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1 infects bovine mammary epithelial cells (MAC-T cell line).
2 cleic acid (DNA) from an HIV-infected Jurkat T cell line.
3 onotype found in the poly(F,Y,A,K)n-specific T cell line.
4 and proliferation by an epitope-specific CD4 T cell line.
5 essed in primary cells and an IL-2-dependent T cell line.
6 of the Notch target gene Hes1 in a leukemia T cell line.
7 ncrease in transfer of HIV-1(BaL) to a human T cell line.
8 from a peptide-independent alloreactive CD8+ T cell line.
9 active Cre recombinase into a loxP-reporter T cell line.
10 on factors indicated that this is a CD4-1(+) T cell line.
11 establishment of an IL-15-dependent CD4-1(+) T cell line.
12 ncorporation in HeLa cells and in the Jurkat T-cell line.
13 mma interferon (IFN-gamma) production by the T-cell line.
14 ng to the GATA3 promoter in the human Jurkat T-cell line.
15 n that against the Cdt-hypersensitive Jurkat T-cell line.
16 e occupancy of three ETS proteins in a human T-cell line.
17 (mac239)) replication in a transformed human T-cell line.
18 apoptotic cell death of the Tax2-established T cell lines.
19 ion in latently infected primary T cells and T cell lines.
20 ppaB kinase and JNK activation in both B and T cell lines.
21 that human GIMAP6 is expressed primarily in T cell lines.
22 primary human T cells but not in transformed T cell lines.
23 through luciferase reporter assays in Jurkat T cell lines.
24 CYLD silencing increases HIV replication in T cell lines.
25 CD4(+) T lymphocytes, but not in some CD4(+) T cell lines.
26 peptide specificity of the in vitro induced T cell lines.
27 ress membrane TRAIL, and induce apoptosis of T-cell lines.
28 n purified CD4+ T cells and Jurkat and HSB-2 T-cell lines.
29 ral blood mononuclear cells and EBV-specific T-cell lines.
30 of both integrins in murine lymphocytes and T-cell lines.
31 orylated in a panel of HTLV-1-infected human T-cell lines.
32 s infectious, yet it spreads poorly in other T-cell lines.
33 compared to the other five SIV-specific CD8+ T-cell lines.
34 o a small number of allergic subject-derived T-cell lines.
35 eases and their functional targets in B- and T-cell lines.
36 in a manner comparable to established mouse TS cell lines.
37 ells, and failure to yield trophoblast stem (TS) cell lines.
39 more limited neutralizing capacity against a T-cell line-adapted SIV compared to those of the milk Ig
40 positive and -negative clones of the WEHI7.2 T cell line after T cell receptor (TCR) activation by an
43 ns decreased the survival of HTLV-1-infected T-cell lines, although no cell death was observed after
44 ing RNA in a VEGF receptor-expressing Jurkat T cell line and by SU5416, a pharmacological KDR inhibit
46 lock proliferation of an IL-1alpha-dependent T cell line and inhibit production of TNF-alpha by activ
49 proliferation of intestinal gliadin-specific T cell lines and clones were measured as evidence of T c
52 drugs that primed latent HIV-1 infection in T cell lines and in primary T cells for reactivation and
55 0-induced apoptosis was further confirmed in T cell lines and peripheral blood mononuclear cells usin
57 from infecting multiple human macrophage and T cell lines and primary cells by hT5Cyp, as were HIV-2R
58 letion or overexpression of hnRNPLL in B and T cell lines and primary T cells resulted in reciprocal
59 lowed the quantitative comparison of the two T cell lines and provided predictions for the conversion
61 of Bim partially protected an IL-7-dependent T-cell line and peripheral T cells, especially cells wit
62 udy, we expressed HDAC7 mutant proteins in a T-cell line and use DNA microarrays to identify transcri
63 ects on the functional phenotype of specific T-cell lines and clones by means of flow cytometry, real
66 with myeloma and generated peptide-specific T-cell lines and clones from HLA-A*0201-positive (HLA-A*
