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1 improved and finally turned to conjunctival scarring.
2 thout scarring; and (4) non-keratoconus with scarring.
3 r of aHSCs induced by injury but suppressing scarring.
4 ormal healing and prevention of hypertrophic scarring.
5 evaluating myocardial function, volumes, and scarring.
6 ion, in association with tarsal conjunctival scarring.
7 ts in the prevention and treatment of keloid scarring.
8 from the epidermis is associated with dermal scarring.
9 he profibrotic response leading to excessive scarring.
10 atory-mediated podocyte death and glomerular scarring.
11 currently available to stratify the risk of scarring.
12 is a potential therapeutic target for dermal scarring.
13 9-14.38) were also associated with new renal scarring.
14 L/MpJ 'healer' mice heal similar injuries by scarring.
15 cs, bowel and bladder dysfunction, and renal scarring.
16 to minimise the development of hypertrophic scarring.
17 nephrectomy (SNx) model of progressive renal scarring.
18 station and markers of myocardial injury and scarring.
19 al of 35 children (7.2%) developed new renal scarring.
20 cacious except in 1 case with severe orbital scarring.
21 raft detachments may reattach with interface scarring.
22 ion, in association with tarsal conjunctival scarring.
23 of 28 patients had mild tarsal conjunctival scarring.
24 tually leading to myocardial hypertrophy and scarring.
25 cal trials that promote organ repair without scarring.
26 baseline retinal dysfunction and subsequent scarring.
27 nologic advancement in the treatment of acne scarring.
28 2 inhibitor results in a marked reduction in scarring.
29 aneous wounds might contribute to pathologic scarring.
30 ural circuits or extensive right ventricular scarring.
31 e-related disease featuring progressive lung scarring.
32 ll exercise capacity, and greater myocardial scarring.
33 ound healing results in diminished cutaneous scarring.
34 CNS, which has decreased cell plasticity and scarring.
35 d widespread and confluent right ventricular scarring.
36 e that MC1R genotype may influence post-burn scarring.
37 esulting in submucosal tissue remodeling and scarring.
38 were at risk of progression of trachomatous scarring.
39 e are associated with post-burn pruritus and scarring.
40 ue repair due to accelerated closure without scarring.
41 analyses to evaluate inflammation and renal scarring.
42 ibrogenic cell in the liver, and drive liver scarring.
43 ract can lead to irreversible fallopian tube scarring.
44 ns (pannus and/or HPs) plus any conjunctival scarring.
45 y epidermal appendage neogenesis and lack of scarring.
46 al signs and moderate or severe conjunctival scarring.
47 st patients respond well to steroids without scarring.
48 recent rigid contact lens wear, and corneal scarring.
49 prognosis characterized by unrelenting lung scarring.
50 % vs. 15%; P = 0.01) and less likely to have scarring (17% vs. 36%; P < 0.001) or SHRM (36% vs. 48%;
51 were categorized as (1) keratoconus without scarring; (2) keratoconus with scarring; (3) non-keratoc
53 conus without scarring; (2) keratoconus with scarring; (3) non-keratoconus without scarring; and (4)
54 complications were hearing loss (5.4%), skin scarring (5.4%), amputation (3.4%), renal dysfunction (2
55 c membrane exerts anti-inflammatory and anti-scarring actions, we hypothesized that HC-HA/PTX3 could
57 croptosis and apoptosis, followed by cardiac scarring after antibiotic therapy, in an NHP model of se
59 ilizing drug, epothilone B (epoB), decreased scarring after rodent spinal cord injury (SCI) by abroga
60 ingly, a pericyte subset is essential during scarring after spinal cord injury, and its arrest result
64 ter, adult Pparg(Delta/Delta) mice developed scarring alopecia and severe perifollicular inflammation
65 ures, which modelled the details of fibrotic scarring an order of magnitude below the MRI scan resolu
69 diated inflammatory responses promoted renal scarring and compromised renal function, as indicated by
71 ent understanding of purinergic signaling in scarring and discuss its potential to prevent or decreas
72 s used clinically in ophthalmology to reduce scarring and enhance wound resolution after surgery.
73 sex, and the presence of preoperative apical scarring and environmental allergies in a multivariable
77 with subcortical calcifications; (3) macular scarring and focal pigmentary retinal mottling; (4) cong
78 functional muscle, human hearts are prone to scarring and hypertrophy, which can often lead to fatal
79 s, we quantified the prevalence of permanent scarring and identified clinical features predictive of
80 y response in some individuals that leads to scarring and in-turning of the eyelids in later life.
