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1 c myelocytes that showed abnormal basophilic granulation.
2 the surface of the Sun-a phenomenon known as granulation.
3 unds which provide wound drainage and tissue granulation.
4 poor re-epithelialization, angiogenesis and granulation.
5 s of key parameters such as inflammation and granulation.
6 location and topographical correspondence of granulations.
7 enting the mouse equivalent of the arachnoid granulations.
8 y for lactic acid production from OFIC(350) (granulation 350 um) hydrolysate and OFIFP extract withou
10 bone, which arise as the result of arachnoid granulations' (AG) protruding and causing the resorption
11 model of CSF outflow across human arachnoid granulations (AGs) as an approximation of in vivo condit
12 tion (2-3 weeks after insertion to allow for granulation and fixation of viscera) and formation of th
13 nd on the type of formulating activity, with granulation and mixing being most prone to API losses.
17 samples obtained by traditional moulding and granulation, and also via a novel spray-drying powdering
20 gradation and dissolution loss of LISs after granulation, as well as the low Li(+) concentration in s
21 ipid profile, oxidative stress, carotid IMT, granulations at the IM layer and near-wall low density b
23 0.05) in the SM+BP group (as for the intimal granulation/bubbles) with minimal variations in the comp
24 on, interstitial fibrosis, desquamation, and granulation by an experienced pulmonary pathologist.
25 e particles enhanced reepithelialization and granulation, by 2- and 3-fold respectively, when compare
29 as longer in subjects with lesser degrees of granulation/connective tissue deposition (fibroblastic f
30 res of IPF, i.e., fibrosis, cellularity, the granulation/connective tissue deposition, and the total
32 aphy, we also directly observe dilatancy and granulation effects, which lead to fracture above a crit
33 a model using human arachnoid membrane with granulations for the study of conditions such as Alzheim
34 nflammation, epidermis re-epithelialization, granulation formation, and proper wound healing in mice.
39 in ANAMMOX-mediated systems, focusing on (i) granulation; (ii) biofilm formation on carrier materials
40 defies typically postulated requirements for granulation in biotechnology, i.e., the need for hydrody
43 er in the arachnoid membrane adjacent to the granulations, in addition to the flow through the AGs.
45 promotes quench granulation, suggesting that granulation is modulated by heterogeneous stress fields
47 tion, and that it reduces vascularization of granulation issue, probably through disabling of the sho
48 inhibiting cell proliferation, angiogenesis, granulation maturation, collagen deposition, and muscula
49 te granulocytic differentiation with profuse granulation, mature, clumped chromatin, and myeloperoxid
51 red by vacuum drying, freeze drying or spray granulation of aqueous mixtures of omega-3 oil and beta-
56 s prevents PRD formation and promotes quench granulation, suggesting that granulation is modulated by
57 variations on timescales of hours arise from granulation, then such variations should correlate with
61 e assessment of wound area and percentage of granulation tissue (PGT) are important for optimizing wo
62 ounds curetted on day 5 were 23% filled with granulation tissue 1 day later and 99% filled 3 days lat
65 afts demonstrated significantly less lumenal granulation tissue 35.3%+/-32 than the allograft implant
66 roup demonstrated significantly less lumenal granulation tissue 48.3%+/-23.7 when compared with the i
67 kinking managed intraoperatively (0% vs 7%), granulation tissue after 12 weeks (1% vs 11%), and sutur
68 histologic response (three of four with >95% granulation tissue and <5% necrosis, one of four with 95
69 the number of myofibroblasts present in the granulation tissue and accelerates wound closure and con
70 inases are rapidly induced in the dermis and granulation tissue and at the leading edge of the epider
71 alse-positive findings due to enhancement of granulation tissue and benign breast tissue remain limit
72 , cryopyrin, and caspase-1, localized to the granulation tissue and cardiomyocytes bordering the infa
73 reases in blood flow and permeability in rat granulation tissue and corresponding vascular changes in
75 wiss mice resulted in a large stimulation of granulation tissue and fibrosis at the site of injection
76 of wound-site macrophages to fibroblasts in granulation tissue and impairment of such response in di
77 ontrol), especially in cells re-epithelizing granulation tissue and in mucosa in proximity to the ulc
81 serve as a "barrier," limiting expansion of granulation tissue and protecting the noninfarcted myoca
82 ration, and vessel formation to form a thick granulation tissue and re-epithelialization of the wound
83 9.5 were expressed by fibroblasts during the granulation tissue and remodeling phases wound healing.
