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1 sted of fludarabine (90 mg/m2) and 2 to 3 Gy total body irradiation.
2 e transplanted after varying doses of cGy of total body irradiation.
3 tion of IL-22 enhanced thymic recovery after total body irradiation.
4 ipheral blood compartments of mice post-4 Gy total body irradiation.
5  VCA recipients with 200-, 300-, and 400-cGy total body irradiation.
6 yclophosphamide, fludarabine, and 200 cGy of total body irradiation.
7  test abnormalities among those who received total body irradiation.
8 ell receptor monoclonal antibody followed by total body irradiation.
9 20 lymphoma in mice preconditioned with 6 Gy total body irradiation.
10 -identical marrow transplantation after 1 Gy total body irradiation.
11 with (131)I-BC8 Ab and fludarabine plus 2 Gy total body irradiation.
12  exhibit enhanced survival following 8-10 Gy total body irradiation.
13 ltered urine from cancer patients undergoing total body irradiation.
14 and responded to antigenic stimulation after total body irradiation.
15 tical donors after conditioning with 920 cGy total body irradiation.
16 ation therapy in mice with anemia induced by total body irradiation.
17 ative conditioning with fludarabine and 2 Gy total body irradiation.
18 e marrow after conditioning with 100-300 cGy total body irradiation.
19 these biomarker genes in patients undergoing total body irradiation.
20 conditioning, primarily cyclophosphamide and total body irradiation.
21 e given HSCT after conditioning with 920 cGy total body irradiation.
22 s were conditioned with cyclophosphamide and total body irradiation.
23  and hematopoietic radioprotection following total body irradiation.
24 ft and a conditioning regimen with > 450 cGy total body irradiation.
25 autologous bone marrow transplantation after total body irradiation.
26  depletion-based conditioning with 1 or 3 Gy total body irradiation.
27 increases survival of mice exposed to lethal total body irradiation.
28 occurred within the IFRT site and five after total-body irradiation.
29 ustained engraftment can be achieved without total-body irradiation.
30                Conditioning therapy involved total body irradiation 2 Gy +/- fludarabine 30 mg/m2.
31 oablative conditioning regimen consisting of total-body irradiation (2 Gy) with or without fludarabin
32            RIC regimens included fludarabine/total body irradiation 200 cGy (n = 5) or 450 cGy (n = 1
33 phamide (50 mg/kg), and a single fraction of total body irradiation (200 cGy) with cyclosporine and m
34 underwent conditioning with a single dose of total-body irradiation (200 cGy).
35 g of alemtuzumab (1 mg/kg in divided doses), total-body irradiation (300 cGy), sirolimus, and infusio
36                Eight recipient dogs received total body irradiation (4.5 cGy), hematopoietic cell tra
37 hosphamide 14.5 mg/kg on days -6 and -5, and total body irradiation 400 cGy administered as a single
38 D154/rapamycin plus 100, 200, and 300 cGy of total body irradiation, 42.9%, 85.7%, and 100% of mice e
39 5% CI 2.3-7.7), ifosfamide (24.9, 7.4-83.5), total body irradiation (6.9, 2.3-21.1), and mean kidney
40                                HDIT included total body irradiation (800 cGy) with lung shielding, cy
41                                We found that total body irradiation, a conditioning regimen required
42 ere hypoplastic and more apoptotic 24 h post-total body irradiation, a time when stem cell survival i
43 men involving anti-CD154 and low dose (3 Gy) total body irradiation, allowing achievement of mixed ch
44 = 498) or unrelated (n = 336) HCT after 2 Gy total body irradiation alone (n = 171) or combined with
45 nstitutions using conditioning with low-dose total body irradiation alone or combined with fludarabin
46 ated donors following conditioning with 2 Gy total body irradiation alone or in combination with flud
47 ne-refractory CLL were conditioned with 2 Gy total-body irradiation alone or combined with fludarabin
48                        Our results show that total body irradiation alters intracellular signaling an
49 oietic cells using a combination of low-dose total body irradiation and a short course of immunosuppr
50 n (BMT) following conditioning with low-dose total body irradiation and anti-CD154 antibody.
