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1 anti-CD14, anti-HLA-DR, anti-CD54, and anti-interleukin 2 receptor.
2 body directed against the alpha chain of the interleukin 2 receptor.
3 activated cells expressing the high-affinity interleukin 2 receptor.
4 is directed against the alpha subunit of the interleukin 2 receptor.
5 FR, VEGFR, PDGFR, NGFR and IGF1R, as well as interleukin-2 receptor.
6 -activated T cells express the high-affinity interleukin-2 receptor.
7 sor-cytotoxic, and natural killer cells) and interleukin 2 receptors.
8 , and serum samples were assayed for soluble interleukin-2 receptors.
9 or and also interacts with the CD4, CD8, and interleukin-2 receptors.
10 , or a combination (29/37), elevated soluble interleukin 2 receptor (20/21), and elevated VEGF (16/20
11 in the expression of CD25, the low-affinity interleukin 2 receptor (34% +/- 15% versus 40% +/- 16%).
12 r burden and the presence of soluble (serum) interleukin-2 receptor, a marker associated with a subse
14 nistered intravenously (i.v.) to bind to the interleukin 2 receptor alpha (IL-2R alpha; CD25)-express
15 the type 1 diabetes (T1D) association in the interleukin 2 receptor alpha (IL2RA) gene region to two
18 te (gamma interferon [IFN-gamma] and soluble interleukin 2 receptor alpha [sIL-2Ralpha]) and adaptive
19 co-expressing a chimeric receptor containing interleukin 2 receptor alpha and GP Ibalpha cytoplasmic
20 T-MMP), nor a chimeric MT-MMP containing the interleukin 2 receptor alpha chain (IL-2R) TM and cytopl
22 reased expression of the CD25 marker and the interleukin 2 receptor alpha chain and perturbation of C
23 le-negative CD4-8- thymocytes expressing the interleukin 2 receptor alpha chain, CD25, was also obser
24 stocompatibility complex class I (MHCI), and interleukin 2 receptor alpha subunit (Tac) was compared
26 h humanized anti-Tac (HAT) directed to CD25 (interleukin 2 receptor alpha) or with MEDI-507 directed
27 le tumor necrosis factor receptor 2, soluble interleukin 2 receptor alpha, soluble gp130, soluble CD2
28 in the absence of CD4(+) T cells express the interleukin 2 receptor alpha-chain (CD25) at lower level
29 hen transferred to the lumenal domain of the interleukin 2 receptor alpha-chain (Tac protein), the cy
30 s of T-cell activation, such as induction of interleukin 2 receptor alpha-chain expression and cytoki
33 zed anti-Tac (HAT) directed toward CD25, the interleukin-2 receptor alpha (IL-2Ralpha) using a human
34 tosis reporter system using a chimera of the interleukin-2 receptor alpha (previously referred to as
37 iggered proliferation and of upregulation of interleukin-2 receptor alpha chain (CD25) molecules, but
38 alphabeta T cells expressing high levels of interleukin-2 receptor alpha chain (IL-2R alpha) and maj
40 measured for soluble KIT (sKIT) and soluble interleukin-2 receptor alpha chain (sCD25), which are kn
41 tracellular and transmembrane domains of the interleukin-2 receptor alpha chain (Tac) and the cytopla
42 ) showed a decrease in the expression of the interleukin-2 receptor alpha chain following PMA stimula
43 manized monoclonal antibody specific for the interleukin-2 receptor alpha chain, was safe and efficac
45 I interferon signaling and the interleukin-2/interleukin-2 receptor alpha pathway for the induction o
47 ochemical routes by expression of a chimeric interleukin-2 receptor alpha subunit (Tac)-FcepsilonRI g
48 sterase release, gamma interferon secretion, interleukin-2 receptor alpha upregulation) were neverthe
49 t of a CD8-Nef chimera or in a fusion of the interleukin-2 receptor alpha with an 11-amino-acid regio
50 ts chromatin remodelling to the IL-2Ralpha ('interleukin-2 receptor alpha') gene, which is ectopicall
51 express FasL and Fas, but not CD69 or CD25 (interleukin-2 receptor alpha) and eventually die via apo
52 n, soluble interleukin-1 receptor I, soluble interleukin-2 receptor alpha, and tumor necrosis factor
53 any genes expressed in the thymus, including interleukin-2 receptor alpha, c-myc, and those encoded b
57 orting signal to the cytoplasmic tail of the interleukin-2 receptor alpha-chain caused significant ba
58 2Mit80, an interval that includes Il2ra (for interleukin 2 receptor, alpha chain), a gene that is kno
60 s in interleukin-7 receptor-alpha (IL7RA*C), interleukin-2 receptor-alpha (IL2RA*T), MGAT1 (IV(A)V(T-
61 1beta, and interleukin-7) as well as soluble interleukin-2 receptor-alpha were significantly elevated
62 ry group, whereas interleukin-1beta, soluble interleukin-2 receptor-alpha, interleukin-4, interleukin
63 d a composite biomarker panel of 4 proteins (interleukin-2-receptor-alpha, tumor-necrosis-factor-rece
64 rease induced monocyte expression of surface interleukin 2 receptors and increased expression of HLA-
65 binds specifically to the alpha chain of the interleukin-2 receptor and may thus reduce the risk of r
66 ody that binds to CD25 (alpha subunit of the interleukin-2 receptor) and modulates interleukin-2 sign
67 nd endothelin-1), T cell activation (soluble interleukin-2 receptors), and collagen synthesis (carbox
68 ion through the T cell antigen receptor, the interleukin-2 receptor, and by stimulation of protein ki
69 tients correlate with interleukin-6, soluble interleukin-2 receptor, and interleukin-10 concentration
70 rsely correlated with interleukin-6, soluble interleukin-2 receptor, and interleukin-10 concentration
72 e clearance was also similar between groups (interleukin-2 receptor antagonist group 56 +/- 20 mL/min
73 e low and similar between groups (10% in the interleukin-2 receptor antagonist group vs 6% in the RAT
74 /plasmapheresis preconditioning regimen with interleukin-2 receptor antagonist induction along with t
75 an 60 min, absence of recipient splenectomy, interleukin-2 receptor antagonist induction, and era.
