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1 1b series (GT1b), but not by a non-1b series ganglioside (GM3).
2  with EGFR requires the presence of CD82 and ganglioside GM3.
3 nant ECD from insect cells bound directly to ganglioside GM3.
4 amide (LacCer) to produce the monosialylated ganglioside GM3.
5 yed milder PKD, revealing a pivotal role for ganglioside GM3.
6               The ST3GAL5 enzyme synthesizes ganglioside GM3, a glycosophingolipid enriched in neural
7                                              Ganglioside GM3, a host-derived glycosphingolipid incorp
8 characterized by the predominant presence of ganglioside GM3 and adhere to lactosylceramide- or Gg3-c
9  its receptor (FGFR), stably associated with ganglioside GM3 and TSPs CD9 and CD81 in the ganglioside
10 SSEA3) and SSEA4 in hiPSCs toward the simple gangliosides GM3 and GD3 in hiPSC-CMs.
11 osylceramide, globotriaosylceramide, and the gangliosides GM3 and GM1 were significantly elevated in
12                                              Gangliosides GM3 and GT1b both inhibit epithelial cell a
13 t out to address the role of a specific GSL (ganglioside GM3) and signaling SL (sphingosine-1-phospha
14 lysobisphosphatidic acid, sphingomyelin, the ganglioside GM3, and cholesterol esters, all of which su
15 ontaining the CD169/Siglec-1 binding ligand, ganglioside GM3, and the non-binding ligand, ganglioside
16  tyrosine kinase is known to be inhibited by ganglioside GM3, but to a much lesser degree by other gl
17 A synthesis in a reversible manner, although ganglioside GM3 could not reverse the effects of FB1 on
18                                    Synthetic ganglioside GM3 derivatives further distinguished lectin
19 found that caveolin-1, tetraspanin CD82, and ganglioside GM3 enable the association of EGFR with PKC-
20  morphology could be reversed by addition of ganglioside GM3 even in the presence of FB1, whereas the
21 ) we generated mice that express only simple gangliosides (GM3/GD3) and examined their central and pe
22 s including several sphingolipids (ceramide, ganglioside GM3, GM2, GM1, GD3 and GD1a), cardiolipin, c
23 oly-lactic acid nanoparticles expressing the ganglioside, GM3 (GM3-NPs) and incorporating dual ARVs,
24 ids, such as ceramide, glucosylceramide, and ganglioside GM3, have been implicated in various aspects
25                                              Ganglioside GM3 inhibits EGFR autophosphorylation and ma
26                                              Ganglioside GM3 inhibits epidermal growth factor (EGF)-d
27 nd the chicken fibroblast cell line DF1, the ganglioside GM3 is the major glycosphingolipid component
28 te that kidney glucosylceramide (GlcCer) and ganglioside GM3 levels are higher in human and mouse PKD
29                                              Ganglioside GM3 mediates adipocyte insulin resistance, b
30 eaction) as well as ceramide trihexoside and ganglioside GM3 (products distal to the GlcCer synthase
31 th the specificity of soluble ECD binding to gangliosides, GM3 specifically inhibited EGFR autophosph
32 ) L612, specific to a tumor-related antigen (ganglioside) GM3 that is expressed on the cell surface o
33 h FB1 resulted in a decrease in synthesis of ganglioside GM3, the major glycosphingolipid in 3T3 fibr
34                             Using a model of ganglioside GM3 uptake in brain vessel endothelial cells
35                                          The ganglioside GM3, used by sialyltransferase II (ST-II) as
36  the sialidase-positive clones, the level of ganglioside GM3 was diminished, and little change was ob
37         The EPEN tumor cells synthesize only ganglioside GM3, whereas the CT-2A tumor cells synthesiz
38      The major difference is in the level of ganglioside GM3, which is several times higher in KK47 t