51 rance are achieved in mice receiving 3 Gy of total body irradiation and anti-CD154 mAb followed by al
52 ents received a single fraction dose of 2 Gy total body irradiation and HC transplants from HLA-ident
53 ient Tregs after a conditioning regimen with total body irradiation and led to a TGF-beta-dependent i
54 -ibritumomab tiuxetan, fludarabine, and 2 Gy total body irradiation and matched-related (15) or unrel
55  of pretransplant T cell depletion, low-dose total body irradiation and posttransplant (donor) bone m
56                                              Total body irradiation and radiation proctitis were moni
57 r nonmyeloablative (3 Gy) and minimal (1 Gy) total body irradiation and treatment with costimulation
58 clophosphamide (CY) and busulfan (BU) (67%), total-body irradiation and CY (21%), BU-fludarabine (10%
59            The conditioning regimen included total-body irradiation and cyclophosphamide (n = 3), bus
60  preconditioning or after 200 cGy or 900 cGy total-body irradiation and evaluated after 4 months.
61 etic stem-cell transplantation that includes total-body irradiation and treatment with alemtuzumab an
62 smoking history, conditioning with high-dose total body irradiation, and an absolute lymphocyte count
63 globulin, fludarabine, cyclophosphamide, and total body irradiation, and graft-versus-host disease pr
64 nsolidation with myeloablative chemotherapy, total-body irradiation, and ABMT versus three cycles of
65    NOD mice received various combinations of total body irradiation, anti-CD154, anti-CD8alpha, anti-
66  recipients who receive conditioning without total body irradiation are not well known.
67 al cell apoptosis after they were exposed to total body irradiation as compared with TNFR1-deficient
68 13)Bi)-labeled anti-CD45 antibody to replace total body irradiation as conditioning for hematopoietic
69                                   The use of total body irradiation as part of conditioning regimens
70 re enriched early after TLI/ATS + BMT versus total body irradiation/ATS + BMT.
71 X compared with TLI/ATS, lethal or sublethal total body irradiation/ATS/CTX, or CTX/ATS conditioning.
72 s the antileukemic benefits of myeloablative total body irradiation-based conditioning and unrelated
73 cantly higher rate of DC was associated with total body irradiation-based conditioning and with acute
74  critical to the induction of tolerance in a total body irradiation-based model.
75 sed with hematologic malignancies received a total body irradiation-based myeloablative conditioning
76 te deletional tolerance as the mechanism for total body irradiation-based nonmyeloablative conditioni
77  in patients conditioned with a fractionated total body irradiation-based regimen has shown encouragi
78 blastic leukemia 10) were conditioned with a total body irradiation-based regimen.
79 hocytic leukemia patients treated with 12 Gy total body irradiation-based regimens and allogeneic tra
80 ted donor transplantation with myeloablative total body irradiation-based regimens.
81  lymphoma who were considered ineligible for total-body irradiation because of older age or prior rad
82 shed in dogs given a sublethal dose (1-2 Gy) total body irradiation before and a short course of immu
83 ditioning of neonates with 100 to 400 cGy of total body irradiation before normal donor marrow transp
84 mg/kg, fludarabine 200 mg/m2, and 200 cGy of total body irradiation (Bu/Flu/TBI).
85 tumoral proliferation of T-effector cells in total body irradiation-conditioned recipients.
86                              The toxicity of total body irradiation conditioning and potential for gr
87 e marrow (BM) cells or through myeloablative total body irradiation conditioning and reconstitution w
88 Furthermore, this procedure usually requires total body irradiation conditioning of recipients.
89 day pulmonary metastases of MCA 205 received total body irradiation conditioning or were nonirradiate
90   However, when mice were given more intense total body irradiation conditioning regimens combined wi
91                       To reduce or eliminate total body irradiation conditioning regimens, we have so
92  ex vivo antigen stimulation irrespective of total body irradiation conditioning.
93  CD34+ cells can engraft even after low-dose total body irradiation conditioning.
94                                              Total body irradiation-containing preparative regimen wa
95              When used with cyclophosphamide/total body irradiation (Cy/TBI) conditioning, sirolimus
96               Cyclophosphamide combined with total body irradiation (Cy/TBI) or busulfan (BuCy) are t
97 nditioning regimens of cyclophosphamide plus total body irradiation (CY/TBI), busulfan plus cyclophos
98 ioned with cyclophosphamide and fractionated total-body irradiation (Cy/TBI) or busulfan and cyclopho
99 ransplantation conditioning regimen (2 Gy of total-body irradiation, cyclophosphamide, and fludarabin
100 receptor and anti-CD8 monoclonal antibodies, total body irradiation, cyclosporine A and mycophenolate
101          Although the addition of 600 rad of total body irradiation delayed tumor growth, further ado
102 ll transplantation with cyclophosphamide and total body irradiation develop wide-spectrum manifestati
103 erance, significantly decreasing the minimum total body irradiation dose required.
