152 related articles for article (PubMed ID: 33539287)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
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. 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]
11. 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]
12. A simple screening assay for the most common JK*0 alleles revealed compound heterozygosity in Jk(a-b-) probands from Guam.
Wester ES; Gustafsson J; Snell B; Spruell P; Hellberg A; Olsson ML; Storry JR
Immunohematology; 2009; 25(4):165-9. PubMed ID: 20406024
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. The Kidd (JK) Blood Group System.
Lawicki S; Covin RB; Powers AA
Transfus Med Rev; 2017 Jul; 31(3):165-172. PubMed ID: 28065763
[TBL] [Abstract][Full Text] [Related]
15. Production of human monoclonal anti-Jk3, recognising an epitope including the Jk(a) /Jk(b) polymorphic site of the Kidd glycoprotein.
Toyoda C; Suzuki Y; Tsuneyama H; Onodera T; Masuno A; Yabe R; Ogasawara K; Okuda M; Nakajima K; Uchikawa M
Transfus Med; 2014 Oct; 24(5):286-91. PubMed ID: 25180691
[TBL] [Abstract][Full Text] [Related]
16. A case series highlighting a common approach to identifying anti-Jk3.
Talabong DJAM; Kelley WE
Immunohematology; 2021 Jun; 37(2):84-88. PubMed ID: 34170639
[TBL] [Abstract][Full Text] [Related]
17. Partial deletion in the JK locus causing a Jk(null) phenotype.
Lucien N; Chiaroni J; Cartron JP; Bailly P
Blood; 2002 Feb; 99(3):1079-81. PubMed ID: 11807016
[TBL] [Abstract][Full Text] [Related]
18. [DNA sequence analysis of Jk(a-b-) phenotype of blood donors from Chengdu].
Hong Y; Gong TX; Zhou CH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Dec; 29(6):697-700. PubMed ID: 23225053
[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. Two new JK silencing alleles identified by single molecule sequencing with 20-Kb long-reads.
Isa K; Takada S; Takeda H; Tsuneyama H; Ogasawara K; Takahashi D; Miyazaki T; Miyata S; Satake M
Transfusion; 2023 Aug; 63(8):1441-1446. PubMed ID: 37165957
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]