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Items: 1 to 20 of 86

1.

A novel JK null allele associated with typing discrepancies among African Americans.

Billingsley KL, Posadas JB, Moulds JM, Gaur LK.

Immunohematology. 2013;29(4):145-8.

PMID:
24689685
2.
3.

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. doi: 10.1111/j.1537-2995.2011.03399.x.

PMID:
22023394
4.

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. doi: 10.1111/j.1537-2995.2012.03750.x.

PMID:
22738189
5.

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.

PMID:
18028269
6.

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.

PMID:
24877238
7.

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. doi: 10.2450/2011.0038-11.

8.

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.

PMID:
9734652
9.

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. doi: 10.1111/j.1537-2995.2008.01958.x.

PMID:
18980618
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.

PMID:
11841450
11.

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. doi: 10.1111/tme.12185.

PMID:
25807964
12.
13.

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. doi: 10.1111/j.1537-2995.2010.02795.x.

PMID:
21309779
14.

Improved allele-specific PCR technique for Kidd blood group genotyping.

Intharanut K, Grams R, Bejrachandra S, Sriwanitchrak P, Nathalang O.

J Clin Lab Anal. 2013 Jan;27(1):53-8. doi: 10.1002/jcla.21561.

PMID:
23325744
15.

Kidd blood group system: a review.

Hamilton JR.

Immunohematology. 2015;31(1):29-35. Review.

PMID:
26308468
16.

Partial deletion in the JK locus causing a Jk(null) phenotype.

Lucien N, Chiaroni J, Cartron JP, Bailly P.

Blood. 2002 Feb 1;99(3):1079-81.

17.

DNA-based typing of blood groups for the management of multiply-transfused sickle cell disease patients.

Castilho L, Rios M, Bianco C, Pellegrino J Jr, Alberto FL, Saad ST, Costa FF.

Transfusion. 2002 Feb;42(2):232-8.

PMID:
11896340
18.

Elucidation of apparent non-maternity with DNA probes detecting highly polymorphic single locus systems.

Fischer GF, Pickl WF, Faé I, Pausch V, Speiser P.

Vox Sang. 1991;60(3):181-3.

PMID:
1677792
19.

The Jk(a-b-) phenotype in New Zealand Polynesians.

Woodfield DG, Douglas R, Smith J, Simpson A, Pinder L, Staveley JM.

Transfusion. 1982 Jul-Aug;22(4):276-8.

PMID:
7101419
20.

Duffy blood group phenotype-genotype correlations using high-resolution melting analysis PCR and microarray reveal complex cases including a new null FY*A allele: the role for sequencing in genotyping algorithms.

Lopez GH, Morrison J, Condon JA, Wilson B, Martin JR, Liew YW, Flower RL, Hyland CA.

Vox Sang. 2015 Oct;109(3):296-303. doi: 10.1111/vox.12273.

PMID:
25900316
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