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1 inflammatory infiltrate on the subepithelial connective tissue.
2 ined by aberrant accumulation of collagenous connective tissue.
3 transport to the development of skeletal and connective tissue.
4 lls were detected both in the epithelium and connective tissue.
5 and is the most common inherited disease of connective tissue.
6 ral proteins that are prevalent in mammalian connective tissue.
7 y determines the properties and functions of connective tissue.
8 trix and provide biomechanical properties to connective tissues.
9 hole, governs ectopic mineralization in soft connective tissues.
10 sparsely in the stroma of subcutaneous loose connective tissues.
11 anding control of collagen mineralization in connective tissues.
12 ate, highlighting the effect of succinate on connective tissues.
13 tion of multiscale force transmission within connective tissues.
14 ition of calcium phosphate complexes in soft connective tissues.
15 ms a distinct microfibrillar network in most connective tissues.
16 tebral disc and potentially other pathogenic connective tissues.
17 he bulk of the extracellular matrix (ECM) in connective tissues.
19 elevates plasma Hcy-thiolactone and leads to connective tissue abnormalities that affect the cardiova
20 ould be evaluated routinely in patients with connective tissue abnormalities, which will enable a bet
22 sis, a disease in which excessive amounts of connective tissue accumulate in response to physical dam
23 l epithelium length; epithelium on the root; connective tissue adaptation; and soft tissue thickness
24 ssues, including muscles, blood vessels, and connective tissues, adapts to mechanical strains in the
25 lance and wound-healing response of gingival connective tissues affected by diabetes mellitus or agin
27 derived from the liver extracellular matrix, connective tissue and epithelium, and proteins related t
28 smoplastic reaction through the synthesis of connective tissue and extracellular matrix, inducing loc
29 ed by inflammatory infiltrates, necrosis and connective tissue and fat replacement of the affected mu
31 1.2-1.5]), liver disease (RR 2.2 [1.6-2.9]), connective tissue and rheumatic diseases (RR 1.5 [1.3-1.
32 ZB was predominantly localized to endomysial connective tissue and to a lesser extent muscle membrane
33 files of mast cells isolated from peripheral connective tissues and basophils isolated from spleen an
34 w that 3D collagen gels, major components of connective tissues and extracellular matrix (ECM), are s
35 w that 3D collagen gels, major components of connective tissues and extracellular matrix, are signifi
36 re is to link a fundamental understanding of connective tissues and their multiscale properties to be
38 nimmunological features, including skeletal, connective tissue, and vascular abnormalities, poor post
39 ese mechanisms may be of importance in other connective tissues, and the key to unraveling cell-matri
45 er bone porosity, trabecular separation, and connective tissue attachment loss (CTAL) as well as redu
46 D100 presented greater bone volume and lower connective tissue attachment loss (CTAL) than group EP (
49 s in the collagen and glycoprotein phases of connective tissues by exploiting the spatially distinct
50 fan syndrome (MFS) is a systemic disorder of connective tissue caused by pathogenic variants in the f
51 an syndrome (MFS) is a heritable disorder of connective tissue, caused by mutations in the fibrillin-
53 deposition, inflammatory cell retention, and connective tissue cell differentiation, respectively.
