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Mary Ellen K. Salyan

Researcher at Bristol-Myers Squibb

Publications -  17
Citations -  588

Mary Ellen K. Salyan is an academic researcher from Bristol-Myers Squibb. The author has contributed to research in topics: Mass spectrometry & Fast atom bombardment. The author has an hindex of 13, co-authored 17 publications receiving 580 citations.

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Journal ArticleDOI

Monosialogangliosides of human myelogenous leukemia HL60 cells and normal human leukocytes. 2. Characterization of E-selectin binding fractions, and structural requirements for physiological binding to E-selectin.

TL;DR: The E-selectin binding epitope in HL60 cells is carried by unbranched terminally alpha 2-->3 sialylated polylactosamines having at least 10 monosaccharide units (4 N-acetyllactosamine units) with internal multiple fucosylation at GlcNAc.
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Monosialogangliosides of Human Myelogenous Leukemia HL60 Cells and Normal Human Leukocytes. 1. Separation of E-Selectin Binding from Nonbinding Gangliosides, and Absence of Sialosyl-Lex Having Tetraosyl to Octaosyl Core†

TL;DR: Isolation and chemical characterization of ganglioside structures I-XI are described in this paper, which suggest that sialosyl-Le(x) (SLex) is a ligand expressed in human neutrophils and myelogenous leukemia HL60 cells which binds to E-selectin and possibly P- selectin.
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Novel tri-and tetrasialosylpoly-N-acetyllactosaminyl gangliosides of human placenta: structure determination of pentadeca- and eicosaglycosylceramides by methylation analysis, fast atom bombardment mass spectrometry, and 1H NMR spectroscopy.

TL;DR: A series of highly polar neolacto series (poly-N-acetyllactosaminyl) gangliosides were isolated from human placenta tissue and purified by HPLC and preparative HPTLC, among the highest molecular weight glycosphingolipids whose detailed oligosaccharide structures are presently known.
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Structural characterization of x2 glycosphingolipid, its extended form, and its sialosyl derivatives: accumulation associated with the rare blood group p phenotype.

TL;DR: Application of MAb TH2 on TLC immunoblotting together with chemical analysis indicates the following points of interest: (i) the existence of extended type GSLs having the same x2 terminal structure; (ii) the chemical quantities of x2, sialosyl-x2, and extended x2 found in blood cells and in various tissues including carcinomas being nearly the same.
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Discovery of a potent and novel motilin agonist.

TL;DR: A novel series of dihydro- and tetrahydrotriazolopyridazine-1,3-dione-based amino acid derivatives were identified as very potent motilin receptor agonists and compound 11A was shown to have a significantly reduced tendency to cause receptor desensitization as compared with the motilIn receptor agonist ABT-229.