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1  test abnormalities among those who received total body irradiation.
2 ell receptor monoclonal antibody followed by total body irradiation.
3 20 lymphoma in mice preconditioned with 6 Gy total body irradiation.
4 -identical marrow transplantation after 1 Gy total body irradiation.
5 with (131)I-BC8 Ab and fludarabine plus 2 Gy total body irradiation.
6  exhibit enhanced survival following 8-10 Gy total body irradiation.
7 and responded to antigenic stimulation after total body irradiation.
8 tical donors after conditioning with 920 cGy total body irradiation.
9 ation therapy in mice with anemia induced by total body irradiation.
10 ative conditioning with fludarabine and 2 Gy total body irradiation.
11 e marrow after conditioning with 100-300 cGy total body irradiation.
12 these biomarker genes in patients undergoing total body irradiation.
13 conditioning, primarily cyclophosphamide and total body irradiation.
14 e given HSCT after conditioning with 920 cGy total body irradiation.
15 s were conditioned with cyclophosphamide and total body irradiation.
16 ophic skeletal muscle even in the absence of total body irradiation.
17 s on each of 2 consecutive days, followed by total body irradiation.
18 s were conditioned with cyclophosphamide and total body irradiation.
19 ft and a conditioning regimen with > 450 cGy total body irradiation.
20 autologous bone marrow transplantation after total body irradiation.
21  depletion-based conditioning with 1 or 3 Gy total body irradiation.
22 increases survival of mice exposed to lethal total body irradiation.
23 e transplanted after varying doses of cGy of total body irradiation.
24 tion of IL-22 enhanced thymic recovery after total body irradiation.
25  and hematopoietic radioprotection following total body irradiation.
26 ipheral blood compartments of mice post-4 Gy total body irradiation.
27  VCA recipients with 200-, 300-, and 400-cGy total body irradiation.
28 yclophosphamide, fludarabine, and 200 cGy of total body irradiation.
29 occurred within the IFRT site and five after total-body irradiation.
30 ustained engraftment can be achieved without total-body irradiation.
31 olgus monkeys were conditioned with low-dose total body irradiation (1.5 Gy on days -6 and -5), suppl
32                Conditioning therapy involved total body irradiation 2 Gy +/- fludarabine 30 mg/m2.
33 oablative conditioning regimen consisting of total-body irradiation (2 Gy) with or without fludarabin
34            RIC regimens included fludarabine/total body irradiation 200 cGy (n = 5) or 450 cGy (n = 1
35 phamide (50 mg/kg), and a single fraction of total body irradiation (200 cGy) with cyclosporine and m
36 underwent conditioning with a single dose of total-body irradiation (200 cGy).
37 g of alemtuzumab (1 mg/kg in divided doses), total-body irradiation (300 cGy), sirolimus, and infusio
38                Eight recipient dogs received total body irradiation (4.5 cGy), hematopoietic cell tra
39                                HDIT included total body irradiation (800 cGy) with lung shielding, cy
40                                We found that total body irradiation, a conditioning regimen required
41              Using nonmyeloablative doses of total body irradiation, a short course of immunosuppress
42 ere hypoplastic and more apoptotic 24 h post-total body irradiation, a time when stem cell survival i
43  anti-CD45 and an otherwise inactive dose of total-body irradiation allowed engraftment of H2 fully a
44 men involving anti-CD154 and low dose (3 Gy) total body irradiation, allowing achievement of mixed ch
45 = 498) or unrelated (n = 336) HCT after 2 Gy total body irradiation alone (n = 171) or combined with
46 nstitutions using conditioning with low-dose total body irradiation alone or combined with fludarabin
47 ated donors following conditioning with 2 Gy total body irradiation alone or in combination with flud
48 ne-refractory CLL were conditioned with 2 Gy total-body irradiation alone or combined with fludarabin
49                        Our results show that total body irradiation alters intracellular signaling an
50 oietic cells using a combination of low-dose total body irradiation and a short course of immunosuppr
51 n (BMT) following conditioning with low-dose total body irradiation and anti-CD154 antibody.
