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1  are nectin-1, HveA, and a specific O-linked sulfated proteoglycan.
2 ed synthesis of matrix molecules, especially sulfated proteoglycans.
3  to the cell surface via naturally occurring sulfated proteoglycans.
4 n to the sLex carbohydrate, P-selectin binds sulfated proteoglycan, 3-sulfated galactosyl ceramide (s
5             The interaction was inhibited by sulfated proteoglycans and by antibodies against GP Ibal
6 curring amyloid deposits are associated with sulfated proteoglycans and other factors.
7  embedded in an extracellular matrix rich in sulfated proteoglycans and type II collagen.
8      Collectively, these studies reveal that sulfated proteoglycans are one determinant used for subs
9 s indicated that elastase treatment released sulfated proteoglycan from the cell surface in a time- a
10             Heparan and chondroitin/dermatan sulfated proteoglycans have a wide range of roles in cel
11                                              Sulfated proteoglycans have been shown to be involved in
12                                              Sulfated proteoglycans have important structural and sig
13 ) and may influence binding of Vn to heparan-sulfated proteoglycans (HSPGs).
14  which we have ablated the binding sites for sulfated proteoglycans in glycoproteins B and C, replace
15 faster than Nodal, with evidence that intact sulfated proteoglycans in the ECM facilitate the remarka
16 potential for interactions with membranes or sulfated proteoglycans is lacking and it is possible tha
17 ited and cell spreading was independent of a sulfated proteoglycan-mediated mechanism.
18 parin binding protein, may also interact via sulfated proteoglycan molecular bridges with a number of
19 oid formation by promoting interactions with sulfated proteoglycans of the extracellular matrix, whic
20 nd infection via Ca(2+)-dependent binding to sulfated proteoglycans on intestinal epithelial cells.
21 ellular assays, we demonstrate that both the sulfated proteoglycans on the cell surface and the corre
22 H. somnus could serve as initial adhesins to sulfated proteoglycans on the endothelial cell surface,
23                                     Instead, sulfated proteoglycans play a role in the storage of sec
24 re was significantly less total collagen and sulfated proteoglycans present in the type VI collagen-d
25  nonspecific electrostatic interactions with sulfated proteoglycans present on the surface of most ma
26                            The importance of sulfated proteoglycan recognition was further supported
27  (but not TGFbeta-induced) proliferation and sulfated proteoglycan synthesis, and it inhibited ligand
28 ked fibronectin fibrillogenesis and required sulfated proteoglycans to mediate cell spreading.
29 rter that promotes a ventral accumulation of sulfated proteoglycans, which is required for ventral PM