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1 ns, and may drive the autoimmune response in systemic autoimmune disease.
2 and elements necessary for the initiation of systemic autoimmune disease.
3 es may develop, and perhaps be prevented, in systemic autoimmune disease.
4 ht to trigger the pathogenic consequences of systemic autoimmune disease.
5 specificities in sera from 58 patients with systemic autoimmune disease.
6 The MHC exerts an important influence on systemic autoimmune disease.
7 llogeneic CAR-T cells in three patients with systemic autoimmune disease.
8 Rheumatoid arthritis (RA) is a chronic systemic autoimmune disease.
9 rs and patients with rheumatoid arthritis, a systemic autoimmune disease.
10 s that affect the priming and progression of systemic autoimmune disease.
11 and function and that H2S deficiency led to systemic autoimmune disease.
12 entral to the pathogenesis of this prototype systemic autoimmune disease.
13 on inhibits inflammatory pathology caused by systemic autoimmune disease.
14 lupus erythematosus (SLE) is the prototypic systemic autoimmune disease.
15 arthritis as well as other manifestations of systemic autoimmune disease.
16 CD4+ T cells in both spontaneous and induced systemic autoimmune disease.
17 Rheumatoid arthritis is a systemic autoimmune disease.
18 o the contribution of Toll-like receptors in systemic autoimmune disease.
19 within the kappa locus may be shared with a systemic autoimmune disease.
20 athway may be related to the pathogenesis of systemic autoimmune disease.
21 our in the search for effective treatment of systemic autoimmune diseases.
22 oantibodies), resulting in organ-specific or systemic autoimmune diseases.
23 ntigen targeted by autoantibodies in several systemic autoimmune diseases.
24 ich is the cellular signature of a subset of systemic autoimmune diseases.
25 sis include nuclear autoantigens targeted in systemic autoimmune diseases.
26 the feature of autoantibody production with systemic autoimmune diseases.
27 e transformed the treatment options for many systemic autoimmune diseases.
28 ne responses and might also be pathogenic in systemic autoimmune diseases.
29 and the putative pathogenic role of LDGs in systemic autoimmune diseases.
30 been linked with autoimmune retinopathy and systemic autoimmune diseases.
31 the treatment of multiple organ fibrosis and systemic autoimmune diseases.
32 city in relation to disease heterogeneity in systemic autoimmune diseases.
33 rols effector T cell function in people with systemic autoimmune diseases.
34 mic lupus erythematosus (SLE) and many other systemic autoimmune diseases.
35 mmune responses to viral pathogens and other systemic autoimmune diseases.
36 epresent a large fraction of autoantigens in systemic autoimmune diseases.
37 mains, with PCS scores in the range of other systemic autoimmune diseases.
38 nts useful in rheumatoid arthritis and other systemic autoimmune diseases.
39 ipheral B-cell development in the context of systemic autoimmune diseases.
40 ies the production of many autoantibodies in systemic autoimmune diseases.
41 likely play a key role in the development of systemic autoimmune diseases.
42 ed not only organ-specific diseases but also systemic autoimmune diseases.
43 arding occupational exposures that may cause systemic autoimmune diseases.
44 he treatment of multiple sclerosis and other systemic autoimmune diseases.
45 rol sera and with sera from 21 patients with systemic autoimmune diseases.
46 n why intracellular antigens are targeted in systemic autoimmune diseases.
47 l remission from organ-specific-, as well as systemic, autoimmune diseases.
