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1 n complete Freund's adjuvant (CFA/incomplete Freund's adjuvant).
2 itoneally with sheep IgG (0.2 mg in complete Freund's adjuvant).
3 ture of antigens which characterize Complete Freund's Adjuvant.
4 retinoid-binding protein (IRBP) in complete Freund's adjuvant.
5 All mice were immunized with TAChR in Freund's adjuvant.
6 mAb MK2-23 conjugated to KLH and given with Freund's adjuvant.
7 istration of capsaicin, formalin or complete Freund's adjuvant.
8 DNA or 5gP protein emulsified in ISA 720 or Freund's adjuvant.
9 to be more effective than emulsification in Freund's adjuvant.
10 humans, with immunization of 5gP protein in Freund's adjuvant.
11 sponsive to rechallenge with OVA in complete Freund's adjuvant.
12 nduced by intraplantar injection of complete Freund's adjuvant.
13 o tolerant to challenge with OVA in complete Freund's adjuvant.
14 ith 1 mg of immunogen emulsified in complete Freund's adjuvant.
15 inflammatory stimuli, formalin and complete Freund's adjuvant.
16 e obtained by formulation of the vaccines in Freund's adjuvant.
17 nimals immunized with ovalbumin and complete Freund's adjuvant.
18 eous injections of CM emulsified in complete Freund's adjuvant.
19 animals with recombinant phogrin in complete Freund's adjuvant.
20 h this epitope when administered in complete Freund's adjuvant.
21 d-binding protein (IRBP) mixed with complete Freund's adjuvant.
22 s were immunized with ovalbumin and complete Freund's adjuvant.
23 nant protein consisting of the C terminus in Freund's adjuvant.
24 to that seen in mice immunized with complete Freund's adjuvant.
25 routes and even in the presence of complete Freund's adjuvant.
26 injection of P gamma emulsified in complete Freund's adjuvant.
27 ining the 36 kDa protein (p-36) and complete Freund's adjuvant.
28 inactivated influenza virus formulated with Freund's adjuvant.
29 rons during inflammation induced by complete Freund's adjuvant.
30 with 100 micrograms of rgp120SF2 in complete Freund's adjuvant.
31 of myeloid cells upon injection of complete Freund's adjuvant.
32 ng immunization with OVA protein in complete Freund's adjuvant.
33 nduced by MF59 but not by alum or incomplete Freund's adjuvant.
34 lpha-myosin heavy chain peptide and complete Freund's adjuvant.
35 zation with PLP(139-151) peptide in complete Freund's adjuvant.
36 saccharide, aluminium hydroxide and complete Freund's adjuvant.
37 in either incomplete (IFA) or complete (CFA) Freund's adjuvant.
38 rat hindpaw 2 d after injection of complete Freund's adjuvant.
39 cell was given subcutaneously in incomplete Freund's adjuvant.
40 eliminates all undesired side effects of the Freund's adjuvants.
41 rabbits immunized with 2/6/7- or 2/6-VLPs in Freund's adjuvants.
42 us CpG 1826, 0 of 4 (0%) with CFA/incomplete Freund's adjuvant, 0 of 4 (0%) with CpG 1826 mixed with
43 (HLA-A-like) peptides emulsified in complete Freund's adjuvant 7 d before transplantation (n = 5 to 7
44 nd paw swelling to paw injection of complete Freund's adjuvant, a model of peripheral inflammatory pa
45 intraperitoneal immunization with incomplete Freund's adjuvant, a protocol previously thought to indu
46 a high dose of HEL emulsified in incomplete Freund's adjuvant, a strong splenic proliferative respon
49 pheral nerve injury or injection of Complete Freund's Adjuvant, although they display intact nocicept
50 llowing a subcutaneous injection of complete Freund's adjuvant, an inducer of chronic inflammation.
