar
Kawabata K, Uchikawa M, Ohto H, et al. Anti-KANNO: a novel alloantibody against a red cell antigen of high frequency. Transfus Med Rev 2014;28:23–8.KawabataKUchikawaMOhtoHAnti-KANNO: a novel alloantibody against a red cell antigen of high frequency.2014;28:23–8.10.1016/j.tmrv.2013.12.00124485899Search in Google Scholar
Byrne KM, Mercado CMC, Nnabue TN, Paige TD, Flegel WA. Inhibition of blood group antibodies by soluble substances. Immunohematology 2019;35:19–22. PMID: 30908075. PMCID: PMC6436639.ByrneKMMercadoCMCNnabueTNPaigeTDFlegelWA.Inhibition of blood group antibodies by soluble substances.2019;35:19–22. PMID: 30908075. PMCID: PMC6436639.10.21307/immunohematology-2020-008Search in Google Scholar
Omae Y, Ito S, Takeuchi M, et al. Integrative genome analysis identified the KANNO blood group antigen as prion protein. Transfusion 2019;59:2429–35.OmaeYItoSTakeuchiMIntegrative genome analysis identified the KANNO blood group antigen as prion protein.2019;59:2429–35.10.1111/trf.1531931020675Search in Google Scholar
Miura T, Sasaki S, Toyama A, Takeuchi H. Copper reduction by the octapeptide repeat region of prion protein: pH dependence and implications in cellular copper uptake. Biochemistry 2005;44:8712–20.MiuraTSasakiSToyamaATakeuchiH.Copper reduction by the octapeptide repeat region of prion protein: pH dependence and implications in cellular copper uptake.2005;44:8712–20.10.1021/bi050178415952778Search in Google Scholar
Biljan I, Giachin G, Ilc G, Zhukov I, Plavec J, Legname G. Structural basis for the protective effect of the human prion protein carrying the dominant-negative E219K polymorphism. Biochem J 2012;446:243–51.BiljanIGiachinGIlcGZhukovIPlavecJLegnameG.Structural basis for the protective effect of the human prion protein carrying the dominant-negative E219K polymorphism.2012;446:243–51.10.1042/BJ2011194022676969Search in Google Scholar
Rudd PM, Endo T, Colominas C, et al. Glycosylation differences between the normal and pathogenic prion protein isoforms. Proc Natl Acad Sci U S A 1999;96:13044–9.RuddPMEndoTColominasCGlycosylation differences between the normal and pathogenic prion protein isoforms.1999;96:13044–9.10.1073/pnas.96.23.130442389710557270Search in Google Scholar
Kirshner KN, Yongye AB, Tschampel SM, et al. GLYCAM06: a generalizable biomolecular force field. Carbohydrates. J Comput Chem 2008;29:622–55.KirshnerKNYongyeABTschampelSMGLYCAM06: a generalizable biomolecular force field. Carbohydrates.2008;29:622–55.10.1002/jcc.20820442354717849372Search in Google Scholar
Jones B, Karamatic Crew V, Musa R, et al. The first evidence of the KANNO– phenotype and anti-KANNO in an individual of Indian origin [abstract]. Vox Sang 2018;113(Suppl 1):232.JonesBKaramaticCrew VMusaRThe first evidence of the KANNO– phenotype and anti-KANNO in an individual of Indian origin [abstract].2018;113(Suppl 1):232.Search in Google Scholar
Shibuya S, Higuchi J, Shin R-W, et al. Codon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob disease. Ann Neurol 1998;43:826–8.ShibuyaSHiguchiJShinR-WCodon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob disease.1998;43:826–8.10.1002/ana.4104306189629853Search in Google Scholar
George MR. Cartwright blood group system review. Immunohematology 2012;28:49–54.GeorgeMR.Cartwright blood group system review.2012;28:49–54.10.21307/immunohematology-2019-149Search in Google Scholar
Storry JR, Lomas-Francis C. The Cromer blood group system: an update. Immunohematology 2021;37:118–21.StorryJRLomas-FrancisC.The Cromer blood group system: an update.2021;37:118–21.10.21307/immunohematology-2021-01734591381Search in Google Scholar
Yuan Z, Wei Y, Chen X, et al. Anti-JMH alloantibody inherited JMH-negative patients leads to immunogenic destruction of JMH-positive RBCs. Clin Exp Immunol 2021;205:182–97YuanZWeiYChenXAnti-JMH alloantibody inherited JMH-negative patients leads to immunogenic destruction of JMH-positive RBCs.2021;205:182–97.10.1111/cei.13622827416334021913Search in Google Scholar
Lane WJ, Aeschlimann J, Vege S, et al. PIGG defines the EMM blood group system. Sci Rep 2021;11:18545.LaneWJAeschlimannJVegeSPIGG defines the EMM blood group system.2021;11:18545.10.1038/s41598-021-98090-w844872834535746Search in Google Scholar
Duval R, Nicolas G, Willemetz A, et al. Inherited glyco-sylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders. Blood 2021; 137:3660–9.DuvalRNicolasGWillemetzAInherited glyco-sylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders.2021;137:3660–9.10.1182/blood.202000981033763700Search in Google Scholar
Reid ME. The Dombrock blood group system: a review. Transfusion 2003;43:107–14.ReidME.The Dombrock blood group system: a review.2003;43:107–14.10.1046/j.1537-2995.2003.00283.x12519438Search in Google Scholar
Donadio S, Alfaidy N, De Keukeleire B, et al. Expression and localization of cellular prion and COMMD1 proteins in human placenta throughout pregnancy. Placenta 2007;28:907–11.DonadioSAlfaidyNDe KeukeleireBExpression and localization of cellular prion and COMMD1 proteins in human placenta throughout pregnancy.2007;28:907–11.10.1016/j.placenta.2006.11.00617254632Search in Google Scholar
Panigaj M, Brouckova A, Glierova H, et al. Underestimation of the expression of cellular prion protein on human red blood cells. Transfusion 2011;51:1012–21.PanigajMBrouckovaAGlierovaHUnderestimation of the expression of cellular prion protein on human red blood cells.2011;51:1012–21.10.1111/j.1537-2995.2010.02924.x21058954Search in Google Scholar
Reiten MR, Bakkebø MK, Brun-Hansen H, et al. Hematological shift in goat kids naturally devoid of prion protein. Front Cell Dev Biol 2015;3:44.ReitenMRBakkebøMKBrun-HansenHHematological shift in goat kids naturally devoid of prion protein.2015;3:44.10.3389/fcell.2015.00044449534026217662Search in Google Scholar
Salvesen Ø, Espenes A, Reiten MR, et al. Goats naturally devoid of PrPC are resistant to scrapie. Vet Res 2020;51:1.SalvesenØEspenesAReitenMRGoats naturally devoid of PrPC are resistant to scrapie.2020;51:1.10.1186/s13567-019-0731-2695462631924264Search in Google Scholar
Glier H, Simak J, Panigaj M, et al. Expression of the cellular prion protein affects posttransfusion recovery and survival of red blood cells in mice. Transfusion 2015;55:2590–6.GlierHSimakJPanigajMExpression of the cellular prion protein affects posttransfusion recovery and survival of red blood cells in mice.2015;55:2590–6.10.1111/trf.1319026033638Search in Google Scholar