56 to create 3D open scaffolds for adhesion of connective tissue cells through well-defined adhesion pl
57 ces appeared as fluid filled sacculi between connective tissue compartments accountable for distendin
58 sis is defined as an excessive deposition of connective tissue components and can affect virtually ev
59 etal muscle and instead consisted of fibrous connective tissue composed of type I and type III collag
60 The palatal donor site of the epithelialized connective tissue (CT) graft significantly influences th
61 rcentages of vital bone, residual graft, and connective tissue (CT)/other were determined via histomo
62 s, modulation of infrastructural components (connective tissue, CT; glycocalyx) of donor organs, and
65 es cellular proliferation, angiogenesis, and connective tissue deposition, suggesting vessel healing
66 HC revealed disrupted junctional epithelium, connective tissue destruction, bacterial invasion, incre
68 f a 3D human lymphatic network within native connective tissue devoid of any exogenous material such
69 Loeys-Dietz syndrome (LDS) is a systemic connective tissue disease (CTD) associated with a predis
71 biopsies from 30 patients with idiopathic or connective tissue disease (CTD)-related ILD and 13 contr
72 using multivariable Cox regression analysis: connective tissue disease (hazard ratio [HR] 2.94, 95% c
74 ral bridges may be pathologically altered in connective tissue disease as evidenced by the ultrastruc
77 r Ehlers-Danlos syndrome is a rare inherited connective tissue disease secondary to mutations within
78 s-Danlos syndrome (vEDS) is a rare inherited connective tissue disease secondary to mutations within
79 was 49+/-14 years, 78% were female, 33% had connective tissue disease, 52% were in New York Heart As
80 od for IPF (kappaw=0.71 [IQR 0.64-0.77]) and connective tissue disease-related interstitial lung dise
87 anti-SSA/Ro-positive sera from patients with connective tissue diseases showed high reactivity to the
89 highest cause-specific mortality of all the connective tissue diseases, and the aetiology of this co
90 ease that presents mixed features with other connective tissue diseases, such as systemic lupus eryth
93 digestive diseases; (6) musculoskeletal and connective tissue diseases; and (7) genitourinary diseas
94 temic sclerosis is a systemic autoimmune and connective tissue disorder associated with the human leu
95 enesis imperfecta (Col1a2(oim)), a heritable connective tissue disorder caused by abnormalities in th
96 los syndrome (vEDS) is an autosomal-dominant connective tissue disorder caused by heterozygous mutati
99 syndrome (MFS) is a highly variable genetic connective tissue disorder caused by mutations in the ca
102 pathogenesis of systemic sclerosis (SSc), a connective tissue disorder characterized by autoimmunity
104 ibromuscular dysplasia was present in 62.7%, connective tissue disorder in 4.9%, and systemic inflamm
105 ers-Danlos syndrome (vEDS) is a rare genetic connective tissue disorder secondary to pathogenic varia
107 MTSL2 mutations cause an autosomal recessive connective tissue disorder, geleophysic dysplasia 1 (GPH
109 s, with the exception of musculoskeletal and connective tissue disorders (992 [8.69% per annum] vs 83
110 myocarditis, and myocarditis associated with connective tissue disorders and may be beneficial in chr
111 s crucial for elucidating pathomechanisms of connective tissue disorders characterized by ECM deficie
112 with respiratory, musculoskeletal system and connective tissue disorders is more prevalent in Whites.
113 molecularly heterogeneous group of inherited connective tissue disorders that share similar skeletal
114 ed with MCVD (cardiomyopathies, arrhythmias, connective tissue disorders, and familial hypercholester
115 gthen the overlap between SCAD and renal and connective tissue disorders, and we highlight several ne
116 ants in several genes, such as those causing connective tissue disorders, have been implicated; howev
118 eatment of several major systemic autoimmune connective tissue disorders: systemic lupus erythematosu
119 nt a series of genetic evaluations for known connective-tissue disorders, but the evaluations were un
122 ease of serum amyloid P associated with lung connective tissue during acute respiratory distress synd
123 factors, aging, and trauma all contribute to connective tissue dysfunction and motivate the need for
126 ation in wdSCCs; yet tenascin C retention in connective tissue extracellular matrix suggests the rigi
127 ts from the maxillary tuberosity are rich in connective tissue fibers, with minimal presence of fatty
129 ize and enhanced tissue repair (strengthened connective tissue formation, improved microvascular form
130 he complexities of cell migration in fibrous connective tissues from three separate but interdependen
132 The present study shows 2-year results of a connective tissue graft (CTG) associated with LLLT in th
133 of this trial was to assess the outcome of a connective tissue graft (CTG) in the esthetic zone of si
134 redictability of the free gingival graft and connective tissue graft (CTG) techniques are highlighted
135 uccal gingival recession (bREC), effect of a connective tissue graft (CTG) when combined with a bucca