51 h purified recombinant LppQ-N' formulated in Freund's adjuvant and challenged them with M. mycoides s
52 rived protein extract emulsified in complete Freund's adjuvant and found that these mice developed ca
55 of sera from immunized mice in the complete Freund's adjuvant and Montanide ISA51 groups and after a
58 e were immunized with cardiac myosin (CM) in Freund's adjuvant and received heterotopic, minor antige
59 211 suppressed allodynia induced by complete Freund's adjuvant and the chemotherapeutic agent paclita
60 d groups of rabbits (n = 7) with each MAP in Freund's adjuvant and then exposed all rabbits to a 200-
62 t proteins from NTHi, or saline (control) in Freund's adjuvant and then were challenged by intrabulla
64 These two antigens were each emulsified with Freund's adjuvant and used to vaccinate Aotus nancymai m
65 or G9-154 (KTWGQYWQV) peptides in Incomplete Freund's Adjuvant and were tested for the ability to be
66 vaccines, we tested gD2 in alum/MPL, gD2 in Freund's adjuvant, and dl5-29 (a replication-defective H
67 oved for use in humans, was as protective as Freund's Adjuvant, and protective vaccination correlated
68 num hydroxide, calcium phosphate, incomplete Freund's adjuvant, and the oil-in-water emulsion MF59.
72 PBS and Freund's adjuvant or with PPSV23 and Freund's adjuvant at 48 hours after infection (P </= 0.0
73 h, once immediately post- and again 2 h post-Freund's adjuvant at GB 30, at the junction of the later
74 Select CpG ODN were as effective as complete Freund's adjuvant at inducing an antigen-specific antibo
76 oPn) major outer membrane protein (MOMP) and Freund's adjuvant can protect mice against a genital cha
78 th antigen, compared favorably with complete Freund's adjuvant (CFA) and alum in eliciting tt specifi
79 culture filtrate antigen (CneF) in complete Freund's adjuvant (CFA) and the other heat-killed Crypto
81 pain: (i) intraplantar injection of complete Freund's adjuvant (CFA) as a model of adjuvant- and path
83 with Arg(12) mutant ras peptide in complete Freund's adjuvant (CFA) develop T cells within 10 d that
85 C harvested from mice injected with complete Freund's adjuvant (CFA) enhanced type-1 cytokine respons
86 th a uveitogenic regimen of IRBP in complete Freund's adjuvant (CFA) exhibited CD25+ regulatory cells
87 ed with a single dose of vaccine in complete Freund's adjuvant (CFA) generated antigen-specific gamma
88 isolated from rats with or without complete Freund's adjuvant (CFA) hindpaw inflammation, in respons
90 more efficient than free peptide in complete Freund's adjuvant (CFA) in inducing T cell activation an
95 persistent inflammation induced by complete Freund's adjuvant (CFA) increased GABAergic miniature IP
96 d dose-dependently potently reduced complete Freund's adjuvant (CFA) induced chronic inflammatory pai
98 ng hindlimb inflammation induced by complete Freund's adjuvant (CFA) injections in the hindpaw and hi
102 ng this model, induced by injecting complete Freund's adjuvant (CFA) into one hind paw, we systematic
103 induced by subcutaneously injecting complete Freund's adjuvant (CFA) into the hind paws of rats.
105 nduced by a unilateral injection of complete Freund's adjuvant (CFA) into the masseter muscle under m
107 rats were injected bilaterally with complete Freund's adjuvant (CFA) into the TMJ or served as uninje
110 ced thermal hypersensitivity in the complete Freund's adjuvant (CFA) model of inflammatory pain (1.3-
112 persistent inflammation induced by Complete Freund's adjuvant (CFA) modulates GABA signaling differe
113 ated mechanical hyperalgesia in the complete Freund's adjuvant (CFA) mouse model of inflammatory pain
114 low-pathology BL/6 mice with SEA in complete Freund's adjuvant (CFA) once before, and once again duri
115 hed mechanical allodynia induced by complete Freund's adjuvant (CFA) or by partial sciatic nerve liga
117 myelin basic protein emulsified in complete Freund's adjuvant (CFA) or passively by the transfer of
118 s the protective response, CneF, in complete Freund's adjuvant (CFA) or the immunogen that induces th
119 rough preinjection with beta-gal in complete Freund's adjuvant (CFA) or through preinjection with sol
120 Hindpaw intraplantar injection of complete Freund's adjuvant (CFA) produced peripheral inflammation
121 in rodents by hindpaw injection of complete Freund's adjuvant (CFA) produces anhedonia and dysregula
123 face adhesin A (PsaA) emulsified in complete Freund's adjuvant (CFA) provides protection against syst
124 -4 weeks on their respective diets, complete Freund's adjuvant (CFA) was injected in one hindpaw to i
126 used a model of arthritis in which complete Freund's adjuvant (CFA) was injected into the rat ankle
129 usly injection of (1) GA mixed with complete Freund's adjuvant (CFA), (2) CFA alone, or (3) saline.
