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1 -reperfusion-injured adult nonobese diabetic-severe combined immunodeficient mice.
2 gnals as shown in chimeric nonobese diabetic/severe combined immunodeficient mice.
3         LAPC-4 cells were injected into male severe combined immunodeficient mice.
4 antation into the mammary fat pads of female severe combined immunodeficient mice.
5 ndrogen-independent DU145 prostate cancer in severe combined immunodeficient mice.
6  MET-1 leukemic cells into nonobese diabetic/severe combined immunodeficient mice.
7 s when these cells were inoculated s.c. into severe combined immunodeficient mice.
8 into cardiomyocytes in the injured hearts of severe combined immunodeficient mice.
9 ) from an ATL patient into nonobese diabetic/severe combined immunodeficient mice.
10  colonization potential after injection into severe combined immunodeficient mice.
11 by a neutralizing antibody to human CXCR4 in severe combined immunodeficient mice.
12 econstitute the marrow of non-obese diabetic severe combined immunodeficient mice.
13 ited lung colonization of the tumor cells in severe combined immunodeficient mice.
14 nt tumor shrinkage of melanoma xenografts in severe combined immunodeficient mice.
15 lets were transplanted in nonobese diabetic, severe combined immunodeficient mice.
16  artery was performed by thermal ligation in severe combined immunodeficient mice.
17 al vector expressing SDF1alpha (AdSDF1) into severe combined immunodeficient mice.
18 urgical specimens and grown as xenografts in severe combined immunodeficient mice.
19 f tumorigenicity after s.c. inoculation into severe combined immunodeficient mice.
20 n into the left subrenal capsule of diabetic severe combined immunodeficient mice.
21 mary fat pad tumors or distant metastases in severe combined immunodeficient mice.
22  to form colonies in soft agar and tumors in severe combined immunodeficient mice.
23 .c. injection of human melanoma LOX cells in severe combined immunodeficient mice.
24 overt AML-like disease in nonobese diabetic--severe combined immunodeficient mice.
25  implanted into the right ovarian pedicle of severe combined immunodeficient mice.
26 ents were performed with tumor xenografts in severe combined immunodeficient mice.
27 del with a composite skin model also made on severe combined immunodeficient mice.
28 s the growth of human soft-tissue sarcoma in severe combined immunodeficient mice.
29 ll lymphoma and multiple myeloma xenografted severe combined immunodeficient mice.
30 lized to infiltrating leukocytes in diseased severe combined immunodeficient mice.
31 ression was studied in nonobese diabetic and severe combined immunodeficient mice.
32 ransparent dorsal skin-fold chambers in male severe combined immunodeficient mice.
33 d immunodeficient mice or non-obese diabetic/severe combined immunodeficient mice.
34 leukemia in vitro and suppress its growth in severe combined immunodeficient mice.
35  in slowing human myeloid leukemia growth in severe combined immunodeficient mice.
36  cells in transparent dorsal skin windows in severe combined immunodeficient mice.
37 low TF and VEGF producer, were grown s.c. in severe combined immunodeficient mice.
38 or, which was injected into the tail vein of severe combined immunodeficient mice.
39 Ak-positive) and LS174T tumor-bearing BALB/c severe combined immunodeficient mice.
40 nd A-2 human prostatic cancers when grown in severe combined immunodeficient mice.
41 n experimental cryptococcosis in outbred and severe combined immunodeficient mice.
42 hibits growth of a human breast carcinoma in severe combined immunodeficient mice.
43 in a transparent dorsal skin fold chamber in severe combined immunodeficient mice.
44 ent and lost their ability to form tumors in severe combined immunodeficient mice.
45 we implanted human-derived glioma cells into severe combined immunodeficient mice.
46         No airway hyperractivity occurred in severe combined immunodeficient mice.
47 40L-deficient animals prevented infection in severe combined immunodeficient mice.
48 ling of human coronary artery transplants in severe combined immunodeficient mice.
49 nd also in tumors in prostate-tumor-bearing, severe combined immunodeficient mice.
50 or supplemented (GFS) matrigel into diabetic severe combined immunodeficient mice.
51 reotactically injected into the subcortex of severe combined immunodeficient mice.
52 tail vein of MDA-MB-231 tumor-bearing female severe combined immunodeficient mice.