84 ed transgene expression in myofibroblasts in granulation tissue and responsiveness to transforming gr
87 dified papilla preservation technique, where granulation tissue and visible calculus were removed wit
89 ed wound closure, decreased inflammation and granulation tissue area, and normalized mechanical prope
92 chondrification centers and persisted within granulation tissue at the expanding soft callus front.
94 r-BB protein (n = 2) resulted in only modest granulation tissue at the margin, but no significant dif
95 lized in the preliminary matrix organized in granulation tissue before trabecular bone formation in t
97 film infection in wounds results in impaired granulation tissue collagen leading to compromised wound
98 and platelet releasate were 14% filled with granulation tissue compared with less than 4% granulatio
99 concept that IL-1Ra modulates MCL-localized granulation tissue components and cytokine production to
100 ing by enhancing basement membrane proteins, granulation tissue components, and angiogenic factors.
102 he fibrin inside the chambers is replaced by granulation tissue consisting of new blood vessels, macr
103 examination revealed a characteristic cap of granulation tissue covering tortuous nondysplastic crypt
104 is a significant reduction in the extent of granulation tissue deposition and the subsequent formati
105 ing agent, enhancing reepithelialization and granulation tissue deposition by 64+/-5 and 83+/-12% ove
106 in response to injury, resulting in delayed granulation tissue deposition in PKCalpha-/- wounds.
107 analysis showed that epithelium ingrowth and granulation tissue deposition were significantly impaire
108 ithelialization, angiogenesis, inflammation, granulation tissue deposition, and enhanced collagen org
110 thrombus deposition and acute inflammation, granulation tissue development, and ultimately smooth mu
114 exhibited impaired development of functional granulation tissue due to severely reduced differentiati
115 in vessels that developed in sponge-induced granulation tissue during 1 month derived from circulati
117 the organization and vascularization of the granulation tissue during healing, possibly by modulatin
118 tly stimulates neovascularization within the granulation tissue during the first week of treatment, f
119 y and function in specific cell types in the granulation tissue during the healing process is unknown
121 fter receiving the lower viral dose, cardiac granulation tissue expressed MyoD mRNA and protein, but
125 increased keratinocyte migration (7.5-fold), granulation tissue formation (2.8-fold), cell proliferat
126 ology are currently limited by stent-induced granulation tissue formation adjacent to the stent.
127 using AuNP-coated SEMS successfully treated granulation tissue formation after stent placement in th
128 nsgenic mice and was associated with reduced granulation tissue formation and highly diminished wound
129 imulatory effect of overexpressed activin on granulation tissue formation and reepithelialization of
133 into the fibrin-laden wound is critical for granulation tissue formation and subsequent healing.
134 into the fibrin-laden wound is critical for granulation tissue formation and subsequent healing.
135 e, or response to infection, but it promoted granulation tissue formation and suppressed leukocyte ne
136 analysis of skin wounds demonstrated delayed granulation tissue formation and vascularization during
137 cellular/ultrastructural studies and in vivo granulation tissue formation assays combined with transc
138 synthesis or action reduces TGF-beta-induced granulation tissue formation by inhibiting both collagen
139 GA-LL37 NP-treated wounds displayed advanced granulation tissue formation by significant higher colla
141 to the fibrin matrix significantly increased granulation tissue formation in a dose-dependent manner.
144 onists of alphaVbeta3 specifically inhibited granulation tissue formation in a transient manner durin
145 pendent increase in epithelial migration and granulation tissue formation in both murine and porcine
147 complete re- epithelialization and profound granulation tissue formation in excisional and incisiona
150 the myocardial scar, suggesting expansion of granulation tissue formation into the noninfarcted terri
155 ial cell chemotaxis, vascular sprouting, and granulation tissue formation upon skin injury, these act
156 ared to their wild-type littermates although granulation tissue formation was nonhomogeneous and ther
159 g was induced by rapid re-epithelialization, granulation tissue formation, and accompanied by angioge
160 uced, and careful analysis of wound closure, granulation tissue formation, and angiogenesis revealed
161 with compromised wound closure, insufficient granulation tissue formation, and blunted induction of M
162 fibroblast activation is a limiting step of granulation tissue formation, and continued cell stimula
163 t mice show suppressed inflammation, delayed granulation tissue formation, and markedly reduced colla
164 g delayed contraction, decreased and delayed granulation tissue formation, and reduced new blood vess
166 ed to accelerate wound re-epithelialization, granulation tissue formation, and synergistically improv
167 telets and macrophages, is not important for granulation tissue formation, and that it reduces vascul
168 are known to be associated with significant granulation tissue formation, and this property provides
169 l-thickness, cutaneous wounds, with enhanced granulation tissue formation, angiogenesis, cell prolife
171 PO and observed dose-dependent inhibition of granulation tissue formation, consistent with an importa
172 ccelerated reepithelialization and increased granulation tissue formation, fibroblast migration, and
173 with reepithelialization and is followed by granulation tissue formation, including neutrophil and m
174 hese studies show that re-epithelialization, granulation tissue formation, including the establishmen
184 is study provided histological evidence that granulation tissue forming under clinically exposed and
185 In 14 and 21 d incised wounds and in chronic granulation tissue from nonhealing ulcers there was stro
186 sions, nail dystrophy and exuberant vascular granulation tissue in certain epithelia, especially conj
189 at in wild-type mice, the early formation of granulation tissue in fibrinogen-deficient mice was edem
190 roximately 1600 mum within wound (neodermis)/granulation tissue in lesions made on the skin of mice.