52 rance are achieved in mice receiving 3 Gy of total body irradiation and anti-CD154 mAb followed by al
53 ents received a single fraction dose of 2 Gy total body irradiation and HC transplants from HLA-ident
54 nfused into 3 adult baboons following lethal total body irradiation and hematopoietic support or with
55 ient Tregs after a conditioning regimen with total body irradiation and led to a TGF-beta-dependent i
56 -ibritumomab tiuxetan, fludarabine, and 2 Gy total body irradiation and matched-related (15) or unrel
57  of pretransplant T cell depletion, low-dose total body irradiation and posttransplant (donor) bone m
58                                              Total body irradiation and radiation proctitis were moni
59 -Furth rats were conditioned with 950 cGy of total body irradiation and transplanted with ACI bone ma
60 r nonmyeloablative (3 Gy) and minimal (1 Gy) total body irradiation and treatment with costimulation
61 clophosphamide (CY) and busulfan (BU) (67%), total-body irradiation and CY (21%), BU-fludarabine (10%
62            The conditioning regimen included total-body irradiation and cyclophosphamide (n = 3), bus
63  preconditioning or after 200 cGy or 900 cGy total-body irradiation and evaluated after 4 months.
64 etic stem-cell transplantation that includes total-body irradiation and treatment with alemtuzumab an
65 smoking history, conditioning with high-dose total body irradiation, and an absolute lymphocyte count
66                        Patient or donor age, total body irradiation, and graft-versus-host disease or
67 globulin, fludarabine, cyclophosphamide, and total body irradiation, and graft-versus-host disease pr
68 nsolidation with myeloablative chemotherapy, total-body irradiation, and ABMT versus three cycles of
69    NOD mice received various combinations of total body irradiation, anti-CD154, anti-CD8alpha, anti-
70  recipients who receive conditioning without total body irradiation are not well known.
71 al cell apoptosis after they were exposed to total body irradiation as compared with TNFR1-deficient
72 13)Bi)-labeled anti-CD45 antibody to replace total body irradiation as conditioning for hematopoietic
73 re enriched early after TLI/ATS + BMT versus total body irradiation/ATS + BMT.
74 X compared with TLI/ATS, lethal or sublethal total body irradiation/ATS/CTX, or CTX/ATS conditioning.
75 s the antileukemic benefits of myeloablative total body irradiation-based conditioning and unrelated
76 cantly higher rate of DC was associated with total body irradiation-based conditioning and with acute
77  critical to the induction of tolerance in a total body irradiation-based model.
78 sed with hematologic malignancies received a total body irradiation-based myeloablative conditioning
79 te deletional tolerance as the mechanism for total body irradiation-based nonmyeloablative conditioni
80  in patients conditioned with a fractionated total body irradiation-based regimen has shown encouragi
81 blastic leukemia 10) were conditioned with a total body irradiation-based regimen.
82 hocytic leukemia patients treated with 12 Gy total body irradiation-based regimens and allogeneic tra
83 ted donor transplantation with myeloablative total body irradiation-based regimens.
84  lymphoma who were considered ineligible for total-body irradiation because of older age or prior rad
85 shed in dogs given a sublethal dose (1-2 Gy) total body irradiation before and a short course of immu
86 ditioning of neonates with 100 to 400 cGy of total body irradiation before normal donor marrow transp
87 mg/kg, fludarabine 200 mg/m2, and 200 cGy of total body irradiation (Bu/Flu/TBI).
88 tumoral proliferation of T-effector cells in total body irradiation-conditioned recipients.
89                              The toxicity of total body irradiation conditioning and potential for gr
90 e marrow (BM) cells or through myeloablative total body irradiation conditioning and reconstitution w
91 Furthermore, this procedure usually requires total body irradiation conditioning of recipients.
92 day pulmonary metastases of MCA 205 received total body irradiation conditioning or were nonirradiate
93 eral strain combinations irrespective of the total body irradiation conditioning regime.
