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2. A novel mutation at the JK locus causing Jk null phenotype in a Chinese family. Meng Y; Zhou X; Li Y; Zhao D; Liang S; Zhao X; Yang B Sci China C Life Sci; 2005 Dec; 48(6):636-40. PubMed ID: 16483143 [TBL] [Abstract][Full Text] [Related]
3. Kidd blood group and urea transport function of human erythrocytes are carried by the same protein. Olivès B; Mattei MG; Huet M; Neau P; Martial S; Cartron JP; Bailly P J Biol Chem; 1995 Jun; 270(26):15607-10. PubMed ID: 7797558 [TBL] [Abstract][Full Text] [Related]
4. Urea transport and Kidd blood groups. Cartron JP; Ripoche P Transfus Clin Biol; 1995; 2(4):309-15. PubMed ID: 8542029 [TBL] [Abstract][Full Text] [Related]
5. Antigenic and functional properties of the human red blood cell urea transporter hUT-B1. Lucien N; Sidoux-Walter F; Roudier N; Ripoche P; Huet M; Trinh-Trang-Tan MM; Cartron JP; Bailly P J Biol Chem; 2002 Sep; 277(37):34101-8. PubMed ID: 12093813 [TBL] [Abstract][Full Text] [Related]
6. Kidd blood group system: a review. Hamilton JR Immunohematology; 2015; 31(1):29-35. PubMed ID: 26308468 [TBL] [Abstract][Full Text] [Related]
7. Urinary concentrating ability in patients with Jk(a-b-) blood type who lack carrier-mediated urea transport. Sands JM; Gargus JJ; Fröhlich O; Gunn RB; Kokko JP J Am Soc Nephrol; 1992 Jun; 2(12):1689-96. PubMed ID: 1498276 [TBL] [Abstract][Full Text] [Related]
8. Photoaffinity labeling of the human red-blood-cell urea-transporter polypeptide components. Possible homology with the Kidd blood group antigen. Neau P; Degeilh F; Lamotte H; Rousseau B; Ripoche P Eur J Biochem; 1993 Dec; 218(2):447-55. PubMed ID: 8269933 [TBL] [Abstract][Full Text] [Related]
9. A Caucasian JK*A/JK*B woman with Jk(a+b-) red blood cells, anti-Jkb, and a novel JK*B allele c.1038delG. Ramsey G; Sumugod RD; Lindholm PF; Zinni JG; Keller JA; Horn T; Keller MA Immunohematology; 2016 Sep; 32(3):91-95. PubMed ID: 27834480 [TBL] [Abstract][Full Text] [Related]
10. Erythroid urea transporter deficiency due to novel JKnull alleles. Wester ES; Johnson ST; Copeland T; Malde R; Lee E; Storry JR; Olsson ML Transfusion; 2008 Feb; 48(2):365-72. PubMed ID: 18028269 [TBL] [Abstract][Full Text] [Related]
11. Clinical aspects of urea transporters. Ran J; Wang H; Hu T Subcell Biochem; 2014; 73():179-91. PubMed ID: 25298346 [TBL] [Abstract][Full Text] [Related]
12. Novel alleles at the JK blood group locus explain the absence of the erythrocyte urea transporter in European families. Irshaid NM; Eicher NI; Hustinx H; Poole J; Olsson ML Br J Haematol; 2002 Feb; 116(2):445-53. PubMed ID: 11841450 [TBL] [Abstract][Full Text] [Related]
14. The molecular basis of the Kidd blood group polymorphism and its lack of association with type 1 diabetes susceptibility. Olivès B; Merriman M; Bailly P; Bain S; Barnett A; Todd J; Cartron JP; Merriman T Hum Mol Genet; 1997 Jul; 6(7):1017-20. PubMed ID: 9215669 [TBL] [Abstract][Full Text] [Related]
16. Methods for the detection of Jk heterozygotes: interpretations and applications. Edwards-Moulds J; Kasschau MR Transfusion; 1988; 28(6):545-8. PubMed ID: 3194929 [TBL] [Abstract][Full Text] [Related]
17. Genomic typing of the Kidd blood group locus by a single-tube allele-specific primer PCR technique. Irshaid NM; Thuresson B; Olsson ML Br J Haematol; 1998 Sep; 102(4):1010-4. PubMed ID: 9734652 [TBL] [Abstract][Full Text] [Related]
18. Jk:-3 red cells have a defect in urea transport: a new urea-dependent lysis test. McDougall DC; McGregor M Transfusion; 1988; 28(2):197-8. PubMed ID: 3214487 [No Abstract] [Full Text] [Related]
19. Molecular genetic analysis of the Jk(a-b-) phenotype in Chinese: A novel silent recessive JK allele. Zhang A; Chi Q; Lin H; She Y Transfus Apher Sci; 2016 Apr; 54(2):232-4. PubMed ID: 26969102 [TBL] [Abstract][Full Text] [Related]
20. JK null alleles identified from Japanese individuals with Jk(a−b−) phenotype. Onodera T; Sasaki K; Tsuneyama H; Isa K; Ogasawara K; Satake M; Tadokoro K; Uchikawa M Vox Sang; 2014 May; 106(4):382-4. PubMed ID: 24877238 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]