53 sed invasiveness of MCF10.DCIS xenografts in severe combined immunodeficient mice.
54 ng highly invasive HCC in nonobese diabetic, severe combined immunodeficient mice.
55 raftment of these cells in nonobese diabetic/severe combined immunodeficient mice.
56  tumor formation and inhibited metastasis in severe combined immunodeficient mice.
57 nt growth in soft agar, and tumorigenesis in severe combined immunodeficient mice.
58 an carcinomas implanted in immunocompromised severe combined immunodeficient mice.
59 ity in prostate cancer tumors implanted into severe combined immunodeficient mice.
60 sicles in a model of glycerol-induced AKI in severe combined immunodeficient mice.
61 ompetitive repopulation of nonobese diabetic/severe combined immunodeficient mice.
62 homa cells were intravitreally injected into severe combined immunodeficient mice.
63 ction on PLC/PRF/5 human tumor xenografts in severe combined immunodeficient mice.
64 in soft agar as well as s.c. tumor growth in severe combined immunodeficient mice.
65 on, led to the formation of larger tumors in severe combined immunodeficient mice.
66 mor cell growth and invasion in vitro and in severe combined immunodeficient mice.
67  and these cells were grown as xenografts in severe combined immunodeficient mice.
68 f resistant multiple myeloma tumors (MM1) in severe combined immunodeficient mice.
69 tibody targeted to HER2-expressing tumors in severe combined immunodeficient mice.
70 variant of SN12C) tumors grown in kidneys of severe combined immunodeficient mice.
71 cells were injected intratibially in C3H and severe-combined immunodeficient mice.
72  C1 was seen toward H460 tumor xenografts in severe-combined immunodeficient mice.
73 te could be transplanted to irradiated SCID (severe combined immunodeficient) mice.
74 eotide-binding oligomerization domain)/SCID (severe combined immunodeficient) mice.
75 edium before transfer to Prkdc(scid)-mutant (severe combined immunodeficient) mice.
76  line (EGI-1) after xenotransplantation into severe-combined-immunodeficient mice, (3) expression of
77 cause combined therapy is not efficacious in severe combined immunodeficient mice; (3) the rejection
78  model originating from footpad injection in severe combined immunodeficient mice, 95% of the resulti
79 antation of these cells in nonobese diabetic-severe combined immunodeficient mice (a) generated xenog
80                 Finally, immunocompetent and severe combined immunodeficient mice administered CXCR2
81 ntitumor effects were markedly diminished in severe combined immunodeficient mice and (b) CD8+ T cell
82          Human fetal bones were implanted in severe combined immunodeficient mice and after 4 weeks,
83 laxis to hu-peripheral blood leukocyte (PBL)-severe combined immunodeficient mice and chimpanzees.
84 aneously implanted into the left shoulder of severe combined immunodeficient mice and evaluated.
85 l blood leukocytes (PBL) were implanted into severe combined immunodeficient mice and infected with h
86                            Experiments using severe combined immunodeficient mice and mice depleted o
87 nted tumors when transplanted into syngeneic severe combined immunodeficient mice and normal mice.
88 MDMs were injected into the basal ganglia of severe combined immunodeficient mice and then Li was adm
89 owth of malignant mesothelioma xenografts in severe-combined immunodeficient mice and extended host s
90 ere injected directly into the peritoneum of severe combined immunodeficient mice, and in a syngeneic
91 neither resulted in weight loss nor death in severe combined immunodeficient mice, and pock lesions w
92 s were implanted into the cranial windows in severe combined immunodeficient mice, and VEGF promoter
93 ation in soft agar, tumor formation in SCID (severe combined immunodeficient) mice, and adhesion.
