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 o the cellular immune landscape of psoriatic arthritis.
2 ctive inhibition of IL-23 to treat psoriatic arthritis.
3 transition from autoimmunity to inflammatory arthritis.
4 and IL17F, in patients with active psoriatic arthritis.
5 stinct way to control joint inflammation and arthritis.
6 of upadacitinib in patients with rheumatoid arthritis.
7 infected, leading to severe and debilitating arthritis.
8 on and prevents joint damage in inflammatory arthritis.
9 int and gut inflammation during inflammatory arthritis.
10 isease progression in mice with inflammatory arthritis.
11 safety profiles, particularly in rheumatoid arthritis.
12 of bimekizumab as a treatment for psoriatic arthritis.
13 echanism during early stages of inflammatory arthritis.
14 zed by debilitating musculoskeletal pain and arthritis.
15 ly inflammatory bowel disease and rheumatoid arthritis.
16 recommended first-line agent for rheumatoid arthritis.
17 s including schistosomiasis, sarcoidosis and arthritis.
18 dylitis, and seronegative erosive rheumatoid arthritis.
19 s to confer a circadian signature to chronic arthritis.
20 t causes both acute and chronic debilitating arthritis.
21 of regulatory T cells and recovery from Lyme arthritis.
22 ntally different immunobiology to rheumatoid arthritis.
23 aged at least 18 years with active psoriatic arthritis.
24 ed light into the pathogenesis of autoimmune arthritis.
25 on of the sEH is a promising target to treat arthritis.
26 s a crucial function for bone erosion during arthritis.
27 c-9 was comparable to (18)F-FDG in detecting arthritis.
28 lammation and contribute to tissue damage in arthritis.
29 receptor agonist inhibits the development of arthritis.
30 hat VR23 can be selective against rheumatoid arthritis.
31 target in therapy of psoriasis and psoriatic arthritis.
32 ch as sepsis or systemic juvenile idiopathic arthritis.
33 can depict the inflamed synovial membrane in arthritis.
34 in the management of patients with psoriatic arthritis.
35 issue-protective actions during inflammatory arthritis.
36 e Janus kinase inhibitor to treat rheumatoid arthritis.
37 roidal anti-inflammatory drugs for psoriatic arthritis.
38 , 10 male) anti-TNF therapy for inflammatory arthritis.
39 ther strain, C57BL/6, develops minimal to no arthritis.
40 GM-CSF in autoantibody-mediated inflammatory arthritis.
41 , including spondyloarthritis and rheumatoid arthritis.
42 on of joint inflammation during inflammatory arthritis.
43 f psoriasis, Crohn's disease, and rheumatoid arthritis.
44 mine the ability of the new tracer to detect arthritis.
45 role of SAP in T1D and autoantibody-mediated arthritis.
46 sis of residual viral antigen-driven chronic arthritis.
47 nd safety for the management of inflammatory arthritis.
48 s inflammation and pathology in inflammatory arthritis.
49 own promoter of cancer growth, fibrosis, and arthritis.
50 tral event in the pathogenesis of rheumatoid arthritis.
51 ly events in the development of inflammatory arthritis.
52 tial novel therapeutic approach in psoriatic arthritis.
53 hose targeted in the treatment of rheumatoid arthritis.
54 ation, and mitigates experimental autoimmune arthritis.
55 e-dependent efficacy in rat collagen-induced arthritis.
56 effective and safe treatment of inflammatory arthritis.
57 ated the role of PON1 in murine inflammatory arthritis.
58 f people older than 60 years are affected by arthritis.
59 oint symptoms, which may evolve into chronic arthritis.
60 ls in 19 additional patients with rheumatoid arthritis.
61 rferi results in prolonged nonresolving Lyme arthritis.
62 he concerns of people living with rheumatoid arthritis?
63 common cause of secondary SS was rheumatoid arthritis (98.1%), followed by systemic lupus erythemato
64 and compared in vivo in an adjuvant-induced arthritis (AA) rat model in order to identify the ideal
65 activity correlated with lower BLM and lower arthritis activity in both K/BxN mice and RA patients.