104                    The omission of high-dose total body irradiation, dose adjustments of busulfan to
105 ent regimens:fludarabine-melphalan (n = 46); total body irradiation-etoposide (n = 28), and busulfan-
106                 Rabbits exposed to 10 cGy of total body irradiation exhibited T cell deficiency, with
107 eparative regimen of nonmyeloablating (5 Gy) total body irradiation experienced the rapid rejection o
108 ancies conditioned with fludarabine and 2 Gy total body irradiation followed by HLA-matched unrelated
109 in which the marrow recipients received 2 Gy total body irradiation followed by marrow infusions from
110 ated with a nonmyeloablative dose of 200 cGy total body irradiation followed by matched-littermate SC
111 of a specific anti-CD44 mAb (S5) and 200 cGy total body irradiation followed by postgrafting immunosu
112                                              Total body irradiation followed by transplantation with
113 d MCA-205 tumors were treated with sublethal total body irradiation, followed by adoptive transfer of
114 were uniformly cured after administration of total body irradiation, followed by the transplantation
115 e were conditioned with 1000 cGy single dose total body irradiation, followed by transplantation of 1
116 (P=0.01) and, in multivariate analysis, with total body irradiation for all lineages (P<0.01).
117 ne tumor recipients were preconditioned with total body irradiation from 0 to 500 cGy or with a 30-da
118 is study, we investigated whether increasing total body irradiation from 200 cGy to 400 cGy would imp
119 matched sibling donors received fractionated total body irradiation (FTBI) and high-dose VP16, wherea
120 n consisted of 90 mg/m2 fludarabine and 2 Gy total body irradiation given before and mycophenolate mo
121 ludarabine and targeted busulfan (n = 25) or total body irradiation (&gt;/=12 Gy; n = 18).
122 nner, with the administration of DA prior to total body irradiation having the greatest protective ef
123 ctive regimen consisted of hyperfractionated total body irradiation (HFTBI), thiotepa, and fludarabin
124 T was seen only in patients conditioned with total-body irradiation (HR, 3.9 [95% CI, 2.6-6.8]).
125 losuppressive regimen, consisting of 100 cGy total body irradiation, immunotoxin mediated T-cell depl
126 ry of young BM ECs along with HSCs following total body irradiation improved HSC engraftment and enha
127 esus macaques conditioned with myeloablative total body irradiation in the absence or presence of sin
128                        Conditioning included total-body irradiation in 92% of patients.
129 unotherapy targeting CD45 may substitute for total-body irradiation in hematopoietic cell transplanta
130 ive preparative regimen that did not involve total-body irradiation in young children with Hurler's s
131      In contrast, no significant increase in total body irradiation-induced apoptosis or tissue injur
132 iation-induced gastrointestinal syndrome and total body irradiation-induced hematopoietic failure.
133  show that p50-/- mice are more sensitive to total body irradiation-induced lethality than wild-type
134  examined the role of NFkappaB activation in total body irradiation-induced tissue damage.
135                          Exposure of mice to total body irradiation induces nuclear factor kappaB (NF
136 g from the combined effects of cyclosporine, total body irradiation, infections, high-dose chemothera
137 reert2)/Met(+/+)/LacZ) were exposed to 10 Gy total body irradiation; intestinal tissues were collecte
138                                              Total body irradiation is a component in various host co
139 hematopoietic regeneration in vivo following total body irradiation is dependent upon EGFR-mediated r
140 experimental and clinical scenarios in which total body irradiation is involved.
141 approach requires conditioning regimens with total body irradiation, lymphodepleting chemotherapy, an
142                        NFkappaB activated by total body irradiation mainly consists of NFkappaB p50/R
143                                         Upon total body irradiation, medullary complexity was partial
144 D154 (MR1) and rapamycin (Rapa) plus 100 cGy total body irradiation (MR1/Rapa/100 cGy) and transplant
145  were conditioned with cyclophosphamide with total body irradiation (n = 39) or busulfan (n = 1).
146  4, 3, and 2 days before receiving 2 or 3 Gy total body irradiation on the day of HSCT (day 0).