94                                        scid (severe combined immunodeficient) mice are unable to effi
95 uman skin is orthotopically transferred onto severe combined immunodeficient mice, autologous immunoc
96 vir had marked antitumor efficacy in vivo in severe combined immunodeficient mice bearing A2780OSP-1-
97                When flavopiridol was used in severe combined immunodeficient mice bearing disseminate
98 e studied the effects of THMAM-MD in vivo in severe combined immunodeficient mice bearing HT-29 colon
99                         In nonobese diabetic/severe combined immunodeficient mice bearing human EBV l
100  "coaguligand." After i.v. administration to severe combined immunodeficient mice bearing human Hodgk
101                We found that pretreatment of severe combined immunodeficient mice bearing human intes
102 ncer and significantly prolonged survival of severe combined immunodeficient mice bearing LAPC-4 xeno
103  activity of 8H9(scFv)-PE38 was evaluated in severe combined immunodeficient mice bearing MCF-7 breas
104                                              Severe combined immunodeficient mice bearing NB4 cells s
105 se implant delivery of 4-hydroxytamoxifen to severe combined immunodeficient mice bearing Rat-1-MycER
106                                              Severe combined immunodeficient mice bearing s.c. BL tum
107                        In the current study, severe combined immunodeficient mice bearing s.c. tumors
108                                           In severe combined immunodeficient mice bearing SKOV3 tumor
109 PET/CT small-animal imaging was performed in severe combined immunodeficient mice bearing solid and d
110                                              Severe combined immunodeficient mice bearing U87MG xenog
111 g 125I- and (131)I-labeled CTX injected into severe combined immunodeficient mice bearing xenografted
112  the growth of TPras transgenic melanomas in severe combined immunodeficient mice, blocked invasive b
113 -gamma had a markedly reduced growth rate in severe combined immunodeficient mice, but IFN-gamma did
114  which can be transmitted to naive syngeneic severe combined immunodeficient mice by adoptive transfe
115 e drug combination decreased tumor volume in severe combined immunodeficient mice by approximately 60
116  totally interrupted the infection of hu-PBL-severe combined immunodeficient mice by PBL-grown HIV-1
117 fts in three genetically isolated strains of severe combined immunodeficient mice (C.B-17, C57BL/6J,
118  model established by tail vein injection in severe combined immunodeficient mice, clonality of lung
119  growth and the gain in mean tumor volume in severe combined immunodeficient mice compared with vehic
120         T cell transfer experiments into NOD/severe combined immunodeficient mice demonstrated the pr
121                          P. carinii-infected severe combined immunodeficient mice displayed little ev
122 nd engraft immunodeficient nonobese diabetes/severe combined immunodeficient mice during both primary
123                                           In severe combined immunodeficient mice, Ebp1 overexpressio
124                                              Severe combined immunodeficient mice engrafted with huma
125   Spleen cells from normal and nude, but not severe combined immunodeficient mice, exhibited strong p
126 6Mre11(ATLD1/ATLD1) and C57BL/6(Prkdc/SCID) (severe combined immunodeficient) mice exposed to low-dos
127 cific neutralizing anti-CXCL12 antibodies to severe combined immunodeficient mice expressing human no
128 ether with normal BALB/c B cells into C.B-17 severe combined immunodeficient mice failed to generate
129 ropagated as serial subcutaneous implants in severe combined immunodeficient mice for >4 years.
130 on of late-passage H-Ras-expressing cells in severe combined immunodeficient mice formed carcinomas w
131 eplication in nontumor tissues and protected severe combined immunodeficient mice from developing let
132  was used in vivo to treat nonobese diabetic/severe combined immunodeficient mice given injections of
133                             This report uses severe-combined immunodeficient mice given injections of
134 2F LMP transfectants were non-tumorigenic in severe combined immunodeficient mice, HaCaT LMP transfec
135                                              Severe combined immunodeficient mice harboring U87 xenog
136 uction of the human HGF ligand in transgenic severe combined immunodeficient mice (hHGF(tg)-SCID mice
137 odinated, and their clearance was studied in severe combined immunodeficient mice hosts by whole-body
138 d not express uPAR formed palpable tumors in severe combined immunodeficient mice; however, metastase
139                                              Severe combined immunodeficient mice implanted with CBS-
140 he marrow space of the bone implanted in the severe combined immunodeficient mice implanted with feta
141 0530 profoundly inhibits tumor metastasis in severe combined immunodeficient mice implanted with GRP-
142 opic HIV-1(JR-CSF) isolate (JR-CSF mice) and severe combined immunodeficient mice implanted with huma
143               An in vivo efficacy trial with severe combined immunodeficient mice implanted with subc
144 nst both PC-3 and DU-145 tumor xenografts in severe combined immunodeficient mice in a dose-dependent
145 implanted as xenografts in nonobese diabetic/severe combined immunodeficient mice in vivo.