48 7 (TLR7) signalling as a mechanism of human systemic autoimmune disease(1-7), evidence of lupus-caus
49 Sera from 639 subjects (417 patients with systemic autoimmune disease, 13 with sarcoidosis, 44 wit
50 Rheumatoid arthritis (RA) is the most common systemic autoimmune disease, affecting approximately 1%
53 alpha deficient mice (IL-2Ralpha-KO) develop systemic autoimmune disease and die from severe anemia b
54 daptive immune systems in the development of systemic autoimmune disease and explain the preponderanc
55 paired Treg suppressive function, leading to systemic autoimmune disease and strong anti-tumor immuni
56 terial disease in allograft vasculopathy and systemic autoimmune diseases and involve pathogenic Abs
58 ssociations have also been reported in other systemic autoimmune diseases and suggest that there are
59 ations between occupation and death from any systemic autoimmune disease, and from RA, SLE, and syste
61 beta T cell-dependent mechanisms can induce systemic autoimmune disease, and to address the roles of
62 (5 for hematologic malignant diseases, 4 for systemic autoimmune diseases, and 2 following organ tran
63 phatidylcholine (LPC) in atherosclerosis and systemic autoimmune disease are well recognized, LPC has
68 tigens targeted across the spectrum of human systemic autoimmune diseases are efficiently cleaved by
69 d concomitant thrombosis risk factors and/or systemic autoimmune disease at the time of thrombosis.
70 stem, and mice lacking TAM receptors develop systemic autoimmune diseases because of inefficient nega
71 autoantigens targeted across the spectrum of systemic autoimmune diseases (but not nonautoantigens) a
72 ated the requirements for the development of systemic autoimmune disease by using bone marrow chimera
74 rome has become the prototype for an aseptic systemic autoimmune disease caused by a known environmen
77 n development of Sjogren's syndrome (SjS), a systemic autoimmune disease characterized by a progressi
78 temic lupus erythematosus (SLE) is a complex systemic autoimmune disease characterized by a wide rang
80 mic lupus erythematosus (SLE) is a prototype systemic autoimmune disease characterized by flares of h
81 s(lpr)) mice develop a rapidly fatal form of systemic autoimmune disease characterized by glomerulone
84 lupus erythematosus (SLE) is a prototypical systemic autoimmune disease characterized by the product
85 temic lupus erythematosus (SLE) is a chronic systemic autoimmune disease characterized by the product
89 tomyositis, and inclusion body myositis) are systemic autoimmune diseases defined by chronic muscle w
90 Patients with juvenile dermatomyositis, a systemic autoimmune disease, displayed a profound skewin
92 me sequencing of two unrelated kindreds with systemic autoimmune disease featuring antinuclear antibo
93 sease occurring in association with a second systemic autoimmune disease for which classification cri
94 B has been implicated in the development of systemic autoimmune disease; however, there has been no
95 s erythematosus is considered a prototype of systemic autoimmune diseases; however, despite considera
96 PK (HR = 4.28, 95% CI 2.38-7.71), history of systemic autoimmune disease (HR = 2.83, 95% CI 1.63-4.90
98 autoantibodies, especially anti-dsDNA, from systemic autoimmune disease in MRL, NZB/W, and motheaten
100 ptor or its ligand (FasL) lead to lupus-like systemic autoimmune diseases in mice and in some humans.
102 y arthritis, as assessed histologically, and systemic autoimmune disease, including glomerulonephriti
103 upations were associated with death from any systemic autoimmune disease, including mining machine op
104 f occupations was associated with death from systemic autoimmune diseases, including several of a pri
105 Ab-dependent and Ab-independent functions in systemic autoimmune diseases, including systemic lupus e
107 The findings reveal that injury-induced systemic autoimmune disease is exacerbated in the absenc
110 ic lupus erythematosus (SLE), the prototypic systemic autoimmune disease, is a debilitating multisyst
111 nts is considered to be the primary cause of systemic autoimmune diseases, like systemic lupus erythe
112 cells maturing to produce autoantibodies in systemic autoimmune diseases, like those in normal immun
114 Systemic sclerosis, or scleroderma, is a systemic autoimmune disease manifest by vascular damage
116 ment of corneal ulceration in the setting of systemic autoimmune disease may represent progression of
118 both foreign Ag-driven immune responses and systemic autoimmune diseases mediated by B lymphocytes.
