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1 with no difference in collagen expression or reepithelialization.
2 omitant with activation of keratinocytes for reepithelialization.
3 trix and dynamic cell-matrix adhesion during reepithelialization.
4  injured lung, one of which is to facilitate reepithelialization.
5 calization of CD44 in the rat corneas during reepithelialization.
6 eractions that mediate cell migration during reepithelialization.
7 nism to maintain their directionality during reepithelialization.
8 xpress collagenase-1 during normal cutaneous reepithelialization.
9 n, stimulating vascularization, and enabling reepithelialization.
10 blast migration and proliferation, and wound reepithelialization.
11 m eccrine sweat glands parallels the rate of reepithelialization.
12  of corneal haze were apparent shortly after reepithelialization.
13 d of subepithelial haze begins shortly after reepithelialization.
14 proximal keratinocytes and maintained during reepithelialization.
15 sociated with a trend toward delayed corneal reepithelialization.
16 important for skin differentiation and wound reepithelialization.
17 ved cells from the follicles aiding in wound reepithelialization.
18 cutaneous wounds heal with an acute delay in reepithelialization.
19 stasis, epithelial cell migration, and wound reepithelialization.
20 .9- to 7.7-week specimens exhibited complete reepithelialization.
21 activation, limited keratinization, and slow reepithelialization.
22 e genes not previously associated with wound reepithelialization.
23  an increase in inflammation and the rate of reepithelialization, a finding consistent with the pheno
24 scle atrophy, osteoporosis, and reduction of reepithelialization ability in wound-healing.
25                                    Effective reepithelialization after injury is essential for correc
26 orts have been focused on accelerating wound reepithelialization and closure.
27 One treatment with Ac-PHSRN-NH(2) stimulates reepithelialization and contraction of dermal wounds in
28                  MRL mice showed accelerated reepithelialization and decreased corneal opacity compar
29 icacy of keratinocyte growth factor (KGF) in reepithelialization and elastin in dermal wound healing.
30 -C motif) ligands 17 and 22, promoting wound reepithelialization and extracellular matrix deposition
31 ffective as a wound healing agent, enhancing reepithelialization and granulation tissue deposition by
32 use skin showed a decrease in wound healing (reepithelialization and granulation) compared to the wil
33 r(db) diabetic mice these particles enhanced reepithelialization and granulation, by 2- and 3-fold re
34 pic wound healing defects, including lack of reepithelialization and granulation, dampened angiogenes
35 proved healing, characterized by accelerated reepithelialization and increased granulation tissue for
36 ofoundly accelerated wound closure mainly by reepithelialization and increased keratinocyte migration
37 ate impaired wound healing marked by delayed reepithelialization and increased neutrophil extracellul
38 betes are at higher risk for delayed corneal reepithelialization and infection.
39 und repair, new tissue formation starts with reepithelialization and is followed by granulation tissu
40 fter lesion healing in concert with complete reepithelialization and loss of HSV DNA from skin biopsi
41                          EMD and P2 promoted reepithelialization and neovascularization in full-thick
42                                              Reepithelialization and neovascularization were assessed
43  was quantified through area measurements of reepithelialization and neovascularization.
44                                        Rapid reepithelialization and reduced keratitis/iritis were al
45      Wound healing kinetics, including wound reepithelialization and wound contraction as well as mic
46 on causes impaired immune cell infiltration, reepithelialization, and angiogenesis.
47                           The wound closure, reepithelialization, and collagen deposition were accele
48 s their healing by stimulating angiogenesis, reepithelialization, and collagen deposition, and by sup
49 aged and specific pattern of cell migration, reepithelialization, and cytokine expression.
50 d CF integrated into the dermis, accelerated reepithelialization, and improved the outcome of CK tran
51 ediated modulation of KC migration and wound reepithelialization, and may aid the development of nove
52 efect, the number of specimens with complete reepithelialization, and rate of closure were evaluated
53 nocyte colonies in the wound and accelerated reepithelialization as compared with CK alone.
54            Transplantation of CF accelerated reepithelialization as determined from wound histologies
55 diminution in size at 3 months, and complete reepithelialization at 6 months.
56 EMD maintained a significant acceleration of reepithelialization at day 3 (P = 0.004).
57    Cx43 decline was delayed until 48 h, when reepithelialization began.
58          Secondary outcomes included rate of reepithelialization, best spectacle-corrected visual acu
59  keratinocyte migration is not essential for reepithelialization but suggest instead that alpha3beta1
60 ays, in part by increasing the rate of wound reepithelialization by 35% compared to control.
61 ta4 topically or intraperitoneally increased reepithelialization by 42% over saline controls at 4 d a
62 ize of the index lesion by 42 days, complete reepithelialization by 98 days, and absence of relapse b
63 e extracellular matrix (ECM), and stimulates reepithelialization by keratinocytes.
64 , is required in the epidermis to facilitate reepithelialization by remodeling the basement membrane,
65  receptors in in vitro and in vivo models of reepithelialization by subtype-selective antagonists, sm
66                     Abnormalities in corneal reepithelialization caused by second-hand cigarette smok
67 goline on the rate of complete corneal ulcer reepithelialization (CCUR) in diabetic rats with diabeti
68 tory cell content, growth factor production, reepithelialization, collagen synthesis, and angiogenesi
69                            The rate of wound reepithelialization, collagen synthesis, and angiogenesi
70 ores driven by lower inflammation and higher reepithelialization compared to NovoSorb BTM.
71 at were receiving NTX had an acceleration in reepithelialization compared with diabetic animals that
72 re, increasing epidermal differentiation and reepithelialization, despite the reduced proliferation.
