| Guanosine diphosphate-mannose:GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutations. Dupre T., Vuillaumier-Barrot S., Chantret I., Yaye H.S., Le Bizec C., Afenjar A., Altuzarra C., Barnerias C., Burglen L., de Lonlay P. et al.
J. Med. Genet. 47:729-735(2010) · Mapped (2) |
| Identification of roles for peptide: N-glycanase and endo-beta-N-acetylglucosaminidase (Engase1p) during protein N-glycosylation in human HepG2 cells. Chantret I., Fasseu M., Zaoui K., Le Bizec C., Yaye H.S., Dupre T., Moore S.E.
PLoS ONE 5:e11734-e11734(2010) · Mapped (2) |
| Activity, splice variants, conserved peptide motifs, and phylogeny of two new alpha1,3-fucosyltransferase families (FUT10 and FUT11). Mollicone R., Moore S.E., Bovin N., Garcia-Rosasco M., Candelier J.J., Martinez-Duncker I., Oriol R.
J. Biol. Chem. 284:4723-4738(2009) · Mapped (5) |
| Characterisation of 5-HT3C, 5-HT3D and 5-HT3E receptor subunits: evolution, distribution and function. Holbrook J.D., Gill C.H., Zebda N., Spencer J.P., Leyland R., Rance K.H., Trinh H., Balmer G., Kelly F.M., Yusaf S.P. et al.
J. Neurochem. 108:384-396(2009) · UniProtKB (1) |
| Two proteins homologous to the N- and C-terminal domains of the bacterial glycosyltransferase Murg are required for the second step of dolichyl-linked oligosaccharide synthesis in Saccharomyces cerevisiae. Chantret I., Dancourt J., Barbat A., Moore S.E.H.
J. Biol. Chem. 280:9236-9242(2005) · UniProtKB (2) |
| Mitochondrial enzyme content in the muscles of high-performance fish: evolution and variation among fiber types. Dalziel A.C., Moore S.E., Moyes C.D.
Am. J. Physiol. 288:R163-R172(2005) · UniProtKB (5) |
| Free-oligosaccharide control in the yeast Saccharomyces cerevisiae: roles for peptide:N-glycanase (Png1p) and vacuolar mannosidase (Ams1p). Chantret I., Frenoy J.-P., Moore S.E.H.
Biochem. J. 373:901-908(2003) · UniProtKB (2) |
| A deficiency in dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase defines a new subtype of congenital disorders of glycosylation. Chantret I., Dancourt J., Dupre T., Delenda C., Bucher S., Vuillaumier-Barrot S., Ogier de Baulny H., Peletan C., Danos O., Seta N. et al.
J. Biol. Chem. 278:9962-9971(2003) · UniProtKB (1) |
| Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferase. Chantret I., Dupre T., Delenda C., Bucher S., Dancourt J., Barnier A., Charollais A., Heron D., Bader-Meunier B., Danos O. et al.
J. Biol. Chem. 277:25815-25822(2002) · UniProtKB (1) · Mapped (6) |
| Perturbation of free oligosaccharide trafficking in endoplasmic reticulum glucosidase I-deficient and castanospermine-treated cells. Durrant C., Moore S.E.
Biochem. J. 365:239-247(2002) · Mapped (5) |
| Neuropilin-2 is required in vivo for selective axon guidance responses to secreted semaphorins. Giger R.J., Cloutier J.F., Sahay A., Prinjha R.K., Levengood D.V., Moore S.E., Pickering S., Simmons D., Rastan S., Walsh F.S. et al.
Neuron 25:29-41(2000) · Mapped (17) |
| Inhibitor of neurite outgrowth in humans. Prinjha R., Moore S.E., Vinson M., Blake S., Morrow R., Christie G., Michalovich D., Simmons D.L., Walsh F.S.
Nature 403:383-384(2000) · UniProtKB (1) |
| Complete sequence and in vitro expression of a tissue-specific phosphatidylinositol-linked N-CAM isoform from skeletal muscle. Barton C.H., Dickson G., Gower H.J., Rowett L.H., Putt W., Elsom V., Moore S.E., Goridis C., Walsh F.S.
Development 104:165-173(1988) · UniProtKB (1) |
| Alternative splicing generates a secreted form of N-CAM in muscle and brain. Gower H.J., Barton C.H., Elsom V.L., Thompson J., Moore S.E., Dickson G., Walsh F.S.
Cell 55:955-964(1988) · UniProtKB (1) |
| Human muscle neural cell adhesion molecule (N-CAM): identification of a muscle-specific sequence in the extracellular domain. Dickson G., Gower H.J., Barton C.H., Prentice H.M., Elsom V.L., Moore S.E., Cox R.D., Quinn C., Putt W., Walsh F.S.
Cell 50:1119-1130(1987) · UniProtKB (1) |
| Cloning and characterization of a myoblast cell surface antigen defined by 24.1D5 monoclonal antibody. Gower H.J., Moore S.E., Dickson G., Elsom V.L., Nayak R., Walsh F.S.
Development 105:723-731(1989) · UniProtKB (1) |
| N-cadherin gene maps to human chromosome 18 and is not linked to the E-cadherin gene. Walsh F.S., Barton C.H., Putt W., Moore S.E., Kelsell D., Spurr N., Goodfellow P.N.
J. Neurochem. 55:805-812(1990) · UniProtKB (1) |