146 ndent growth in vitro and tumor formation in severe combined immunodeficient mice in vivo.
147 CDV) and octadecyloxyethyl-CVD (ODE-CDV)--in severe combined immunodeficient mice in which either hum
148 sgene expression was substantially higher in severe combined immunodeficient mice, indicating that in
149 as far less efficacious in immunocompromised severe combined immunodeficient mice, indicating the req
150 5(+) T cells to infected macrophage-depleted severe combined immunodeficient mice induced CNS demyeli
151 ionship between phospho-AKT and FAS in vivo, severe combined immunodeficient mice injected intraperit
152 meliorated adoptively transferred ileitis in severe combined immunodeficient mice injected with CD4 +
153 the agents, named TH-1177, was used to treat severe combined immunodeficient mice inoculated with the
154                            Nonobese diabetic severe combined immunodeficient mice lacking the cytokin
155 to repopulate human bone grafts implanted in severe combined immunodeficient mice, MSCV-directed NGFR
156                             Groups 1 to 4 of severe combined immunodeficient mice (n = 5-7 per group)
157 weeks old abortuses were xenografted s.c. to severe combined immunodeficient mice (n = 52).
158 nder the kidney capsule of nonobese diabetic-severe combined immunodeficient mice (n=4-7 per group/ti
159 and then transplanted into nonobese diabetic severe combined immunodeficient mice (NOD SCID).
160 onset of diabetes in young nonobese diabetic-severe combined immunodeficient mice (NOD.scid).
161 dies, BMSCs and ECs were cotransplanted into severe combined immunodeficient mice on biodegradable po
162                                          The severe combined immunodeficient mice, on the other hand,
163 t study, we induced EAE in T-cell-deficient, severe combined immunodeficient mice or in immunocompete
164 ting factor, and stem cell factor genes with severe combined immunodeficient mice or non-obese diabet
165  the administration of TNF-alpha to infected severe combined immunodeficient mice or to infected cult
166 t VEGF111 addition before transplantation to severe combined immunodeficient mice ovaries.
167                                     In SCID (severe combined immunodeficient) mice, proper assembly o
168                              However, unlike severe combined immunodeficient mice, radiation-induced
169 macrophages (MDMs) into the basal ganglia of severe combined immunodeficient mice recapitulates histo
170 ally injected into the basal ganglia of CB17 severe combined immunodeficient mice, received daily int
171 th a targeted deletion of the T-bet gene and severe combined immunodeficient mice receiving CD4+ cell
172 er growth was evaluated in hu-PBL-SCID mice (severe combined immunodeficient mice reconstituted with
173                                              Severe combined immunodeficient mice remained persistent
174 ed in the dorsal skinfold chamber in C3H and severe combined immunodeficient mice, respectively, and
175 uman ovarian tumor cells into the ovaries of severe combined immunodeficient mice resulted in periton
176 mum tolerated dose of 2L-Rap-hLL1-gamma4P in severe combined immunodeficient mice (SCID) or BALB/c mi
177  infection in human intestinal xenografts in severe combined immunodeficient mice (SCID-HU-INT mice).
178 racranial implantation of human gliomas into severe combined immunodeficient mice showed a marked red
179  The standard adoptive transfer study in NOD-severe combined immunodeficient mice showed that periphe
180 nts using a human pancreatic cancer model in severe combined immunodeficient mice showed that there w
181 Split-thickness pig skin was transplanted on severe combined immunodeficient mice so that pig dermal
182  silicone chambers implanted on the backs of severe combined immunodeficient mice sorts out to recons
183         When Cyno-1 cells were injected into severe combined immunodeficient mice, teratomas with der
184 LAPC-9) propagated by serial passage in male severe combined immunodeficient mice that expresses pros
185                                              Severe combined immunodeficient mice that received purge
186 severity of HSK in CD4+ T cell-reconstituted severe combined immunodeficient mice that were depleted
187  following immunization of nonobese diabetic-severe combined immunodeficient mice that were repopulat
188                                           In severe combined immunodeficient mice, the antitumor effi
189                         When inoculated into severe combined immunodeficient mice, the trx-transfecte
190   When injected into the mammary fat pads of severe combined immunodeficient mice, the tumors formed
191                         In the tumor-bearing severe combined immunodeficient mice, the vast majority
192          Additionally, in in vivo studies in severe combined immunodeficient mice, there was signific
193 an peripheral blood leukocytes (hu PBL-SCID [Severe Combined Immunodeficient] mice) to test the hypot
194 marrow of human bones that were implanted in severe combined immunodeficient mice, tumors formed by c
