These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
130 related articles for article (PubMed ID: 26969102)
1. 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]
2. 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]
3. Characterization of the gene encoding the human Kidd blood group/urea transporter protein. Evidence for splice site mutations in Jknull individuals. Lucien N; Sidoux-Walter F; Olivès B; Moulds J; Le Pennec PY; Cartron JP; Bailly P J Biol Chem; 1998 May; 273(21):12973-80. PubMed ID: 9582331 [TBL] [Abstract][Full Text] [Related]
4. Jk Allhoff W; Weidner L; Lindlbauer N; Grüner L; Libisch M; Schistal E; Jungbauer C Blood Transfus; 2021 May; 19(3):237-243. PubMed ID: 33539287 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. Genotyping and serotyping profiles showed weak Jk Wu PC; Chyan TW; Feng SH; Chen MH; Pai SC Vox Sang; 2019 Apr; 114(3):268-274. PubMed ID: 30820956 [TBL] [Abstract][Full Text] [Related]
7. Development of anti-Jk3 associated with silenced Kidd antigen expression and a novel single nucleotide variant of the Manrai PA; Siddon AJ; Hager KM; Hendrickson JE; Keller MA; Tormey CA Immunohematology; 2021 Sep; 37(3):109-112. PubMed ID: 34591379 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed Program. Dinardo CL; Oliveira TGM; Kelly S; Ashley-Koch A; Telen M; Schmidt LC; Castilho S; Melo K; Dezan MR; Wheeler MM; Johnsen JM; Nickerson DA; Jain D; Custer B; Pereira AC; Sabino EC; Transfusion; 2021 Feb; 61(2):603-616. PubMed ID: 33231305 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Two novel Jk(null) alleles derived from 222C>A in Exon 5 and 896G>A in Exon 9 of the JK gene. Liu HM; Lin JS; Chen PS; Lyou JY; Chen YJ; Tzeng CH Transfusion; 2009 Feb; 49(2):259-64. PubMed ID: 18980618 [TBL] [Abstract][Full Text] [Related]
12. The mutation spectrum of the JK-null phenotype in the Chinese population. Guo Z; Wang C; Yan K; Xie J; Shen W; Li Q; Zhang J; Ye L; Zhu Z Transfusion; 2013 Mar; 53(3):545-53. PubMed ID: 22738189 [TBL] [Abstract][Full Text] [Related]
13. A novel missense mutation nt737T>G of JK gene with Jk(a-b-) phenotype in Chinese blood donors. Ma L; Liu YC; Zhu SW; Hu WJ; Chen X; Xue M; Zhen L; Wu MH; Liu Y; Sun J Transfus Med; 2015 Feb; 25(1):38-41. PubMed ID: 25807964 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Genomic characterisation of the Jk(a-b-) phenotype in Thai blood donors. Sriwanitchrak P; Sriwanitchrak K; Tubrod J; Kupatawintu P; Kaset C; Nathalang O Blood Transfus; 2012 Apr; 10(2):181-5. PubMed ID: 22153692 [TBL] [Abstract][Full Text] [Related]
16. Genomic characterization of the kidd blood group gene:different molecular basis of the Jk(a-b-) phenotype in Polynesians and Finns. Irshaid NM; Henry SM; Olsson ML Transfusion; 2000 Jan; 40(1):69-74. PubMed ID: 10644814 [TBL] [Abstract][Full Text] [Related]
17. Breakpoint regions of an RHD-CE(4-9)-D allele and a rare JK allele in a Pacific Islander individual. Srivastava K; Bueno MU; Flegel WA Blood Transfus; 2024 May; 22(3):189-197. PubMed ID: 37677094 [TBL] [Abstract][Full Text] [Related]
18. A novel JKA allele, nt561C>A, associated with silencing of Kidd expression. Horn T; Castilho L; Moulds JM; Billingsley K; Vege S; Johnson N; Westhoff CM Transfusion; 2012 May; 52(5):1092-6. PubMed ID: 22023394 [TBL] [Abstract][Full Text] [Related]
19. Characterization of Jk(a+(weak)): a new blood group phenotype associated with an altered JK*01 allele. Wester ES; Storry JR; Olsson ML Transfusion; 2011 Feb; 51(2):380-92. PubMed ID: 21309779 [TBL] [Abstract][Full Text] [Related]
20. Kidd blood group system: a review. Hamilton JR Immunohematology; 2015; 31(1):29-35. PubMed ID: 26308468 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]