81 benefits were associated with suppression of scarring and infiltration of inflammatory/immune cells i
83 mulation reveals a novel mechanism of genome scarring and is critical to exploring therapies to count
84 derived from skin biopsy studies that cause scarring and may be impractical in large-scale clinical
87 characterized by confluent right ventricular scarring and patchy left ventricular scarring capable of
91 or ductular regeneration, demonstrating that scarring and regeneration can be uncoupled in adult bili
92 mate human biology, as well as comparison of scarring and regenerative phenotypes to uncover master r
93 bullous keratopathy, postinfectious corneal scarring and thinning and keratoconus were the most comm
97 Due to the substantial improvement in skin scarring and well-established clinical safety profile, l
98 ling in limiting the genital tract fibrosis, scarring, and chronic inflammation often associated with
99 es are invasive and result in pain, anxiety, scarring, and disfigurement of patients, which can add a
105 a significant difference in symptom control, scarring, and occurrence of vulvar carcinoma between com
108 an's layer level, and the absence of stromal scarring are associated with a high risk of developing c
111 uring open revision which lead to additional scarring around the stent and subsequent raised intraocu
112 undescribed pattern of interface astroglial scarring at boundaries between brain parenchyma and flui
114 we introduce a noninvasive method to prevent scarring based on nonthermal partial irreversible electr
115 Cs into mice with liver injury reduced liver scarring based on picrosirius red staining (49.7% reduct
117 ot only poised to prevent progressive tissue scarring, but also have the potential to reverse establi
118 g in oral mucosa is faster and produces less scarring, but the mechanisms involved are incompletely u
119 UWFI; P < .001) and chorioretinal atrophy or scarring by 116% (50 eyes [0.6%] by NMFP vs 101 eyes [1.
122 ricular scarring and patchy left ventricular scarring capable of sustaining a large number of re-entr
123 severity of dryness, corneal ulceration and scarring, cataract, and glaucoma are factors associated
124 hibited an acute inflammatory response, with scarring characterized by stronger myeloperoxidase activ
126 significant corneal injuries and subsequent scarring collectively represent a major global human hea
130 are required to exclude the other causes of scarring conjunctivitis until more sensitive and specifi
131 fibroblasts (OFs) were treated with the pro-scarring cytokine, transforming growth factor beta (TGFb
132 Trabeculectomies in eyes without previous scarring decreased 52% from 54 224 in 1994 to 25 758 in
135 iopathic pulmonary fibrosis is a progressive scarring disease characterized by extracellular matrix a
136 st that genetic associations with chlamydial scarring disease may be focussed on processes relating t
138 lmonary fibrosis encompasses a group of lung-scarring disorders that occur owing to known or unknown
141 Eleven showed progression of conjunctival scarring during a median follow-up of 42 months (range,
143 val scarring on presentation or worsening of scarring during follow-up, even in the setting of negati
144 d hepatic stellate cells (aHSCs) orchestrate scarring during liver injury, with putative quiescent pr
149 diameter was found to significantly increase scarring for glass implants, as well as increase local B
150 diameter and cell wall thickness in the pre-scarring fossilized wood show a response similar to that
152 pro-fibrotic myofibroblast phenotype, limits scarring from different hepatic insults and represents a
154 tologic findings suggest that improvement in scarring from this treatment goes beyond remodeling of c
157 q to probe unsorted cells from regenerating, scarring, homeostatic, and developing skin, we identifie
158 netic determinants of post-burn hypertrophic scarring (HTS) are unknown, and melanocortin 1 receptor
162 P = 0.01) in PLTR and baseline conjunctival scarring in BLTR (OR, 1.72; 95% CI, 1.06-2.81; P = 0.03)
169 we demonstrate increased latency and corneal scarring in LTalpha(-/-) infected mice, independent of t
171 resents a morphological analysis of fibrotic scarring in non-ischemic dilated cardiomyopathy, and its
172 eased 50% lethal dose, and decreased corneal scarring in ocularly infected mice compared to the NgK o
183 implants were found to significantly reduce scarring in vivo, compared to hard implants of identical
187 onic tissues heal wounds rapidly and without scarring, in a process conserved across species and driv
188 etry, corneal transplantation rates, corneal scarring incidence, and patient-reported outcome measure
189 factors, such as bacterial infection, tissue scarring, inflammation, and vasculature damage, as well
190 standing why adult mammals develop extensive scarring instead of regeneration is a crucial goal for r
194 beyond the material yielding threshold, and scarring is thus a by-product of the folding dynamics th
196 s replication in the eyes, levels of corneal scarring, latency-reactivation in the trigeminal ganglia
199 on of CD80 has a detrimental role in corneal scarring, likely by increasing CD8(+) T cell recruitment
200 d neovascularization, postherpetic keratitis scarring, lipid keratopathy, and limbal stem cell defici
202 ces of cranial implants, which include glial scarring, meningeal lymphangiogenesis, and increased gly
203 gnosis of LyP and were also required to have scarring, more than 10 lesions, or active lesions on the
204 y during regeneration (Acomys cahirinus) and scarring (Mus musculus), we found that both species exhi
206 ccal ophthalmia neonatorum can cause corneal scarring, ocular perforation, and blindness as early as
