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1 ifferentiation are substantially enhanced by B cell-activating factor.
2 family protein, which is inhibited by excess B cell-activating factor.
3 associated with liver inflammation and serum B cell-activating factor.
4 ly prolonged survival ex vivo independent of B cell activating factor and showed increased amounts of
5                             Remarkably, both B cell-activating factor and CD40 ligand do not signific
6 eads to systemic inflammation with increased B cell-activating factor and IFN levels and induction of
7 for an abrogation of tolerance, no increased B cell-activating factor and IFN, and no IFN signature.
8 d B-cell counts, B-cell subset distribution, B cell-activating factor and immunoglobulin levels, and
9 d salivary glands and abnormal expression of B cell-activating factor and its receptors.
10 he formation of ectopic lymphoid structures (B-cell activating factor and B cell-attracting chemokine
11 ls are activated and primed for survival via B-cell activating factor and B-cell receptor-associated
12                             The emergence of B-cell-activating factor and its related family members
13  incorporating the molecular adjuvants BAFF (B cell activating factor) and APRIL (a proliferation-ind
14 ers, as well as B-cell survival factor BAFF (B-cell activating factor) and antiapoptotic molecule Bcl
15 lammation, splenic plasma cells, circulating B cell activating factor, and intragraft transcripts for
16 or activator of NF-kB (RANK)-RANK ligand and B cell-activating factor-APRIL (a proliferation-inducing
17          Activation of the type I interferon/B cell-activating factor axis in SS has recently attract
18 ently to wild type in response to IgM, CD40, B cell-activating factor/B lymphocyte stimulator, CpG, a
19         At 2 years from transplantation, the B-cell activating factor/B-cell ratio was significantly
20                                          The B cell activating factor BAFF (BlyS/TALL-1/zTNF4) is a t
21 mbinant RABV-based vaccine expressing murine B cell activating factor (BAFF) (rRABV-mBAFF).
22                                 The cytokine B cell activating factor (BAFF) and its receptor, BAFF r
23 he tumor necrosis factor (TNF) family member B cell activating factor (BAFF) binds B cells and enhanc
24                                              B cell activating factor (BAFF) is a crucial survival fa
25 gulation of signals received through BCR and B cell activating factor (BAFF) receptor.
26                                              B cell activating factor (BAFF) signals through BAFF-R t
27                                              B cell activating factor (BAFF) stimulation of the BAFF
28  member 13B (B lymphocyte stimulator (BLyS), B cell activating factor (BAFF)) promotes primary B cell
29                                              B cell activating factor (BAFF), a ligand belonging to t
30  cells proliferate to the prosurvival factor B cell activating factor (BAFF).
31                            We show here that B cell-activating factor (BAFF) activates this second pa
32 roteins and B cell tropic factors, including B cell-activating factor (BAFF) and a proliferation-indu
33 iated IgG-PB differentiation is dependent on B cell-activating factor (BAFF) and IL-10, whereas IgA-P
34 mpaired receptor editing and increased serum B cell-activating factor (BAFF) concentrations.
35                                          The B cell-activating factor (BAFF) is critical for B cell d
36 ents with cGVHD have significantly increased B cell-activating factor (BAFF) levels and that their B
37 e presence of alloantibodies and high plasma B cell-activating factor (BAFF) levels in patients with
38  show that Btk also couples the receptor for B cell-activating factor (BAFF) of the TNF family (BAFF-
39 independent survival signals provided by the B cell-activating factor (BAFF) receptor (BAFF-R).
40 am of both the B cell receptor (BCR) and the B cell-activating factor (BAFF) receptor.
41 ets, elevated IgG autoantibody reactivity to B cell-activating factor (BAFF) was associated with SLE
42 ey found autoantibodies directed against the B cell-activating factor (BAFF) were associated with gre
43                                Expression of B cell-activating factor (BAFF), a critical B cell survi
44 cathelicidin, interleukin 1 (IL-1), IL-4 and B cell-activating factor (BAFF), after IgD crosslinking.
