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1 ross-reactivity with the high-affinity human laminin receptor.
2 eration with the alpha6 integrin, a specific laminin receptor.
3 ltage-gated calcium channel as well as a new laminin receptor.
4 o infect mammalian cells using the Mr 67,000 laminin receptor.
5  alpha(6) integrin is a 140-kDa (nonreduced) laminin receptor.
6  a precursor for the Mr 67,000 high-affinity laminin receptor.
7 a6beta4 integrin, beta1 integrins, and an E3 laminin receptor.
8 erves as a cell surface collagen or collagen/laminin receptor.
9 1 and beta 4 subunits to form a subfamily of laminin receptors.
10 dy/dy mice lacking LN-alpha2, but expressing laminin receptors.
11 atural antagonist of the integrin-associated laminin receptor 1 (LAMR1) known to mediate metastatic t
12               EGCG interacts with the 67-kDa laminin receptor 1 (LR1), which is significantly elevate
13 osine phosphatase kappa (RPTP-kappa) and the laminin receptor 1 (ribosomal protein SA) pseudogene 1 l
14          The screen was extended to identify laminin receptor 1 as a functional partner in regards to
15 lipoprotein C-III, and the gene encoding the laminin receptor 1 were only found in the samples from p
16 ly associated with malignancy, including the laminin receptor-1 and the multidrug-resistance channel
17            Two of the known genes, the 67-kd laminin receptor (67LR) and tumor-associated trypsin inh
18 1) interaction with its receptor, the 67-kDa laminin receptor (67LR), and host signaling molecules in
19 zoe et al. report that EGCG activates 67-kDa laminin receptor (67LR), elevates cGMP levels, and induc
20        These include six known genes, 67-kDa laminin receptor (67LR), endothelin receptor B (ENDRB),
21 -induced preconditioning required the 67-kDa laminin receptor (67LR), to which EGCG binds with high a
22 RP) of HBMEC, which is a precursor of 67-kDa laminin receptor (67LR).
23 -3-gallate (EGCG) signals ECs via the 67 kDa laminin-receptor (67LR) resulting in protein kinase A de
24 ecreased membrane localization of the 67 kDa laminin receptor, 67LR, and inhibition of the functional
25 RA induced expression of alpha 6 integrin (a laminin receptor alpha-chain) and enabled more advanced
26 tastatic, expresses three potential integrin laminin receptors: alpha 2 beta 1, alpha 3 beta 1, and a
27 pithelial cells deficient in their prominent laminin receptor, alpha3beta1, were found to have a mark
28                            We found that the laminin receptor alpha6beta1 integrin, which is expresse
29 m the VZ express high levels of the integrin laminin receptor alpha6beta1.
30 eolar epithelial cells (AECs) expressing the laminin receptor alpha6beta4, but little or no pro-surfa
31 ly, myotubes lacking integrin alpha7beta1, a laminin-receptor, also show a significant increase in pS
32                 Furthermore, our analyses of laminin receptor, an in vivo substrate of ST3 in the int
33 preference for cancer cells that overexpress laminin receptor and safeguard RNA prior their delivery
34 ns act as links among pre- and post-synaptic laminin receptors and alpha-DG and pikachurin in the syn
35 thetic review on loss-of-function studies of laminin receptors and foster the formation and testing o
36 in multiple sclerosis (MS) lesions, integrin laminin receptors and laminin were analyzed in central n
37 e alpha6beta1 integrin, a well characterized laminin receptor, and that alpha6beta1 expression levels
38 t, key signaling pathways downstream of each laminin receptor are summarized and compared.
39          Therefore, while other cell surface laminin receptors are likely responsible for myocardial
40 in astrocyte endfeet) and integrin-alpha6 (a laminin receptor), are upregulated in Apcdd1-/- retinas
41 nduced new expression of alpha 6 integrin, a laminin receptor, as assessed by reverse transcription-p
42 ulation of human SS RBC adhesiveness via the laminin receptor, basal cell adhesion molecule/Lutheran
43            Another synaptically concentrated laminin receptor, Bcam, is dispensable.
44 , prior exposure to 100 microg ml-1 YIGSR, a laminin receptor-binding peptide, restored ACh-induced s
45 gainst the alpha6 subunit of the alpha6beta1 laminin receptor blocked matrix induction of uPA without
46 od group A and precursors of blood antigens; laminin receptor; c-erbB1/epidermal growth factor recept
47 anism whereby the integrin alpha 6 beta 1, a laminin receptor, can affect cell motility and induce mi
48 endently of choline binding protein A (CbpA)/laminin receptor, CbpA/polymeric immunoglobulin receptor
49 strate of ST3 in the intestine, suggest that laminin receptor cleavage may be an underlying mechanism
50                                 Internalized laminin receptors colocalized with receptor recycling ve
51 fish suggests the existence of an additional laminin receptor complex that anchors muscle fibers to t
52 ract with, amongst others, the transmembrane laminin receptor dystroglycan, cytoskeletal actin and, i
53                            Another potential laminin receptor, dystroglycan, is at the post-synaptic
54 the function of dystroglycan, a cell-surface laminin receptor expressed by cells contacting basement
55 lar signaling by the alpha6beta4 integrin, a laminin receptor expressed in basal keratinocytes and ot
56   The alpha(2)beta(1) integrin is a collagen/laminin receptor expressed on platelets, endothelial cel
57 dystroglycan are essential for high-affinity laminin-receptor function.
58 nes encoding laminin subunits as well as the laminin receptor gene Itga7, which encodes the alpha7 in
59  those of fibronectin, fibronectin receptor, laminin receptor homolog, beta-tubulin, insulin-like gro
60 ggests that this protein may also serve as a laminin receptor in malignant tumors.