77 364), antithymocyte globulin (ATG; n=4,930), interleukin-2 receptor antagonists (IL-2RA; n=4,378), or
79 antithymocyte globulin (RATG) compared with interleukin-2 receptor antagonists in a racially diverse
81 tandard induction immunosuppression was with interleukin-2 receptor antagonists, and antithymocyte gl
83 match, rabbit antithymocyte globulin (RATG), interleukin-2 receptor antagonists, tacrolimus (FK), cyc
84 n cells activated in vitro with MTg and anti-interleukin-2 receptor (anti-IL-2R), anti-IL-2, or anti-
85 is more effective than Thymoglobulin or anti-interleukin 2 receptor antibodies cannot be answered at
86 .1%) when compared with those receiving anti-interleukin-2 receptor antibodies (2%) and non-induction
87 splantation outcomes between alemtuzumab and interleukin-2 receptor antibodies (IL-2RA) in living don
88 isk of BPAR compared with induction with the interleukin-2 receptor antibodies (IL-2RAs): basiliximab
90 lso distinguished patients who received anti-interleukin-2 receptor antibodies from those who receive
92 polyclonal antibody or OKT3 (n = 62, 33.5%), interleukin-2 receptor antibody (n = 61, 33%), and no in
93 unosuppressive protocol consisted of an anti-interleukin-2 receptor antibody for induction, and mycop
94 phenolate mofetil, corticosteroids, and anti-interleukin-2 receptor antibody induction, results in im
95 phenolate mofetil, corticosteroids, and anti-interleukin-2 receptor antibody induction, was associate
99 on the cell surface such as Fas and CD69 and interleukin 2 receptor, at comparable levels as those T
100 n of a chimeric cytokine receptor (the mouse interleukin 2 receptor beta chain [IL-2Rbeta] extracellu
101 n a lymphopenic host upregulate CD44, CD122 (interleukin 2 receptor beta) and Ly6C expression, acquir
103 be relevant in vivo, since p12(I) binds the interleukin-2 receptor beta and gammac chains, raising t
105 sion of the antiapoptotic molecule Bcl-2 and interleukin-2 receptor beta chain and diminished IL-15-d
106 s are indistinguishable, except for enhanced interleukin 2 receptor-beta (IL-2Rbeta) and suppressed i
109 e-1 diabetes, baseline femoral neck T-score, interleukin-2 receptor blockade, and proteinuria (HR 2.0
110 tandard immunosuppression with Thymoglobulin/interleukin 2 receptor blocker and mycophenolate mofetil
111 Daclizumab, a highly humanized, specific interleukin-2 receptor blocker, may be efficacious to th
112 tion treatments (alemtuzumab, thymoglobulin, interleukin-2 receptor blockers, and no induction) given
113 nt reports have demonstrated the efficacy of interleukin-2-receptor blockers in lowering the incidenc
114 lung transplant subjects also expressed the interleukin-2 receptor, but only during the early post-t
115 body directed against the alpha-chain of the interleukin 2 receptor (CD25), has been extensively eval
116 dy directed against the alpha chain of human interleukin-2 receptor (CD25), reduces the incidence of
117 disorders expressing Tac (alpha chain of the interleukin 2 receptor; CD25), physiologic shedding of t
118 organ-based disease, serum levels of soluble interleukin-2 receptor, collagen propeptides (N propepti
119 ed, SIN lentiviral vector encoding the human interleukin 2 receptor common gamma chain (IL2RG) gene a
121 a humanized monoclonal antibody recognizing interleukin-2 receptor (daclizumab), which has proven to
122 onal antibodies that block the high-affinity interleukin-2 receptor expressed on alloantigen-reactive
123 e CD4:CD8 inversion, and marked reduction in interleukin-2 receptor expression by CD4(+) T cells.