147  simulated weightlessness and space-relevant total-body irradiation on vascular responsiveness in mic
148 mice were lymphodepleted by nonmyeloablative total body irradiation or a myeloablative regimen that r
149 e latter treatment, however, did not require total body irradiation or adoptive cell transfer and res
150  there was no difference between receiving a total body irradiation or busulfan based regimens (P = .
151 yclophosphamide associated with fractionated total body irradiation or busulfan.
152  myeloablative regimens, ie, those including total body irradiation or high-dose busulfan.
153 l HCT, where recipients are conditioned with total body irradiation or high-dose chemotherapy.
154 philia A BALB/c mice after reduced-intensity total body irradiation or nonmyeloablative chemotherapy
155 t differences in hazards were observed after total-body irradiation or receipt of an allogeneic versu
156  male sexual function domains declined after total body irradiation (P < .05).
157 m(2) x 5, cyclophosphamide 50 mg/kg, 200 cGy total body irradiation), patients received either matche
158         Patients treated with C-HDT received total body irradiation plus chemotherapy (70%) or chemot
159 h busulfan plus cyclophosphamide and 12 with total body irradiation plus chemotherapy.
160             The patients received 300 cGy of total-body irradiation plus alemtuzumab before transplan
161 iation of conditioning therapy (fractionated total-body irradiation plus high-dose chemotherapy) and
162 sk for osteoporosis and bone fractures after total body irradiation preconditioning.
163                     Although nonmyeloblative total body irradiation prevented organ graft rejection,
164  depletion with CD3-immunotoxin, and 100 cGy total body irradiation prior to hematopoietic cell trans
165  A single injection of CBLB502 before lethal total-body irradiation protected mice from both gastroin
166 Univariate analysis showed that fractionated total body irradiation, race, and use of cytarabine sign
167                                      However total-body irradiation, radiation to the gonads, and che
168                                              Total body irradiation reduced numbers of proliferating
169 r without T-cell lymphodepletion reduced the total body irradiation requirement to 100 cGy for establ
170                                              Total body irradiation (RR = 0.6) provided a protective
171                            Mice subjected to total body irradiation showed alterations in glucose met
172 or-bearing mice with DMA 2 hours before 8 Gy total body irradiation showed an impressive rescue of ra
173 nti-FVIII immune response, and together with total body irradiation, suppresses anti-FVIII immune res
174 serum at 10 mg at day +10 (single dose), and total-body irradiation t 300 cGy (day 0) before bone-mar
175 s 11.0%, higher among survivors who received total body irradiation (TBI) (17%) than those who did no
176 ence indicates that the addition of low-dose total body irradiation (TBI) (2-4 Gy) to reduced intensi
177 ed: (1) myeloablative conditioning (MA) with total body irradiation (TBI) + PBSCs, (2) MA + TBI + BM,
178 that antithymocyte globulin (ATG) given with total body irradiation (TBI) 200 cGy and fludarabine res
179 re we use bone marrow transplantation (BMT), total body irradiation (TBI) and abdominal irradiation (
180                        Lymphodepletion using total body irradiation (TBI) and administering high-dose
181  littermate recipients consisting of 450 cGy total body irradiation (TBI) and anti-CD44 monoclonal an
182 man urine data sets from patients undergoing total body irradiation (TBI) and from a colorectal cance
183 mone (GH) deficiency are complications after total body irradiation (TBI) and hematopoietic cell tran
184 ce were conditioned with decreasing doses of total body irradiation (TBI) and reconstituted with bone
185 ) cell recovery in rhesus macaques following total body irradiation (TBI) and reinfusion of vector-tr
186                BALB/c mice were treated with total body irradiation (TBI) and then infused with C57Bl
187 onmyeloablative chemotherapy with or without total body irradiation (TBI) before adoptive T-cell tran
188                                              Total body irradiation (TBI) before allogeneic hematopoi
189 anti-CD45 radioimmunotherapy (RIT) replacing total body irradiation (TBI) before haploidentical HCT i
190                   Four dogs received 920 cGy total body irradiation (TBI) before infusion of autologo
