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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
13 r mechanism explains the cooperation between extracellular matrix receptors during cell adhesion.
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
19 findings suggest dystroglycan function as an extracellular matrix receptor in cardiac myocytes plays
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
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
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
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
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
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
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