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1 provided new information about many of these specific autoantibodies.
2 dromes of which many are closely linked with specific autoantibodies.
3 ausally related to the deposition of antigen-specific autoantibodies.
4 creened to identify peptides targeted by MGO-specific autoantibodies.
5 of microarrays was used to identify disease-specific autoantibodies.
6 sting of T1D subjects with and without organ-specific autoantibodies.
7 therothrombotic status, further modulated by specific autoantibodies.
8 solid supports for the selective capture of specific autoantibodies.
9 tion recognized by rheumatoid arthritis (RA)-specific autoantibodies.
10 d spinal cords of MHV-infected mice with CNS-specific autoantibodies.
11 titer of anti-RNA binding protein (anti-RBP)-specific autoantibodies.
12 CVD in APS and SLE; 2) assess the effects of specific autoantibodies.
13 y as demonstrated by the presence of disease-specific autoantibodies.
14 to isolate several dozen unique IgG platelet-specific autoantibodies.
15 haracterized by a variety of circulating SSc-specific autoantibodies.
16 produced lower levels of mouse thyroglobulin-specific autoantibodies after immunization with MTg and
17 patients with chronic prostatitis possessed specific autoantibodies against the human SVS2-like semi
19 re, and have provided evidence that myositis-specific autoantibodies and autoreactive T cells are pre
21 e SSc families tend to be concordant for SSc-specific autoantibodies and HLA haplotypes; familial SSc
22 O mice is preceded by the development of OVA-specific autoantibodies and is delayed in B cell-deficie
23 lude recent findings related to the myositis-specific autoantibodies and magnetic resonance imaging o
24 ter criteria is proposed to include myositis-specific autoantibodies and magnetic resonance imaging.
26 treated with anti-CD20 Ab at a time when PG-specific autoantibodies and T cell activation were evide
27 ether IFNalpha induction was associated with specific autoantibodies and/or clinical features of the
29 plement-dependent pathogenic role of dry-eye-specific autoantibodies, and suggest autoantibody deposi
30 atched for both genetic ancestry and disease-specific autoantibodies (anti-citrullinated protein anti
31 y index, a history of nephritis, and disease-specific autoantibodies (anti-dsDNA, anti-Smith (Sm), an
33 Anti-GP2 IgG and IgA, constituting novel CD specific autoantibodies, appear to be associated with di
34 ve been recently associated with the disease-specific autoantibody aquaporin-4, thought to be pathoge
36 port a role for a complement activating AQP4-specific autoantibody as the initiator of the NMO lesion
37 anding of immunopathogenesis, histology, and specific autoantibody associations has broadened our und
38 subjects, including the presence of pancreas-specific autoantibodies, autoreactive CD4+ and CD8+ T ce
39 e course, with a progressive accumulation of specific autoantibodies before the onset of SLE, while p
40 e, myelin oligodendrocyte glycoprotein (MOG)-specific autoantibodies can initiate disease bouts by co
41 ta demonstrate that a precursor of a disease-specific autoantibody can be present in the preimmune re
42 oma, or both for clinical features and organ-specific autoantibodies characteristic of APS-I patients
43 We hypothesized that the presence of antigen-specific autoantibodies could be used as a "surrogate ma
45 ce produce high level of serum TNF-alpha and specific autoantibodies deposited onto brain blood vesse
46 en accompanied by the development of disease-specific autoantibodies directed against the SNF2-superf
50 he families of SLE probands, suggesting that specific autoantibody formation is partly genetically de
52 t to other inflammatory myopathies, myositis-specific autoantibodies had not been found in sIBM patie
53 specific and sensitive determination of p53-specific autoantibodies has been developed for the first
54 In dogs with inflammatory myopathy, muscle-specific autoantibodies have been found, especially in m
55 nd tested for association with seven disease-specific autoantibodies in a large cross-sectional cohor
57 ical activity of SP077 in the recognition of specific autoantibodies in multiple sclerosis patients'
62 once disease was evident, we detected heart specific autoantibodies in PD-L1(-/-);MRL-Fas(lpr) mice.
65 self tolerance, including the deposition of specific autoantibodies in the respective target organs,
66 is extremely sensitive in detecting disease-specific autoantibodies in the sera of bullous pemphigoi
70 Here we show that TrkA-, TrkB-, and TrkC-specific autoantibodies isolated from the sera of four i
73 we define a causal mechanism whereby beta1AR-specific autoantibodies mediate noninflammatory cardiomy
74 mphigus vulgaris (PV) is a prototypic tissue-specific autoantibody-mediated disease, in which anti-de
75 1, detected by DNA oligotyping) and myositis-specific autoantibodies (MSA) were determined in 224 pat
76 ong correlations between particular myositis-specific autoantibodies (MSAs) and clinical subsets.
79 differences in the proportion of DM- and DM-specific autoantibodies observed around the world are no
81 autoantibodies, revealed the presence of MOG-specific autoantibodies over vesiculated myelin networks
83 he treatment of juvenile DM in both myositis-specific autoantibody-positive and -negative patients.
84 , and TrkC, but not T. cruzi, are targets of specific autoantibodies present in the sera of patients
85 attenuate, but did not completely abolish HA-specific autoantibody production in an adoptive transfer
89 se symptoms and clinical course, scleroderma-specific autoantibody profiles associate strongly with d
92 from a multiple sclerosis patient and by MBP-specific autoantibodies purified from multiple sclerosis
93 phy that these glucose-6-phosphate isomerase-specific autoantibodies rapidly localize to distal joint
94 lular staining patterns were determined, and specific autoantibody reactivities were assessed by immu
96 study reveals features of a disease- and Ag-specific autoantibody repertoire with preferred VH:VL us
97 rol sera by ELISA, we found a consistent and specific autoantibody response against Dsg1 and other ke
104 l autoimmunity is presented in which epitope-specific autoantibody stimulates de novo autoimmune path
108 ic thrombocytopenic purpura caused by a GPVI-specific autoantibody that mediates clearance of the GPV
109 eth cells and were seropositive for defensin-specific autoantibodies; the presence of autoantibodies
110 highlights the recent work on novel myositis-specific autoantibodies, their autoantigen targets, the
112 is the presence of high-titer and extremely specific autoantibodies to the E2 component of the pyruv
113 in-4 (AQP4) antibody (AQP4-antibody), an NMO-specific autoantibody to AQP4, the dominant water channe
114 been described recently in which an epitope-specific autoantibody to murine zona pellucida 3 induces
115 adic IIM, although the frequency of myositis-specific autoantibodies was lower in familial than in sp
116 patterns were seen in 6.1%; the most common specific autoantibodies were anti-Ro (3.9%) and anti-Su
119 with active SLE, although the association of specific autoantibodies with chemokine score, a combined
120 l studies have implicated the association of specific autoantibodies with morphea subtype or severity
121 tures, such as autoimmune manifestations and specific autoantibodies, with patients affected by autoi
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