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Items: 1 to 50 of 83

1.

Effects in Cancer Cells of the Recombinant l-Methionine Gamma-Lyase from Brevibacterium aurantiacum. Encapsulation in Human Erythrocytes for Sustained l-Methionine Elimination.

Machover D, Rossi L, Hamelin J, Desterke C, Goldschmidt E, Chadefaux-Vekemans B, Bonnarme P, Briozzo P, Kopečný D, Pierigè F, Magnani M, Mollicone R, Haghighi-Rad F, Gaston-Mathé Y, Dairou J, Boucheix C, Saffroy R.

J Pharmacol Exp Ther. 2019 Jun;369(3):489-502. doi: 10.1124/jpet.119.256537. Epub 2019 Apr 2.

PMID:
30940696
2.

Enhancement of 5-Fluorouracil Cytotoxicity by Pyridoxal 5'-Phosphate and Folinic Acid in Tandem.

Machover D, Goldschmidt E, Mollicone R, Haghighi-Rad F, Desterke C, Gaston-Mathé Y, Saffroy R, Boucheix C, Dairou J.

J Pharmacol Exp Ther. 2018 Aug;366(2):238-243. doi: 10.1124/jpet.118.249367. Epub 2018 Jun 1.

PMID:
29858389
3.

A functional splice variant of the human Golgi CMP-sialic acid transporter.

Salinas-Marín R, Mollicone R, Martínez-Duncker I.

Glycoconj J. 2016 Dec;33(6):897-906. Epub 2016 Jul 7.

PMID:
27387429
4.

Activation of human naïve Th cells increases surface expression of GD3 and induces neoexpression of GD2 that colocalize with TCR clusters.

Villanueva-Cabello TM, Mollicone R, Cruz-Muñoz ME, López-Guerrero DV, Martínez-Duncker I.

Glycobiology. 2015 Dec;25(12):1454-64. doi: 10.1093/glycob/cwv062. Epub 2015 Aug 11.

PMID:
26263924
5.

Activity, splice variants, conserved peptide motifs, and phylogeny of two new alpha1,3-fucosyltransferase families (FUT10 and FUT11).

Mollicone R, Moore SE, Bovin N, Garcia-Rosasco M, Candelier JJ, Martinez-Duncker I, Oriol R.

J Biol Chem. 2009 Feb 13;284(7):4723-38. doi: 10.1074/jbc.M809312200. Epub 2008 Dec 16.

6.

Evolutionary history of the alpha2,8-sialyltransferase (ST8Sia) gene family: tandem duplications in early deuterostomes explain most of the diversity found in the vertebrate ST8Sia genes.

Harduin-Lepers A, Petit D, Mollicone R, Delannoy P, Petit JM, Oriol R.

BMC Evol Biol. 2008 Sep 23;8:258. doi: 10.1186/1471-2148-8-258.

7.

Glycosylation status of the membrane protein CD9P-1.

André M, Morelle W, Planchon S, Milhiet PE, Rubinstein E, Mollicone R, Chamot-Rooke J, Le Naour F.

Proteomics. 2007 Nov;7(21):3880-95.

PMID:
17960739
8.

Transferrin and apolipoprotein C-III isofocusing are complementary in the diagnosis of N- and O-glycan biosynthesis defects.

Wopereis S, Grünewald S, Huijben KM, Morava E, Mollicone R, van Engelen BG, Lefeber DJ, Wevers RA.

Clin Chem. 2007 Feb;53(2):180-7. Epub 2006 Dec 14.

9.

Phylogenetic and mutational analyses reveal key residues for UDP-glucuronic acid binding and activity of beta1,3-glucuronosyltransferase I (GlcAT-I).

Fondeur-Gelinotte M, Lattard V, Oriol R, Mollicone R, Jacquinet JC, Mulliert G, Gulberti S, Netter P, Magdalou J, Ouzzine M, Fournel-Gigleux S.

Protein Sci. 2006 Jul;15(7):1667-78.

10.

The animal sialyltransferases and sialyltransferase-related genes: a phylogenetic approach.

Harduin-Lepers A, Mollicone R, Delannoy P, Oriol R.

Glycobiology. 2005 Aug;15(8):805-17. Epub 2005 Apr 20. Erratum in: Glycobiology. 2005 Sep;15(9):21G.

PMID:
15843597
11.

Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter.

Martinez-Duncker I, Dupré T, Piller V, Piller F, Candelier JJ, Trichet C, Tchernia G, Oriol R, Mollicone R.

Blood. 2005 Apr 1;105(7):2671-6. Epub 2004 Dec 2.

PMID:
15576474
12.

Cytogenetics, conserved synteny and evolution of chicken fucosyltransferase genes compared to human.

Coullin P, Crooijmans RP, Fillon V, Mollicone R, Groenen MA, Adrien-Dehais C, Bernheim A, Zoorob R, Oriol R, Candelier JJ.

Cytogenet Genome Res. 2003;103(1-2):111-21.

PMID:
15004473
13.

Activity and tissue distribution of splice variants of alpha6-fucosyltransferase in human embryogenesis.

