ライフサイエンスコーパス: laminin receptor

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 ns act as links among pre- and post-synaptic laminin receptors and alpha-DG and pikachurin in the syn

34 in multiple sclerosis (MS) lesions, integrin laminin receptors and laminin were analyzed in central n

35 e alpha6beta1 integrin, a well characterized laminin receptor, and that alpha6beta1 expression levels

36 Therefore, while other cell surface laminin receptors are likely responsible for myocardial

37 nduced new expression of alpha 6 integrin, a laminin receptor, as assessed by reverse transcription-p

38 ulation of human SS RBC adhesiveness via the laminin receptor, basal cell adhesion molecule/Lutheran

39 Another synaptically concentrated laminin receptor, Bcam, is dispensable.

40 , prior exposure to 100 microg ml-1 YIGSR, a laminin receptor-binding peptide, restored ACh-induced s

41 gainst the alpha6 subunit of the alpha6beta1 laminin receptor blocked matrix induction of uPA without

42 od group A and precursors of blood antigens; laminin receptor; c-erbB1/epidermal growth factor recept

43 anism whereby the integrin alpha 6 beta 1, a laminin receptor, can affect cell motility and induce mi

44 endently of choline binding protein A (CbpA)/laminin receptor, CbpA/polymeric immunoglobulin receptor

45 strate of ST3 in the intestine, suggest that laminin receptor cleavage may be an underlying mechanism

46 Internalized laminin receptors colocalized with receptor recycling ve

47 fish suggests the existence of an additional laminin receptor complex that anchors muscle fibers to t

48 ract with, amongst others, the transmembrane laminin receptor dystroglycan, cytoskeletal actin and, i

49 Another potential laminin receptor, dystroglycan, is at the post-synaptic

50 the function of dystroglycan, a cell-surface laminin receptor expressed by cells contacting basement

51 lar signaling by the alpha6beta4 integrin, a laminin receptor expressed in basal keratinocytes and ot

52 The alpha(2)beta(1) integrin is a collagen/laminin receptor expressed on platelets, endothelial cel

53 dystroglycan are essential for high-affinity laminin-receptor function.

54 those of fibronectin, fibronectin receptor, laminin receptor homolog, beta-tubulin, insulin-like gro

55 ggests that this protein may also serve as a laminin receptor in malignant tumors.

56 Since the alpha7beta1 integrin is a major laminin receptor in skeletal muscle, we determined if th

57 nduced by laminin, thereby implicating an E3 laminin receptor in this function.

58 trophin glycoprotein complexes are the major laminin receptors in skeletal muscle.

59 nvolvement of the alpha 6 beta a integrin, a laminin receptor, in breast carcinoma progression needs

60 Together, our findings indicate that the laminin receptor integrin alpha6beta1 promotes the survi

61 t with an increase in the alpha 6-containing laminin receptor integrin.

62 A potential laminin receptor, integrin alpha3, is at the presynaptic

63 he levels of RNA and surface protein for two laminin receptors, integrin alpha6beta1 and alpha3beta1,

64 monstrate that alpha3beta1 integrin, a major laminin receptor involved in the development of the kidn

65 quiescent retinal vessels suggests that this laminin receptor is an important and novel target for fu

66 mical staining of tumor cells indicates that laminin receptor is elevated in tumor versus normal cell

67 Here, we show that the beta1-Integrin laminin receptor is required for RGC positioning and reo

68 after depletion of precursors, expression of laminin receptors is upregulated.

69 The alpha2beta1 integrin, a collagen/laminin receptor, is expressed at high level in the basa

70 The alpha2beta1 integrin, a collagen/laminin receptor, is expressed by a variety of cell type

71 We showed that Lu/BCAM, the unique erythroid laminin receptor, is overexpressed and highly phosphoryl

72 The human laminin receptor (LamR) interacts with many ligands, inc

73 The 37/ 67-kDa human laminin receptor (LamR) is a cell surface receptor for l

74 electively targets tumors through the 67-kDa laminin receptor (LAMR).

75 a cellular receptor for AAV8, the 37/67-kDa laminin receptor (LamR).

76 te copy (97.9% identical) of the transcribed laminin receptor (LAMR1) with all the introns precisely

77 itecture, is a cooperative process requiring laminin- receptor ligation, receptor-facilitated self-as

78 teracting proteins and identified the 67-kDa laminin receptor (LR), a nonintegrin matrix protein rece

79 and certain neurotropic viruses, bind to the laminin receptor (LR), and this determines tropism to th

80 ivation by binding with a 67 kDa nonintegrin laminin receptor (LR).

81 noma cells acting via 37/67 kDa non-integrin laminin receptor (LR/37/67 kDa) and downstream ERK1/2, P

82 Tumor overexpression of the laminin receptor may explain the specificity and efficac

83 are cross-reactive antigens that bind to the laminin receptor of the blood-brain barrier as a molecul

84 nt in mice and humans, oncofetal Ag/immature laminin receptor (OFA/iLRP)-specific Th1, CTL, and IL-10

85 at a synaptic vesicle component may act as a laminin receptor on the presynaptic plasma membrane; the

86 esin choline-binding protein A that binds to laminin receptor on vascular endothelial cells and bindi

87 Expression of alpha(6) integrin, a laminin receptor, on tumor cell surfaces is associated w

88 A functional role for the nonintegrin laminin receptor p67 has been described for cancer metas

89 e linked the overexpression of the Mr 37,000 laminin receptor precursor (37-LRP) to tumor cell growth

90 invasion of HBMEC and interacts with 37-kDa laminin receptor precursor (37LRP) of HBMEC, which is a

91 Here, we identified 37-kDa laminin receptor precursor (LRP) as the receptor for CNF

92 g of the toxin to its cellular receptor, the laminin receptor precursor protein (LRP), a series of CN

93 the cell surface GBC-3 antigen is the 40 kDa laminin receptor precursor protein.

94 of CNF1+ E. coli K1 with recombinant 37-kDa laminin receptor precursor reduced the invasion rate to

95 her and over 60% identity with the human p40/laminin receptor precursor.

96 de proteins closely related to mammalian p40/laminin receptor precursors (LRPs).

97 A highly conserved laminin receptor processed pseudogene (LAMRL5) that has

98 an evolutionarily conserved 37-kDa immature laminin receptor protein (OFA-iLRP), a nonimmunogenic em

99 ll to purified OFA or 32- to 44-kDa immature laminin receptor protein.

100 We sought to identify the specific laminin receptor(s) mediating the multiple cell response

101 neuropathies, results attributed to loss of laminin-receptor signaling.

102 Suppression of integrin alpha3, a laminin receptor subunit, in cells synthesizing normal a

103 (fibronectin receptor), and alpha3 (collagen/laminin receptor) subunits were the most abundant.

104 ss of the dystrophin-glycoprotein complex, a laminin receptor that connects the myofiber to its surro

105 beta 1 integrin (VLA-1) is a major collagen/laminin receptor that regulates fibroblast proliferation

106 The integrin alpha6beta4, a laminin receptor that stabilizes epithelial cell adhesio

107 a central component of the DGC, serves as a laminin receptor via its extracellular alpha subunit, an

108 tive binding activity toward the alpha7beta1 laminin receptor, we have found that overexpression of M

109 Down-regulated expression of laminin receptor with small interfering RNA significantl