119 pothesis that induction of autoantibodies in systemic autoimmune diseases might be triggered by a T c
120 ontrast to oligoclonal expansion observed in systemic autoimmune disease models, insulin-binding B ce
122 s (SSc), or scleroderma, is a rare, complex, systemic autoimmune disease of unknown aetiology, charac
123 ccupation was associated with death from any systemic autoimmune disease (OR 1.3 [95% CI 1.2-1.4]), a
124 is (SSc) remains a challenging and enigmatic systemic autoimmune disease, owing to its complex pathog
126 of morbidity and mortality in patients with systemic autoimmune diseases, particularly systemic lupu
128 blic, such as teachers, were associated with systemic autoimmune disease-related death, whereas other
130 ty in vivo; the mice rapidly developed fatal systemic autoimmune disease resembling the FoxP3 KO phen
132 oplasmic autoantibody (ANCA) vasculitis is a systemic autoimmune disease resulting in small-vessel in
133 (the most common form), associated to other systemic autoimmune diseases (SAD-APS), and catastrophic
136 osaccharide chains (N-glycans), results in a systemic autoimmune disease similar to human systemic lu
138 H are caused by capillaritis associated with systemic autoimmune diseases such as antineutrophil cyto
142 adaptive immunity that is characteristic of systemic autoimmune diseases such as systemic lupus eryt
143 uced by IFNs during viral. infections and in systemic autoimmune diseases such as systemic lupus eryt
144 ay be of benefit in the treatment of chronic systemic autoimmune diseases such as systemic lupus eryt
145 s strongly implicated in the pathogenesis of systemic autoimmune diseases, such as lupus, and rare mo
146 y self-NA also underlies the pathogenesis of systemic autoimmune diseases, such as systemic lupus ery
147 nd their contribution to the pathogenesis of systemic autoimmune diseases suggest new opportunities f
148 Autoimmunity to DNA in mouse models for the systemic autoimmune disease systemic lupus erythematosus
150 G production, as well as in the serum of the systemic autoimmune disease systemic lupus erythematosus
152 temic lupus erythematosus (SLE) is a chronic systemic autoimmune disease that disproportionately affe
154 Systemic lupus erythematosus (SLE) is a systemic autoimmune disease that is accompanied by the e
155 erythematosus (SLE) is a heterogenous multi-systemic autoimmune disease that is associated with cons
158 ot MHC class I, permitted the development of systemic autoimmune disease that is indistinguishable fr
161 Systemic lupus erythematosus (SLE) is a systemic autoimmune disease that predominantly affects w
162 mic lupus erythematosus (SLE) is a prototype systemic autoimmune disease that results from a break in
163 d autoimmunity (mHgIA) is a T cell-dependent systemic autoimmune disease that shares a number of comm
164 in healthy individuals and in patients with systemic autoimmune diseases that affect the kidney will
165 opathies (IIMs) are a heterogeneous group of systemic autoimmune diseases that affect the skeletal mu
166 ic inflammatory myopathies (IIMs), which are systemic autoimmune diseases that are characterized by m
167 r, many chemokines have been associated with systemic autoimmune diseases that have chronic IFN signa
169 Tim-1(Deltamucin) mice did not develop frank systemic autoimmune disease unless they were crossed ont
170 , including infectious, most commonly viral, systemic autoimmune diseases, vaccine-associated process
173 antiphospholipid syndrome (PAPS), a nonlupus systemic autoimmune disease, were hyporesponsive to P2X7
174 s to DNA and nucleoproteins are expressed in systemic autoimmune diseases, whereas B cells producing
175 stemic lupus erythematosus (SLE) is a common systemic autoimmune disease with complex etiology but st
180 Mixed connective tissue disease (MCTD) is a systemic autoimmune disease with significant morbidity a
181 i-dsDNA Id(+) B cells in mice suffering from systemic autoimmune disease with SLE-like features.
182 rtk (TAM) triply knockout (TKO) mice exhibit systemic autoimmune diseases, with characteristics of in