コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 d replacement of injured cardiomyocytes with granulation tissue.
2 in myofibroblasts and smooth muscle cells of granulation tissue.
3 tion of necrotic tissue and replacement with granulation tissue.
4 nificantly inhibited in vivo angiogenesis in granulation tissue.
5 f inducible nitric oxide synthase protein in granulation tissue.
6 ermal wound margin and over fibronectin-rich granulation tissue.
7 skin wounds and impaired angiogenesis in the granulation tissue.
8 gnificantly reduced vascularity of the wound granulation tissue.
9 growth factor, is highly expressed in dermal granulation tissue.
10 tion of fibroblasts, and angiogenesis in the granulation tissue.
11 emonstrated peripheral flow at US because of granulation tissue.
12 rregularly organized and highly vascularized granulation tissue.
13 th the abnormal collagen organization in the granulation tissue.
14 d associated with the formation of abdominal granulation tissue.
15 ce re-epithelialization and the formation of granulation tissue.
16 placement by a thin layer of highly vascular granulation tissue.
17 h increased risk of aspiration and laryngeal granulation tissue.
18 necrotic areas, connective tissue stroma or granulation tissue.
19 e the site of injury with newly vascularized granulation tissue.
20 service independently traced wound area and granulation tissue.
21 ient has chronic refractory otorrhea and ear granulation tissue.
22 epithelialization and increased formation of granulation tissue.
23 cterized by more inflammatory, necrotic, and granulation tissue.
24 ement of an intrauterine device, and vaginal granulation tissue.
25 g the formation of new arterioles within the granulation tissue.
26 r, increasingly in antigen-negative areas of granulation tissue.
27 d regulates their cytokine production in the granulation tissue.
28 elimination of tumor cells and formation of granulation tissue.
29 ar density of MRL-MSC-generated experimental granulation tissue.
30 lar weight S100A7 in human wound exudate and granulation tissue.
31 activation of alpha-SMA in myofibroblasts in granulation tissue.
32 d replacement of injured cardiomyocytes with granulation tissue.
33 of alpha-SMA expression in myofibroblasts in granulation tissue.
34 ounds curetted on day 5 were 23% filled with granulation tissue 1 day later and 99% filled 3 days lat
37 afts demonstrated significantly less lumenal granulation tissue 35.3%+/-32 than the allograft implant
38 roup demonstrated significantly less lumenal granulation tissue 48.3%+/-23.7 when compared with the i
40 kinking managed intraoperatively (0% vs 7%), granulation tissue after 12 weeks (1% vs 11%), and sutur
41 ts show that Cyr61 is inducibly expressed in granulation tissues after wounding and that Cyr61 activa
43 zone beneath neutrophil and macrophage-rich granulation tissue, an active lesion core of FAS cells a
44 histologic response (three of four with >95% granulation tissue and <5% necrosis, one of four with 95
45 the number of myofibroblasts present in the granulation tissue and accelerates wound closure and con
46 inases are rapidly induced in the dermis and granulation tissue and at the leading edge of the epider
47 alse-positive findings due to enhancement of granulation tissue and benign breast tissue remain limit
48 , cryopyrin, and caspase-1, localized to the granulation tissue and cardiomyocytes bordering the infa
49 reases in blood flow and permeability in rat granulation tissue and corresponding vascular changes in
51 wiss mice resulted in a large stimulation of granulation tissue and fibrosis at the site of injection
52 of wound-site macrophages to fibroblasts in granulation tissue and impairment of such response in di
53 ontrol), especially in cells re-epithelizing granulation tissue and in mucosa in proximity to the ulc
57 serve as a "barrier," limiting expansion of granulation tissue and protecting the noninfarcted myoca
58 ration, and vessel formation to form a thick granulation tissue and re-epithelialization of the wound
59 9.5 were expressed by fibroblasts during the granulation tissue and remodeling phases wound healing.
60 ed transgene expression in myofibroblasts in granulation tissue and responsiveness to transforming gr
63 dified papilla preservation technique, where granulation tissue and visible calculus were removed wit
64 crypt destruction, erosions, ulcerations, or granulation tissue) and clinical endpoints at the end of
65 ialization, presence or absence of swelling, granulation tissue, and bleeding on gentle palpation wer
66 latelet and fibrin deposition, inflammation, granulation tissue, and finally, fibrous encapsulation.
70 ed wound closure, decreased inflammation and granulation tissue area, and normalized mechanical prope
73 chondrification centers and persisted within granulation tissue at the expanding soft callus front.
