Oriol R - 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: oriol r. 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

Expression of Lewis histo-blood group glycolipids in the plasma of individuals of Le(a+b+) and partial secretor phenotypes.

Henry SM, Oriol R, Samuelsson BE. Henry SM, et al. Among authors: oriol r. Glycoconj J. 1994 Dec;11(6):593-9. doi: 10.1007/BF00731311. Glycoconj J. 1994. PMID: 7696863

3

Plasma and red-cell glycolipid patterns of Le(a+b+) and Le(a+b-) Polynesians as further evidence of the weak secretor gene Se(w).

Henry SM, Woodfield DG, Samuelsson BE, Oriol R. Henry SM, et al. Among authors: oriol r. Vox Sang. 1993;65(1):62-9. doi: 10.1111/j.1423-0410.1993.tb04527.x. Vox Sang. 1993. PMID: 8362517

4

Lewis histo-blood group system and associated secretory phenotypes.

Henry S, Oriol R, Samuelsson B. Henry S, et al. Among authors: oriol r. Vox Sang. 1995;69(3):166-82. doi: 10.1111/j.1423-0410.1995.tb02591.x. Vox Sang. 1995. PMID: 8578728 Review.

5

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. Among authors: oriol r. Vox Sang. 1996;71(4):233-41. doi: 10.1046/j.1423-0410.1996.7140233.x. Vox Sang. 1996. PMID: 8958648

6

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: oriol r. Glycoconj J. 1996 Dec;13(6):985-93. doi: 10.1007/BF01053194. Glycoconj J. 1996. PMID: 8981090

7

Significance of individual point mutations, T202C and C314T, in the human Lewis (FUT3) gene for expression of Lewis antigens by the human alpha(1,3/1,4)-fucosyltransferase, Fuc-TIII.

Elmgren A, Mollicone R, Costache M, Börjeson C, Oriol R, Harrington J, Larson G. Elmgren A, et al. Among authors: oriol r. J Biol Chem. 1997 Aug 29;272(35):21994-8. doi: 10.1074/jbc.272.35.21994. J Biol Chem. 1997. PMID: 9268337 Free article.

8

Identification of two functionally deficient plasma alpha 3-fucosyltransferase (FUT6) alleles.

Elmgren A, Börjeson C, Mollicone R, Oriol R, Fletcher A, Larson G. Elmgren A, et al. Among authors: oriol r. Hum Mutat. 2000 Dec;16(6):473-81. doi: 10.1002/1098-1004(200012)16:6<473::AID-HUMU4>3.0.CO;2-T. Hum Mutat. 2000. PMID: 11102976

9

Immunochemical and immunohistological expression of Lewis histo-blood group antigens in small intestine including individuals of the Le(a+b+) and Le(a-b-) nonsecretor phenotypes.

Henry SM, Samuelsson BE, Oriol R. Henry SM, et al. Among authors: oriol r. Glycoconj J. 1994 Dec;11(6):600-7. doi: 10.1007/BF00731312. Glycoconj J. 1994. PMID: 7696864

10

Detection and characterization of Lewis antigens in plasma of Lewis-negative individuals. Evidence of chain extension as a result of reduced fucosyltransferase competition.

Henry SM, Oriol R, Samuelsson BE. Henry SM, et al. Among authors: oriol r. Vox Sang. 1994;67(4):387-96. doi: 10.1111/j.1423-0410.1994.tb01279.x. Vox Sang. 1994. PMID: 7701811

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