67 tential of [(18)F]fluoro-PEG-folate to image arthritis activity in RA with favourable imaging charact
69 as rheumatoid arthritis, juvenile idiopathic arthritis, adult-onset Still's disease, giant cell arter
71 diabetes, cancer, neurological disorders and arthritis, among others, for >150 years, RGD has always
72 VTE risk is 4.7% in patients with rheumatoid arthritis and 2.5% in those without), and inherited thro
73 n used for decades to treat human rheumatoid arthritis and benefits from 70-y hindsight on medical us
74 inflammation in vivo during antigen-induced arthritis and experimental autoimmune encephalomyelitis,
76 a regulator of pathologic bone resorption in arthritis and highlight its potential as a target for fu
78 r human autoimmune disorders like rheumatoid arthritis and inflammatory bowel disease yet increases s
79 e the biodistribution, potential for imaging arthritis and kinetic properties of [18F]fluoro-PEG-fola
81 is a target for the treatment of rheumatoid arthritis and multiple sclerosis and is re-emerging as a
82 67269.FUNDINGNIAID and National Institute of Arthritis and Musculoskeletal and Skin Diseases of the N
83 Institutes of Health, National Institute of Arthritis and Musculoskeletal and Skin Diseases; the Nat
84 ty of musculoskeletal manifestations such as arthritis and non-inflammatory pain as well as with meta
86 rom pathological bone loss during rheumatoid arthritis and osteoporosis, whose pathogenesis is associ
87 inical outcomes for patients with rheumatoid arthritis and other chronic autoimmune diseases; however
88 line drug for the treatment of RA, psoriatic arthritis and other forms of inflammatory arthritis, and
90 n rheumatoid arthritis, as well as psoriatic arthritis and spondyloarthritis, is bringing new insight
91 Systemic diagnosis with juvenile idiopathic arthritis and spondyloarthropathy were also associated w
92 s or older with active adult-onset psoriatic arthritis and symptoms for at least 6 months were random
93 asome activation contributes to inflammatory arthritis and systemic inflammation not only in RA, but
96 sh, and colitis, gastritis, pancreatitis and arthritis, and diabetic ketoacidosis each occurring in o
97 iated diseases, including SLE and rheumatoid arthritis, and following IgG Fcgamma receptor cross-link
98 ate-to-severe plaque psoriasis and psoriatic arthritis, and further agents are currently in clinical
100 ic arthritis and other forms of inflammatory arthritis, and it enhances the effect of most biologic a
101 iency virus infection, psoriasis, rheumatoid arthritis, and systemic lupus erythematosus predispose t
107 in larger group of patients with rheumatoid arthritis, as is planned for the next phase of clinical
108 ization of the synovial tissue in rheumatoid arthritis, as well as psoriatic arthritis and spondyloar
109 tic arthritis (PsA), reactive arthritis, the arthritis associated with inflammatory bowel disease inc
110 iologic-naive patients with active psoriatic arthritis (at least five swollen joints, at least five t
111 M-CSF signaling not only during inflammatory arthritis but also in experimental allergic encephalomye
112 familial linkage study of SLE and rheumatoid arthritis, but the association has not been explored fur
114 number of comorbidities including psoriatic arthritis, cardiometabolic diseases, and depression.
115 orbidity and increased rates of inflammatory arthritis, cardiometabolic diseases, and mental health d
117 , BLT1(-/-) mice developed nonresolving Lyme arthritis characterized by increased neutrophils in the
118 uded: hypertension, coronary artery disease, arthritis, chronic kidney disease, heart failure, stroke
119 y common medical conditions (such as cancer, arthritis, chronic obstructive pulmonary disease (COPD),
120 plications including oncology and rheumatoid arthritis, could also be exploited in future DMD therapi
122 with numerous conditions such as rheumatoid arthritis, diabetes, systemic lupus erythematosus, infla
123 iologic-naive patients with active psoriatic arthritis (DISCOVER-2): a double-blind, randomised, plac
124 c autoantibodies in patients with rheumatoid arthritis display a shift toward the pro-inflammatory Ig
125 k drives rhythmic repression of inflammatory arthritis during the night in mice, but mechanisms under
127 that can affect peripheral and axial joints (arthritis), entheses, skin (psoriasis) and other structu
128 he in vivo efficacy of auranofin (rheumatoid arthritis FDA-approved drug) in a CDI mouse model and es
130 s a challenge for patients with inflammatory arthritis for several reasons, in particular, the safety
131 outcomes for many patients with inflammatory arthritis; for others, however, these agents do not subs
132 c drug (DMARD) treatment in the inflammatory arthritis groups (i.e. RA and UA) and confirmed by qRT-P
135 ht/obesity and risk of developing rheumatoid arthritis, however, the evidence is not entirely consist
136 ndary panuveitis (HR = 4.21), and rheumatoid arthritis (HR = 3.30) were significantly associated with
143 vivo, AdA treatment significantly alleviated arthritis in an LTB(4)-dependent murine arthritis model.