130 to the epitope peptide delivered in complete Freund's adjuvant (CFA), and IgM production was even gre
132 inducing liver histologic change as complete Freund's adjuvant (CFA), the standard adjuvant used for
133 g protein1-20 peptide (IRBP1-20) in complete Freund's adjuvant (CFA), with or without a preceding ATR
134 jection of formalin, carrageenan or complete Freund's adjuvant (CFA), without affecting basal pain pe
135 ted in the K/BxN serum-transfer and complete Freund's adjuvant (CFA)-evoked active immunization model
137 f the mTOR signaling pathway during complete Freund's adjuvant (CFA)-induced chronic inflammatory pai
139 r findings were that 48 h following complete Freund's adjuvant (CFA)-induced inflammation, the propor
140 mined the relative contributions of complete Freund's adjuvant (CFA)-induced inflammatory pain and op
141 ates inflammatory hyperalgesia in a complete Freund's adjuvant (CFA)-induced inflammatory pain rat mo
142 tional deletion of Orai1 attenuates Complete Freund's adjuvant (CFA)-induced pain hypersensitivity in
143 tional deletion of Orai1 attenuates complete Freund's adjuvant (CFA)-induced pain hypersensitivity.
145 PD) mRNA than did the adults during complete Freund's adjuvant (CFA)-induced peripheral inflammation.
146 use formalin assay and also reduced complete Freund's adjuvant (CFA)-induced thermal hyperalgesia and
147 The 3d mutation slightly reduced complete Freund's adjuvant (CFA)-mediated antigen presentation, b
160 ion induced by hindpaw injection of complete Freund's adjuvant (CFA): artemin expression increased 10
162 onferred by yMSP1(19) emulsified in complete Freund's adjuvant (CFA/incomplete Freund's adjuvant).
163 llowing paw inflammation induced by complete Freund's adjuvant (CFA; 1:1 injected s.c. in a 0.01 ml v
164 (8-60 min), carrageenan (3 hr), and complete Freund's adjuvant (CFA; 3 d) into the rat hindpaw as wel
166 on with schistosome egg antigens in complete Freund's adjuvant, coinfection with the nematodes also r
167 n were noted, for dams immunized with gB and Freund's adjuvant, compared with dams immunized with gB
169 rculosis, an essential component of complete Freund's adjuvant, converted CD11b(hi)CD11c(-) monocytes
170 odendrocyte glycoprotein peptide in complete Freund's adjuvant, correlating with milder experimental
172 c antibody; only those animals given PYC2 in Freund's adjuvant demonstrated a significant degree of p
173 unized with a P55 fusion protein in complete Freund's adjuvant developed anti-P55 antibodies, detecta
174 x rabbits vaccinated with the MAP peptide in Freund's adjuvant developed high-titer, high-avidity ant
175 injection of donor splenocytes and complete Freund's adjuvant eliminates autoimmunity and permanentl
176 istration of the B9-23 peptide in incomplete Freund's adjuvant enhanced their insulin autoantibody re
177 When WEB2170 was added to OVA in complete Freund's adjuvant, enhanced IgG2a but not IgG1 productio
178 were immunized with IRBP mixed with complete Freund's adjuvant; eyes were enucleated on day 7 after i
179 ), whereas rabbits immunized with PPSV23 and Freund's adjuvant failed to show differences in clinical
180 ith pneumococcal capsular polysaccharide and Freund's adjuvant fails to produce opsonizing antibodies
181 e fragments of target antigens in incomplete Freund's adjuvant has resulted in severe anaphylactic re
184 ccine administered to neonates in incomplete Freund's adjuvant (IFA) induced such cells in reduced nu
186 d) mice, immunization with HEL in incomplete Freund's adjuvant (IFA) resulted in Th2-dominated immune
187 -chain peptide 9-23 emulsified in incomplete Freund's adjuvant (IFA) was also potent at preventing on
188 BP KO mice immunized with IRBP in incomplete Freund's adjuvant (IFA), lacking mycobacteria (whereas t
189 Treatment with E2 peptide2 in incomplete Freund's adjuvant (IFA), resulted in higher antibody pro
195 ntradermal injections of gliadin in complete Freund's adjuvant (immunization) or of soluble gliadin o
196 e subcutaneous route with rHag B in complete Freund's adjuvant, immunized with rHag B and orally infe
197 quent challenge with the peptide in complete Freund's adjuvant in adult life, although this neonatal
198 cord slices from rats injected with complete Freund's adjuvant in one hindpaw and from uninflamed con