67 s their recognition by EphA2-specific CD8(+) T-cell lines and clones in vitro via a mechanism that is
68 A panel of human GAD (hGAD65)-specific CD4 T-cell lines and hybridomas was generated to serve as de
69 miRNA expression in HTLV-1-transformed human T-cell lines and primary peripheral blood mononuclear ce
70 oduced robust cytotoxicity against malignant T-cell lines and primary tumors and were protective in a
72 -cell responses against gluten by generating T-cell lines and T-cell clones from intestinal biopsies
73 l-2 family, is restricted to HTLV-1-infected T-cell lines and to T-cells expressing both Tax and HBZ
74 oth resting T cells and the nonactivated EL4 T cell line, and was up-regulated in both types of T cel
75 ding HIV-1 infection was also normal in most T cell lines, and flap mutant viruses replicated equival
76 cytokines produced by IFX-specific T cells, T cell lines, and T cell clones were evaluated at the mR
77 n increased Rac1 activity in both B-cell and T-cell lines, and its suppression was able to abrogate p
79 9 induced the greatest proliferation in CD4+ T-cell lines, and VirB9-specific CD4+ T-cell clones resp
80 n activation, however, some of the malignant T-cell lines are able to coexpress IL-17A and IL-17F, le
81 assays were performed using the Jurkat E6.1 T cell line as a model of T lymphocytes and Caco2-BBE mo
82 s associated with Tam resistance in the MCF7-T cell line as opposed to the Tam-sensitive MCF7 cell li
87 ltivars Ayacuchana and Pasankalla stimulated T cell lines at levels similar to those for gliadin and
88 cassette with flanking loxP sites in a human T-cell line at the precise location of vector integratio
89 rived from rabbits immunized with the Jurkat T-cell line (ATG-Fresenius) or thymus cells (Thymoglobul
90 ify the APOBEC3 repertoire in multiple human T-cell lines, bulk leukocytes and leukocyte subsets, and
91 ecent phosphoproteomic studies of the Jurkat T cell line but difficult to reconcile with former bioch
94 the CD4 T cell response to CCNB1, we derived T cell lines by multiple weekly rounds of stimulation wi
95 by hamster kidney)-21 and an HTLV-1-infected T cell line, C8166, physiologically relevant to HTLV-1-i
96 m, we show that autologous BK virus-specific T cell lines can be reliably generated from viremic KTR.
99 mRNAs indicated that, compared to the human T-cell lines CEM and H9, prostate cell lines LNCaP and D
100 parental Jurkat cells or an unrelated human T cell line (CEM391) inhibited SOCE and led to sensitiza
101 ral blood mononuclear cells (PBMC) and a CD4 T-cell line compared to monocyte-derived macrophages, or
104 ased in a single round of replication from a T cell line containing A3G complexes (CEM cells) after i
105 ipid C-stimulated mouse iNKT cells and human T-cell lines containing NKTs primed with CD1d+C1R transf
106 re autoantigen-nonspecific, in that the same T cell line could suppress autoimmunity induced by three
107 28-35)SL8- and Gag(181-189)CM9-specific CD8+ T-cell lines could suppress the replication of an escape
109 of mutant CARD11 expression constructs into T cell lines demonstrated both loss-of-function and domi
110 n experiments using latently infected Jurkat T-cell lines demonstrated that the HKMT enhancer of Zest
113 ix mutant replicated efficiently in the MT-4 T-cell line despite maintaining an MVB-targeting phenoty
114 d therefore these findings and the new model T cell line developed will contribute to a greater under
115 viral efficacies of 26 epitope-specific CD8+ T-cell lines directed against seven SIV epitopes in Tat,
116 processed A. fumigatus and the multispecific T-cell lines, directed against all 3 proteins, especiall
125 NS5 protein inhibits HIV replication, CD4(+) T cell lines expressing this protein were generated.
127 , in contrast to its parental virus, infects T-cell lines expressing low levels of cell surface CCR5.