75 r-BB protein (n = 2) resulted in only modest granulation tissue at the margin, but no significant dif
76 lized in the preliminary matrix organized in granulation tissue before trabecular bone formation in t
78 film infection in wounds results in impaired granulation tissue collagen leading to compromised wound
79 and platelet releasate were 14% filled with granulation tissue compared with less than 4% granulatio
80 concept that IL-1Ra modulates MCL-localized granulation tissue components and cytokine production to
81 ing by enhancing basement membrane proteins, granulation tissue components, and angiogenic factors.
83 he fibrin inside the chambers is replaced by granulation tissue consisting of new blood vessels, macr
84 examination revealed a characteristic cap of granulation tissue covering tortuous nondysplastic crypt
86 is a significant reduction in the extent of granulation tissue deposition and the subsequent formati
87 ing agent, enhancing reepithelialization and granulation tissue deposition by 64+/-5 and 83+/-12% ove
89 analysis showed that epithelium ingrowth and granulation tissue deposition were significantly impaire
90 ithelialization, angiogenesis, inflammation, granulation tissue deposition, and enhanced collagen org
92 y aimed to compare global gene expression in granulation tissue derived from different types of perio
93 is study aimed to compare gene expression in granulation tissue derived from different types of perio
94 thrombus deposition and acute inflammation, granulation tissue development, and ultimately smooth mu
98 exhibited impaired development of functional granulation tissue due to severely reduced differentiati
99 in vessels that developed in sponge-induced granulation tissue during 1 month derived from circulati
101 the organization and vascularization of the granulation tissue during healing, possibly by modulatin
102 tly stimulates neovascularization within the granulation tissue during the first week of treatment, f
103 y and function in specific cell types in the granulation tissue during the healing process is unknown
104 of TGF beta leading to enhanced formation of granulation tissue, even in the absence of obvious infec
107 fter receiving the lower viral dose, cardiac granulation tissue expressed MyoD mRNA and protein, but
109 istology showed channel remnants composed of granulation tissue, fibrosis, and new vessels (NV).
112 increased keratinocyte migration (7.5-fold), granulation tissue formation (2.8-fold), cell proliferat
113 ology are currently limited by stent-induced granulation tissue formation adjacent to the stent.
114 using AuNP-coated SEMS successfully treated granulation tissue formation after stent placement in th
115 nsgenic mice and was associated with reduced granulation tissue formation and highly diminished wound
116 imulatory effect of overexpressed activin on granulation tissue formation and reepithelialization of
120 into the fibrin-laden wound is critical for granulation tissue formation and subsequent healing.
121 into the fibrin-laden wound is critical for granulation tissue formation and subsequent healing.
122 e, or response to infection, but it promoted granulation tissue formation and suppressed leukocyte ne
123 analysis of skin wounds demonstrated delayed granulation tissue formation and vascularization during
124 cellular/ultrastructural studies and in vivo granulation tissue formation assays combined with transc
125 synthesis or action reduces TGF-beta-induced granulation tissue formation by inhibiting both collagen
126 GA-LL37 NP-treated wounds displayed advanced granulation tissue formation by significant higher colla
128 to the fibrin matrix significantly increased granulation tissue formation in a dose-dependent manner.
131 onists of alphaVbeta3 specifically inhibited granulation tissue formation in a transient manner durin
132 pendent increase in epithelial migration and granulation tissue formation in both murine and porcine
134 complete re- epithelialization and profound granulation tissue formation in excisional and incisiona
136 uNP)-coated stent for treating stent-induced granulation tissue formation in the rat esophagus was in
138 the myocardial scar, suggesting expansion of granulation tissue formation into the noninfarcted terri
143 ial cell chemotaxis, vascular sprouting, and granulation tissue formation upon skin injury, these act
144 ared to their wild-type littermates although granulation tissue formation was nonhomogeneous and ther
147 an result in a larger ostium size, decreased granulation tissue formation, and a decreased number of
148 g was induced by rapid re-epithelialization, granulation tissue formation, and accompanied by angioge
149 uced, and careful analysis of wound closure, granulation tissue formation, and angiogenesis revealed
150 with compromised wound closure, insufficient granulation tissue formation, and blunted induction of M
151 fibroblast activation is a limiting step of granulation tissue formation, and continued cell stimula
152 t mice show suppressed inflammation, delayed granulation tissue formation, and markedly reduced colla
153 g delayed contraction, decreased and delayed granulation tissue formation, and reduced new blood vess
155 ed to accelerate wound re-epithelialization, granulation tissue formation, and synergistically improv
156 telets and macrophages, is not important for granulation tissue formation, and that it reduces vascul
157 are known to be associated with significant granulation tissue formation, and this property provides
158 l-thickness, cutaneous wounds, with enhanced granulation tissue formation, angiogenesis, cell prolife
160 PO and observed dose-dependent inhibition of granulation tissue formation, consistent with an importa
161 ccelerated reepithelialization and increased granulation tissue formation, fibroblast migration, and
162 with reepithelialization and is followed by granulation tissue formation, including neutrophil and m
163 hese studies show that re-epithelialization, granulation tissue formation, including the establishmen
173 is study provided histological evidence that granulation tissue forming under clinically exposed and
174 In 14 and 21 d incised wounds and in chronic granulation tissue from nonhealing ulcers there was stro
175 of active wounds of living T1D subjects, and granulation tissues from mice with streptozotocin-induce
177 tor (VEGF), Flk1, and VE-cadherin in ECs and granulation tissues (GTs) of full-thickness wounds.