199 search for an adjuvant that is comparable to Freund's adjuvant in potency and is safe for use in huma
202 n A/J mice immunized with myosin in complete Freund's adjuvant in that myosin-specific antibodies and
203 nduced by subcutaneous injection of Complete Freund's Adjuvant in the left hind paw of Sprague-Dawley
204 by 6 wk after a challenge with human GAA and Freund's adjuvant; in contrast, administration of the AA
205 fic IgG responses when immunized in complete Freund's adjuvant, indicating that B7-1 and B7-2 can hav
206 ection and not when administered in complete Freund's adjuvant, indicating that molecular mimicry-ind
207 nization with the same antigen in incomplete Freund's adjuvant induced a strong IgG1 response with on
208 H1 conjugated with keyhole limpet hemocyanin Freund's adjuvant induced humoral and cellular anti-3H1
209 n of transgenic animals with MBP in complete Freund's adjuvant induced IFN-gamma-secreting Th1 cells
210 , and immunization with antigen and complete Freund's adjuvant induced interferon-gamma-secreting, an
211 ice with myocarditogenic peptide in complete Freund's adjuvant induced the infiltration of IL-17A-pro
212 agonist of TRPA1) and reversed CFA (Complete Freund's Adjuvant)-induced inflammation and thermal hype
213 alin-induced spontaneous behaviors, complete Freund's adjuvant-induced heat and mechanical hypersensi
214 ete Freund's adjuvant), intradermal complete Freund's adjuvant-induced hindlimb inflammation 1 and 4
217 s-like immunoreactivity in a rodent complete Freund's adjuvant-induced peripheral inflammatory model
218 (ED50 = 30 micromolkg s.c.) reduced complete Freund's adjuvant-induced thermal hyperalgesia in the ra
219 pain models, we found no change in Complete Freund's adjuvant-induced thermal or mechanical hypersen
220 bovine collagen (CII) emulsified in complete Freund's adjuvant inhibited T helper type 1 differentiat
221 mal hyperalgesia after intraplantar complete Freund's adjuvant injection (ED(50) = 41 mg/kg, i.p.).
222 sed thermal hyperalgesia induced by complete Freund's adjuvant injection and reduced response to acid
223 e phase inflammatory pain following complete Freund's adjuvant injection and the late phase neuropath
225 mation was produced by injection of complete Freund's adjuvant into one hindpaw in rats, and neurons
226 injection of an inflammatory agent, complete Freund's adjuvant, into the masseter muscle and perfused
227 -inducing chromic gut; and (4) CFA (complete Freund's adjuvant), intradermal complete Freund's adjuva
228 toreceptor retinoid-binding protein/complete Freund's adjuvant (IRBP/CFA) or adoptive transfer of T c
230 e conserved protein virulence factor PLY and Freund's adjuvant is able to reduce corneal inflammation
231 ipheral inflammation (intraplanatar complete Freund's adjuvant) is substantially diminished in the nu
232 nalysis of allografts from vimentin/complete Freund's adjuvant mice demonstrated increased numbers of
233 d White rabbits were actively immunized with Freund's adjuvant mixed with pneumolysin toxoid (psiPLY)
234 ted antiallodynic efficacy in a rat complete Freund's adjuvant model for inflammatory pain showing im
235 Several agonists were active in the complete Freund's adjuvant model of chronic inflammatory thermal
237 in the tail immersion assay, in the complete Freund's adjuvant model of inflammatory pain and in the
239 mulated as a stable emulsion with incomplete Freund's adjuvant (Montanide ISA 51; Seppic SA, Paris, F
240 dose) or gp100:209-217(210M) plus incomplete Freund's adjuvant (Montanide ISA-51) once per cycle, fol
241 tion with ESO(157-170) mixed with incomplete Freund's adjuvant (Montanide ISA51) in 18 HLA-DP4+ EOC p
242 njection of capsaicin, formalin, or complete Freund's adjuvant more effectively than unconjugated CGR
243 DO11.10) along with OVA peptide and complete Freund's adjuvant, observing a dramatic increase in OVA-
244 livered singly or in combination with either Freund's adjuvant or alum, indicated that augmented bact
249 abbits that were mock immunized with PBS and Freund's adjuvant or with PPSV23 and Freund's adjuvant a
251 s in immunogenic formulations based on alum, Freund's adjuvant, or two different types of liposomes.