136 lly advanced tunnel flap (TUN) combined with connective tissue graft (CTG) when compared to the trape
137 d patient-centered outcomes of subepithelial connective tissue graft (CTG) with and without enamel ma
139 r dermal matrix [ADM], collagen matrix [CM], connective tissue graft [CTG]) are able to significantly
140 ques in combination with soft tissue grafts (connective tissue graft [CTG], collagen matrix [CM], and
141 of clinical long-term results 20 years after connective tissue grafting (CTG) or guided tissue regene
144 Combination therapy of papilla preservation, connective tissue grafting, and coronally advanced flaps
145 tions at palatal donor area of subepithelial connective tissue grafts (CTG) between cyanoacrylates ti
146 this study was to compare thick versus thin connective tissue grafts (CTG) for the treatment of ging
148 ted a greater GR reduction for subepithelial connective tissue grafts (SCTG) + coronally advanced fla
149 ompared two different types of subepithelial connective tissue grafts (SCTG) considering clinical par
150 ound healing of donor sites of subepithelial connective tissue grafts (SCTG), harvested by the single
151 tes have been proposed to replace autogenous connective tissue grafts, therefore the aims of this stu
157 cytosol, increase expression of YAP and TAZ connective tissue growth factor (CTGF) and Cyr61 target
158 he protein levels of 2 profibrosis proteins, connective tissue growth factor (CTGF) and TGF-beta1, in
159 ed the signaling of Smad3 and p53 to produce connective tissue growth factor (CTGF) and then resulted
168 expression of YAP-regulated genes, including connective tissue growth factor (CTGF), and cysteine-ric
169 in-1, collagen I, alpha-smooth muscle actin, connective tissue growth factor (CTGF), and plasminogen
170 TGF-beta), TGF-beta receptor 1 (TGF-betaR1), connective tissue growth factor (CTGF), E-cadherin, SRY-
171 jury markers such as interleukin-18 (IL-18), connective tissue growth factor (CTGF), neutrophil gelat
178 Several lines of evidence indicate that connective tissue growth factor (CTGF/CCN2) stimulates c
179 collagen VI, myocilin), matricellular genes (connective tissue growth factor [CTGF], secreted protein
180 expression of two TEAD-dependent genes, the connective tissue growth factor and amphiregulin genes.
181 in the levels of alpha-smooth muscle actin, connective tissue growth factor and fibronectin, and dec
182 collagen/fibronectin deposition, as well as connective tissue growth factor and matrix metalloprotei
183 ic RHOA effector, and elevated expression of connective tissue growth factor and smooth muscle actin.
184 mRNA levels of profibrotic genes, including connective tissue growth factor and tissue inhibitor of
185 e myosins, NotchR and Wnt pathway genes, and connective tissue growth factor by Pofut1 in skeletal mu
187 at were capable of dose-dependently reducing connective tissue growth factor gene expression in vitro
188 that cysteine-rich protein 61 (CYR61)/CYR61 connective tissue growth factor nephroblastoma overexpre
189 -fibronectin, alpha smooth muscle actin, and connective tissue growth factor) and stabilized or impro
191 P1(-/-)) in mice disinhibited TGFbeta1-CTGF (connective tissue growth factor) signaling, leading to s
192 transforming growth factor-beta-1) and CTGF (connective tissue growth factor), reduced fibroblast pro
195 ding fibronectin, alpha-smooth muscle actin, connective tissue growth factor, collagen I, and TGF-bet
196 cation network factor 2, previously known as connective tissue growth factor, CTGF) using a specific
197 t plasminogen activator inhibitor-1 (PAI-1), connective tissue growth factor, fibronectin, and p21 in
198 ents within individual target mRNAs, such as connective tissue growth factor, induced hyper-adhesive,
199 ransforming growth factor-beta1 (TGF-beta1), connective tissue growth factor, matrix metalloproteinas
200 agonists of transforming growth factor-beta, connective tissue growth factor, several tyrosine kinase
201 decorin, important for the interaction with connective tissue growth factor, was detected predominan
203 stoma overexpressed/cysteine-rich protein 61/connective tissue growth factor/nephroblastoma overexpre
204 Our work shows that muscle and cartilage connective tissues harbor progenitor cells capable of fu
205 thelial cells play a key role in stimulating connective tissue healing through a FOXO1-dependent mech
207 These novel data redefine adaptation in connective tissue, highlighting the fundamental importan
212 e same processes, which specify the basis of connective tissue impairment observed in DS patients, po
215 SPGs) are important structural components of connective tissues in essentially all metazoan organisms
217 With recent advances in the engineering of connective tissues, including arteries, we are on the cu
218 emical evaluation to determine the extent of connective tissue inflammatory infiltrate (CTII) using t
221 redefined the cellular origins of periocular connective tissues interacting with the EOMs, which do n
222 asal epithelium positioned at the epithelial-connective tissue interface (ECTI), separating the basal
223 er, the majority of the bone, cartilage, and connective tissue is derived from the neural crest.
