ライフサイエンスコーパス: sulfated proteoglycan

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1 are nectin-1, HveA, and a specific O-linked sulfated proteoglycan.

2 to the cell surface via naturally occurring sulfated proteoglycans.

3 n to the sLex carbohydrate, P-selectin binds sulfated proteoglycan, 3-sulfated galactosyl ceramide (s

4 The interaction was inhibited by sulfated proteoglycans and by antibodies against GP Ibal

5 curring amyloid deposits are associated with sulfated proteoglycans and other factors.

6 embedded in an extracellular matrix rich in sulfated proteoglycans and type II collagen.

7 Collectively, these studies reveal that sulfated proteoglycans are one determinant used for subs

8 s indicated that elastase treatment released sulfated proteoglycan from the cell surface in a time- a

9 Heparan and chondroitin/dermatan sulfated proteoglycans have a wide range of roles in cel

10 Sulfated proteoglycans have been shown to be involved in

11 Sulfated proteoglycans have important structural and sig

12 ) and may influence binding of Vn to heparan-sulfated proteoglycans (HSPGs).

13 which we have ablated the binding sites for sulfated proteoglycans in glycoproteins B and C, replace

14 faster than Nodal, with evidence that intact sulfated proteoglycans in the ECM facilitate the remarka

15 potential for interactions with membranes or sulfated proteoglycans is lacking and it is possible tha

16 ited and cell spreading was independent of a sulfated proteoglycan-mediated mechanism.

17 parin binding protein, may also interact via sulfated proteoglycan molecular bridges with a number of

18 oid formation by promoting interactions with sulfated proteoglycans of the extracellular matrix, whic

19 nd infection via Ca(2+)-dependent binding to sulfated proteoglycans on intestinal epithelial cells.

20 H. somnus could serve as initial adhesins to sulfated proteoglycans on the endothelial cell surface,

21 Instead, sulfated proteoglycans play a role in the storage of sec

22 re was significantly less total collagen and sulfated proteoglycans present in the type VI collagen-d

23 nonspecific electrostatic interactions with sulfated proteoglycans present on the surface of most ma

24 The importance of sulfated proteoglycan recognition was further supported

25 (but not TGFbeta-induced) proliferation and sulfated proteoglycan synthesis, and it inhibited ligand

26 ked fibronectin fibrillogenesis and required sulfated proteoglycans to mediate cell spreading.

27 rter that promotes a ventral accumulation of sulfated proteoglycans, which is required for ventral PM

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