Larson G - Search Results

1

Homozygous expression of a missense mutation at nucleotide 385 in the FUT2 gene associates with the Le(a+b+) partial-secretor phenotype in an Indonesian family.

Henry S, Mollicone R, Fernandez P, Samuelsson B, Oriol R, Larson G. Henry S, et al. Among authors: larson g. Biochem Biophys Res Commun. 1996 Feb 27;219(3):675-8. doi: 10.1006/bbrc.1996.0293. Biochem Biophys Res Commun. 1996. PMID: 8645240

2

Blood group type glycosphingolipids of human cord blood erythrocytes.

Larson G, Samuelsson BE. Larson G, et al. J Biochem. 1980 Sep;88(3):647-57. doi: 10.1093/oxfordjournals.jbchem.a133015. J Biochem. 1980. PMID: 7419515 Free article.

3

Genotypic heterogeneity among Lewis negative individuals.

Elmgren A, Rydberg L, Larson G. Elmgren A, et al. Among authors: larson g. Biochem Biophys Res Commun. 1993 Oct 29;196(2):515-20. doi: 10.1006/bbrc.1993.2280. Biochem Biophys Res Commun. 1993. PMID: 8240322

4

Anti-carbohydrate antibodies associated with hyperacute rejection in a vascularized mouse heart-to-rat xenotransplantation model.

Gustavsson ML, Gannedahl G, Bäcker AE, Larson G, Olling A, Tufveson G, Samuelsson BE. Gustavsson ML, et al. Among authors: larson g. Transplantation. 1996 Mar 27;61(6):957-63. doi: 10.1097/00007890-199603270-00019. Transplantation. 1996. PMID: 8623166

5

A missense mutation in the FUT6 gene results in total absence of alpha3-fucosylation of human alpha1-acid glycoprotein.

Brinkman-Van der Linden EC, Mollicone R, Oriol R, Larson G, Van den Eijnden DH, Van Dijk W. Brinkman-Van der Linden EC, et al. Among authors: larson g. J Biol Chem. 1996 Jun 14;271(24):14492-5. doi: 10.1074/jbc.271.24.14492. J Biol Chem. 1996. PMID: 8662894 Free article.

6

DNA sequencing and screening for point mutations in the human Lewis (FUT3) gene enables molecular genotyping of the human Lewis blood group system.

Elmgren A, Börjeson C, Svensson L, Rydberg L, Larson G. Elmgren A, et al. Among authors: larson g. Vox Sang. 1996;70(2):97-103. doi: 10.1111/j.1423-0410.1996.tb01300.x. Vox Sang. 1996. PMID: 8801770

7

A second nonsecretor allele of the blood group alpha(1,2)fucosyl-transferase gene (FUT2).

Henry S, Mollicone R, Lowe JB, Samuelsson B, Larson G. Henry S, et al. Among authors: larson g. Vox Sang. 1996;70(1):21-5. doi: 10.1111/j.1423-0410.1996.tb00991.x. Vox Sang. 1996. PMID: 8928486 Free article.

8

Identification of a new plasma alpha(1,3)fucosyltransferase (FUT6) allele requires an extended genotyping strategy.

Larson G, Börjeson C, Elmgren A, Kernholt A, Henry S, Fletcher A, Aziz A, Mollicone R, Oriol R. Larson G, et al. Vox Sang. 1996;71(4):233-41. doi: 10.1046/j.1423-0410.1996.7140233.x. Vox Sang. 1996. PMID: 8958648

9

Molecular basis for erythrocyte Le(a+ b+) and salivary ABH partial-secretor phenotypes: expression of a FUT2 secretor allele with an A-->T mutation at nucleotide 385 correlates with reduced alpha(1,2) fucosyltransferase activity.

Henry S, Mollicone R, Fernandez P, Samuelsson B, Oriol R, Larson G. Henry S, et al. Among authors: larson g. Glycoconj J. 1996 Dec;13(6):985-93. doi: 10.1007/BF01053194. Glycoconj J. 1996. PMID: 8981090

10

Structural and immunochemical identification of Le(a), Le(b), H type 1, and related glycolipids in small intestinal mucosa of a group O Le(a-b-) nonsecretor.

Henry S, Jovall PA, Ghardashkhani S, Elmgren A, Martinsson T, Larson G, Samuelsson B. Henry S, et al. Among authors: larson g. Glycoconj J. 1997 Feb;14(2):209-23. doi: 10.1023/a:1018541821819. Glycoconj J. 1997. PMID: 9111138

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