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1 her response and lower dose were labelled as radiosensitive.
2 ozygotes in the human population may also be radiosensitive.
3 l that assumes all tumor cells are uniformly radiosensitive.
4  growth defects and are generally considered radiosensitive.
5 radioresistant, while Lgr5(+) stem cells are radiosensitive.
6 ere unable to resolve DNA damage, and became radiosensitive.
7 tributions, and the mutants were only mildly radiosensitive.
8  Lgr5(-) reserve stem cells are surprisingly radiosensitive.
9 l lines lacking functional ATM are extremely radiosensitive.
10 s, we conclude that CLL and non-CLL are both radiosensitive.
11 radiation therapy, as hypoxic cells are less radiosensitive.
12 r human papillomavirus (HPV) are exquisitely radiosensitive.
13 tradicts this model, in that they are highly radiosensitive.
14 ssion of ATG5 and Beclin-1 made the WT cells radiosensitive.
15 (cs) and, like Atm(-/-) mice, are viable and radiosensitive [4-8].
16 uring the G2 delay when compared to the more radiosensitive A2780 cell line.
17 mary malignant brain tumor in children, is a radiosensitive and chemosensitive tumor.
18             In addition, Artemis mutants are radiosensitive and chromosomally unstable, which has bee
19  gene that encodes nibrin, and NBS cells are radiosensitive and defective in S-phase checkpoint activ
20       Tumor growth inhibition was relatively radiosensitive and dependent on host-derived CD8+ T cell
21 ermal Langerin(+) dendritic cells (DCs) were radiosensitive and displayed a distinct cell surface phe
22 that NHEJ-deficient 2BN cells derived from a radiosensitive and immune-deficient patient lack XLF due
23 atterns, however, discriminated well between radiosensitive and more resistant lines, possibly being
24             Female BALB/c mice are unusually radiosensitive and more susceptible than C57BL/6 and oth
25 tion was of indeterminate origin, being both radiosensitive and not replenished by donor bone marrow.
26                             We observed that radiosensitive and radioresistant cells played distinct
27 aH2AX focus formation or immunoreactivity in radiosensitive and radioresistant human tumor cell lines
28                               One subset was radiosensitive and rapidly replaced from hematogenous pr
29  even at very high levels, remained as chemo/radiosensitive and repair deficient as the parental cell
30                      ATM-deficient cells are radiosensitive and show impaired cell cycle arrest and i
31 ost markedly in mammary tissue, and are both radiosensitive and susceptible to radiogenic mammary can
32 ta argue that Lgr5(-) reserve stem cells are radiosensitive and that Lgr5(+) cells are crucial for ro
33    Mutant rhp6-788 is slightly HU sensitive, radiosensitive, and exhibits normal checkpoint responses
34  against either class I or class II Ags, was radiosensitive, and required cell-cell contact.
35  and clinical features, F96-224 cells are as radiosensitive as Artemis null cell lines.
36                      However, in contrast to radiosensitive Atm-/- fibroblasts and radioresistant Atm
37                 In contrast, TCR revision is radiosensitive, B cell, CD28, and inducible costimulator
38  potential protective effect of receptors on radiosensitive, bone marrow-derived cells.
39 that these DNA-PKcs null mutants were highly radiosensitive but also that upon IR treatment, p53 accu
40  that has the interesting phenotype of being radiosensitive, but having only a modest defect in VDJ r
41              Malignant plasma cells are very radiosensitive, but the potential role of radioimmunothe
42 ataxia telangiectasia gene are indeed highly radiosensitive, but their numbers are very small.
43                                   Cells from radiosensitive, cancer-prone BALB/c mice showed ineffici
44                             Testing in other radiosensitive cancers is warranted.
45 es revealed that the IL-1R was required in a radiosensitive cell in the sensitization phase of the CH
46                                   180BR is a radiosensitive cell line defective in DSB repair, which
47                               We show that a radiosensitive cell line, mutant for the RAD51 homolog X
48              In the third group, composed of radiosensitive cell lines derived from tumors associated
49                             In addition, the radiosensitive cell populations (crypt or stem cells) ar
50 cceptance is associated with the presence of radiosensitive cells in the donor liver that may interac
51              The simulated absorbed doses to radiosensitive cells in the GI tract for 99mTc and 123I
52 ls and PAFR engagement on radioresistant and radiosensitive cells in the lung promote allergic respon
53 n the innate response to flagellin, with the radiosensitive cells producing the majority of the TNF-a
54  TLR and RLH signaling of radioresistant and radiosensitive cells was required for efficient protecti
55    IL-1beta blockade, IL-1beta deficiency in radiosensitive cells, and CCR2/CCR7 double deficiency bu
56 Ifitm3 functioned in both radioresistant and radiosensitive cells, as higher levels of WNV were obser
57 ined with a layer of endosteum that contains radiosensitive cells.
58 oietic (radioresistant) and the hemopoietic (radiosensitive) compartments, we measured both innate an
59 is directly required for the accumulation of radiosensitive dermal-derived langerin(+)CD103(+) DCs in
60                                            A radiosensitive DNA repair-deficient xrs-5 cell line was
61 rminal modification renders mice exquisitely radiosensitive due to defects in HSC/progenitor prolifer
62 ts suggest that there may be a donor-derived radiosensitive element that enhances allograft survival
63                                              Radiosensitive elements in kidney allograft may be respo
64                      Although the disease is radiosensitive, external beam radiation leads to signifi
65 p53 or interfering RNA to inhibit p21 stayed radiosensitive for 24 hours after drug treatment.