45  a proliferation-inducing ligand (APRIL) and B cell-activating factor (BAFF), tumor necrosis factor l
46 B cell dysfunctions, and one of these is the B cell-activating factor (BAFF).
47 ubsets, mirroring deficiency of the cytokine B cell-activating factor (BAFF).
48 is a novel splicing isoform of the regulator B cell-activating factor (BAFF, BLyS), a TNF family prot
49               The cytokine TNF family member B cell-activating factor (BAFF; also termed BLyS) is ess
50 ectively evaluated B-cell subpopulations and B-cell activating factor (BAFF) in 136 patients (46 BOS,
51                            We measured serum B-cell activating factor (BAFF) in 46 cGVHD patients rec
52                                              B-cell activating factor (BAFF) is an important cytokine
53                                              B-cell activating factor (BAFF) single nucleotide polymo
54                                              B-cell activating factor (BAFF), a member of the TNF fam
55 pa B ligand (sRANKL), osteoprotegerin (OPG), B-cell activating factor (BAFF), and a proliferation-ind
56 G), a proliferation-inducing ligand (APRIL), B-cell activating factor (BAFF), interleukin (IL)-6, and
57  of APRIL (a proliferation-inducing ligand), B-cell activating factor (BAFF), tumor necrosis factor-a
58 SF13B, encoding the cytokine and drug target B-cell activating factor (BAFF), was associated with mul
59 tor receptor (BAFFR) expression and inhibits B-cell activating factor (BAFF)-induced B-cell survival
60 e stimulator (BLyS), also referred to as the B-cell activating factor (BAFF).
61 e genes included Tnfsf13b, which encodes the B-cell activating factor (BAFF).
62                                              B-cell-activating factor (BAFF) and its receptor BAFF-R
63                        Sustained increase in B-cell-activating factor (BAFF) mRNA in the CNS and BAFF
64    As a result, mutant TWEAK associated with B-cell-activating factor (BAFF) protein and down-regulat
65 -142(-/-) B cells express elevated levels of B-cell-activating factor (BAFF) receptor (BAFF-R) and as
66 ivation, as well as a defect in BCR-mediated B-cell-activating factor (BAFF) receptor up-regulation a
67  Recent studies have underscored the role of B-cell-activating factor (BAFF), a member of the tumor n
68  a proliferation-inducing ligand (APRIL) and B-cell-activating factor (BAFF), whereas removal of term
69 apacity of a therapeutic mAb and blockade of B-cell-activating factor (BAFF)-BR3 B-cell survival.
70                                          The B-cell-activating factor (BAFF)-receptor (BAFF-R) is res
71                                     Elevated B-cell-activating factor (BAFF; TNFSF13B) levels have be
72 e mated with mice transgenic (Tg) for CD257 (B-cell activating factor, BAFF) developed CD5(+) B-cell
73                                          The B cell activating factor belonging to the tumor necrosis
74                                              B cell-activating factor belonging to the TNF family (BA
75 ly sensitive to the combination of IL-21 and B cell-activating factor belonging to the TNF family (BA
76               Constitutive overexpression of B cell-activating factor belonging to the TNF family (BA
77 3dg-binding CD21/CD19 costimulatory complex, B cell-activating factor belonging to the TNF family (BA
78                      The TNF-related ligand, B cell-activating factor belonging to the TNF family (BA
79                                              B cell-activating factor belonging to the TNF family (BA
80                      The TNF family cytokine B cell-activating factor belonging to the TNF family (BA
81                                              B cell-activating factor belonging to the TNF family (BA
82  to influence Mvarphi phenotype by mediating B cell-activating factor belonging to the TNF family (BA
83 pecificity, NF-kappaB activation through the B cell-activating factor belonging to the TNF family (BA
84                               The effects of B cell-activating factor belonging to the TNF family (BA
85                                              B cell-activating factor belonging to the TNF family rec
86 y, superimposing genetic deficiency of BAFF (B cell-activating factor belonging to the TNF family) on
87 nd is resistant to the survival factor BAFF (B cell-activating factor belonging to the TNF family).