94   However, when mice were given more intense total body irradiation conditioning regimens combined wi
95                       To reduce or eliminate total body irradiation conditioning regimens, we have so
96  ex vivo antigen stimulation irrespective of total body irradiation conditioning.
97  CD34+ cells can engraft even after low-dose total body irradiation conditioning.
98                                              Total body irradiation-containing preparative regimen wa
99              When used with cyclophosphamide/total body irradiation (Cy/TBI) conditioning, sirolimus
100               Cyclophosphamide combined with total body irradiation (Cy/TBI) or busulfan (BuCy) are t
101 nditioning regimens of cyclophosphamide plus total body irradiation (CY/TBI), busulfan plus cyclophos
102 ioned with cyclophosphamide and fractionated total-body irradiation (Cy/TBI) or busulfan and cyclopho
103                            HDIT consisted of total body irradiation, cyclophosphamide, and antithymoc
104 receptor and anti-CD8 monoclonal antibodies, total body irradiation, cyclosporine A and mycophenolate
105          Although the addition of 600 rad of total body irradiation delayed tumor growth, further ado
106 ll transplantation with cyclophosphamide and total body irradiation develop wide-spectrum manifestati
107 erance, significantly decreasing the minimum total body irradiation dose required.
108                    The omission of high-dose total body irradiation, dose adjustments of busulfan to
109 ent regimens:fludarabine-melphalan (n = 46); total body irradiation-etoposide (n = 28), and busulfan-
110                 Rabbits exposed to 10 cGy of total body irradiation exhibited T cell deficiency, with
111 eparative regimen of nonmyeloablating (5 Gy) total body irradiation experienced the rapid rejection o
112 ution and toxicity in baboons that underwent total body irradiation followed by autologous transplant
113 ancies conditioned with fludarabine and 2 Gy total body irradiation followed by HLA-matched unrelated
114 in which the marrow recipients received 2 Gy total body irradiation followed by marrow infusions from
115 ated with a nonmyeloablative dose of 200 cGy total body irradiation followed by matched-littermate SC
116 of a specific anti-CD44 mAb (S5) and 200 cGy total body irradiation followed by postgrafting immunosu
117                                              Total body irradiation followed by transplantation with
118 d MCA-205 tumors were treated with sublethal total body irradiation, followed by adoptive transfer of
119 were uniformly cured after administration of total body irradiation, followed by the transplantation
120 (P=0.01) and, in multivariate analysis, with total body irradiation for all lineages (P<0.01).
121 ne tumor recipients were preconditioned with total body irradiation from 0 to 500 cGy or with a 30-da
122 matched sibling donors received fractionated total body irradiation (FTBI) and high-dose VP16, wherea
123 n consisted of 90 mg/m2 fludarabine and 2 Gy total body irradiation given before and mycophenolate mo
124 ludarabine and targeted busulfan (n = 25) or total body irradiation (&gt;/=12 Gy; n = 18).
125 nner, with the administration of DA prior to total body irradiation having the greatest protective ef
126 ctive regimen consisted of hyperfractionated total body irradiation (HFTBI), thiotepa, and fludarabin
127 T was seen only in patients conditioned with total-body irradiation (HR, 3.9 [95% CI, 2.6-6.8]).
128 losuppressive regimen, consisting of 100 cGy total body irradiation, immunotoxin mediated T-cell depl
129 ry of young BM ECs along with HSCs following total body irradiation improved HSC engraftment and enha
130               Conditioning regimens included total body irradiation in 199 (44%) cases.
131 esus macaques conditioned with myeloablative total body irradiation in the absence or presence of sin
132                        Conditioning included total-body irradiation in 92% of patients.
133 unotherapy targeting CD45 may substitute for total-body irradiation in hematopoietic cell transplanta
134 ive preparative regimen that did not involve total-body irradiation in young children with Hurler's s
135      In contrast, no significant increase in total body irradiation-induced apoptosis or tissue injur
136 iation-induced gastrointestinal syndrome and total body irradiation-induced hematopoietic failure.
