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1 tion of fibroblasts, and angiogenesis in the granulation tissue.
2 f inducible nitric oxide synthase protein in granulation tissue.
3 ermal wound margin and over fibronectin-rich granulation tissue.
4 skin wounds and impaired angiogenesis in the granulation tissue.
5 gnificantly reduced vascularity of the wound granulation tissue.
6 growth factor, is highly expressed in dermal granulation tissue.
7 emonstrated peripheral flow at US because of granulation tissue.
8 epithelialization and increased formation of granulation tissue.
9 rregularly organized and highly vascularized granulation tissue.
10 th the abnormal collagen organization in the granulation tissue.
11 d associated with the formation of abdominal granulation tissue.
12 placement by a thin layer of highly vascular granulation tissue.
13 necrotic areas, connective tissue stroma or granulation tissue.
14 cterized by more inflammatory, necrotic, and granulation tissue.
15 ement of an intrauterine device, and vaginal granulation tissue.
16 g the formation of new arterioles within the granulation tissue.
17 r, increasingly in antigen-negative areas of granulation tissue.
18 d regulates their cytokine production in the granulation tissue.
19 ce re-epithelialization and the formation of granulation tissue.
20 elimination of tumor cells and formation of granulation tissue.
21 ar density of MRL-MSC-generated experimental granulation tissue.
22 lar weight S100A7 in human wound exudate and granulation tissue.
23 activation of alpha-SMA in myofibroblasts in granulation tissue.
24 d replacement of injured cardiomyocytes with granulation tissue.
25 of alpha-SMA expression in myofibroblasts in granulation tissue.
26 d replacement of injured cardiomyocytes with granulation tissue.
27 ient has chronic refractory otorrhea and ear granulation tissue.
28 in myofibroblasts and smooth muscle cells of granulation tissue.
29 tion of necrotic tissue and replacement with granulation tissue.
30 nificantly inhibited in vivo angiogenesis in granulation tissue.
31 ounds curetted on day 5 were 23% filled with granulation tissue 1 day later and 99% filled 3 days lat
34 afts demonstrated significantly less lumenal granulation tissue 35.3%+/-32 than the allograft implant
35 roup demonstrated significantly less lumenal granulation tissue 48.3%+/-23.7 when compared with the i
37 ts show that Cyr61 is inducibly expressed in granulation tissues after wounding and that Cyr61 activa
39 histologic response (three of four with >95% granulation tissue and <5% necrosis, one of four with 95
40 the number of myofibroblasts present in the granulation tissue and accelerates wound closure and con
41 inases are rapidly induced in the dermis and granulation tissue and at the leading edge of the epider
42 alse-positive findings due to enhancement of granulation tissue and benign breast tissue remain limit
43 , cryopyrin, and caspase-1, localized to the granulation tissue and cardiomyocytes bordering the infa
44 reases in blood flow and permeability in rat granulation tissue and corresponding vascular changes in
46 wiss mice resulted in a large stimulation of granulation tissue and fibrosis at the site of injection
47 ontrol), especially in cells re-epithelizing granulation tissue and in mucosa in proximity to the ulc
50 serve as a "barrier," limiting expansion of granulation tissue and protecting the noninfarcted myoca
51 ration, and vessel formation to form a thick granulation tissue and re-epithelialization of the wound
52 9.5 were expressed by fibroblasts during the granulation tissue and remodeling phases wound healing.
53 ed transgene expression in myofibroblasts in granulation tissue and responsiveness to transforming gr
55 latelet and fibrin deposition, inflammation, granulation tissue, and finally, fibrous encapsulation.
58 ed wound closure, decreased inflammation and granulation tissue area, and normalized mechanical prope
61 chondrification centers and persisted within granulation tissue at the expanding soft callus front.
63 r-BB protein (n = 2) resulted in only modest granulation tissue at the margin, but no significant dif
64 lized in the preliminary matrix organized in granulation tissue before trabecular bone formation in t
66 and platelet releasate were 14% filled with granulation tissue compared with less than 4% granulatio
67 concept that IL-1Ra modulates MCL-localized granulation tissue components and cytokine production to
68 ing by enhancing basement membrane proteins, granulation tissue components, and angiogenic factors.
70 he fibrin inside the chambers is replaced by granulation tissue consisting of new blood vessels, macr
72 is a significant reduction in the extent of granulation tissue deposition and the subsequent formati
73 ing agent, enhancing reepithelialization and granulation tissue deposition by 64+/-5 and 83+/-12% ove
75 analysis showed that epithelium ingrowth and granulation tissue deposition were significantly impaire
76 ithelialization, angiogenesis, inflammation, granulation tissue deposition, and enhanced collagen org
78 thrombus deposition and acute inflammation, granulation tissue development, and ultimately smooth mu
81 exhibited impaired development of functional granulation tissue due to severely reduced differentiati
82 in vessels that developed in sponge-induced granulation tissue during 1 month derived from circulati
84 the organization and vascularization of the granulation tissue during healing, possibly by modulatin
85 tly stimulates neovascularization within the granulation tissue during the first week of treatment, f
86 y and function in specific cell types in the granulation tissue during the healing process is unknown
87 of TGF beta leading to enhanced formation of granulation tissue, even in the absence of obvious infec
88 fter receiving the lower viral dose, cardiac granulation tissue expressed MyoD mRNA and protein, but
93 increased keratinocyte migration (7.5-fold), granulation tissue formation (2.8-fold), cell proliferat
94 nsgenic mice and was associated with reduced granulation tissue formation and highly diminished wound
95 imulatory effect of overexpressed activin on granulation tissue formation and reepithelialization of
100 into the fibrin-laden wound is critical for granulation tissue formation and subsequent healing.