191                                              Total body irradiation (TBI) can induce lethal myelosupp
192 lantation (BMT), but this procedure requires total body irradiation (TBI) conditioning of the recipie
193  engraftment was only transient with 100 cGy total body irradiation (TBI) conditioning, indicating su
194 at under myeloablative and reduced-intensity total body irradiation (TBI) conditioning, transplantati
195                                              Total body irradiation (TBI) damages hematopoietic cells
196                    We examined the impact of total body irradiation (TBI) dose and fractionation on r
197 eic transplantation with regimens of varying total body irradiation (TBI) doses (0-1575 cGy), with an
198                                              Total body irradiation (TBI) exposure was associated wit
199 equires the recipient mice to undergo lethal total body irradiation (TBI) followed by rescue with who
200 BMT, rats were treated with varying doses of total body irradiation (TBI) followed by transplantation
201 not been compared with cyclophosphamide plus total body irradiation (TBI) in adults with advanced ref
202 emission at the time of allo-HSCT and use of total body irradiation (TBI) in patients with non-Hodgki
203 rs of 2 articles have compared busulfan with total body irradiation (TBI) in preparative regimens for
204                         Lymphodepletion with total body irradiation (TBI) increases the efficacy of a
205 ood, Shao et al report that a side effect of total body irradiation (TBI) is long-term bone marrow in
206                      Fractionated, high-dose total body irradiation (TBI) is used therapeutically to
207 myeloablative conditioning regimens--200 cGy total body irradiation (TBI) or 10 mg/kg busulfan--with
208  (BMT) after conditioning with either lethal total body irradiation (TBI) or an established nonmyeloa
209  in the bone marrow (BM) as a consequence of total body irradiation (TBI) or granulocyte colony-stimu
210                Mice were subjected to either total body irradiation (TBI) or partial body irradiation
211 s studies showed that treatment of mice with total body irradiation (TBI) or total lymphoid tissue ir
212 monoclonal antibody before conditioning with total body irradiation (TBI) prevents GVHD but retains G
213  nonmyeloablative chemotherapeutic agents or total body irradiation (TBI) prior to adoptive transfer
214  inhibition using AZ31 prior to 9 or 9.25 Gy total body irradiation (TBI) reduced median time to mori
215 treatment, we determined the minimal dose of total body irradiation (TBI) required when added to anti
216 C57BL/6 mice to a sublethal dose (6.5 Gy) of total body irradiation (TBI) resulted in a sustained qua
217 requency of side effects caused by high-dose total body irradiation (TBI) the nonmyeloablative regime
218              Addition and intensification of total body irradiation (TBI) to the preparative lymphode
219                                       Lethal total body irradiation (TBI) triggers multifactorial hea
220 ) given conventional conditioning, high-dose total body irradiation (TBI) was associated with an incr
221                                              Total body irradiation (TBI) was associated with develop
222 ft rejection after conditioning with 1 Gy of total body irradiation (TBI) was consistently seen in hi
223 e NSG host environment using preconditioning total body irradiation (TBI) was indispensable for effic
224 ynomolgus monkeys, cyclophosphamide (CP) and total body irradiation (TBI) were compared as part of a
225 l HSCT in which 27 patients conditioned with total body irradiation (TBI) were given a fixed dose of
226 single-exposure, high dose rate (30 cGy/min) total body irradiation (TBI) with cyclophosphamide as co
227 6 transplantation model and ascertained that total body irradiation (TBI) with establishment of chime
228 yeloablative conditioning consisting of 2 Gy total body irradiation (TBI) with or without added fluda
229 of fludarabine, anti-thymocyte globulin, and total body irradiation (TBI) would enable reduction of t
230 itioned with CD45-SAP, CD45-SAP plus 2 Gy of total body irradiation (TBI), 2 Gy of TBI, 8 Gy of TBI,
231 al antibodies (mAbs) on Days -6 and -1, 3 Gy total body irradiation (TBI), and 7 Gy thymic irradiatio
232 eived cyclophosphamide (CY), single fraction total body irradiation (TBI), and antithymocyte globulin
233 re treated with cyclophosphamide, etoposide, total body irradiation (TBI), and PBSCT.
