Olsson ML - Search Results

1

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: olsson ml. 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.

2

A rapid and simple ABO genotype screening method using a novel B/O2 versus A/O2 discriminating nucleotide substitution at the ABO locus.

Olsson ML, Chester MA. Olsson ML, et al. Vox Sang. 1995;69(3):242-7. doi: 10.1111/j.1423-0410.1995.tb02602.x. Vox Sang. 1995. PMID: 8578738

3

Evidence for a new type of O allele at the ABO locus, due to a combination of the A2 nucleotide deletion and the Ael nucleotide insertion.

Olsson ML, Chester MA. Olsson ML, et al. Vox Sang. 1996;71(2):113-7. doi: 10.1046/j.1423-0410.1996.7120113.x. Vox Sang. 1996. PMID: 8873422

4

Frequent occurrence of a variant O1 gene at the blood group ABO locus.

Olsson ML, Chester MA. Olsson ML, et al. Vox Sang. 1996;70(1):26-30. doi: 10.1111/j.1423-0410.1996.tb00992.x. Vox Sang. 1996. PMID: 8928487

5

Heterogeneity of the O alleles at the blood group ABO locus in Amerindians.

Olsson ML, Santos SE, Guerreiro JF, Zago MA, Chester MA. Olsson ML, et al. Vox Sang. 1998;74(1):46-50. Vox Sang. 1998. PMID: 9481861

6

A clinically applicable method for determining the three major alleles at the Duffy (FY) blood group locus using polymerase chain reaction with allele-specific primers.

Olsson ML, Hansson C, Avent ND, Akesson IE, Green CA, Daniels GL. Olsson ML, et al. Transfusion. 1998 Feb;38(2):168-73. doi: 10.1046/j.1537-2995.1998.38298193099.x. Transfusion. 1998. PMID: 9531948

7

Different genotypes causing indiscernible patterns of A expression on A(el) red blood cells as visualized by scanning immunogold electron microscopy.

Hansen T, Namork E, Olsson ML, Chester MA, Heier HE. Hansen T, et al. Among authors: olsson ml. Vox Sang. 1998;75(1):47-51. Vox Sang. 1998. PMID: 9745153

8

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. 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.

9

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: olsson ml. 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.

10

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: olsson ml. 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.

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