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3 radiographic knee osteoarthritis, the intra-articular administration of 100 mug of sprifermin every
6 ates osteoarthritis development, while intra-articular administration of recombinant gremlin-1 exacer
8 d the CD4(+) T-cell DNA methylome of 68 poly-articular and extended oligo-articular JIA patients, bef
14 l accounting for differential effects, intra-articular and topical therapies were superior to oral tr
15 istopathologic evaluation confirmed osseous, articular, and neurovascular invasion in 8.6%, 2.9%, and
17 Collectively, our data suggest that intra-articular BMNC could increase synovial macrophage counts
18 y (3), medial circumflex femoral artery (2), articular branch of descending genicular artery (1), per
19 has been focused on the intervening tissue, articular calcified cartilage (ACC) and its role in the
25 xpression level of ADAM12 protein in the KBD articular cartilage (average positive chondrocyte rate =
26 rate = 47.59 +/- 7.79%) compared to healthy articular cartilage (average positive chondrocyte rate =
27 evated ratio of calcified cartilage to total articular cartilage (CC/TAC), and synovial hyperplasia w
28 ture, ultrastructure and function of hyaline articular cartilage (HAC) and subchondral bone (SCB), an
29 abnormalities or morphologic defects in the articular cartilage (mean age, 54 years +/- 5; 51% women
30 development of synthetic composite gel-based articular cartilage analog suggests new avenues to explo
31 ctures include a skeletal element lined with articular cartilage and a synovial cavity, and we demons
33 ure of osteoarthritis is the gradual loss of articular cartilage and bone deformation, resulting in t
35 oint motion via adsorption to the surface of articular cartilage and its lubricating properties in so
37 duced joint pathology, including thinning of articular cartilage and loss of proteoglycans in the car
40 ence was found in morphological thickness of articular cartilage and menisci in early osteoarthritis
42 nologies that are being developed for use in articular cartilage and meniscus repair and regeneration
44 potential in amelioration of degeneration of articular cartilage and subchondral bone microarchitectu
45 erestingly, IL-3 reduces the degeneration of articular cartilage and subchondral bone microarchitectu
46 OA) is a progressive degenerative disease of articular cartilage and surrounding tissues, and is asso
48 r findings suggest that Gdf5 upregulation in articular cartilage and synovium is a generic response t
50 ochondral defects contain damage to both the articular cartilage and underlying subchon- dral bone, w
53 uciate ligament (ACL) remnants compared with articular cartilage at the cellular and tissue level.
54 nlike the well-defined zonal organization of articular cartilage attributed to postnatal biomechanica
55 escribe physiological benchmarks for healthy articular cartilage behavior during walking and provide
56 sion to show that chondrocytes isolated from articular cartilage biopsies of patients and subjected t
58 hyaluronan, anchored at the outer surface of articular cartilage by lubricin molecules, complexes wit
59 arthritis and its hallmark is degradation of articular cartilage by proteolytic enzymes leading to lo
60 t, similar to transient cartilage, embryonic articular cartilage cells also originate from the prolif
61 ignificantly greater agent uptake of CA4+ in articular cartilage compared to that of similar anionic
64 tion of lentiviral Wnt7a strongly attenuated articular cartilage damage induced by destabilization of
65 , in spite of the protection from structural articular cartilage damage, the postnatal growth plates
66 he progeny of these cells reconstitute adult articular cartilage de novo, entirely substituting fetal
68 termine the incidence with which morphologic articular cartilage defects develop over 48 months in ca
70 uated hedgehog-induced or surgically induced articular cartilage degeneration in mouse models of OA.