137  show that p50-/- mice are more sensitive to total body irradiation-induced lethality than wild-type
138  examined the role of NFkappaB activation in total body irradiation-induced tissue damage.
139                          Exposure of mice to total body irradiation induces nuclear factor kappaB (NF
140 g from the combined effects of cyclosporine, total body irradiation, infections, high-dose chemothera
141 reert2)/Met(+/+)/LacZ) were exposed to 10 Gy total body irradiation; intestinal tissues were collecte
142                                              Total body irradiation is a component in various host co
143 experimental and clinical scenarios in which total body irradiation is involved.
144 at liver toxicity after cyclophosphamide and total body irradiation is related to cyclophosphamide th
145 approach requires conditioning regimens with total body irradiation, lymphodepleting chemotherapy, an
146                        NFkappaB activated by total body irradiation mainly consists of NFkappaB p50/R
147                                         Upon total body irradiation, medullary complexity was partial
148 D154 (MR1) and rapamycin (Rapa) plus 100 cGy total body irradiation (MR1/Rapa/100 cGy) and transplant
149  were conditioned with cyclophosphamide with total body irradiation (n = 39) or busulfan (n = 1).
150  simulated weightlessness and space-relevant total-body irradiation on vascular responsiveness in mic
151 mice were lymphodepleted by nonmyeloablative total body irradiation or a myeloablative regimen that r
152 e latter treatment, however, did not require total body irradiation or adoptive cell transfer and res
153  there was no difference between receiving a total body irradiation or busulfan based regimens (P = .
154 yclophosphamide associated with fractionated total body irradiation or busulfan.
155  myeloablative regimens, ie, those including total body irradiation or high-dose busulfan.
156 l HCT, where recipients are conditioned with total body irradiation or high-dose chemotherapy.
157 philia A BALB/c mice after reduced-intensity total body irradiation or nonmyeloablative chemotherapy
158 t differences in hazards were observed after total-body irradiation or receipt of an allogeneic versu
159  male sexual function domains declined after total body irradiation (P < .05).
160 m(2) x 5, cyclophosphamide 50 mg/kg, 200 cGy total body irradiation), patients received either matche
161         Patients treated with C-HDT received total body irradiation plus chemotherapy (70%) or chemot
162 h busulfan plus cyclophosphamide and 12 with total body irradiation plus chemotherapy.
163             The patients received 300 cGy of total-body irradiation plus alemtuzumab before transplan
164 iation of conditioning therapy (fractionated total-body irradiation plus high-dose chemotherapy) and
165 sk for osteoporosis and bone fractures after total body irradiation preconditioning.