144 f arthritogenic K/BxN serum triggered robust arthritis in HoxB8 chimeras, but not in irradiated, nont
146 tion of sPLA(2) promoted K/BxN serum-induced arthritis in mice, whereby ankle swelling was partially
149 hted imaging (DWI) was accurate in detecting arthritis in pediatric participants with juvenile idiopa
150 5% confidence intervals (CIs) for rheumatoid arthritis in relation to different measures of adiposity
152 ovium in osteoarthritis, the most widespread arthritis in the world, using the powerful tool of singl
153 experiences of pain among older adults with arthritis include the center of daily living, a lonely p
154 igger for some forms of chronic inflammatory arthritis, including spondyloarthritis and rheumatoid ar
155 recision medicine approaches in inflammatory arthritis, including strategies for predicting response
156 ased, dizziness, aphthous ulcer, arthralgia, arthritis, increased appetite, increased weight, restles
158 llagen antibody transfer (CAIA) was used for arthritis induction in B6 mice homozygous for the PON1 h
159 and baricitinib in patients with rheumatoid arthritis, inflammatory bowel diseases, psoriasis, or an
160 mouse model of antigen-induced inflammatory arthritis, intraarticular injection of Sdc3(-/-) MSCs yi
164 iatric participants with juvenile idiopathic arthritis (JIA) or suspected of having JIA and showed ag
165 ment among patients with juvenile idiopathic arthritis (JIA)-associated uveitis treated with topical
166 rious rheumatic diseases, such as rheumatoid arthritis, juvenile idiopathic arthritis, adult-onset St
169 es MSC adhesion and efficacy in inflammatory arthritis, likely via induction of the AKT pathway.
171 thritis (RA) and other forms of inflammatory arthritis, low-dose methotrexate therapy remains the gol
172 ckade decreased inflammation in a rheumatoid arthritis model without reducing circulating autoantibod
173 vivo activity in a collagen antibody-induced arthritis model, where it showed biologic-like in vivo e
177 triction improves outcome in multiple murine arthritis models and its removal induces preosteoclast m
178 mpelling data from in vitro and experimental arthritis models demonstrating its pro-inflammatory effe
179 vo, articular knockdown of miR-132 in murine arthritis models reduces the number of osteoclasts in th
180 nd unique CCL17-driven inflammatory pain and arthritis models, the latter permitting a radiation chim
181 Using a TNF-alpha-induced TMJ inflammatory arthritis mouse model, we found that the expression of N
182 pathogenesis of autoimmune diseases (such as arthritis, multiple sclerosis, psoriasis, inflammatory b
183 atory bowel disease (n = 27,739), rheumatoid arthritis (n = 25,324), systemic lupus erythematosus (n
184 disease (n = 8; 42%) and juvenile idiopathic arthritis (n = 6; 32%) were the commonest underlying con
187 a debilitating immune-mediated inflammatory arthritis of unknown pathogenesis commonly affecting pat
188 y team determined the presence or absence of arthritis on the basis of clinical, laboratory, and imag
189 On day 14 after Y. enterocolitica infection (arthritis onset), we found that under TNFRp55 deficiency
192 ients with acute Crohn's disease, rheumatoid arthritis, or sepsis were susceptible to both IgA- and I
193 ect older adults' experiences of living with arthritis pain across diverse ethnicities and cultures.
194 ' perceptions and experiences of living with arthritis pain can benefit healthcare experts in designi
196 be sensitive to older adults' experience of arthritis pain, realize the importance of providers' sup
199 an emerging Alzheimer's disease, cancer, and arthritis pathogen and established agent of periodontiti
202 ely, increased C3 expression by T cells from arthritis patients correlated with disease severity.
203 n the primary synovial cells from rheumatoid arthritis patients than those from healthy donors, sugge
204 ase-modifying antirheumatic drug-naive early arthritis patients, we assessed whether autocitrullinate
207 ompassing conditions, such as low back pain, arthritis, persistent post-surgical pain, fibromyalgia,
209 ) mice were infected with B. burgdorferi and arthritis progression was monitored by ankle swelling ov
211 0% of the patients with PS develop psoriatic arthritis (PsA), a condition characterized by inflammato
212 or apremilast in psoriasis (PSOR), psoriatic arthritis (PsA), and ankylosing spondylitis (AS) from 52
213 clude ankylosing spondylitis (AS), psoriatic arthritis (PsA), reactive arthritis, the arthritis assoc
214 uently used for the management of rheumatoid arthritis (RA) and other chronic conditions, but the saf
215 nsively in clinical management of rheumatoid arthritis (RA) and other chronic inflammatory diseases.
216 logic agents for the treatment of rheumatoid arthritis (RA) and other forms of inflammatory arthritis
218 r treating non-resistant malaria, rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE).