61    Since the alpha7beta1 integrin is a major laminin receptor in skeletal muscle, we determined if th
62 nduced by laminin, thereby implicating an E3 laminin receptor in this function.
63 tudies have described the essential roles of laminin receptors in both physiological and pathologic c
64 trophin glycoprotein complexes are the major laminin receptors in skeletal muscle.
65 nvolvement of the alpha 6 beta a integrin, a laminin receptor, in breast carcinoma progression needs
66 pathology and loss-of-function phenotypes of laminin receptors, including integrin-alpha3, integrin-a
67     Together, our findings indicate that the laminin receptor integrin alpha6beta1 promotes the survi
68 t with an increase in the alpha 6-containing laminin receptor integrin.
69                                  A potential laminin receptor, integrin alpha3, is at the presynaptic
70 he levels of RNA and surface protein for two laminin receptors, integrin alpha6beta1 and alpha3beta1,
71 monstrate that alpha3beta1 integrin, a major laminin receptor involved in the development of the kidn
72 quiescent retinal vessels suggests that this laminin receptor is an important and novel target for fu
73 mical staining of tumor cells indicates that laminin receptor is elevated in tumor versus normal cell
74        Here, we show that the beta1-Integrin laminin receptor is required for RGC positioning and reo
75 after depletion of precursors, expression of laminin receptors is upregulated.
76         The alpha2beta1 integrin, a collagen/laminin receptor, is expressed at high level in the basa
77         The alpha2beta1 integrin, a collagen/laminin receptor, is expressed by a variety of cell type
78 We showed that Lu/BCAM, the unique erythroid laminin receptor, is overexpressed and highly phosphoryl
79                                    The human laminin receptor (LamR) interacts with many ligands, inc
80                         The 37/ 67-kDa human laminin receptor (LamR) is a cell surface receptor for l
81 identified decreased expression of 37/67 kDa laminin receptor (LAMR), which binds laminin-beta1, in h
82 electively targets tumors through the 67-kDa laminin receptor (LAMR).
83  a cellular receptor for AAV8, the 37/67-kDa laminin receptor (LamR).
84 te copy (97.9% identical) of the transcribed laminin receptor (LAMR1) with all the introns precisely
85 itecture, is a cooperative process requiring laminin- receptor ligation, receptor-facilitated self-as
86 teracting proteins and identified the 67-kDa laminin receptor (LR), a nonintegrin matrix protein rece
87 and certain neurotropic viruses, bind to the laminin receptor (LR), and this determines tropism to th
88 ivation by binding with a 67 kDa nonintegrin laminin receptor (LR).
89 noma cells acting via 37/67 kDa non-integrin laminin receptor (LR/37/67 kDa) and downstream ERK1/2, P
90                  Tumor overexpression of the laminin receptor may explain the specificity and efficac
91 are cross-reactive antigens that bind to the laminin receptor of the blood-brain barrier as a molecul
92 nt in mice and humans, oncofetal Ag/immature laminin receptor (OFA/iLRP)-specific Th1, CTL, and IL-10
93 at a synaptic vesicle component may act as a laminin receptor on the presynaptic plasma membrane; the
94 esin choline-binding protein A that binds to laminin receptor on vascular endothelial cells and bindi
95           Expression of alpha(6) integrin, a laminin receptor, on tumor cell surfaces is associated w
96        A functional role for the nonintegrin laminin receptor p67 has been described for cancer metas
97 e linked the overexpression of the Mr 37,000 laminin receptor precursor (37-LRP) to tumor cell growth
98  invasion of HBMEC and interacts with 37-kDa laminin receptor precursor (37LRP) of HBMEC, which is a
99                   Here, we identified 37-kDa laminin receptor precursor (LRP) as the receptor for CNF
100 g of the toxin to its cellular receptor, the laminin receptor precursor protein (LRP), a series of CN
101 the cell surface GBC-3 antigen is the 40 kDa laminin receptor precursor protein.
102  of CNF1+ E. coli K1 with recombinant 37-kDa laminin receptor precursor reduced the invasion rate to
103 her and over 60% identity with the human p40/laminin receptor precursor.
104 de proteins closely related to mammalian p40/laminin receptor precursors (LRPs).
105                           A highly conserved laminin receptor processed pseudogene (LAMRL5) that has
106  an evolutionarily conserved 37-kDa immature laminin receptor protein (OFA-iLRP), a nonimmunogenic em
107 ll to purified OFA or 32- to 44-kDa immature laminin receptor protein.
108 ted redox-induced downstream expression of a laminin receptor, Ribosomal Protein SA, following RFGDT.
109           We sought to identify the specific laminin receptor(s) mediating the multiple cell response
110  neuropathies, results attributed to loss of laminin-receptor signaling.
111            Suppression of integrin alpha3, a laminin receptor subunit, in cells synthesizing normal a
112 (fibronectin receptor), and alpha3 (collagen/laminin receptor) subunits were the most abundant.
113 ss of the dystrophin-glycoprotein complex, a laminin receptor that connects the myofiber to its surro
114  beta 1 integrin (VLA-1) is a major collagen/laminin receptor that regulates fibroblast proliferation
115                  The integrin alpha6beta4, a laminin receptor that stabilizes epithelial cell adhesio
116 onal redundancy/compensation among different laminin receptors, the phenotypes of compound knockout m
117  a central component of the DGC, serves as a laminin receptor via its extracellular alpha subunit, an
118 tive binding activity toward the alpha7beta1 laminin receptor, we have found that overexpression of M
119                                              Laminin receptors were blocked, and TEa T-cell migration
120                 Down-regulated expression of laminin receptor with small interfering RNA significantl

 
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