73        Keratinocyte migration is critical to reepithelialization during wound repair.
74 d a reduced median time to 50 and 100% ulcer reepithelialization for ACT1-treated ulcers.
75 The primary end point was mean percent ulcer reepithelialization from baseline to 12 weeks.
76  stripping, MK6a(-/-) mice showed a delay in reepithelialization from the hair follicle.
77                               Wound closure, reepithelialization, granulation tissue formation, and r
78                               Once allograft reepithelialization has occurred, immunosuppression can
79 nce of events from the point of injury until reepithelialization in axolotl skin explant model and sh
80                Blockade of VEGF also blocked reepithelialization in both the postmenstrual endometriu
81 one (NTX; 30 mg/kg, twice daily) can restore reepithelialization in diabetic cornea, we induced diabe
82 ereas miR193b-3p knockdown accelerated wound reepithelialization in human ex vivo and diabetic murine
83 vivo blockade of Smad7 increased the rate of reepithelialization in Itga3(-/-) and WT wounds to simil
84             We have shown here that retarded reepithelialization in Itga3(-/-) mouse skin wounds is d
85 , extracellular matrix (ECM) deposition, and reepithelialization in porcine skin wounds.
86 cts in keratinocyte proliferation and tissue reepithelialization in the absence of wild-type DETCs.
87  hydroxamate inhibitor, and in mouse tissue, reepithelialization in trachea from matrilysin-null mice
88 umented function for Smad7 as a regulator of reepithelialization in vivo and implicates Smad7 as a po
89 rs, including EGFR ligands, accelerate wound reepithelialization in vivo and in vitro.
90 However, the precise function of MMPs during reepithelialization in vivo has been elusive in mammalia
91 particularly MMP-1 in migration and possibly reepithelialization in vivo.
92 llular protein, has an important role during reepithelialization in wound healing and is critical for
93                              EGFR-stimulated reepithelialization is highly dependent on Slug, as demo
94    Wounds were histologically processed, and reepithelialization, leukocyte infiltration, and angioge
95    This resulted in a novel extending shield reepithelialization mechanism, which we confirmed by com
96 sion was examined in vivo by using a corneal reepithelialization model in mice heterozygous for a Pax
97 nisms of lung repair, which include alveolar reepithelialization, myofibroblast differentiation/activ
98                                       During reepithelialization of cutaneous wounds, keratinocytes d
99 nd found that A. faecalis treatment promotes reepithelialization of diabetic keratinocytes, a process
100 y, expression of wild-type MEKK1 accelerates reepithelialization of full-thickness skin and corneal d
101                                              Reepithelialization of induced full-thickness skin wound
102  of molecules reported to be associated with reepithelialization of mucosal and cutaneous wounds.
103  activin on granulation tissue formation and reepithelialization of skin wounds nor its protumorigeni
104 ergo a dramatic phenotypic conversion during reepithelialization of skin wounds to become hyperprolif
105  underlying matrix may influence the rate of reepithelialization of skin wounds.
106 ally significant effects on healing rates or reepithelialization of skin wounds.
107 ptor-mediated, negative growth factor during reepithelialization of the abraded human cornea.
108                                              Reepithelialization of the Col1a1(r/r) wounds took 7 d l
109 estoration of transepithelial resistance and reepithelialization of the denuded epithelium.
110 sary for the morphogenesis, homeostasis, and reepithelialization of the stratified epidermis.
111 factor (PAF), and interferes with the normal reepithelialization of wounded cornea.
112 tified to play an inhibitory role during the reepithelialization of wounds.
113                         During monitoring of reepithelialization over fourteen days, the barrier full
114 oporation, the wound bed showed an increased reepithelialization rate, collagen synthesis, and angiog
115  MRL mice than in B6 mice, by means of rapid reepithelialization, reduced inflammation, and reduced f
116 pression is necessary for an EGFR-stimulated reepithelialization response.
117                                     In vitro reepithelialization stimulated by ectopic Slug expressio
118 e expression of CD44 correlates with corneal reepithelialization, suggesting that CD44 may be involve
119  of keratinocyte alpha3beta1 integrin during reepithelialization suggests that this adhesion molecule
120  0.601) or weight (P = 0.322) on the corneal reepithelialization (survival) curve.
121            These results indicate a delay in reepithelialization that is dependent on the duration of
122 plied topically every hour while awake until reepithelialization, then 4 times daily for at least 3 w
123 rticipates in skin healing and corneal wound reepithelialization through enhancement of epithelial mi
124                           The median mucosal reepithelialization time was 3 weeks.
125                               The process of reepithelialization was apparent by 12 h, however, the w
126                                        Wound reepithelialization was assessed using immunohistochemis
127 tion of CD44 on cell surfaces during corneal reepithelialization was consistent with the pattern of m
128                    At 4 and 8 weeks, corneal reepithelialization was markedly subnormal, with delays
129                                              Reepithelialization was measured by fluorescein staining
130                                              Reepithelialization was monitored by fluorescein stainin
131                                              Reepithelialization was the dominant mode of wound closu
132 ity, leader cell formation and inhibition of reepithelialization, we developed an integrative 2D cont
133              By adapting HSEs to study wound reepithelialization, we found that the extended passage
134                       KC migration and wound reepithelialization were facilitated by M4 and inhibited
135 upregulation of Cx43 and doubled the rate of reepithelialization, which exceeded control levels.
136                          We hypothesize that reepithelialization will also prevent chronic rejection
137             Treatment success was defined as reepithelialization with infiltrate resolution, and trea
138  on PRCP(gt/gt) mice had delayed closure and reepithelialization with reduced PECAM staining, but inc

 
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