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Kidd blood group and urea transport function of human erythrocytes are carried on the same protein
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Olives B, Mattei MG, Huet M, Neau P, Martial S, Cartron JP, Bailly P,. Kidd blood group and urea transport function of human erythrocytes are carried on the same protein. J Biol Chem 1995; 270: 15607-10.
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Olives, B.1
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2
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0033569732
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At physiological expression levels the Kidd blood group/urea transporter protein is not a water channel
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Sidoux-Walter F, Lucien N, Olives B, Gobin R, Rousselet G, Kamsteeg EJ, Ripoche P, Deen PM, Cartron JP, Bailly P,. At physiological expression levels the Kidd blood group/urea transporter protein is not a water channel. J Biol Chem 1999; 274: 30228-35.
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Sidoux-Walter, F.1
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Bailly, P.10
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0030750176
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The molecular basis of the Kidd blood group polymorphism and its lack of association with type 1 diabetes susceptibility
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Olives B, Merriman M, Bailly P, Bain S, Barnett A, Todd J, Cartron JP, Merriman T,. 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.
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Olives, B.1
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Cartron, J.P.7
Merriman, T.8
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0346096786
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Allelic genes of blood group antigens: A source of human mutations and cSNPs documented in the Blood Group Antigen Gene Mutation Database
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Blumenfeld OO, Patnaik SK,. Allelic genes of blood group antigens: a source of human mutations and cSNPs documented in the Blood Group Antigen Gene Mutation Database. Hum Mutat 2004; 23: 8-16.
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Blumenfeld, O.O.1
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CASE STUDY: A JK:-3 phenotype in an African American family
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Oliver CK, Sexton T, Joyner J,. CASE STUDY: a JK:-3 phenotype in an African American family. Transfusion 1993; 33 Suppl.: 23S.
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Oliver, C.K.1
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Erythroid urea transporter deficiency due to novel JKnull alleles
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Wester ES, Johnson ST, Copeland T, Malde R, Lee E, Storry JR, Olsson ML,. Erythroid urea transporter deficiency due to novel JKnull alleles. Transfusion 2008; 48: 365-72.
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Lee, E.5
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Olsson, M.L.7
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8
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0036174928
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Novel alleles at the JK blood group locus explain the absence of the erythrocyte urea transporter in European families
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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.
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Irshaid, N.M.1
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Olsson, M.L.5
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9
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0036464690
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Partial deletion in the JK locus causing a Jk(null) phenotype
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Lucien N, Chiaroni J, Cartron JP, Bailly P,. Partial deletion in the JK locus causing a Jk(null) phenotype. Blood 2002; 99: 1079-81.
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Lucien, N.1
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10
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0033863024
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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
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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. Transfusion 2000; 40: 888-9.
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Ekman, G.C.1
Hessner, M.J.2
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11
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0032557563
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Characterization of the gene encoding the human Kidd blood group/urea transporter protein. Evidence for splice site mutations in Jknull individuals
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Lucien N, Sidoux-Walter F, Olives B, Moulds J, Le Pennec PY, Cartron JP, Bailly P,. 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.
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Lucien, N.1
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Cartron, J.P.6
Bailly, P.7
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12
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58849118154
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Two novel Jk(null) alleles derived from 222C>A in Exon 5 and 896G>A in Exon 9 of the JK gene
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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.
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Liu, H.M.1
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Lyou, J.Y.4
Chen, Y.J.5
Tzeng, C.H.6
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33746396737
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A novel mutation at the JK locus causing Jk null phenotype in a Chinese family
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Meng Y, Zhou X, Li Y, Zhao D, Liang S, Zhao X, Yang B,. A novel mutation at the JK locus causing Jk null phenotype in a Chinese family. Sci China C Life Sci 2005; 48: 636-40.
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Meng, Y.1
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Li, Y.3
Zhao, D.4
Liang, S.5
Zhao, X.6
Yang, B.7
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14
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0034663333
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Molecular heterogeneity of the Jk(null) phenotype: Expression analysis of the Jk(S291P) mutation found in Finns
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Sidoux-Walter F, Lucien N, Nissinen R, Sistonen P, Henry S, Moulds J, Cartron JP, Bailly P,. Molecular heterogeneity of the Jk(null) phenotype: expression analysis of the Jk(S291P) mutation found in Finns. Blood 2000; 96: 1566-73.
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Sidoux-Walter, F.1
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Nissinen, R.3
Sistonen, P.4
Henry, S.5
Moulds, J.6
Cartron, J.P.7
Bailly, P.8
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