195 R, and DeltaB-Raf:ER cells to form tumors in severe combined immunodeficient mice was compared.
196 demonstrated that less neovascularization in severe combined immunodeficient mice was observed with c
197 poietic cells engrafted in nonobese diabetic/severe combined immunodeficient mice was obtained.
198 tion of human fetal thymus/liver implants in severe combined immunodeficient mice was used to investi
199               Intratibial tumor injection in severe combined immunodeficient mice was used to simulat
200      Finally, using an angiogenesis assay in severe combined immunodeficient mice, we demonstrate tha
201 lls, bone marrow chimeras, and reconstituted severe combined immunodeficient mice, we identify the pr
202 and adoptive transfer of CD4(+) T cells into severe combined immunodeficient mice, we show that anti-
203 drogen-dependent Shionogi carcinoma grown in severe combined immunodeficient mice, we show that castr
204 igh-avidity CTLs adoptively transferred into severe combined immunodeficient mice were 100- to 1000-f
205  cells harvested from carcinoma formation in severe combined immunodeficient mice were designated caM
206                                       Female severe combined immunodeficient mice were fed a low-fat/
207 cific cellular and humoral immune responses, severe combined immunodeficient mice were given an adopt
208                                              Severe combined immunodeficient mice were given injectio
209                                         When severe combined immunodeficient mice were injected with
210                                              Severe combined immunodeficient mice were reconstituted
211                                              Severe combined immunodeficient mice were reconstituted
212 tin-expressing tumors grown as xenografts in severe combined immunodeficient mice were responsive to
213                      cTVT fragments grown in severe combined immunodeficient mice were successfully i
214                 M21 (human melanoma)-bearing severe combined immunodeficient mice were used for biodi
215 atalase was also seen in tumor xenografts in severe combined immunodeficient mice when compared with
216  human stem cell-engrafted nonobese diabetic/severe combined immunodeficient mice, where 24% of the h
217 sfectants produced no intracranial tumors in severe combined immunodeficient mice, whereas parental U
218  by analyzing early passage fibroblasts from severe combined immunodeficient mice, which are deficien
219 et organs of immunocompetent BALB/c mice and severe combined immunodeficient mice, which are exquisit
220                                              Severe combined immunodeficient mice, which lack B and T
221 ive, Fc-dependent, passive immunity, even in severe combined immunodeficient mice with an established
222                                 Infection of severe combined immunodeficient mice with Babesia sp. st
223        Furthermore, treatment of LCL-bearing severe combined immunodeficient mice with Bcl-2 antisens
224  in situ zymography, in colonic tissues from severe combined immunodeficient mice with colitis induce
225 inst subcutaneous B-cell tumor xenografts in severe combined immunodeficient mice with comparable or
226 KLMS-1 and rhabdomyosarcoma RD xenografts in severe combined immunodeficient mice with DC101 resulted
227  dementia, dexamethasone was administered to severe combined immunodeficient mice with HIV-1 encephal
228 HCV-infected urokinase plasminogen activator-severe combined immunodeficient mice with livers repopul
229 ficient NOD/SCID (nonobese diabetic/X-linked severe combined immunodeficient) mice with human cord bl
230 ation of SKOV3ip1 cells in nonobese diabetic/severe combined immunodeficient mice, with increased pho
231  cell lines grow as solitary nodules in nude/severe combined immunodeficient mice without manifesting
232                                           In severe combined immunodeficient mice, xenograft tumors e
233 asion assays, and/or injected into flanks of severe combined immunodeficient mice; xenograft tumor gr
234  Furthermore, Kp-10 inhibits tumor growth in severe combined immunodeficient mice xenografted with hu
235                                              Severe combined immunodeficient mice xenografted with M2
236 volume, rate of metastasis, and mortality of severe combined immunodeficient mice xenografted with PC

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