88 microenvironment, including signals from the B cell-activating factor belonging to the TNF family/BLy
89                                        BAFF (B cell-activating factor belonging to the tumor necrosis
90  studies have defined a crucial role for the B cell-activating factor belonging to TNF family (BAFF;
91 pril (a proliferation-inducing ligand)/BAFF (B cell-activating factor belonging to TNF), albumin, cho
92 2 cells released the B-cell survival factor, B-cell activating factor belonging to the TNF family (BA
93                                              B-cell activating factor belonging to the tumor necrosis
94 ults suggest that macrophage- and DC-derived B-cell-activating factor belonging to the TNF family (BA
95 ith the potent B-cell survival factor BAFF ('B-cell-activating factor belonging to the TNF family') p
96  B-cell survival and maturation factor BAFF (B-cell-activating factor belonging to the tumor necrosis
97 w discusses some of the pertinent aspects of B-cell-activating factor biology and considers how recen
98  involved in B lymphocyte development, BAFF (B cell activating factor, BlyS, TALL-1, CD257, TNFSF13B)
99 ection from spontaneous apoptosis induced by B cell-activating factors CD40L, TNF-alpha, and fibronec
100             Total airway IgE correlated with B-cell activating factor concentrations.
101                              Serum levels of B-cell activating factor correlate with laboratory indic
102 s were maintained in a manner different from B-cell-activating-factor-dependent p52/RelB regulation.
103 its absence relieved B cells of the need for B cell activating factor for survival.
104 ession, and rendering B cells independent of B cell activating factor for survival.
105 family kinases, whereas it is independent of B-cell activating factor, IFN, and Toll-like receptor si
106                              By neutralizing B cell-activating factor in vivo, we found an arrest in
107 ction after B-cell receptor stimulation, and B-cell activating factor-induced nuclear factor kappaB2/
108 fic cytokines (insulin-like growth factor-1, B-cell activating factor, interleukin-6, interleukin-10)
109 (-) and CD21(low) B cells and a reduction in B cell-activating factor levels.
110 s against double-stranded DNA, and increased B cell-activating factor levels.
111 ere reduced despite slightly increased serum B cell-activating factor levels.
112  (eg, zoledronic acid, anti-DKK-1 MoAb, anti-B-cell activating factor MoAb and bortezomib, Btk inhibi
113                          Mice overexpressing B cell activating factor of the TNF family (BAFF) develo
114                                              B cell activating factor of the TNF family (BAFF), also
115                                        BAFF (B cell activating factor of the TNF family, also known a
116                                              B cell activating factor of the tumor necrosis factor fa
117 e mice results in the elevated production of B cell-activating factor of the TNF family ((BAFF) also
118 d the functions of the TNF family cytokines, B cell-activating factor of the TNF family (BAFF) and a
119 non-Hodgkin's lymphoma (NHL) B cells express B cell-activating factor of the TNF family (BAFF) and a
120                       The TNF family members B cell-activating factor of the TNF family (BAFF) and it
121  a proliferation-inducing ligand (APRIL) and B cell-activating factor of the TNF family (BAFF) but th
122 ther augmentation in mitogenic responses and B cell-activating factor of the TNF family (BAFF) recept
123                   Herein we demonstrate that B cell-activating factor of the TNF family (BAFF), a B c
124 volved in the immunopathology of RA, such as B cell-activating factor of the TNF family (BAFF), ICOS
125 n requires additional signals from BCR and a B cell-activating factor of the TNF family (BAFF), produ
126  that they stained with mAb specific for the B cell-activating factor of the TNF family (BAFF; also c
127  is also associated with increased levels of B cell-activating factor of the TNF family (BAFF; also k
128                                              B cell-activating factor of the TNF family and a prolife
129 In addition, LMP1 induces B cells to express B cell-activating factor of the TNF family and a prolife
130         DC-produced survival factors such as B cell-activating factor of the TNF family and a prolife
131                                          The B cell-activating factor of the TNF family receptor (BAF
132 function are completely independent of BAFF (B cell-activating factor of the TNF family) or APRIL (a
133 IgG and IgA production was enhanced by BAFF (B cell-activating factor of the TNF family), an innate m
134 -4 or IL-10, whereas Ab secretion requires a B cell-activating factor of the TNF family.