226 peutic avenue for functional rejuvenation of connective tissue is reprogrammed fibroblast replacement
228 r invasive malignant epithelial cells in the connective tissue, keratin pearls in the OSCC, and ducts
229 ults revealed less gingival inflammation and connective tissue loss in the L+H groups compared with t
230 a family with a congenital-onset disorder of connective tissue, manifesting as early-onset joint hype
232 ls were used as "surrogates" for mucosal and connective tissue mast cells, respectively, and their re
233 e number of blood vessels and sub-epithelial connective tissue matrix components within the wound bed
235 osphate/phosphate ratio is the cause of soft connective tissue mineralization in these disorders.
236 dered in patients presenting with congenital connective tissue/myopathy overlap disorders with joint
237 by Menninghaus et al. fails because its main connective tissue - "negative emotions" - is beyond the
241 To describe the clinical characteristics of connective tissue nevi on the trunk and extremities of p
244 We observed a decrease in a cerebriform connective tissue nevus and a reduction in pain in child
245 [19-70] years) with TSC (56%) had at least 1 connective tissue nevus on the trunk or thighs; of these
247 a precursor protein that is expressed by the connective tissues of the craniofacial skeleton, namely,
248 SIL, without significant down-regulation of connective tissue or transforming growth factor-beta sig
249 ed stromal progenitor performance related to connective tissue organization as well as muscle develop
250 ne = 20.47%, porcine = 19.52%, P = 0.82) and connective tissue/other (bovine = 43.32%, porcine = 49.2
251 bone formation, residual graft material, and connective tissue/other when ridge preservation is accom
253 ining revealed a greater proportion of dense connective tissue (P=0.02) in women compared with men.
254 doexfoliation (PEX) syndrome exhibit various connective tissue pathologies associated with dysregulat
257 l delay, visceral and cardiac malformations, connective tissue presentations with arterial involvemen
258 apamycin (90.3% and 82.9%), respectively, 2) connective tissue progenitor cells, 3) platelet-derived
260 formed blastema, the spatial coordinates of connective tissue progenitors are predictive of their ul
261 ogether with kidney, smooth muscle, and limb connective tissue progenitors from the lateral plate mes
262 protease hydrolysis of meat myofibrillar and connective tissue protein extracts produces bioactive pe
263 r ability to hydrolyse meat myofibrillar and connective tissue protein extracts to produce bioactive
264 and thermal denaturation temperature of the connective tissue proteins (second peak in the DSC therm
268 ndicate that muscle functions as a planarian connective tissue, raising the possibility of broad role
272 Fibroblasts are then cultured to produce connective tissue rich in extracellular matrix (stage 2)
275 hat selective breeding has resulted in lower connective tissue stability of Atlantic salmon fillets.
277 es have been described in various species as connective tissue structures "bridging" small cranio-cer
278 as greater in the alveolar septa than in the connective tissue surrounding the airways or vessels.
280 ease in Sox9 expression in muscle-associated connective tissues, tendons, and bones led to hypoplasia
281 ndon and bone are attached by a transitional connective tissue that is morphologically graded from te
282 Fibrosis, the progressive accumulation of connective tissue that occurs in response to injury, cau
284 e localized fibrotic disorders of the penile connective tissues that can substantially impair a patie
285 nce the majority of the bones, cartilage and connective tissues that comprise the head and face are d
286 ucture-function relationships in native soft connective tissues that may be used to guide material de
288 nd clinical management of three intermediate connective tissue tumors: desmoid tumor (DT) or aggressi
289 & Microbe, Pundir et al. (2019) report that connective-tissue-type mast cells spy on bacterial commu
290 Our findings indicate that injury to dense connective tissues under prestrain alters boundary const
291 tly increased new bone formation and reduced connective tissue volume after 42 days demonstrating tha
292 tissue as either skin, fat, glands, ducts or connective tissue was demonstrated with an overall accur
293 ecently to genetic diseases characterized by connective tissue wasting (Penttinen syndrome) or overgr
294 this feat by means of elastic compliance of connective tissue, which passively redistributes the ove
295 essential for inducing the formation of new connective tissue, which requires the generation of sign
298 terogeneous group of hereditary disorders of connective tissue, with common features including joint
300 ight at harvesting, softer texture and lower connective tissue yield compared with the WP group.