128 was highlighted by data showing that CEM-SS T-cell lines expressing near-physiologic levels of APOBE
132 itopes, establishing antigen-specific memory T-cell lines for identifying CD8(+) and CD4(+) T-cell ep
133 ated a large number of MAGE-A3-specific CD4+ T cell lines from all individuals tested, enabling full
134 oted that all bronchoalveolar lavage-derived T cell lines from HLA-DP2-expressing CBD patients contai
139 esent study, we established cytotoxic CD4(+) T cell lines from VV-immune donors, which recognize epit
144 significantly less frequent in EBV-specific T-cell lines from patients with EBV-associated nasophary
149 is of 50 of a total of 236 CD4(+) and CD8(+) T cell lines grown from individual handpicked islets or
153 These findings demonstrate that in human T cell lines, HIV-1 and simian immunodeficiency virus ca
155 oth kill thymocytes, peripheral T cells, and T cell lines; however, we have found that galectin-9 and
157 stimulation in PBMCs, CD4(+) T cells, or the T cell line HuT78 activates the Notch pathway by nuclear
160 ectrometry was performed on the human Jurkat T cell line in the presence of U0126, an inhibitor of ER
162 , we analyzed the dynamics of the two CD4(+) T cell lines in mice during infection with L. monocytoge
163 enuate the proliferation of disease-specific T cell lines in response to gluten antigens and, therefo
164 ng DSBs, in benign Barrett's epithelial (BAR-T) cell lines in vitro and in patients with Barrett's es
165 t and in response to signaling in a cultured T-cell line in a manner which temporally correlates with
166 HDR donors in hESCs to generate an isogenic TS cell line in a scarless manner and to model the 16p11
168 cific overexpression of either SOD in Jurkat T cell lines increases intracellular production of H2O2
169 eceptors from the regulatory IL-10-secreting T cell line induced by the random amino acid copolymers
171 OCS1 and SOCS3, but not SOCS2, in the Jurkat T cell line inhibited IFN-alpha-induced phosphorylated S
172 -tRNA(Val) observed in the homoplasmic 1624C>T-cell lines is caused by a rapid degradation of the dea
173 driving IL-17 secretion in short-term CD4(+) T cell lines isolated from human peripheral blood, altho
174 ramer(+) cells and cloned them from uncloned T cell lines isolated from spleen and lymph nodes of dia
175 nes were derived from HIV-reactive CD28+CD8+ T-cell lines isolated from 7 HIV+ HAART-treated patients
178 on of endogenous c-Myc by Runx1 in the human T cell line Jurkat and murine primary hematopoietic cell
179 s increased after restimulation in the human T cell line Jurkat, in human memory and Th2 cells, and i
182 GBV-C NS5A proteins were expressed in a CD4+ T cell line (Jurkat), and both induced a potent, dose-de
183 ent with SS, an acute lymphoblastic leukemia T-cell line (Jurkat), and JFL (a FAS-low variant of Jurk
184 (LBRM-33), similar to its effects on a human T-cell line (Jurkat), but did not inhibit IL-2 productio
185 en analyzed in physiologically more relevant T-cell lines (Jurkat and CEM), NC mutant viruses remaine
187 f the herpesvirus saimiri-transformed CD8(+) T-cell line, K#1 50K, has potent HIV-1-inhibitory activi
188 interleukin-2 (IL-2) production by a murine T-cell line (LBRM-33), similar to its effects on a human
189 , two different murine CD4(+) TCR transgenic T cell lines, LLO118 and LLO56, both specific for the sa
192 d Ag-specific cytotoxic activity of a CD8(+) T cell line manifested in a 4-h assay (10-20% increase),
195 B-HCV") has been shown to infect established T cell lines (Molt-4 and Jurkat) and primary human naive
199 and irradiated cells of an HTLV-1-producing T-cell line, MT2 was used to determine the permissivity
201 e also analyzed A3 editing of HTLV-1 in five T-cell lines obtained from HTLV-1-infected patients.
202 44 internalization varied among cultured CD8 T cell lines of different specificities, and correlated
203 using HLA-A2 matched effector cells (CD8(+) T cell line or clone) and target cells supporting full H
204 al strains in pairwise competition assays in T-cell lines, primary cells, and the ecotropic human imm
209 we demonstrate that M. leprae-specific mouse T-cell lines recognize several of these antigens, with t
210 exogenous NY-ESO-1 protein, only one CD4(+) T cell line recognized NY-ESO-1(+) HLA class II-expressi
213 e, we showed that silencing IFN-lambda1 in T/T cell line reduced basal ISG expression and improved an
214 te more potently activated a CD1b-restricted T cell line relative to Mo-DCs pulsed with free lipid Ag
217 xt to an "optimal" Kozak sequence in a human T cell line resulted in enhanced translation of a single
218 of complete STLV genome sequences from these T cell lines revealed them to be closely related but dis
224 nalyzed two naturally occurring human CD4(+) T cell lines specific for different peptides from cytoso