166                     Although nonmyeloblative total body irradiation prevented organ graft rejection,
167  depletion with CD3-immunotoxin, and 100 cGy total body irradiation prior to hematopoietic cell trans
168  A single injection of CBLB502 before lethal total-body irradiation protected mice from both gastroin
169                                      However total-body irradiation, radiation to the gonads, and che
170                                              Total body irradiation reduced numbers of proliferating
171 r without T-cell lymphodepletion reduced the total body irradiation requirement to 100 cGy for establ
172                                              Total body irradiation (RR = 0.6) provided a protective
173                            Mice subjected to total body irradiation showed alterations in glucose met
174 or-bearing mice with DMA 2 hours before 8 Gy total body irradiation showed an impressive rescue of ra
175 nti-FVIII immune response, and together with total body irradiation, suppresses anti-FVIII immune res
176 serum at 10 mg at day +10 (single dose), and total-body irradiation t 300 cGy (day 0) before bone-mar
177        Conditioning therapy involved 800 cGy total body irradiation (TBI) (+/- lung shielding to appr
178 s 11.0%, higher among survivors who received total body irradiation (TBI) (17%) than those who did no
179 ence indicates that the addition of low-dose total body irradiation (TBI) (2-4 Gy) to reduced intensi
180 ed: (1) myeloablative conditioning (MA) with total body irradiation (TBI) + PBSCs, (2) MA + TBI + BM,
181 that antithymocyte globulin (ATG) given with total body irradiation (TBI) 200 cGy and fludarabine res
182 re we use bone marrow transplantation (BMT), total body irradiation (TBI) and abdominal irradiation (
183                        Lymphodepletion using total body irradiation (TBI) and administering high-dose
184  littermate recipients consisting of 450 cGy total body irradiation (TBI) and anti-CD44 monoclonal an
185 man urine data sets from patients undergoing total body irradiation (TBI) and from a colorectal cance
186 mone (GH) deficiency are complications after total body irradiation (TBI) and hematopoietic cell tran
187 ce were conditioned with decreasing doses of total body irradiation (TBI) and reconstituted with bone
188 ) cell recovery in rhesus macaques following total body irradiation (TBI) and reinfusion of vector-tr
189                BALB/c mice were treated with total body irradiation (TBI) and then infused with C57Bl
190 onmyeloablative chemotherapy with or without total body irradiation (TBI) before adoptive T-cell tran
191 anti-CD45 radioimmunotherapy (RIT) replacing total body irradiation (TBI) before haploidentical HCT i
192                   Four dogs received 920 cGy total body irradiation (TBI) before infusion of autologo
193 ost uniformly achieved in dogs given 200 cGy total body irradiation (TBI) before, and a short course
194                                              Total body irradiation (TBI) can induce lethal myelosupp
195 lantation (BMT), but this procedure requires total body irradiation (TBI) conditioning of the recipie
196  engraftment was only transient with 100 cGy total body irradiation (TBI) conditioning, indicating su
197 at under myeloablative and reduced-intensity total body irradiation (TBI) conditioning, transplantati
198                                              Total body irradiation (TBI) damages hematopoietic cells
199 eic transplantation with regimens of varying total body irradiation (TBI) doses (0-1575 cGy), with an
200                                              Total body irradiation (TBI) exposure was associated wit
201 patients with refractory cancer with 100 cGy total body irradiation (TBI) followed by infusion of non
202 equires the recipient mice to undergo lethal total body irradiation (TBI) followed by rescue with who
203  are compared with those of adult mice given total body irradiation (TBI) followed by transplantation
204 BMT, rats were treated with varying doses of total body irradiation (TBI) followed by transplantation
205 not been compared with cyclophosphamide plus total body irradiation (TBI) in adults with advanced ref
206 emission at the time of allo-HSCT and use of total body irradiation (TBI) in patients with non-Hodgki
207 rs of 2 articles have compared busulfan with total body irradiation (TBI) in preparative regimens for
208                         Lymphodepletion with total body irradiation (TBI) increases the efficacy of a
