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Items: 1 to 20 of 135

1.

Molecular basis of the Kell (K1) phenotype.

Lee S, Wu X, Reid M, Zelinski T, Redman C.

Blood. 1995 Feb 15;85(4):912-6.

2.

The Kell blood group system.

Redman CM, Lee S.

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

PMID:
8542022
3.

Point mutations characterize KEL10, the KEL3, KEL4, and KEL21 alleles, and the KEL17 and KEL11 alleles.

Lee S, Wu X, Son S, Naime D, Reid M, Okubo Y, Sistonen P, Redman C.

Transfusion. 1996 Jun;36(6):490-4.

PMID:
8669078
4.

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
5.

Molecular basis of the K:6,-7 [Js(a+b-)] phenotype in the Kell blood group system.

Lee S, Wu X, Reid M, Redman C.

Transfusion. 1995 Oct;35(10):822-5.

PMID:
7570911
6.
7.

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
8.

Kell typing by allele-specific PCR (ASP).

Avent ND, Martin PG.

Br J Haematol. 1996 Jun;93(3):728-30.

PMID:
8652402
9.
10.

Prenatal diagnosis of Kell blood group genotypes: KEL1 and KEL2.

Lee S, Bennett PR, Overton T, Warwick R, Wu X, Redman CM.

Am J Obstet Gynecol. 1996 Aug;175(2):455-9.

PMID:
8765268
11.

Molecular defects underlying the Kell null phenotype.

Lee S, Russo DC, Reiner AP, Lee JH, Sy MY, Telen MJ, Judd WJ, Simon P, Rodrigues MJ, Chabert T, Poole J, Jovanovic-Srzentic S, Levene C, Yahalom V, Redman CM.

J Biol Chem. 2001 Jul 20;276(29):27281-9. Epub 2001 May 24.

12.
14.

Development of a PCR-based diagnostic assay for the determination of KEL genotype in donor blood samples.

Murphy MT, Fraser RH, Goddard JP.

Transfus Med. 1996 Jun;6(2):133-7.

PMID:
8809961
15.

Point mutations causing the McLeod phenotype.

Russo DC, Lee S, Reid ME, Redman CM.

Transfusion. 2002 Mar;42(3):287-93.

PMID:
11961232
16.

KEL6 and KEL7 genotyping with sequence-specific primers.

Renoud KJ, Barracchini K, Byrne KM, Adams S, Pickett A, Caruccio L, Stroncek DF.

Transfusion. 2006 Sep;46(9):1510-4.

PMID:
16965577
17.

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
18.

A McLeod phenotype detected by random screening for K:-4 [Kp(b-)] blood donors in Brazil.

Wendel S, Fontão-Wendel R, Levi JE, Aravechia MG, Bordokan RF, Russo D, Haddad MS.

Transfusion. 2004 Nov;44(11):1579-87.

PMID:
15504163
19.

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
20.

Molecular basis of Kell blood group phenotypes.

Lee S.

Vox Sang. 1997;73(1):1-11. Review. Erratum in: Vox Sang 1998;74(1):58.

PMID:
9269063

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