191 by topical application of VEGF and FGF-2 to granulation tissue in skin chambers, and 2) suramin, a c
192 is caused by expansion of microvascular-rich granulation tissue in some locations and collagen-rich s
193 backs of Sprague-Dawley rats and 1 wk later, granulation tissue in the chamber was exposed twice dail
194 aryngeal injury (i.e., mucosal ulceration or granulation tissue in the larynx) was present in 57 pati
202 accelerated replacement of cardiomyocytes by granulation tissue leading to a thin mature scar at 14 d
206 e recipient airway demonstrated less lumenal granulation tissue obstruction and better preservation o
208 dy, we show that CCN3 is highly expressed in granulation tissue of cutaneous wounds 5-7 days after in
209 ntron was expressed in myofibroblasts within granulation tissue of cutaneous wounds in a pattern that
210 showed that, similar to TSP1-null mice, the granulation tissue of double-null mice was not excessive
211 margins of human keloid samples, and in the granulation tissue of newly deposited ECM in a mouse mod
213 round the healing margins and throughout the granulation tissue of superficial ulcerative wounds.
215 in processes involved in development of the granulation tissue of wounds, but little is known about
218 PDGF B-chain did not decrease the extent of granulation tissue or vascular lesion formation, and tha
219 e healing (24days) and exhibited accelerated granulation tissue production, epithelial maturation, an
220 iferation, in vivo engraftment, experimental granulation tissue reconstitution, and tissue vascularit
221 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 ment of wound closure, increased blood flow, granulation tissue thickness (GTT), and CD31 that correl
233 db/db mice markedly increased angiogenesis, granulation tissue thickness, and wound closure rates, w
236 preparation, a palatal mini-flap was raised, granulation tissue was eliminated by means of ultrasonic
237 e angiogenesis and maturation of provisional granulation tissue was enhanced in response to genetic d
238 tion, generation of thick, well-vascularized granulation tissue was enhanced, in parallel with increa
241 analysis of esophageal biopsies demonstrated granulation tissue with acute and chronic inflammation.
242 nt of inflammatory macrophages, formation of granulation tissue with angiogenesis, and finally tissue
244 crypt destruction, erosions, ulcerations, or granulation tissue) and clinical endpoints at the end of
246 ialization, presence or absence of swelling, granulation tissue, and bleeding on gentle palpation wer
247 latelet and fibrin deposition, inflammation, granulation tissue, and finally, fibrous encapsulation.
251 of TGF beta leading to enhanced formation of granulation tissue, even in the absence of obvious infec
252 istology showed channel remnants composed of granulation tissue, fibrosis, and new vessels (NV).
253 e re-surfaced before the formation of normal granulation tissue, leading to a defective epidermal arc
254 ion (loss of respiratory epithelium, luminal granulation tissue, lymphocytic tracheitis) with increas
257 monocyte infiltration/giant cell formation (granulation tissue, the intimal and subintimal synovial
258 alpha-smooth muscle actin and are present in granulation tissue, where they are responsible for wound
292 tor (VEGF), Flk1, and VE-cadherin in ECs and granulation tissues (GTs) of full-thickness wounds.
293 ts show that Cyr61 is inducibly expressed in granulation tissues after wounding and that Cyr61 activa
294 of active wounds of living T1D subjects, and granulation tissues from mice with streptozotocin-induce
295 r, specifically with the transition from the granulation to the remodeling phases of the wound healin
297 heric velocities are dominated by convective granulation (which has been considered before for spicul