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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.
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
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
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.
24 itope pCol(28-40) of noncollagen domain 1 of collagen type IV alpha3 chain not only uniformly induced
26 of extracellular matrix components, such as collagen type IV and fibronectin, and suggests an import
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
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
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
47 ltured beta-cells adhered to and migrated on collagen type IV (Col-IV), and these responses were medi
50 eaved gelatin but was inactive toward type I collagen, type IV collagen, fibronectin, and laminin.
52 lasma membrane polarity; and fibronectin and collagen type IV, constituents of Descemet's membrane.
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
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
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
73 ain of the alpha3 chain of basement membrane collagen (type IV) inhibits the activation of polymorpho
75 lation of PN1 target protease specificity by collagen type IV is a result of the purification protoco
78 on of Roscovitine reduced immunostaining for collagen type IV, laminin, and fibronectin at days 5 and
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
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
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
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
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
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