71 ith losartan both delayed the progression of articular cartilage degeneration induced by DMM compared
72 gery in Cre-negative control mice, including articular cartilage degradation and subchondral sclerosi
76 We conclude that Phd2 is a key regulator of articular cartilage development that acts by inhibiting
78 To simulate osteoarthritis in vitro, human articular cartilage explants were placed in culture and
83 years it has become increasingly clear that articular cartilage harbours a viable pool of progenitor
90 chronic disease characterized by the loss of articular cartilage in synovial joints through a process
100 fering RNAs (siRNAs) in an effective dose to articular cartilage is very challenging as the cartilage
101 nic disease characterized by degeneration of articular cartilage leading to pain and physical disabil
104 used towards the repair of focal defects in articular cartilage or broadly towards widespread biomed
109 at acts by inhibiting the differentiation of articular cartilage progenitors via modulating HIF-1alph
111 Cell and tissue engineering approaches for articular cartilage regeneration increasingly focus on m
114 attractive therapeutic solution for targeted articular cartilage repair, allowing for a controlled an
115 and histologic sections of growth plate and articular cartilage revealed no significant abnormalitie
116 tes taken from paired intact versus degraded articular cartilage samples across 38 patients undergoin
118 y investigated mechano-regulation of miRs in articular cartilage subjected to 'physiological' and 'no
121 It reduces the coefficient of friction of articular cartilage under boundary mode conditions (0.08
123 ion channel transduces mechanical loading of articular cartilage via the generation of intracellular
124 running show higher reductions of knee joint articular cartilage volume after 75 minutes of running.
127 imaging in comparison with the incidence in articular cartilage without signal abnormalities at base
129 res and CC/TAC (calcified cartilage to total articular cartilage), but increased SBP (subchondral bon
130 joints causes profound loss of volume in the articular cartilage, a clinical observation first descri
131 r the correct development and homeostasis of articular cartilage, as evidenced by the fact that aberr
132 findings show that RRV infection damages the articular cartilage, including a loss of proteoglycans w
133 nic joint pain resulting from degradation of articular cartilage, inflammation of the synovial lining
134 ntitative ultrasound grading of knee femoral articular cartilage, osteophytes and meniscal extrusion,
136 ciated with chondrocyte hypertrophy in adult articular cartilage, the lack of which protects from car
138 is a novel adipokine that negatively impacts articular cartilage, triggering catabolic and inflammato
158 esponsible for the remarkable lubrication of articular cartilage; but alone, these molecules cannot e
159 Strategies to deplete these pathogenic intra-articular cell subpopulations could be a therapeutic opt
160 though the off-label administration of intra-articular cell therapies (such as platelet-rich plasma a
161 the interaction between degeneration, intra-articular chemical factors, and pain has further restric
164 distinct synovial cell types and 7 distinct articular chondrocyte phenotypes from matched tissues.
165 Using RNA sequencing we identified a human articular chondrocyte repertoire of lncRNAs from normal
166 ubtypes, CRF-R1 and CRF-R2, in primary human articular chondrocytes (AC) and demonstrate its role as
167 ultures of mesenchymal stem cells (MSCs) and articular chondrocytes (ACs) in PLL-loaded hydrogels.
172 i-induced catabolic gene expression in human articular chondrocytes and is sufficient to attenuate MM
174 n, reduce levels of phosphorylated VEGFR2 in articular chondrocytes and synovial cells and reduce lev
175 nction induces matrix-degrading proteases in articular chondrocytes and synoviocytes, stimulating art
176 so required for postnatal differentiation of articular chondrocytes and the timely ossification of bo
179 lic events and stimulated anabolic events in articular chondrocytes cultured in an inflammatory envir
181 rkA signaling were examined in human healthy articular chondrocytes maintained under conditions suppo
184 50 mM) inhibits Hedgehog signaling in bovine articular chondrocytes such that the induction of GLI1 a
185 e results show that susceptibility of normal articular chondrocytes to lysis by NK cells is modulated
187 nockdown of Hif-1alpha expression in primary articular chondrocytes using lentiviral vectors containi
188 ther with HMWHA inhibits catabolic events in articular chondrocytes via the inhibition of p38 mitogen
189 medium from IL-1beta and P15-1-treated human articular chondrocytes was less inhibitory for chondroge
192 ontribution of growth plate chondrocytes and articular chondrocytes, not only for long bone growth, b
193 oforms 1 and 8 were highly expressed only in articular chondrocytes, suggesting their splice-specific
194 Upon ectopic expression in primary human articular chondrocytes, Wnt7a inhibited IL-1beta-induced
201 whereas 3-T MR imaging with or without intra-articular contrast material appears to improve diagnosti
202 iority of 3-T imaging, with or without intra-articular contrast material compared with 1.5-T imaging,
210 c autoimmune disease that causes progressive articular damage, functional loss, and comorbidity.