208 size, the GG homozygotes demonstrated worse scarring (odds ratio 1.88, P = 0.005) compared to AG het
209 multivariate analysis were keratoconus with scarring (odds ratio [OR] = 3.56, P = .02), non-keratoco
211 retion, ependymal denudation, and damage and scarring of intraventricular and parenchymal (glia-lymph
215 stitial lung disease characterized by patchy scarring of the distal lung with limited therapeutic opt
218 s a clinical disorder characterized by focal scarring of the glomerular capillary tuft, podocyte inju
219 ve kidney diseases are often associated with scarring of the kidney's filtration unit, a condition ca
220 lmonary Fibrosis (IPF), there is unrelenting scarring of the lung mediated by pathological mesenchyma
222 ) is a complex lung disease characterized by scarring of the lung that is believed to result from an
225 atients who have Foster stage 3 conjunctival scarring on presentation or worsening of scarring during
227 nal lesions - congenital dysplasia, acquired scarring or both - are a common cause of childhood hyper
228 of cutaneous surgery contributes to abnormal scarring or delayed wound healing is widely taught and p
229 to be unique among mammals by showing little scarring or fibrosis after skin or muscle injury, but th
230 oderate cases have a low risk of significant scarring or visual sequelae and may be monitored and tre
231 [OR] = 3.56, P = .02), non-keratoconus with scarring (OR = 5.09, P = .002), intraoperative central p
234 cuity risk was 11.1-fold higher with macular scarring (p = 0.001) and 14-fold higher with optic atrop
235 tival corkscrew vessels (P < 0.001), corneal scarring (P = 0.01) and pingueculae under the age of 50
236 ildren for clinical evidence of trachomatous scarring, pannus and Herbert's pits (HPs) or limbal foll
237 re of cardiac fibroblasts, which can lead to scarring, pathological remodelling and functional defici
240 nalysis allowed us to detect the presence of scarring processes resulting from the disappearance of o
241 enes that were significantly associated with scarring progression included those encoding proinflamma
242 A and PDGF were significantly upregulated in scarring progressors relative to in nonprogressors.
243 shown to contribute to myofibroblasts during scarring, promote metaplastic differentiation of airway
248 ic injury, corneal wound healing can cause a scarring response that stiffens the tissue and impairs o
250 l acuity at referral, local therapy, macular scarring, retinal detachment, and hypotony and phthisis
253 The primary efficacy endpoint was average scarring score using visual analog scales evaluating inc
255 gard to visual acuity, dry eye symptoms, and scarring sequelae at least 3 months after the acute illn
259 ata were analyzed in relation to progressive scarring status between baseline and the final time poin
260 ould be more effective in treating excessive scarring than modulation of either therapeutic target al
261 a(-/-) mice had significantly higher corneal scarring than WT mice, and adoptive T cell transfer did
262 ive explanation for some forms of pathologic scarring that are now attributed to truncated telomeres.
263 y development of cardiac fibrosis, a form of scarring that increases muscular tissue rigidity and dec
264 c blast exposure showed prominent astroglial scarring that involved the subpial glial plate, penetrat
265 ealing response that generates collagen-rich scarring that is at first protective but if inappropriat
266 g corneal edema can lead to anterior stromal scarring that may limit visual acuity following Descemet
267 vere cases of pyelonephritis can cause renal scarring that subsequently can lead to progressive failu
268 eta 2 adrenergic receptor (beta2AR) in wound scarring, the ability of beta 2 adrenergic receptor agon
269 imicrobial therapy was associated with renal scarring; the median (25th, 75th percentiles) duration o
271 conjunctival fibroblasts from patients with scarring trachoma and matching control individuals, and
272 ntly no treatment to halt the progression of scarring trachoma due to an incomplete understanding of
275 ered a distinctive molecular fingerprint for scarring trachoma fibroblasts, and identified IL-6- as a
276 FA) is a recently described inflammatory and scarring type of hair loss affecting almost exclusively
277 ), central corneal disease (vascularization, scarring, ulceration, and conjunctivalization), history
279 as determined by the degree of conjunctival scarring (using Tauber staging), central corneal disease
281 otic therapy in those with and without renal scarring was 72 (30, 120) and 48 (24, 72) hours, respect
283 wound inflammation, angiogenesis, and wound scarring was explored in HDFs, zebrafish, chick chorioal
287 healing to attenuate or prevent hypertrophic scarring, well-designed trials to confirm treatment effi
288 inal pigment epithelial atrophy, and macular scarring were associated with increased risk of MVL; and
291 mal fibroblast (HDF ) function contribute to scarring, whereas hyperpigmentation negatively affects s
292 findings contrast with the current model of scarring, whereby collagen deposition is exclusively att
293 position of neural tissue and leads to glial scarring, which inhibits the regrowth of damaged axons.
295 cutive keratoconic eyes without deep stromal scarring, with at least 1 postoperative examination 1 mo
297 aracterized by progressive, unrelenting lung scarring, with death from respiratory failure within 2-4
298 3A)-responsive cells in driving trachomatous scarring, with potential key mechanistic roles for PDGFB
299 dentifies a trend between COMT genotype with scarring, with rs4680 genetic variation constituting an