Martinez-Duncker I, Michalski JC, Bauvy C, Candelier JJ, Mennesson B, Codogno P, Oriol R, Mollicone R.

Glycobiology. 2004 Jan;14(1):13-25. Epub 2003 Sep 26.

PMID:
14514715
14.

A new superfamily of protein-O-fucosyltransferases, alpha2-fucosyltransferases, and alpha6-fucosyltransferases: phylogeny and identification of conserved peptide motifs.

Martinez-Duncker I, Mollicone R, Candelier JJ, Breton C, Oriol R.

Glycobiology. 2003 Dec;13(12):1C-5C. Epub 2003 Sep 9.

PMID:
12966037
15.

The nucleotide-sugar transporter family: a phylogenetic approach.

Martinez-Duncker I, Mollicone R, Codogno P, Oriol R.

Biochimie. 2003 Mar-Apr;85(3-4):245-60.

PMID:
12770764
16.

Schistosome N-glycans containing core alpha 3-fucose and core beta 2-xylose epitopes are strong inducers of Th2 responses in mice.

Faveeuw C, Mallevaey T, Paschinger K, Wilson IB, Fontaine J, Mollicone R, Oriol R, Altmann F, Lerouge P, Capron M, Trottein F.

Eur J Immunol. 2003 May;33(5):1271-81.

17.

Assignment of FUT8 to chicken chromosome band 5q1.4 and to human chromosome 14q23.2-->q24.1 by in situ hybridization. Conserved and compared synteny between human and chicken.

Coullin P, Crooijmans RP, Groenen MA, Heilig R, Mollicone R, Oriol R, Candelier JJ.

Cytogenet Genome Res. 2002;97(3-4):234-8.

PMID:
12438718
18.

Common origin and evolution of glycosyltransferases using Dol-P-monosaccharides as donor substrate.

Oriol R, Martinez-Duncker I, Chantret I, Mollicone R, Codogno P.

Mol Biol Evol. 2002 Sep;19(9):1451-63.

PMID:
12200473
19.

Macrothrombocytopenia with abnormal demarcation membranes in megakaryocytes and neutropenia with a complete lack of sialyl-Lewis-X antigen in leukocytes--a new syndrome?

Willig TB, Breton-Gorius J, Elbim C, Mignotte V, Kaplan C, Mollicone R, Pasquier C, Filipe A, Miélot F, Cartron JP, Gougerot-Pocidalo MA, Debili N, Guichard J, Dommergues JP, Mohandas N, Tchernia G.

Blood. 2001 Feb 1;97(3):826-8.

PMID:
11157507
20.

Expression of fucosyltransferases in skin, conjunctiva, and cornea during human development.

Candelier JJ, Mollicone R, Mennesson B, Coullin P, Oriol R.

Histochem Cell Biol. 2000 Aug;114(2):113-24.

PMID:
11052260
21.

[Cloning and gene expression of alpha-3/4-fucosyltransferase lewis in the chimpanzee] .

Costache M, Iordăchescu D, Oriol R, Mollicone R.

Rom J Physiol. 1998 Jan-Jun;35(1-2):41-54. French. No abstract available.

PMID:
11000864
22.

Molecular genetics of H.

Oriol R, Candelier JJ, Mollicone R.

Vox Sang. 2000;78 Suppl 2:105-8. Review.

PMID:
10938937
23.

FUT4 and FUT9 genes are expressed early in human embryogenesis.

Cailleau-Thomas A, Coullin P, Candelier JJ, Balanzino L, Mennesson B, Oriol R, Mollicone R.

Glycobiology. 2000 Aug;10(8):789-802.

PMID:
10929005
24.

Molecular cloning of a putative alpha3-fucosyltransferase from Schistosoma mansoni.

Trottein F, Mollicone R, Fontaine J, de Mendonça R, Piller F, Pierce R, Oriol R, Capron M.

Mol Biochem Parasitol. 2000 Apr 15;107(2):279-87.

PMID:
10779604
25.

Evolution of alpha 2-fucosyltransferase genes in primates: relation between an intronic Alu-Y element and red cell expression of ABH antigens.

Apoil PA, Roubinet F, Despiau S, Mollicone R, Oriol R, Blancher A.

Mol Biol Evol. 2000 Mar;17(3):337-51.

PMID:
10723735
26.

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

Elmgren A, Börjeson C, Mollicone R, Oriol R, Fletcher A, Larson G.

Hum Mutat. 2000 Dec;16(6):473-81.

PMID:
11102976
28.

Divergent evolution of fucosyltransferase genes from vertebrates, invertebrates, and bacteria.

Oriol R, Mollicone R, Cailleau A, Balanzino L, Breton C.

Glycobiology. 1999 Apr;9(4):323-34. Review.

PMID:
10089206
29.

Point mutations and deletion responsible for the Bombay H null and the Reunion H weak blood groups.

Fernandez-Mateos P, Cailleau A, Henry S, Costache M, Elmgren A, Svensson L, Larson G, Samuelsson BE, Oriol R, Mollicone R.

Vox Sang. 1998;75(1):37-46.