209 ood, Shao et al report that a side effect of total body irradiation (TBI) is long-term bone marrow in
210                      Fractionated, high-dose total body irradiation (TBI) is used therapeutically to
211 myeloablative conditioning regimens--200 cGy total body irradiation (TBI) or 10 mg/kg busulfan--with
212  (BMT) after conditioning with either lethal total body irradiation (TBI) or an established nonmyeloa
213  in the bone marrow (BM) as a consequence of total body irradiation (TBI) or granulocyte colony-stimu
214 s studies showed that treatment of mice with total body irradiation (TBI) or total lymphoid tissue ir
215 monoclonal antibody before conditioning with total body irradiation (TBI) prevents GVHD but retains G
216  nonmyeloablative chemotherapeutic agents or total body irradiation (TBI) prior to adoptive transfer
217  inhibition using AZ31 prior to 9 or 9.25 Gy total body irradiation (TBI) reduced median time to mori
218 treatment, we determined the minimal dose of total body irradiation (TBI) required when added to anti
219 C57BL/6 mice to a sublethal dose (6.5 Gy) of total body irradiation (TBI) resulted in a sustained qua
220 requency of side effects caused by high-dose total body irradiation (TBI) the nonmyeloablative regime
221              Addition and intensification of total body irradiation (TBI) to the preparative lymphode
222 ) given conventional conditioning, high-dose total body irradiation (TBI) was associated with an incr
223                                              Total body irradiation (TBI) was associated with develop
224 ft rejection after conditioning with 1 Gy of total body irradiation (TBI) was consistently seen in hi
225 e NSG host environment using preconditioning total body irradiation (TBI) was indispensable for effic
226 ynomolgus monkeys, cyclophosphamide (CP) and total body irradiation (TBI) were compared as part of a
227 l HSCT in which 27 patients conditioned with total body irradiation (TBI) were given a fixed dose of
228 single-exposure, high dose rate (30 cGy/min) total body irradiation (TBI) with cyclophosphamide as co
229 6 transplantation model and ascertained that total body irradiation (TBI) with establishment of chime
230 yeloablative conditioning consisting of 2 Gy total body irradiation (TBI) with or without added fluda
231 of fludarabine, anti-thymocyte globulin, and total body irradiation (TBI) would enable reduction of t
232 al antibodies (mAbs) on Days -6 and -1, 3 Gy total body irradiation (TBI), and 7 Gy thymic irradiatio
233 eived cyclophosphamide (CY), single fraction total body irradiation (TBI), and antithymocyte globulin
234 ns were impaired by a single dose of 200 cGy total body irradiation (TBI), and both GVH and residual
235 ned with antilymphocyte serum (ALS), 100 cGy total body irradiation (TBI), and given 30 x 10(6) allog
236 re treated with cyclophosphamide, etoposide, total body irradiation (TBI), and PBSCT.
237  unrelated donors were rejected after 9.2 Gy total body irradiation (TBI), and that graft resistance
238 ty conditioning (RIC) consisting of low-dose total body irradiation (TBI), cyclophosphamide, and flud
239 is upregulated during lymphopenia induced by total body irradiation (TBI), cyclophosphamide, or Thy1
240 f the endosteal osteoblastic HSC niche after total body irradiation (TBI), defined as relocalization
241          Nonmyeloablative regimens were 2 Gy total body irradiation (TBI), either alone (n = 40) or c
242 ransplantation regimen consisted of low-dose total body irradiation (TBI), preceded in some patients
243  animals were submitted at 60 days to 9.5-Gy total body irradiation (TBI), reconstituted immediately
244 ests that intense immune suppression using a total body irradiation (TBI)-based regimen and hematopoi
245 ive intravenous busulfan (IV-BU) vs ablative total body irradiation (TBI)-based regimens in myeloid m
246 outcome when patients had undergone previous total body irradiation (TBI)-containing myeloablative tr
247 second relapse was significantly lower after total body irradiation (TBI)-containing transplant regim
248 way as a new mechanism for the mitigation of total body irradiation (TBI)-induced mortality.
249 isease (GVHD) in recipients conditioned with total body irradiation (TBI).
250 sphamide of 60 mg/kg per day for 2 days, and total body irradiation (TBI).
251  recovery in the blood and bone marrow after total body irradiation (TBI).
252 cy, we developed a murine model of sublethal total body irradiation (TBI).
