Poole J - Search Results

1

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

Wester ES, Storry JR, Schneider K, Nilsson Sojka B, Poole J, Olsson ML. Wester ES, et al. Among authors: poole j. Transfusion. 2005 Apr;45(4):545-9. doi: 10.1111/j.0041-1132.2005.04283.x. Transfusion. 2005. PMID: 15819675

2

Molecular basis of the globoside-deficient P(k) blood group phenotype. Identification of four inactivating mutations in the UDP-N-acetylgalactosamine: globotriaosylceramide 3-beta-N-acetylgalactosaminyltransferase gene.

Hellberg A, Poole J, Olsson ML. Hellberg A, et al. Among authors: poole j. J Biol Chem. 2002 Aug 16;277(33):29455-9. doi: 10.1074/jbc.M203047200. Epub 2002 May 21. J Biol Chem. 2002. PMID: 12023287 Free article.

3

Additional molecular bases of the clinically important p blood group phenotype.

Hellberg A, Steffensen R, Yahalom V, Sojka BN, Heier HE, Levene C, Poole J, Olsson ML. Hellberg A, et al. Among authors: poole j. Transfusion. 2003 Jul;43(7):899-907. doi: 10.1046/j.1537-2995.2003.00425.x. Transfusion. 2003. PMID: 12823750

4

Identification of six new alleles at the FUT1 and FUT2 loci in ethnically diverse individuals with Bombay and Para-Bombay phenotypes.

Storry JR, Johannesson JS, Poole J, Strindberg J, Rodrigues MJ, Yahalom V, Levene C, Fujita C, Castilho L, Hustinx H, Olsson ML. Storry JR, et al. Among authors: poole j. Transfusion. 2006 Dec;46(12):2149-55. doi: 10.1111/j.1537-2995.2006.01045.x. Transfusion. 2006. PMID: 17176328

5

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. Irshaid NM, et al. Among authors: poole j. Br J Haematol. 2002 Feb;116(2):445-53. doi: 10.1046/j.1365-2141.2002.03238.x. Br J Haematol. 2002. PMID: 11841450 Free article.

6

The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoprotein.

Olsson ML, Smythe JS, Hansson C, Poole J, Mallinson G, Jones J, Avent ND, Daniels G. Olsson ML, et al. Among authors: poole j. Br J Haematol. 1998 Dec;103(4):1184-91. doi: 10.1046/j.1365-2141.1998.01083.x. Br J Haematol. 1998. PMID: 9886340 Free article.

7

Identification of a novel hybrid glycophorin gene encoding GP.Hop.

Storry JR, Poole J, Condon J, Reid ME. Storry JR, et al. Among authors: poole j. Transfusion. 2000 May;40(5):560-5. doi: 10.1046/j.1537-2995.2000.40050560.x. Transfusion. 2000. PMID: 10827259

8

SERF: a new antigen in the Cromer blood group system.

Banks J, Poole J, Ahrens N, Seltsam A, Salama A, Hue-Roye K, Storry JR, Palacajornsuk P, Ma BW, Lublin DM, Reid ME. Banks J, et al. Among authors: poole j. Transfus Med. 2004 Aug;14(4):313-8. doi: 10.1111/j.0958-7578.2004.00519.x. Transfus Med. 2004. PMID: 15285728

9

The MNS blood group antigens, Vr (MNS12) and Mt(a) (MNS14), each arise from an amino acid substitution on glycophorin A.

Storry JR, Coghlan G, Poole J, Figueroa D, Reid ME. Storry JR, et al. Among authors: poole j. Vox Sang. 2000;78(1):52-6. doi: 10.1159/000031149. Vox Sang. 2000. PMID: 10729812

10

International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Cancun report (2012).

Storry JR, Castilho L, Daniels G, Flegel WA, Garratty G, de Haas M, Hyland C, Lomas-Francis C, Moulds JM, Nogues N, Olsson ML, Poole J, Reid ME, Rouger P, van der Schoot E, Scott M, Tani Y, Yu LC, Wendel S, Westhoff C, Yahalom V, Zelinski T. Storry JR, et al. Among authors: poole j. Vox Sang. 2014 Jul;107(1):90-6. doi: 10.1111/vox.12127. Epub 2013 Dec 27. Vox Sang. 2014. PMID: 24372289 Free PMC article.

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