Olsson ML - Search Results

1

A novel mutation in the complement regulator clusterin in recurrent hemolytic uremic syndrome.

Ståhl AL, Kristoffersson A, Olin AI, Olsson ML, Roodhooft AM, Proesmans W, Karpman D. Ståhl AL, et al. Among authors: olsson ml. Mol Immunol. 2009 Jul;46(11-12):2236-43. doi: 10.1016/j.molimm.2009.04.012. Epub 2009 May 15. Mol Immunol. 2009. PMID: 19446882

2

Shiga toxin-induced complement-mediated hemolysis and release of complement-coated red blood cell-derived microvesicles in hemolytic uremic syndrome.

Arvidsson I, Ståhl AL, Hedström MM, Kristoffersson AC, Rylander C, Westman JS, Storry JR, Olsson ML, Karpman D. Arvidsson I, et al. Among authors: olsson ml. J Immunol. 2015 Mar 1;194(5):2309-18. doi: 10.4049/jimmunol.1402470. Epub 2015 Jan 30. J Immunol. 2015. PMID: 25637016 Free article.

3

The IgG-specific endoglycosidase EndoS inhibits both cellular and complement-mediated autoimmune hemolysis.

Allhorn M, Briceño JG, Baudino L, Lood C, Olsson ML, Izui S, Collin M. Allhorn M, et al. Among authors: olsson ml. Blood. 2010 Jun 17;115(24):5080-8. doi: 10.1182/blood-2009-08-239020. Epub 2010 Mar 31. Blood. 2010. PMID: 20357243 Free PMC article.

4

New and unusual O alleles at the ABO locus are implicated in unexpected blood group phenotypes.

Hosseini-Maaf B, Irshaid NM, Hellberg A, Wagner T, Levene C, Hustinx H, Steffensen R, Chester MA, Olsson ML. Hosseini-Maaf B, et al. Among authors: olsson ml. Transfusion. 2005 Jan;45(1):70-81. doi: 10.1111/j.1537-2995.2005.04195.x. Transfusion. 2005. PMID: 15647021

5

Erythroid urea transporter deficiency due to novel JKnull alleles.

Wester ES, Johnson ST, Copeland T, Malde R, Lee E, Storry JR, Olsson ML. Wester ES, et al. Among authors: olsson ml. Transfusion. 2008 Feb;48(2):365-72. doi: 10.1111/j.1537-2995.2007.01532.x. Epub 2007 Nov 19. Transfusion. 2008. PMID: 18028269

6

Expression of a novel missense mutation found in the A4GALT gene of Amish individuals with the p phenotype.

Hellberg A, Schmidt-Melbye AC, Reid ME, Olsson ML. Hellberg A, et al. Among authors: olsson ml. Transfusion. 2008 Mar;48(3):479-87. doi: 10.1111/j.1537-2995.2007.01552.x. Epub 2007 Dec 7. Transfusion. 2008. PMID: 18067504

7

Glycoproteomic and Phenotypic Elucidation of B4GALNT2 Expression Variants in the SID Histo-Blood Group System.

Stenfelt L, Nilsson J, Hellberg Å, Liew YW, Morrison J, Larson G, Olsson ML. Stenfelt L, et al. Among authors: olsson ml. Int J Mol Sci. 2022 Apr 1;23(7):3936. doi: 10.3390/ijms23073936. Int J Mol Sci. 2022. PMID: 35409292 Free PMC article.

8

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.

9

Platelet concentrate increases bone ingrowth into porous hydroxyapatite.

Siebrecht MA, De Rooij PP, Arm DM, Olsson ML, Aspenberg P. Siebrecht MA, et al. Among authors: olsson ml. Orthopedics. 2002 Feb;25(2):169-72. doi: 10.3928/0147-7447-20020201-22. Orthopedics. 2002. PMID: 11871379

10

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: olsson ml. Transfusion. 2003 Jul;43(7):899-907. doi: 10.1046/j.1537-2995.2003.00425.x. Transfusion. 2003. PMID: 12823750

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