253 d donors received fludarabine and 200 cGy of total body irradiation (TBI); UCB recipients received cy
254 )) rats were conditioned with 600 to 300 cGy total body irradiation (TBI, day-1), and 100 x 10(6) T-c
255 on, a nonmyeloablative regimen using 200 cGy total-body irradiation (TBI) and mycophenolate mofetil (
256              Next, nine dogs received 4.5 Gy total-body irradiation (TBI) and unmodified marrow graft
257 nsplantation-conditioning regimens including total-body irradiation (TBI) at doses 12 Gy or less did
258               Recipient dogs were given 2-Gy total-body irradiation (TBI) before and a short course o
259 ents, certain other leukemogenic agents, and total-body irradiation (TBI) cause chromosomal damage th
260 tion (SCT) for hematologic malignancies with total-body irradiation (TBI) conditioning regimens, and
261                                    Impact of total-body irradiation (TBI) in conditioning regimen on
262 to show that temporarily blocking p53 during total-body irradiation (TBI) not only ameliorates acute
263 ars of age, received either cyclophosphamide/total-body irradiation (TBI) or busulfan/cyclophosphamid
264          Cyclophosphamide (Cy) combined with total-body irradiation (TBI) or with busulfan (Bu) are c
265 ne adults received cyclophosphamide (CY) and total-body irradiation (TBI) supported by autologous bon
266 er 2 (25 patients) or 12 Gy (25 patients) of total-body irradiation (TBI) was administered before cel
267 n diagnosis, type of transplantation, use of total-body irradiation (TBI), and presence of graft-vers
268 with age and after genotoxic stress, such as total-body irradiation (TBI).
269 ool and 100% survival after a lethal dose of total-body irradiation (TBI).
270 d: 4-6 of 6 matched dUCB-TCF (n = 120; TCF = total body irradiation [TBI] 200 cGy + cyclophosphamide
271 ice deficient in both genes survive doses of total-body irradiation that lethally deplete hematopoiet
272 th severe thrombocytopenia induced by 6.5 Gy total body irradiation, thereby markedly abridging the d
273 eted PBSC grafts following conditioning with total body irradiation, thiotepa, and fludarabine.
274 ourteen Cynomolgus monkeys received low dose total body irradiation, thymic irradiation, antithymocyt
275   Furthermore, administering lethal doses of total body irradiation to GF mice produces markedly fewe
276 r synthesis is not detectable in response to total body irradiation unless NaCl is lowered by furosem
277 le protected rodents against lethal doses of total body irradiation up to 13 Gy, whether DIM dosing w
278 de 2 to 4 acute GVHD were cyclophosphamide + total-body irradiation versus busulfan + cyclophosphamid
279 demia (RR = 3.2, P < .01); conditioning with total body irradiation was associated with an increased
280                                              Total body irradiation was associated with higher TRM bu
281         A regimen of fludarabine and 200 cGy total body irradiation was followed by infusion of allog
282                                              Total body irradiation was not required for immunologica
283 In addition, challenge of leukemic mice with total body irradiation was selectively toxic to normal h
284                                              Total-body irradiation was a major determinant for BCC.
285                                              Total-body irradiation was a significant risk factor for
286 red on days -21, -20, and -19 and 200 cGy of total-body irradiation was administered on day -1, follo
287 ter they were exposed to increasing doses of total body irradiation, we additionally examined the rol
288 e marrow and to avoid the adverse effects of total body irradiation, we employed a murine parabiosis
289 gh (myeloablative) doses of chemotherapy and total body irradiation, which have been associated with
290 itioned with T-cell depleting antibodies and total body irradiation with or without cyclophosphamide.
291 nrelated donors after conditioning with 2 Gy total body irradiation with or without fludarabine and p
292 three consecutive patients who received 2 Gy total body irradiation with or without fludarabine were
293   Conditioning was with cyclophosphamide and total body irradiation with or without fludarabine.
294 ted with nonmyeloablative conditioning (2 Gy total-body irradiation with [n = 53] or without [n = 11]
295 = 28) donors after conditioning with 2 Gy of total-body irradiation with or without fludarabine.
296 = 85) grafts after conditioning with 2 Gy of total-body irradiation with or without fludarabine.
297              Rats were subjected to 15 Gy of total-body irradiation with x-rays.
298  courses of myeloablative therapy (including total-body irradiation) with PBSCR.
299 ose melphalan and autograft followed by 2-Gy total body irradiation, with or without fludarabine, and
300 e-unit transplantation in patients receiving total body irradiation without antithymocyte globulin (A

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