135 nate and adaptive immune systems through the B cell-activating factor of the TNF family.
136                    We examined expression of B cell-activating factor of the tumor necrosis factor (T
137                     The ASC survival factors B cell-activating factor of the tumor necrosis factor (T
138 cell life depends critically on the cytokine B cell-activating factor of the tumor necrosis factor fa
139 rs of the B cell-activating TNF superfamily (B cell-activating factor of TNF family (BAFF) and a prol
140 we show that NF-kappaB activation induced by B cell-activating factor of tumor necrosis factor family
141 s express BR3, the specific receptor for the B cell-activating factor of tumor necrosis factor family
142                                              B cell-activating factor of tumor necrosis factor family
143 )) for APRIL and the closely related ligand, B-cell activating factor of the TNF family (BAFF), bind
144                                          The B-cell activating factor of the TNF family (BAFF), nucle
145 aling from the B-cell receptor (BCR) and the B-cell activating factor of the TNF family receptor (BAF
146 n of the effects of rituximab (anti-CD20) on B-cell-activating factor of the tumor necrosis factor fa
147 ein expression of NIK is steadily induced by B cell-activating factor or CD40 ligand, two major physi
148 lls (IgG(+)); and (5) both TNFRSF17 mRNA and B cell-activating factor protein were up-regulated.
149                   Signaling from the BCR and B cell activating factor receptor (BAFF-R or BR3) differ
150 w here that PTP1B negatively regulates CD40, B cell activating factor receptor (BAFF-R), and TLR4 sig
151 eptors sensitive to trophic factors, such as B cell-activating factor receptor (BAFF-R or BR3) during
152 quires cooperative signaling through BCR and B cell-activating factor receptor 3 (BR3).
153 ne production, proliferation of T cells, and B cell-activating factor receptor expression on B cells.
154 e Ptpn22, we show evidence for enhanced BCR, B cell-activating factor receptor, and CD40 coreceptor p
155  induced IL-15 production in B cells through B cell-activating factor receptor, whereas IL-15, a pote
156 sing functional itBreg cells in a CD40L- and B cell-activating factor receptor-dependent manner.
157         Rather, high CD45 expression reduces B-cell activating factor receptor (BAFFR) expression and
158  (dpi) was more dominantly controlled by the B-cell-activating factor receptor (BAFF-R), a gene that
159 nalling of B-cell activation molecules CD69, B-cell-activating factor receptor, and transmembrane act
160                           High-level soluble B-cell activating factor (sBAFF) was observed in kidney
161         The recruited neutrophils secreted a B cell-activating factor that highly accelerated plasma
162                         The approval of anti-B cell activating factor therapy and an increasing body
163 Fo cells responded to AgR stimulation and to B cell activating factor, they displayed decreased survi
164 rated mediators, matrix metalloproteinase-9, B-cell activating factor, transforming growth factor-bet
165 of CLL or normal B cells with CD40-ligand or B-cell-activating factor upregulated miR-155 and enhance
166 ant CXCL13 was up-regulated >1,000-fold, and B cell-activating factor was also detected.
167  chemokines (CXCL13, CCL19, CCL21, CCL1, and B-cell-activating factor) was increased in pancreatic an

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