214 lung disease (which can predate the onset of articular disease by many years) probably originates fro
216 anifestation of rheumatoid arthritis (RA) is articular disease; however, extra-articular disease can
220 , IL-36beta and IL-36gamma) are found in the articular environment during arthritis and often correla
223 d lubricin has been observed following intra-articular fracture in humans and horses and in human lat
224 ars or older with an acute, displaced, extra-articular fracture of the distal tibia from April 2013 t
225 ars or older with an acute, displaced, extra-articular fracture of the distal tibia, neither nail fix
226 sified as juxta-articular haemangioma, intra-articular haemangioma or an intermediate type of hemangi
232 of animal models captures features of intra-articular inflammation, joint overloading, and tissue da
239 odel of post-traumatic osteoarthritis; intra-articular injection of adenosine nanoparticles prevented
240 imental osteoarthritis was elicited by intra-articular injection of collagenase in wild type and Cxcr
242 athology were studied in models of OA (intra-articular injection of monosodium iodoacetate in rats an
243 tory MK2-inhibiting (MK2i) peptide for intra-articular injection to halt inflammation that contribute
244 roinflammatory cytokine IL-6, and, via intra-articular injection, are successfully delivered into the
248 ants were randomized to 1 of 5 groups: intra-articular injections of 100 mug of sprifermin administer
249 nfirmed these findings in vivo through intra-articular injections of lubricin in a rat OA model where
251 ed to a dramatic and progressive loss of TMJ articular integrity and osteoarthritis-like changes.
255 lome of 68 poly-articular and extended oligo-articular JIA patients, before and after anti-TNF therap
256 Osteoarthritis (OA) is a chronic disease of articular joints that leads to degeneration of both cart
257 degeneration of the cartilaginous tissue in articular joints, severely impairs mobility in many peop
261 autologous nature, and potential to generate articular-like cartilage rather than fibrocartilage.
262 ial lung disease (ILD) is a well-known extra-articular manifestation of rheumatoid arthritis (RA).
263 ases that have variable presentations, extra-articular manifestations and clinical outcomes, and that
266 ependently associated with LNJSA, age, intra-articular nonarthroplasty prosthesis, and number of surg
267 lage cells are capable of differentiating as articular or transient cartilage, depending on exposure
269 nodes (differential model) showed that intra-articular placebo (effect size, 0.29 [95% credible inter
274 articular triamcinolone, compared with intra-articular saline, resulted in significantly greater cart
279 model estimated the association of TMJ intra-articular status with the latent measure TMD impact as a
282 omous expression of diphtheria toxin to kill articular surface chondrocytes in mice and determined th
285 , such as prominent rims around the anterior articular surfaces of cervical centra and bifurcated ant
286 the trapezial and proximal first metacarpal articular surfaces of Neanderthals (Homo neanderthalensi
287 riacanthosaurid allosauroids), flat anterior articular surfaces of the cervical centra (also present
289 eal joints, normal human metatarsophalangeal articular tissue and human OA tibial plateau tissues mea
290 ation; however, for the past 20 years, intra-articular treatment options for the management of knee o
296 cebo-controlled, double-blind trial of intra-articular triamcinolone vs saline for symptomatic knee o
297 omatic knee osteoarthritis, 2 years of intra-articular triamcinolone, compared with intra-articular s
299 tiotemporally precise manner, reducing intra-articular vector spread and possible loss of the therape