228 were characterized in vitro by using a human T-cell line specific for the immunodominant epitope of B
229 T-cell receptor (TCR) cDNAs from murine CD8 T-cell lines specific for either pIRS-21097-1105 or pCDC
231 with collagen-induced arthritis (CIA), this T cell line specifically enhanced the severity of autoim
232 ed a CpG island that is methylated in CD4(+) T cell lines (such as Jurkat and Sup-T1), resulting in t
233 timulation of the Fas receptor in the Jurkat T-cell line, suggesting that Hip is a substrate unique t
234 ty of interactions are common to both B- and T-cell lines, suggesting interactions may be highly cell
236 xamined the fine specificity of VSG-specific T-cell lines, T-cell hybridomas, and Th cells activated
238 re detected in 83% of Art v 125-36 -reactive T-cell lines (TCL) from mugwort-allergic individuals, bu
242 rt hairpin RNA in both primary T cells and a T cell line that recapitulates the stability phase of re
243 ical to those recently found in a regulatory T cell line that secretes both IL-4 and IL-10 induced in
244 This approach identified several independent T cell lines that proliferated robustly in response to I
245 s among the drug, HLA, and TCR, we generated T cell lines that react to ALP or its metabolite oxypuri
246 sion with either HSV or VZV enriches for CD4 T cell lines that recognize the other agent at the whole
247 ild-type virus replication, a Tet-off Jurkat T-cell line that expressed approximately 15-fold-higher
248 t express human or macaque CD16 and a CD4(+) T-cell line that expresses luciferase from a Tat-inducib
249 cell carcinoma (RCC), we identified a CD4(+) T-cell line that showed TCR-mediated recognition and lys
251 lus fumigatus proteins, Aspergillus-specific T-cell lines that have a broad specificity and favorable
252 at it is possible to establish clonal CD8(+) T-cell lines that represent the most abundant specificit
253 spleen and lymph node cells in vitro yielded T-cell lines that specifically produced interferon-gamma
254 1) vif compromise virus replication in human T-cell lines that stably express APOBEC3F (A3F) or APOBE
255 by ELF5 will be instrumental to derive human TS cell lines that truly reflect early placental trophob
256 and enables derivation of trophoblast stem (TS) cell lines that, when injected into blastocysts, chi
257 epared M. tuberculosis-specific gamma9delta2 T cell lines to study their direct protective effects an
259 have used an IA(b)/OMP-19(107-122)-specific T-cell line to monitor antigen display ex vivo during ac
260 abilities of different epitope-specific CD8+ T-cell lines to control simian immunodeficiency virus (S
262 firmed the responsiveness of these cytotoxic T-cell lines to seven peptides described previously and
264 ate the effect: an anti-myelin basic protein T-cell line treated with cefuroxime or penicillin was mo
266 olyclonal vaccinia virus-polyspecific CD8(+) T cell line, two conserved vaccinia-derived TAP-independ
267 D147-dependent phosphoproteome in the Jurkat T cell line upon treatment with T cell stimulating agent
268 cytosis in the adherent cell 293T and Jurkat T cell lines using a fusion protein of extracellular CD4
270 f a beryllium-responsive, HLA-DP2-restricted T cell line was seen after the induction of 4-1BB ligand
272 strated that forced expression of GRAIL in a T cell line was sufficient for conversion of these cells
274 +), OT-II CD4+ T cells, and the human Jurkat T cell line, we show that physiological levels of H(2)S
275 human T cells and a reporter assay in Jurkat T cell lines, we dissected the regulation of TLR10, a TL
276 ted CD4(+) T cells from spleen and lung, and T cell lines, we found that the majority of these T cell
278 a/beta pairs cloned from single cells of the T cell line were inserted into a retrovirus vector linke
284 By contrast, the peptide 14-28-specific T cell lines were not stimulated in any of these conditi
289 28-35)SL8- and Gag(181-189)CM9-specific CD8+ T-cell lines were consistently superior at suppressing v
291 chemical genetic inhibitor system in Jurkat T cell lines, where the inhibitor blocked ZAP-70-depende
292 This 9-mer serves to direct cytolysis by T cell lines, whereas a related 10-mer (E7(11-20)), prev
293 Unexpectedly, IL-27 did not inhibit HIV-1 in T cell lines, whereas IL-2 inhibited HIV-1 replication i
294 ired for proliferation and survival of these T cell lines whether or not JAKs or STATs were mutated.
295 gIIFPLA(2) inhibited the proliferation of a T cell line, which was not seen with group IIA PLA(2).
296 interrogated vaccinia-reactive CD4 in vitro T cell lines with vaccinia protein fragments expressed f
297 age is observed upon infection of the Jurkat T-cell line with vesicular stomatitis virus G glycoprote
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