101 e, or response to infection, but it promoted granulation tissue formation and suppressed leukocyte ne
102 synthesis or action reduces TGF-beta-induced granulation tissue formation by inhibiting both collagen
103 GA-LL37 NP-treated wounds displayed advanced granulation tissue formation by significant higher colla
105 to the fibrin matrix significantly increased granulation tissue formation in a dose-dependent manner.
108 onists of alphaVbeta3 specifically inhibited granulation tissue formation in a transient manner durin
109 pendent increase in epithelial migration and granulation tissue formation in both murine and porcine
111 complete re- epithelialization and profound granulation tissue formation in excisional and incisiona
114 the myocardial scar, suggesting expansion of granulation tissue formation into the noninfarcted terri
119 ial cell chemotaxis, vascular sprouting, and granulation tissue formation upon skin injury, these act
120 ared to their wild-type littermates although granulation tissue formation was nonhomogeneous and ther
122 g was induced by rapid re-epithelialization, granulation tissue formation, and accompanied by angioge
123 uced, and careful analysis of wound closure, granulation tissue formation, and angiogenesis revealed
124 with compromised wound closure, insufficient granulation tissue formation, and blunted induction of M
125 fibroblast activation is a limiting step of granulation tissue formation, and continued cell stimula
126 t mice show suppressed inflammation, delayed granulation tissue formation, and markedly reduced colla
127 g delayed contraction, decreased and delayed granulation tissue formation, and reduced new blood vess
129 ed to accelerate wound re-epithelialization, granulation tissue formation, and synergistically improv
130 telets and macrophages, is not important for granulation tissue formation, and that it reduces vascul
131 are known to be associated with significant granulation tissue formation, and this property provides
132 l-thickness, cutaneous wounds, with enhanced granulation tissue formation, angiogenesis, cell prolife
134 PO and observed dose-dependent inhibition of granulation tissue formation, consistent with an importa
135 with reepithelialization and is followed by granulation tissue formation, including neutrophil and m
136 hese studies show that re-epithelialization, granulation tissue formation, including the establishmen
143 is study provided histological evidence that granulation tissue forming under clinically exposed and
144 In 14 and 21 d incised wounds and in chronic granulation tissue from nonhealing ulcers there was stro
145 of active wounds of living T1D subjects, and granulation tissues from mice with streptozotocin-induce
147 tor (VEGF), Flk1, and VE-cadherin in ECs and granulation tissues (GTs) of full-thickness wounds.
148 sions, nail dystrophy and exuberant vascular granulation tissue in certain epithelia, especially conj
151 at in wild-type mice, the early formation of granulation tissue in fibrinogen-deficient mice was edem
152 roximately 1600 mum within wound (neodermis)/granulation tissue in lesions made on the skin of mice.
153 by topical application of VEGF and FGF-2 to granulation tissue in skin chambers, and 2) suramin, a c
154 is caused by expansion of microvascular-rich granulation tissue in some locations and collagen-rich s
155 backs of Sprague-Dawley rats and 1 wk later, granulation tissue in the chamber was exposed twice dail
162 accelerated replacement of cardiomyocytes by granulation tissue leading to a thin mature scar at 14 d
163 ion (loss of respiratory epithelium, luminal granulation tissue, lymphocytic tracheitis) with increas
167 e recipient airway demonstrated less lumenal granulation tissue obstruction and better preservation o
169 dy, we show that CCN3 is highly expressed in granulation tissue of cutaneous wounds 5-7 days after in
170 ntron was expressed in myofibroblasts within granulation tissue of cutaneous wounds in a pattern that
171 showed that, similar to TSP1-null mice, the granulation tissue of double-null mice was not excessive
172 margins of human keloid samples, and in the granulation tissue of newly deposited ECM in a mouse mod
174 round the healing margins and throughout the granulation tissue of superficial ulcerative wounds.
176 in processes involved in development of the granulation tissue of wounds, but little is known about
178 PDGF B-chain did not decrease the extent of granulation tissue or vascular lesion formation, and tha
180 e healing (24days) and exhibited accelerated granulation tissue production, epithelial maturation, an
181 iferation, in vivo engraftment, experimental granulation tissue reconstitution, and tissue vascularit
183 ptozotocin-induced diabetic rats to elicit a granulation tissue response and to collect acute wound f
184 ll surgical sponges to elicit a foreign body granulation tissue response, or by ligating the left com
185 hol sponges were implanted to elicit a naive granulation tissue response, removed at defined time poi
186 N-terminal domain is a key regulator of the granulation tissue response, with important implications
188 ponge implants in Flk-1(LacZ) knock-in mice, granulation tissue showed many more LacZ-positive cells
189 ells/blood vessel lumen, M2 macrophages, and granulation tissue size without compromising the mechani
192 monocyte infiltration/giant cell formation (granulation tissue, the intimal and subintimal synovial
194 preparation, a palatal mini-flap was raised, granulation tissue was eliminated by means of ultrasonic
195 tion, generation of thick, well-vascularized granulation tissue was enhanced, in parallel with increa
198 alpha-smooth muscle actin and are present in granulation tissue, where they are responsible for wound
199 nt of inflammatory macrophages, formation of granulation tissue with angiogenesis, and finally tissue
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