253 ed with gp100 melanoma peptide in incomplete Freund's adjuvant (peptide/IFA), which is commonly used
254 We previously reported that vaccination with Freund's adjuvant plus the recombinant N-terminus of the
255 Unilateral hind paw injections of complete Freund's adjuvant produced inflammation, hyperalgesia of
256 f nonhuman primates with E. coli MSP1(42) in Freund's adjuvant protected six of seven Aotus monkeys f
257 train 35000HP (nHgbAI) and administered with Freund's adjuvant provided complete protection against a
259 G3 2/4/6/7-VLPs) or SA11 simian rotavirus in Freund's adjuvants, QS-21 (saponin adjuvant), or aluminu
260 rom donor hearts placed in vimentin/complete Freund's adjuvant recipients contained anti-vimentin ant
262 ming of recipients with beta-gal in complete Freund's adjuvant resulted in an increased frequency of
263 57BL/6 mice with murine vimentin in complete Freund's adjuvant resulted in anti-vimentin antibodies a
264 tion of Aotus monkeys with BVp42 in complete Freund's adjuvant resulted in high antibody titers again
266 with soluble B. malayi antigen and complete Freund's adjuvant resulted in significantly fewer IL-4-p
268 h schistosome egg antigens (SEA) in complete Freund's adjuvant (SEA/CFA) correlates with elevated pro
270 tus monkeys immunized with BVp42 in complete Freund's adjuvant showed evidence of protection of prote
273 atory pain was induced by injecting complete Freund's adjuvant subcutaneously into one hind paw of ra
274 of antigen-specific IgG2a than did complete Freund's adjuvant, suggesting an enhanced TH1 response.
275 allenged with antigen emulsified in complete Freund's adjuvant, the overall pattern was similar, exce
276 were preimmunized with the KLH in incomplete Freund's adjuvant to induce a population of Th2 memory c
277 albumin with alum or ovalbumin with complete Freund's adjuvant to induce T helper type 2 or T helper
278 eceptor retinoid-binding protein in complete Freund's adjuvant to test their efficacy in suppressing
282 mechanical hyperalgesia induced by complete Freund's adjuvant was accompanied by C5a upregulation an
285 pes when injected subcutaneously in complete Freund's adjuvant was significantly enhanced if administ
289 esence or absence of LT(R192G) or incomplete Freund's adjuvant were not protected against lethal chal
290 eas of the rabbits immunized with psiPLY and Freund's adjuvant were significantly lower than scores o
292 earlier with proteolipid protein in complete Freund's adjuvant, were injected with 3 x 10(6) cells fr
293 inflammatory stimuli, formalin and complete Freund's adjuvant, were reduced or abolished in AC1&8 DK
294 nized and boosted with a GABHS homogenate in Freund's adjuvant, whereas controls received Freund's ad
295 se models require immunization with complete Freund's adjuvant, whereas others suggest that a decreas
296 ore potent than that obtained using Complete Freund's Adjuvant with gp100, whereas no response was ob
298 in saline or intraperitoneally in incomplete Freund's adjuvant, with large quantities of the immunodo
299 rimmune sera of rabbits immunized with PA in Freund's adjuvant, with peak neutralization titers 23-,
300 o the induction of arthritis with incomplete Freund's adjuvant, with similar effects in arthritis ind