179 sions, nail dystrophy and exuberant vascular granulation tissue in certain epithelia, especially conj
182 at in wild-type mice, the early formation of granulation tissue in fibrinogen-deficient mice was edem
183 roximately 1600 mum within wound (neodermis)/granulation tissue in lesions made on the skin of mice.
184 by topical application of VEGF and FGF-2 to granulation tissue in skin chambers, and 2) suramin, a c
185 is caused by expansion of microvascular-rich granulation tissue in some locations and collagen-rich s
186 backs of Sprague-Dawley rats and 1 wk later, granulation tissue in the chamber was exposed twice dail
187 aryngeal injury (i.e., mucosal ulceration or granulation tissue in the larynx) was present in 57 pati
195 accelerated replacement of cardiomyocytes by granulation tissue leading to a thin mature scar at 14 d
196 e re-surfaced before the formation of normal granulation tissue, leading to a defective epidermal arc
197 ion (loss of respiratory epithelium, luminal granulation tissue, lymphocytic tracheitis) with increas
201 e recipient airway demonstrated less lumenal granulation tissue obstruction and better preservation o
203 dy, we show that CCN3 is highly expressed in granulation tissue of cutaneous wounds 5-7 days after in
204 ntron was expressed in myofibroblasts within granulation tissue of cutaneous wounds in a pattern that
205 showed that, similar to TSP1-null mice, the granulation tissue of double-null mice was not excessive
207 margins of human keloid samples, and in the granulation tissue of newly deposited ECM in a mouse mod
209 round the healing margins and throughout the granulation tissue of superficial ulcerative wounds.
211 in processes involved in development of the granulation tissue of wounds, but little is known about
214 PDGF B-chain did not decrease the extent of granulation tissue or vascular lesion formation, and tha
217 e assessment of wound area and percentage of granulation tissue (PGT) are important for optimizing wo
218 e healing (24days) and exhibited accelerated granulation tissue production, epithelial maturation, an
219 iferation, in vivo engraftment, experimental granulation tissue reconstitution, and tissue vascularit
220 retained specifically within the presumptive granulation tissue region of the wound at a higher densi
223 ptozotocin-induced diabetic rats to elicit a granulation tissue response and to collect acute wound f
224 ll surgical sponges to elicit a foreign body granulation tissue response, or by ligating the left com
225 hol sponges were implanted to elicit a naive granulation tissue response, removed at defined time poi
226 N-terminal domain is a key regulator of the granulation tissue response, with important implications
228 ponge implants in Flk-1(LacZ) knock-in mice, granulation tissue showed many more LacZ-positive cells
229 ells/blood vessel lumen, M2 macrophages, and granulation tissue size without compromising the mechani
232 monocyte infiltration/giant cell formation (granulation tissue, the intimal and subintimal synovial
233 ment of wound closure, increased blood flow, granulation tissue thickness (GTT), and CD31 that correl
234 db/db mice markedly increased angiogenesis, granulation tissue thickness, and wound closure rates, w
237 preparation, a palatal mini-flap was raised, granulation tissue was eliminated by means of ultrasonic
238 e angiogenesis and maturation of provisional granulation tissue was enhanced in response to genetic d
239 tion, generation of thick, well-vascularized granulation tissue was enhanced, in parallel with increa
242 alpha-smooth muscle actin and are present in granulation tissue, where they are responsible for wound
243 analysis of esophageal biopsies demonstrated granulation tissue with acute and chronic inflammation.
244 nt of inflammatory macrophages, formation of granulation tissue with angiogenesis, and finally tissue