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1 rmation, and the adhesion of A. baumannii to collagen type IV.
2 t injury for 24 hours induced an increase in collagen type IV.
3 y be required for increased cell adhesion to collagen type IV.
4 to collagen type VI and, to a lesser extent, collagen type IV.
5 egulating adhesion of breast cancer cells to collagen type IV.
6 egulatory elements within matrix-immobilized collagen type IV.
7 d arachidonic acid-mediated cell adhesion to collagen type IV.
8 in and collagen type I (P < 0.01) but not on collagen type IV.
9 otease specificity is under the influence of collagen type IV (1).
10 of SMA (9-fold), fibronectin (2.5-fold), and collagen type IV (2-fold).
11 with diminished MMP-2 activity and increased collagen type IV accumulation.
12 /K+-ATPase, beta3-integrin, fibronectin, and collagen type IV achieved their mature localization patt
13 tronectin, RGD peptide, collagen type I, and collagen type IV) adsorbed to tissue culture plastic was
14 fluence of BL proteins-laminin, fibronectin, collagen type IV, agrin, and perlecan-on adhesion and TE
15                    Heterotrimers composed of collagen type IV alpha 1 (COL4A1) and alpha 2 (COL4A2) c
16 ctor 10, retinoblastoma susceptibility gene, collagen type IV alpha 1), and one additional marker was
17 f Alport syndrome gene COL4A3, which encodes collagen type IV alpha 3, and we present immunohistochem
18                                 Mutations in Collagen type IV alpha-1 (COL4A1) and Beta-1,3-galactosy
19                                              Collagen, type IV, alpha 1 (COL4A1) and alpha 2 (COL4A2)
20 inactivation of fumarate hydratase (FH), and collagen, type IV, alpha 5 and collagen, type IV, alpha
21 ase (FH), and collagen, type IV, alpha 5 and collagen, type IV, alpha 6 (COL4A5-COL4A6) deletions.
22                                              Collagen type IV alpha1 (COL4A1) and alpha2 (COL4A2) for
23          Tyrosine kinase receptor 1 (Tie-1), collagen type IV alpha1 (Col4a1), complement component 1
24 itope pCol(28-40) of noncollagen domain 1 of collagen type IV alpha3 chain not only uniformly induced
25  antibodies against the matrix constituents, collagen type IV and fibronectin (FN).
26  of extracellular matrix components, such as collagen type IV and fibronectin, and suggests an import
27 erstitial accumulation of collagen type III, collagen type IV and fibronectin.
28 ees C-grown E. faecalis OG1RF to immobilized collagen type IV and laminin as well as collagen type I,
29  conditional binding of E. faecalis OG1RF to collagen type IV and laminin in addition to collagen typ
30               The decreased interaction with collagen type IV and laminin was consistent with a reduc
31 ng to these changes, including expression of collagen type IV and laminin, transforming growth factor
32 dothelial cell monolayers as well as through collagen type IV and laminin-coated BD BIOCOAT inserts,
33 32 would be crucial for its interaction with collagen type IV and plasma proteins fibronectin and pla
34 n of whole A. baumannii cells to immobilized collagen type IV and played a role in the survival of A.
35 ltration rate, mesangial cell expansion, and collagen type IV and transforming growth factor-beta exp
36 iance in the level of serum antibody binding collagen types IV and V.
37 ons to varying extents and is most common in collagen types IV and V.
38 y borne gene cluster and mediates binding to collagen types IV and V.
39 U87MG, U251, and LN229 induces expression of collagen types IV and VI and the collagen crosslinking e
40 iating the adhesion of A. baumannii cells to collagen type IV, and contributing to the survival of A.
41 B proteins, including laminin, entactin, and collagen type IV, are elevated in the cerebrospinal flui
42 eratin, the junctional complex protein ZO-1, collagen type IV, as well as UB and collecting duct mark
43 ct that PDLFs adhere well to fibronectin and collagen type IV bound to plastic, and express integrins
44 B-435 cells to the basement membrane protein collagen type IV can be activated by treatment with arac
45                     Six genetically distinct collagen type IV chains have been identified and are dis
46                                          The collagen type IV cleavage fragment tumstatin and its act
47 ltured beta-cells adhered to and migrated on collagen type IV (Col-IV), and these responses were medi
48 es to the self-antigens fibronectin (FN) and collagen type-IV (Col-IV).
49 d tumor epithelial cells, but also to type I collagen, type IV collagen, and laminin.
50 eaved gelatin but was inactive toward type I collagen, type IV collagen, fibronectin, and laminin.
51 NA amounts in cells grown in the presence of collagen type IV compared to the controls.
52 lasma membrane polarity; and fibronectin and collagen type IV, constituents of Descemet's membrane.