234  unrelated donors were rejected after 9.2 Gy total body irradiation (TBI), and that graft resistance
235 ty conditioning (RIC) consisting of low-dose total body irradiation (TBI), cyclophosphamide, and flud
236 is upregulated during lymphopenia induced by total body irradiation (TBI), cyclophosphamide, or Thy1
237 f the endosteal osteoblastic HSC niche after total body irradiation (TBI), defined as relocalization
238          Nonmyeloablative regimens were 2 Gy total body irradiation (TBI), either alone (n = 40) or c
239 ril, an ACE inhibitor, initiated 1-4 h after total body irradiation (TBI), improved Hematopoietic Acu
240 ransplantation regimen consisted of low-dose total body irradiation (TBI), preceded in some patients
241  animals were submitted at 60 days to 9.5-Gy total body irradiation (TBI), reconstituted immediately
242 ests that intense immune suppression using a total body irradiation (TBI)-based regimen and hematopoi
243 ive intravenous busulfan (IV-BU) vs ablative total body irradiation (TBI)-based regimens in myeloid m
244 outcome when patients had undergone previous total body irradiation (TBI)-containing myeloablative tr
245 second relapse was significantly lower after total body irradiation (TBI)-containing transplant regim
246 way as a new mechanism for the mitigation of total body irradiation (TBI)-induced mortality.
247  recovery in the blood and bone marrow after total body irradiation (TBI).
248 cy, we developed a murine model of sublethal total body irradiation (TBI).
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 peutics Inc., in mice exposed to Co-60 gamma total body irradiation (TBI).
252 d donors received fludarabine and 200 cGy of total body irradiation (TBI); UCB recipients received cy
253 )) rats were conditioned with 600 to 300 cGy total body irradiation (TBI, day-1), and 100 x 10(6) T-c
254              Next, nine dogs received 4.5 Gy total-body irradiation (TBI) and unmodified marrow graft
255               Recipient dogs were given 2-Gy total-body irradiation (TBI) before and a short course o
256 ents, certain other leukemogenic agents, and total-body irradiation (TBI) cause chromosomal damage th
257 tion (SCT) for hematologic malignancies with total-body irradiation (TBI) conditioning regimens, and
258 ocoumarin (DAMTC) to mitigate RIII following total-body irradiation (TBI) in C57BL/6 mice and underly
259                                    Impact of total-body irradiation (TBI) in conditioning regimen on
260 to show that temporarily blocking p53 during total-body irradiation (TBI) not only ameliorates acute
261 ars of age, received either cyclophosphamide/total-body irradiation (TBI) or busulfan/cyclophosphamid
262          Cyclophosphamide (Cy) combined with total-body irradiation (TBI) or with busulfan (Bu) are c
263 no administered 24 h before or after 4 Gy of total-body irradiation (TBI) promoted rapid and complete
264 ne adults received cyclophosphamide (CY) and total-body irradiation (TBI) supported by autologous bon
265 er 2 (25 patients) or 12 Gy (25 patients) of total-body irradiation (TBI) was administered before cel
266 n diagnosis, type of transplantation, use of total-body irradiation (TBI), and presence of graft-vers
267 with age and after genotoxic stress, such as total-body irradiation (TBI).
268 ool and 100% survival after a lethal dose of total-body irradiation (TBI).
269 d: 4-6 of 6 matched dUCB-TCF (n = 120; TCF = total body irradiation [TBI] 200 cGy + cyclophosphamide
270 targeted forms of radiotherapy compared with total body irradiation that have the potential to decrea
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                                   Increasing total body irradiation to 400 cGy substantially reduced
276   Furthermore, administering lethal doses of total body irradiation to GF mice produces markedly fewe
277 oned with fludarabine, cyclophosphamide, and total-body irradiation, underwent combined HCT/kidney tr
278 r synthesis is not detectable in response to total body irradiation unless NaCl is lowered by furosem
279 le protected rodents against lethal doses of total body irradiation up to 13 Gy, whether DIM dosing w
280 de 2 to 4 acute GVHD were cyclophosphamide + total-body irradiation versus busulfan + cyclophosphamid
281 nalysis of significant variables showed that total body irradiation was a risk factor for cataract fo
282 demia (RR = 3.2, P < .01); conditioning with total body irradiation was associated with an increased
283         A regimen of fludarabine and 200 cGy total body irradiation was followed by infusion of allog
284                                              Total body irradiation was given with each HSCT.
285                                              Total body irradiation was not required for immunologica
286 In addition, challenge of leukemic mice with total body irradiation was selectively toxic to normal h
287                                              Total-body irradiation was a major determinant for BCC.
288                                              Total-body irradiation was a significant risk factor for
289 ter they were exposed to increasing doses of total body irradiation, we additionally examined the rol
290 e marrow and to avoid the adverse effects of total body irradiation, we employed a murine parabiosis
291 itioned with T-cell depleting antibodies and total body irradiation with or without cyclophosphamide.
292 nrelated donors after conditioning with 2 Gy total body irradiation with or without fludarabine and p
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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