PMID:
9745152
30.

Evolution of fucosyltransferase genes in vertebrates.

Costache M, Apoil PA, Cailleau A, Elmgren A, Larson G, Henry S, Blancher A, Iordachescu D, Oriol R, Mollicone R.

J Biol Chem. 1997 Nov 21;272(47):29721-8.

31.
32.

Advances in molecular genetics of alpha-2- and alpha-3/4-fucosyltransferases.

Costache M, Cailleau A, Fernandez-Mateos P, Oriol R, Mollicone R.

Transfus Clin Biol. 1997 Jul;4(4):367-82. Review.

PMID:
9269717
33.

Molecular cloning and expression of a bovine alpha(1,3)-fucosyltransferase gene homologous to a putative ancestor gene of the human FUT3-FUT5-FUT6 cluster.

Oulmouden A, Wierinckx A, Petit JM, Costache M, Palcic MM, Mollicone R, Oriol R, Julien R.

J Biol Chem. 1997 Mar 28;272(13):8764-73.

35.

How do antibodies and lectins recognize histo-blood group antigens? A 3D-QSAR study by comparative molecular field analysis (CoMFA).

Imberty A, Mollicone R, Mikros E, Carrupt PA, Pérez S, Oriol R.

Bioorg Med Chem. 1996 Nov;4(11):1979-88.

PMID:
9007281
36.

Fucosyltransferase genes are dispersed in the genome: FUT7 is located on 9q34.3 distal to D9S1830.

Reguigne-Arnould I, Wolfe J, Hornigold N, Fauré S, Mollicone R, Oriol R, Coullin P.

C R Acad Sci III. 1996 Sep;319(9):783-8.

PMID:
8952881
37.

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.

J Biol Chem. 1996 Jun 14;271(24):14492-5.

38.

Recognition of the blood group H type 2 trisaccharide epitope by 28 monoclonal antibodies and three lectins.

Mollicone R, Cailleau A, Imberty A, Gane P, Perez S, Oriol R.

Glycoconj J. 1996 Apr;13(2):263-71.

PMID:
8737251
39.

Physical mapping of 49 microsatellite markers on chromosome 19 and correlation with the genetic linkage map.

Reguigne-Arnould I, Faure S, Chery M, Mota-Viera L, Mollicone R, Candelier JJ, Oriol R, Couillin P.

Genomics. 1996 Mar 15;32(3):458-61.

PMID:
8838811
40.

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.

Biochem Biophys Res Commun. 1996 Feb 27;219(3):675-8.

PMID:
8645240
41.

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.

Vox Sang. 1996;71(4):233-41.

PMID:
8958648
42.

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.

Vox Sang. 1996;70(1):21-5.

43.
44.

Molecular genetics of H, Se, Lewis and other fucosyltransferase genes.

Mollicone R, Cailleau A, Oriol R.

Transfus Clin Biol. 1995;2(4):235-42. Review.

PMID:
8542021
45.

Relative positions of two clusters of human alpha-L-fucosyltransferases in 19q (FUT1-FUT2) and 19p (FUT6-FUT3-FUT5) within the microsatellite genetic map of chromosome 19.

Reguigne-Arnould I, Couillin P, Mollicone R, Fauré S, Fletcher A, Kelly RJ, Lowe JB, Oriol R.

Cytogenet Cell Genet. 1995;71(2):158-62.

PMID:
7656588
46.

Molecular basis for Lewis alpha(1,3/1,4)-fucosyltransferase gene deficiency (FUT3) found in Lewis-negative Indonesian pedigrees.

Mollicone R, Reguigne I, Kelly RJ, Fletcher A, Watt J, Chatfield S, Aziz A, Cameron HS, Weston BW, Lowe JB.

J Biol Chem. 1994 Aug 19;269(33):20987-94.

47.

H and B human blood-group antigen expression in cochlear hair cells is modulated by thyroxine.

Gil-Loyzaga P, Remezal M, Mollicone R, Ibáñez A, Oriol R.

Cell Tissue Res. 1994 May;276(2):239-43.

PMID:
8020061
48.

Molecular basis for plasma alpha(1,3)-fucosyltransferase gene deficiency (FUT6).

Mollicone R, Reguigne I, Fletcher A, Aziz A, Rustam M, Weston BW, Kelly RJ, Lowe JB, Oriol R.

J Biol Chem. 1994 Apr 29;269(17):12662-71.

49.

The gene encoding myeloid alpha-3-fucosyl-transferase (FUT4) is located between D1 1S388 and D11S919 on 11q21.

Reguigne I, James MR, Richard CW 3rd, Mollicone R, Seawright A, Lowe JB, Oriol R, Couillin P.

Cytogenet Cell Genet. 1994;66(2):104-6.

PMID:
8287679
50.

Molecular genetics of alpha-L-fucosyltransferase genes (H, Se, Le, FUT4, FUT5 and FUT6).

Mollicone R, Candelier JJ, Reguigne I, Couillin P, Fletcher A, Oriol R.

Transfus Clin Biol. 1994;1(2):91-7. Review.

PMID:
8019653

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