53                                              Collagen type IV degradation results in disruption and b
54 P resulting in collagenase IV activation and collagen type IV degradation.
55                                     Although collagen type IV demonstrated no effect on the associati
56  (highly exposed in the liver sinusoids) and collagen type IV-dependent activation of focal adhesion
57 f human metastatic breast carcinoma cells to collagen type IV depends on the protein kinase C (PKC) p
58 iated with a moderately increased glomerular collagen type IV deposition compared with NS/Pla mice.
59 th tissues is accompanied by a discontinuous collagen type IV expression pattern and decreased lamini
60 eins, including fibrinogen, collagen type I, collagen type IV, fibronectin, and laminin.
61 scle cell adhesion to vitronectin but not to collagen type IV, fibronectin, or laminin, whereas selec
62 on hensin or laminin, but not fibronectin or collagen type IV, formed hemispheric epithelial structur
63 nalysis has determined that viking encodes a collagen type IV gene, alpha2(IV).
64          Integrin alpha2-mediated binding to collagen type IV (highly exposed in the liver sinusoids)
65                     The delicate lacework of collagen type IV immunoreactivity was replaced by bundle
66 lular TIGR immunoreactivity colocalized with collagen type IV immunoreactivity.
67 h as B16F10 melanoma interact with denatured collagen type IV in part by recognizing the HUIV26 crypt
68 cular defects, we examined the deposition of collagen type IV in the basement membrane, and found it
69 sed gelatinolytic activity and low levels of collagen type IV in the basement membranes of TSP-2-null
70 hXA85 was increased to 200 nM, the amount of collagen type IV in the cell layer extract increased by
71 , alpha3(IV), and alpha6(IV) chains of human collagen type IV in the regulation of angiogenesis and t
72 sence of otherwise active substrates such as collagen type IV, indicative of active inhibition.
73 ain of the alpha3 chain of basement membrane collagen (type IV) inhibits the activation of polymorpho
74                                              Collagen type IV is a major component of the basal lamin
75 lation of PN1 target protease specificity by collagen type IV is a result of the purification protoco
76                                              Collagen type IV is the major structural component of th
77 ared with fibronectin (FN), laminin (LN), or collagen type IV (IV).
78 on of Roscovitine reduced immunostaining for collagen type IV, laminin, and fibronectin at days 5 and
79  JCT were confirmed to be made up chiefly of collagen type IV, laminin, and fibronectin.
80 and on several distinct substrates including collagen type IV, laminin, fibronectin, and plastic.
81 indings suggest that specific NC1 domains of collagen type IV may represent an important new class of
82  cell interactions with structurally altered collagen type IV may suppress the expression of insulin-
83 on for a more complete genetic dissection of collagen type IV molecules and their developmental funct
84 eases in protein levels but had no effect on collagen type IV mRNA or protein levels in vitro.
85 -smooth muscle actin (SMA), fibronectin, and collagen type IV mRNA or protein levels.
86 ted the increased expression of TGF-beta and collagen type IV mRNAs and proteins.
87  the common laminin contaminants entactin or collagen type IV, neither of these proteins are likely t
88 fibronectin, nidogens, laminin isoforms, and collagen type IV, occurs in EC-pericyte cocultures, but
89  quiescent A1N4 cells to fibronectin, and to collagen types IV or I, induces the expression of c-Myc
90 ytosis of beads coated with collagen type I, collagen type IV, or thrombospondin or uncoated controls
91                                  Laminin and collagen type IV, other basal lamina proteins commonly f
92 ciency allows an increase in fibronectin and collagen type IV receptor activities.
93              Integrin alpha1beta1, the major collagen type IV receptor, is expressed by endothelial c
94 nce is provided that proteolytic cleavage of collagen type IV results in the exposure of a functional
95 at hBVR is a regulator of the TNF-alpha-GPBP-collagen type IV signaling cascade and uncover a novel b
96                                 The TGFalpha/collagen type IV signaling system that induces LAMP expr
97 n an in vitro assay (laminin > fibronectin > collagen type IV), suggesting that the parasitic cell su
98 I were deposited in a diffuse manner whereas collagen type IV surrounded the clusters of the epitheli
99 overexpression of CCN3 increased adhesion to collagen type IV, the major component of the basement me
100 dental basement membrane (BM) is composed of collagen types IV, VI, VII, and XVII, fibronectin, and l
101 ction of Ace after growth in the presence of collagen type IV was demonstrated by immunofluorescence
102             We show here that Ata binding to collagen type IV was inhibited by antibodies to Ata.
103  arachidonic acid; however, cell adhesion to collagen type IV was not highly sensitive to PD98059, an
104 that mediate the allosteric interaction with collagen type IV, we found that protease specificity was
105 ms of CS meshwork, fibronectin, laminin, and collagen type IV were associated with basement membranes
106 lecular phenotype if grown with TGFalpha and collagen type IV, while other signals fail to induce LAM
107       We also showed in vitro interaction of collagen type IV with Ace from OG1RF mutanolysin extract

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