Olives B, Mattei MG, Huet M, et al. Kidd blood group and urea transport function of human erythrocytes are carried by the same protein. J Biol Chem 1995;270:15607–10.10.1074/jbc.270.26.156077797558Search in Google Scholar
Heaton DC, McLoughlin K. Jk(a-b-) red blood cells resist urea lysis. Transfusion 1982;22:70–1.10.1046/j.1537-2995.1982.22182154224.x7064211Search in Google Scholar
Edwards-Moulds J, Kasschau MR. The effect of 2 molar urea on Jk (a-b-) red cells. Vox Sang 1988;55:181–5.10.1111/j.1423-0410.1988.tb05089.x3238952Search in Google Scholar
Woodfield DG, Douglas R, Smith J, Simpson A, Pinder L, Staveley JM. The Jk(a-b-) phenotype in New Zealand Polynesians. Transfusion 1982;22:276–8.10.1046/j.1537-2995.1982.22482251206.x7101419Search in Google Scholar
Henry S, Woodfield G. Frequencies of the Jk(a-b-) phenotype in Polynesian ethnic groups (letter). Transfusion 1995;35:277.10.1046/j.1537-2995.1995.35395184290.x7878726Search in Google Scholar
Okubo Y, Tomita T, Nagao N, Yamaguchi H, Tanaka M. Mass screening donors for -D- and Jk (a-b-) using the Groupamatic-360 (letter). Transfusion 1983;23:362–3.10.1046/j.1537-2995.1983.23483276884.x6410555Search in Google Scholar
Sareneva H, Pirkola A, Sistonen S, Sistonen P. Exceptional high frequency of a gene for recessive JK blood group null phenotype among Finns. Abstract book from the 6th Regional Congress of the ISBT, Jerusalem, Israel, 1999;96.Search in Google Scholar
McDougall DC, McGregor M. Jk:-3 red cells have a defect in urea transport: a new urea-dependent lysis test (letter). Transfusion 1988;28:197–8 (published erratum appears in Transfusion 1988;28:585).10.1046/j.1537-2995.1988.28288179034.x3214487Search in Google Scholar
Olives B, Merriman M, Bailly P, et al. The molecular basis of the Kidd blood group polymorphism and its lack of association with type 1 diabetes susceptibility. Hum Mol Genet 1997;6:1017–20.10.1093/hmg/6.7.10179215669Search in Google Scholar
Okubo Y, Yamaguchi H, Nagao N, Tomita T, Seno T, Tanaka M. Heterogeneity of the phenotype Jk(a-b-) found in Japanese. Transfusion 1986;26:237–9.10.1046/j.1537-2995.1986.26386209377.x3705140Search in Google Scholar
Lucien N, Sidoux-Walter F, Olives B, et al. Characterization of the gene encoding the human Kidd blood group/urea transporter protein. Evidence for splice site mutations in Jknull individuals. J Biol Chem 1998;273:12973–80.10.1074/jbc.273.21.129739582331Search in Google Scholar
Irshaid NM, Henry SM, Olsson ML. Genomic characterization of the Kidd blood group gene: different molecular basis of the Jk(a-b-) phenotype in Polynesians and Finns. Transfusion 2000;40:69–74.10.1046/j.1537-2995.2000.40010069.x10644814Search in Google Scholar
Sidoux-Walter F, Lucien N, Nissinen R, et al. Molecular heterogeneity of the Jk(null) phenotype: expression analysis of the Jk(S291P) mutation found in Finns. Blood 2000;96:1566–73.10.1182/blood.V96.4.1566Search in Google Scholar
Lucien N, Chiaroni J, Cartron JP, Bailly P. Partial deletion in the JK locus causing a Jk(null) phenotype. Blood 2002;99:1079–81.10.1182/blood.V99.3.1079Search in Google Scholar
Irshaid NM, Eicher NI, Hustinx H, Poole J, Olsson ML. Novel alleles at the JK blood group locus explain the absence of the erythrocyte urea transporter in European families. Br J Haematol 2002;116:445–53.10.1046/j.1365-2141.2002.03238.x11841450Search in Google Scholar
Meng Y, Zhou X, Li Y, et al. A novel mutation at the JK locus causing Jk null phenotype in a Chinese family. Sci China C Life Sci 2005;48:636–40.10.1360/062005-12716483143Search in Google Scholar
Ekman GC, Hessner MJ. Screening of six racial groups for the intron 5 G→A 3’ splice acceptor mutation responsible for the Polynesian Kidd (a-b-) phenotype: the null mutation is not always associated with the JKB allele (letter). Transfusion 2000;40:888–9.10.1046/j.1537-2995.2000.40070888.x10924622Search in Google Scholar
Wester ES, Johnson ST, Copeland T, et al. Erythroid urea transporter deficiency due to novel JKnull alleles. Transfusion 2008;48:365–72.Search in Google Scholar
Liu HM, Lin JS, Chen PS, Lyou JY, Chen YJ, Tzeng CH. Two novel Jk(null) alleles derived from 222C>A in exon 5 and 896G>A in exon 9 of the JK gene. Transfusion 2009;49:259–64.10.1111/j.1537-2995.2008.01958.x18980618Search in Google Scholar
Irshaid NM, Hustinx H, Olsson ML. A novel molecular basis of the Jk(a-b-) phenotype in a Swiss family. Vox Sang 2000;78(Suppl 1):0019.Search in Google Scholar
Irshaid NM, Thuresson B, Olsson ML. Genomic typing of the Kidd blood group locus by a single-tube allele-specific primer PCR technique. Br J Haematol 1998;102:1010–14.10.1046/j.1365-2141.1998.00874.x9734652Search in Google Scholar
Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988;i6:1215.10.1093/nar/16.3.12153347653344216Search in Google Scholar
Yan L, Zhu F, Fu Q. Jk(a-b-) and Kidd blood group genotypes in Chinese people. Transfusion 2003;43:289–91.10.1046/j.1537-2995.2003.t01-1-00362.x12559028Search in Google Scholar