221 rogressive debilitating nature of rheumatoid arthritis (RA) combined with its unknown etiology and in
222 ression signatures to distinguish rheumatoid arthritis (RA) from non-inflammatory arthralgia (NIA), s
227 The primary manifestation of rheumatoid arthritis (RA) is articular disease; however, extra-arti
230 rtant role in the pathogenesis of rheumatoid arthritis (RA) owing to their ability to generate citrul
231 imaging of arthritis activity in rheumatoid arthritis (RA) patients using macrophage PET holds promi
236 one of the main cell types of the rheumatoid arthritis (RA) synovium, possess phenotypic and molecula
239 of advances in the management of rheumatoid arthritis (RA), a substantial minority of patients are e
240 se (CD), multiple sclerosis (MS), rheumatoid arthritis (RA), and others are increasingly recognized a
241 s critical to improve outcomes in rheumatoid arthritis (RA), but current diagnostic tools have limite
242 s in the hands is associated with rheumatoid arthritis (RA), it is unknown whether tenosynovitis of t
243 sociated with osteolysis, such as rheumatoid arthritis (RA), often leading to disability in patients.
244 inflamed joints of patients with rheumatoid arthritis (RA), together with compelling data from in vi
245 implicated in the pathogenesis of rheumatoid arthritis (RA), we evaluated the role of PON1 in murine
246 atient-derived in-vitro assay for Rheumatoid arthritis (RA), which yielded 5 promising genes, one of
247 utrophil extracellular trap (NET) rheumatoid arthritis (RA)-rmAbs derived from CD19(+) B cells within
257 c inflammatory conditions such as rheumatoid arthritis (RA); however, it has only been during the twe
258 multiple sclerosis (MS, n = 147), rheumatoid arthritis (RA, n = 229), Crohn's disease (n = 148), or u
261 ibitor baricitinib, used to treat rheumatoid arthritis, reduces inflammation by modifying the cytokin
262 ation modulator, in patients with rheumatoid arthritis refractory to biologic disease-modifying antir
264 Crohn's disease and ulcerative colitis, the arthritis related to anterior uveitis, and finally, some
265 o assess the effects these cells have on the arthritis-resistant phenotype characteristic of this mou
267 ce were associated with increased rheumatoid arthritis risk, suggesting adiposity could be targeted f
268 it binding, significantly improved psoriatic arthritis signs and symptoms with an acceptable safety p
269 n children with systemic juvenile idiopathic arthritis (sJIA) and cytokine storm syndrome (CSS), a po
270 inflammatory arthralgia (NIA), self-limiting arthritis (SLA), and undifferentiated arthritis (UA) as
271 iographic outcome in patients with psoriatic arthritis, so that stratified medicine approaches can be
273 rus-mediated diseases do not induce clinical arthritis, suggesting that a local inflammatory niche de
274 presence of skin inflammation and the joint arthritis susceptibility in the host are only partially
277 characterized by debilitating arthralgia and arthritis that can endure for months to years following
278 ng undergoes a major expansion in rheumatoid arthritis that is linked to disease activity(3-5); howev
280 is (AS), psoriatic arthritis (PsA), reactive arthritis, the arthritis associated with inflammatory bo
282 s in the blood from patients with rheumatoid arthritis; these cells shared features of inflammatory s
283 lection of blood in patients with rheumatoid arthritis to allow for longitudinal RNA sequencing (RNA-
284 be critical for enabling patients with hand arthritis to effectively use smartphone apps and might f
286 miting arthritis (SLA), and undifferentiated arthritis (UA) as compared to healthy controls as novel
287 joints of patients suffering from rheumatoid arthritis underwent a GM-CSF-independent necroptosis fol
288 f the intestinal barrier in the pre-phase of arthritis using butyrate or a cannabinoid type 1 recepto
289 inflammatory cell infiltrate, and persistent arthritis, via GM-CSF production, as deletion of NK cell
290 In addition, a patient with early rheumatoid arthritis was studied with both (68)Ga-DOTA-Siglec-9 and
292 /spine infections, osteomyelitis, and septic arthritis were labeled as IDRIs if discharge codes inclu
293 halangeal joints was specific for rheumatoid arthritis when compared with findings in patients with o
294 arthritis with features common to psoriatic arthritis, while mice expressing point mutations in A20'
295 sk profile in patients with active psoriatic arthritis who were naive to treatment with biologics.
296 A specific mouse strain, C3H/HeN develops arthritis with B. burgdorferi infection whereas another
297 itin-binding motif uniformly developed digit arthritis with features common to psoriatic arthritis, w
298 sgenic mouse develops spontaneous autoimmune arthritis with joint remodeling and profound bone loss.
299 r 52 weeks in patients with active psoriatic arthritis, with a musculoskeletal primary endpoint of Am
300 n (Western Ontario and McMaster Universities Arthritis [WOMAC] index); study type was randomized cont