戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ive capacity, mediated in part by integrins (extracellular matrix receptors).
2 Bud10p functions in a manner analogous to an extracellular matrix receptor.
3 ains for CD44, a plasma membrane protein and extracellular matrix receptor.
4 lved in activation of the integrin family of extracellular matrix receptors.
5 n and reduced expression of several integrin extracellular matrix receptors.
6 monstrate that dystroglycan and perlecan, an extracellular matrix receptor and its ligand, help local
7 sing mediated through the integrin family of extracellular matrix receptors and linked proteins and d
8 le in either uterine invasion (integrin cell-extracellular matrix receptors and matrix metalloprotein
9 protein interaction subnetworks, enriched by extracellular matrix receptors and modulators or by nucl
10 s and that laminin is crucial for organizing extracellular matrix, receptor and intracellular protein
11 p and others has demonstrated a role for the extracellular matrix receptor CD44 and its ligand hyalur
12          Cranin (dystroglycan), a mucin-like extracellular matrix receptor comprised of two subunits
13 r mechanism explains the cooperation between extracellular matrix receptors during cell adhesion.
14      Post-translational modifications of the extracellular matrix receptor dystroglycan (DG) determin
15                        Here, we show that an extracellular matrix receptor, Dystroglycan, is down-reg
16 ay be a host environmental cue that triggers extracellular matrix receptor expression at a septic sit
17 w that Large(myd) hearts with the loss of DG extracellular matrix receptor function display a cardiom
18       The abnormal glycosylation and loss of extracellular matrix receptor function of the protein dy
19 findings suggest dystroglycan function as an extracellular matrix receptor in cardiac myocytes plays
20        Dystroglycan, which serves as a major extracellular matrix receptor in muscle and the central
21 1 and alphaVbeta3/beta5 integrins, essential extracellular matrix receptors in mesenchymal tumors, wh
22 of the beta1 integrin family of cell surface extracellular matrix receptors in multilineage different
23 rch directions into this important family of extracellular matrix receptors in the myocardium.
24 to the function of this fascinating class of extracellular matrix receptors, in particular in the con
25  exists on how the nanoscale presentation of extracellular matrix receptors influences collective cel
26 slet endocrine cell-specific inactivation of extracellular matrix receptor integrin beta1 disrupted b
27                            By correcting the extracellular matrix-receptor (integrin) signaling and b
28 K) development; however, among the different extracellular matrix receptors, integrin alpha2beta1 and
29 hlighted a unique set of targets involved in extracellular matrix-receptor interaction and focal adhe
30 e important to the OA process, including the extracellular matrix-receptor interaction and the focal
31 with a high enrichment in focal adhesion and extracellular matrix-receptor interaction, in addition t
32  in pathways linked to insulin secretion and extracellular matrix-receptor interaction.
33 atory roles in smooth muscle contraction and extracellular matrix-receptor interaction.
34                                  Conversely, extracellular matrix receptor interactions are upregulat
35 ponse; rather, oxidative phosphorylation and extracellular matrix-receptor interactions are dysregula
36 lative to the DZ included, most prominently, extracellular matrix-receptor interactions, cell adhesio
37 hways in focal adhesion, actin cytoskeleton, extracellular matrix-receptor interactions, multiple lig
38 vous system development), cell adhesion, and extracellular matrix-receptor interactions.
39 time, this work highlights the importance of extracellular matrix receptor nanoscale organization req
40 xpression of keratinocyte integrins or their extracellular matrix receptors occurs after the causativ
41                             In recent years, extracellular matrix receptors of the integrin family ha
42                                              Extracellular matrix receptors on the cell surface media
43    Their results reveal that signaling by an extracellular matrix receptor plays a key role in the di
44 lpha-dystroglycan is a highly O-glycosylated extracellular matrix receptor that is required for ancho
45           Dystroglycan is a widely expressed extracellular matrix receptor that plays a critical role
46                  Integrins are heterodimeric extracellular matrix receptors that are essential for th
47       Integrins are a class of transmembrane extracellular matrix receptors that function as alphabet
48 Integrins comprise a family of heterodimeric extracellular matrix receptors that mediate cell adhesio
49 sociated in oligodendrocytes with integrins, extracellular matrix receptors that regulate target-depe
50 ins of integrins provide attachment of these extracellular matrix receptors to the cytoskeleton and p
51 rotein that is critical for linking integrin extracellular-matrix receptors to the actin cytoskeleton
52 rtantly, they express differential levels of extracellular matrix receptors, with NSCs expressing low