125 composed of Tac antigen, the alpha-chain of interleukin 2-receptor, fused to the first five amino ac
126 odeficiency (SCID-X1) caused by mutations in interleukin 2 receptor gamma (IL2RG) gene threatens the
127 nterferon, CCL5, CXCL1, CXCL2, CXCL7, CXCL9, interleukin 2 receptor gamma (IL2Rgamma), IL21R, CCR2, a
129 is due to mutations in the gene encoding the Interleukin-2 receptor gamma chain (IL-2Rgamma), leading
130 of iCD8alpha cells depends on expression of interleukin-2 receptor gamma chain (IL-2Rgammac), IL-15,
131 se of more highly immunocompromised NOD/SCID interleukin-2 receptor gamma chain null (Il2rg(-/-)) mic
132 rus-based gamma-retrovirus vector expressing interleukin-2 receptor gamma-chain (gammac) complementar
133 se diabetic/severe combined immunodeficiency/interleukin-2 receptor-gamma-null (NOD-SCID IL2Rgamma(nu
134 se diabetic/severe combined immunodeficiency/interleukin-2 receptor-gamma-null (NSgamma) mice with li
135 brane domain of the Tac subunit of the human interleukin 2 receptor (gp55) fused to the cytoplasmic d
136 body directed against the alpha chain of the interleukin 2 receptor, has been shown to reduce the inc
137 genitors by augmenting responsiveness of the interleukin 2 receptor (IL-2R) and transcription factor
138 or (TfR) expression follows the induction of interleukin 2 receptor (IL-2R) expression in a sequence
141 ells), which have abundant expression of the interleukin 2 receptor (IL-2R), are reliant on IL-2 prod
142 of alpha, beta, and gamma(c) subunits of the interleukin 2 receptors (IL-2R) in plasma membranes of K
143 f the erythropoietin receptor (EPO-R) or the interleukin-2 receptor (IL-2-R) by their respective liga
146 was associated with a specific deficiency of interleukin-2 receptor (IL-2R) alpha-chain up-regulation
147 expressed activation markers, as measured by interleukin-2 receptor (IL-2R) and transcription factor
148 immunostaining with DEC-205, B7-1, CD4, and interleukin-2 receptor (IL-2R) antibodies and histopatho
149 12(I) binds to the cytoplasmic domain of the interleukin-2 receptor (IL-2R) beta chain that is involv
154 (SRL) in combination with chimeric (c-) anti-interleukin-2 receptor (IL-2R) monoclonal antibodies (mA
158 IgG1 directed against the alpha chain of the interleukin-2 receptor (IL-2R), is a competitive inhibit
159 cts with the beta and gamma(c) chains of the interleukin-2 receptor (IL-2R), the heavy chain of the m
164 ntibody that binds to the alpha chain of the interleukin-2 receptor (IL-2Ralpha), administered for a
165 pansion of alloreactive donor T cells, their interleukin-2-receptor (IL-2R) alpha-chain expression an
168 mmon cytokine receptor gamma chain (NOD/SCID/interleukin 2 receptor [IL2r] gamma(null)) efficiently s
169 dy directed against the alpha subunit of the interleukin 2 receptor, in reducing acute rejection afte
170 IL2RG, which encodes the gamma-chain of the interleukin-2 receptor, in a mouse model of the disease
175 ited by the fact that CD25, the low-affinity interleukin-2 receptor, is up-regulated on conventional
176 was distinguished by less T-cell activation (interleukin-2 receptor+), less proliferation (proliferat
179 d Nf1-deficient T cells, T-cell receptor and interleukin-2 receptor-mediated proliferation of thymocy
180 mes to the more commonly used combination of interleukin-2 receptor monoclonal antibody induction wit
181 inhibitor, cyclosporine A, the chimeric anti-interleukin-2 receptor monoclonal antibody, basiliximab,
182 ocyte polyclonal antibody or basiliximab, an interleukin-2 receptor monoclonal antibody, is most comm
184 assess whether basiliximab, a chimeric anti-interleukin-2 receptor monoclonal antibody, reduced the
187 the absence of downstream events related to interleukin 2 receptor occupancy and/or cell division.
188 and day 4-was selected to block detection of interleukin-2 receptor on 97% of peripheral blood lympho
190 b (Roche Laboratories, Nutley, NJ) block the interleukin-2 receptor on the surface of activated T cel
191 tively, act by binding to the alpha chain of interleukin-2 receptors on activated T lymphocytes.
193 es composed of R73-positive T cells and rare interleukin-2 receptor-positive cells, which was not obs
194 3-positive cells and 88% for the presence of interleukin-2 receptor-positive or HLA-DR-positive cells
195 tion of IgG anti-HLA class II antibodies and interleukin-2 receptor--positive T-cell outgrowth from b
197 a humanized monoclonal antibody against the interleukin-2 receptor, reduced the risk of rejection wi
202 r-like effector nucleases (TALENs) to target interleukin-2 receptor subunit gamma (IL2RG) in pronucle
205 s enzyme provides a crucial link between the interleukin-2 receptor, the protooncogene PKB, and p70 S
207 ride, interleukin-6, interleukin-10, soluble interleukin-2 receptor, tumor necrosis factor-alpha, and
208 tive cells expressing the alpha chain of the interleukin 2 receptor) were removed by immunomagnetic s
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