Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 117

1.

Three novel alleles in the Kell blood group system resulting in the Knull phenotype and the first in a Native American.

Moulds JM, Persa R, Rierson D, Billingsley KL, Noumsi GT, Hue-Roye K, Reid ME.

Transfusion. 2013 Nov;53(11 Suppl 2):2867-71. doi: 10.1111/trf.12205. Epub 2013 Apr 15.

PMID:
23581548
2.

A KEL gene encoding serine at position 193 of the Kell glycoprotein results in expression of KEL1 antigen.

Poole J, Warke N, Hustinx H, Taleghani BM, Martin P, Finning K, Crew VK, Green C, Bromilow I, Daniels G.

Transfusion. 2006 Nov;46(11):1879-85.

PMID:
17076841
3.

Expansion of the Kell blood group system: two new high-prevalence antigens and two novel K0 (Kellnull ) phenotypes.

Lomas-Francis C, Vege S, Velliquette RW, Fuchisawa A, Uchikawa M, Tani Y, Moro H, Debnath AK, Westhoff CM.

Transfusion. 2013 Nov;53(11 Suppl 2):2887-91. doi: 10.1111/trf.12377. Epub 2013 Aug 22.

PMID:
23968329
4.

Three uncommon KEL alleles in one family with unusual Kell phenotypes explain a 35-year old conundrum.

Karamatic Crew V, Poole J, Burton N, Daniels G.

Vox Sang. 2014 Apr;106(3):242-7.

PMID:
24795954
5.

Molecular basis of two novel and related high-prevalence antigens in the Kell blood group system, KUCI and KANT, and their serologic and spatial association with K11 and KETI.

Velliquette RW, Hue-Roye K, Lomas-Francis C, Gillen B, Schierts J, Gentzkow K, Peyrard T, von Zabern I, Flegel WA, Rodberg K, Debnath AK, Lee S, Reid ME.

Transfusion. 2013 Nov;53(11 Suppl 2):2872-81. doi: 10.1111/trf.12200. Epub 2013 Apr 8.

6.

Identification of novel silent KEL alleles causing KEL:-5 (Ko) phenotype or discordance between KEL:1,-2 phenotype/KEL*01/02 genotype.

Martin-Blanc S, Simon P, Gien D, Kappler-Gratias S, Le Pennec PY, Pham BN.

Transfusion. 2013 Nov;53(11 Suppl 2):2859-66. doi: 10.1111/trf.12206. Epub 2013 Apr 15.

PMID:
23581578
7.

Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman.

Koda Y, Soejima M, Tsuneoka M, Yasumoto K, Higashitani T, Sagawa K, Kimura H.

Br J Haematol. 2002 Apr;117(1):220-5.

PMID:
11918559
8.

Novel alleles at the Kell blood group locus that lead to Kell variant phenotype in the Dutch population.

Ji Y, Veldhuisen B, Ligthart P, Haer-Wigman L, Jongerius J, Boujnan M, Ait Soussan A, Luo G, Fu Y, van der Schoot CE, de Haas M.

Transfusion. 2015 Feb;55(2):413-21. doi: 10.1111/trf.12838. Epub 2014 Aug 25.

PMID:
25156717
9.

KEL*02 alleles with alterations in and around exon 8 in individuals with apparent KEL:1,-2 phenotypes.

Wester ES, Steffensen R, Ligthart PC, Vad J, de Haas M, Storry JR, Olsson ML.

Vox Sang. 2010 Aug 1;99(2):150-7. doi: 10.1111/j.1423-0410.2010.01334.x. Epub 2010 Apr 4.

PMID:
20384970
10.
11.

Possible suppression of fetal erythropoiesis by the Kell blood group antibody anti-Kp(a).

Tuson M, Hue-Roye K, Koval K, Imlay S, Desai R, Garg G, Kazem E, Stockman D, Hamilton J, Reid ME.

Immunohematology. 2011;27(2):58-60.

PMID:
22356520
12.

The Kell blood group system.

Redman CM, Lee S.

Transfus Clin Biol. 1995;2(4):243-9. Review.

PMID:
8542022
13.

A novel KEL*1,3 allele with weak Kell antigen expression confirming the cis-modifier effect of KEL3.

Körmöczi GF, Scharberg EA, Gassner C.

Transfusion. 2009 Apr;49(4):733-9.

PMID:
19347978
14.

Molecular basis for the high-incidence antigens of the Kell blood group system.

Lee S, Naime DS, Reid ME, Redman CM.

Transfusion. 1997 Nov-Dec;37(11-12):1117-22.

PMID:
9426633
15.

The KEL24 and KEL14 alleles of the Kell blood group system.

Lee S, Naime D, Reid M, Redman C.

Transfusion. 1997 Oct;37(10):1035-8.

PMID:
9354821
16.

Genetic diversity of KELnull and KELel: a nationwide Austrian survey.

Körmöczi GF, Wagner T, Jungbauer C, Vadon M, Ahrens N, Moll W, Mühlbacher A, Ozgül-Gülce S, Kleinrath T, Kilga-Nogler S, Schönitzer D, Gassner C.

Transfusion. 2007 Apr;47(4):703-14.

PMID:
17381630
17.

Genetic and functional analyses describe a novel 730delG mutation in the KEL gene causing K0 phenotype in a Taiwanese blood donor.

Yang MH, Li L, Kuo YF, Hung YS, Yu LC, Hung CS, Tsai SJ, Lin KS, Chu DC.

Transfus Med. 2011 Oct;21(5):318-24. doi: 10.1111/j.1365-3148.2011.01084.x. Epub 2011 Jun 26.

PMID:
21707797
18.

Genetic basis of the K(0) phenotype in the Swedish population.

Wester ES, Storry JR, Schneider K, Nilsson Sojka B, Poole J, Olsson ML.

Transfusion. 2005 Apr;45(4):545-9.

PMID:
15819675
19.

Molecular basis of two novel high-prevalence antigens in the Kell blood group system, KALT and KTIM.

Lee S, Debnath AK, Wu X, Scofield T, George T, Kakaiya R, Yogore MG 3rd, Sausais L, Yacob M, Lomas-Francis C, Reid ME.

Transfusion. 2006 Aug;46(8):1323-7. Erratum in: Transfusion. 2006 Oct;46(10):1852.

PMID:
16934067
20.

Supplemental Content

Support Center