66  are hyperproliferative and potentially more radiosensitive) for patients treated with previous chemo
67  inducing a protective autophagy response in radiosensitive gastrointestinal tissues.
68 , TRADD expression was induced in a uniquely radiosensitive GM cell line but not in radioresistant GM
69   The choice of therapeutic modality in this radiosensitive group of patients should be made on a cas
70       However, NOD/LtSz-scid mice are highly radiosensitive, have short life spans, and a small numbe
71 ave not gained success in patients except in radiosensitive hematological neoplasms, or in settings i
72 , nitric oxide synthase 2 production by both radiosensitive hematopoietic and radioresistant stromal
73 licited in the absence of Ag presentation by radiosensitive host hematopoietic-derived APCs after all
74 e reported that in the absence of functional radiosensitive host hematopoietic-derived APCs, H-Y Ag p
75 r T cells will induce GVHD in the absence of radiosensitive host hematopoietic-derived APCs.
76 ld indeed represent a societally-significant radiosensitive human subpopulation.
77 of radioresistant stroma cells as well as of radiosensitive immune cells is needed to effectively pro
78 cond group, composed of cell lines that were radiosensitive in culture (D0 approximately 1 Gy) but de
79 al epithelial (SIE) cells are among the most radiosensitive in the body.
80 ponse to radiation; these animals are highly radiosensitive in the soma and radioresistant in the ger
81 ls expressing AS-IGF1R transcripts were more radiosensitive in vitro and in vivo than controls.
82 the ATM gene (ATM(+/-)) may be slightly more radiosensitive in vitro, it remained to be determined wh
83    We found that these stem cells are highly radiosensitive, in contrast to their isogenic differenti
84 ased localization of radiopharmaceuticals in radiosensitive kidney subregions can potentially lead to
85 tor, but not other innate immune sensors, in radiosensitive leukocytes protects against tumour format
86                                      Another radiosensitive line, mutant for XRCC3 and defective in H
87 ken together, these data identify c-MYC as a radiosensitive locus, implicating this oncogenic transcr
88 rays to survey common CNVs in a cohort of 50 radiosensitive lymphoblastoid cell lines (RS-LCLs) deriv
89 immunosuppressive agent that acts by killing radiosensitive lymphocytes.
90 ance the oncolytic potency of MV-Edm against radiosensitive malignancies and to facilitate noninvasiv
91 eriments and in clinical trials conducted in radiosensitive malignancies, particularly B-cell lymphom
92                        Multiple myeloma is a radiosensitive malignancy that is currently incurable.
93                         On the other hand, a radiosensitive mutant (irs-20) of DNA-PKcs with a defect
94              DNA-PK-deficient cell lines are radiosensitive mutants lacking either the catalytic subu
95  protein carbonylation than is the much more radiosensitive nematode Caenorhabditis elegans.
96 e basis of the DNA repair strategies of more radiosensitive organisms.
97  determine normalized dose data for maternal radiosensitive organs and embryo/fetus from 256-slice CT
98 iminary tests of shielding other superficial radiosensitive organs frequently included at diagnostic
99   Mitochondrial p53 accumulation occurred in radiosensitive organs like thymus, spleen, testis, and b
100           Organ and surface dose to specific radiosensitive organs were estimated by using software f
101 rofile of the cumulative uptake over time of radiosensitive organs.
102 tion is associated with massive apoptosis in radiosensitive organs.
103 nce animal survival or crypt regeneration in radiosensitive p21 KO-recipient mice.
104 in a redistribution of the cells into a more radiosensitive phase of the cell cycle or in an increase
105         Tachpyridine arrested cells at G2, a radiosensitive phase of the cell cycle, and enhanced the
106 ortion of cells in G2-M (27% versus 5%), the radiosensitive phase of the cell cycle.
107 partial synchronisation of cells in the most radiosensitive phase of the cell-cycle.
108 e DNA glycosylases in mutant cells confers a radiosensitive phenotype and an increase in the number o
109 ns in the LRR can only partially reverse the radiosensitive phenotype and V(D)J recombination deficit
110    Initially this was because of the unusual radiosensitive phenotype of cells from A-T patients, and
111  isolated as a second-site suppressor of the radiosensitive phenotype of seeds defective in the repai
112 ulature in wild-type mice that resembled the radiosensitive phenotype of tumor vessels in SCID mice.
113 t mechanisms may be responsible for the more radiosensitive phenotype.
114 of multiple myeloma, an incurable but highly radiosensitive plasma cell malignancy.
115 myelination appears to be mediated by a CD8+ radiosensitive population, which is induced on infection
116                           Interestingly, two radiosensitive primary fibroblast cell lines, derived fr
117 three patient subgroups of radiosensitivity: radiosensitive, radio-normal, and radioresistant groups.
118 g agents and absence of B and T lymphocytes (radiosensitive severe combined immune deficiency [RS-SCI
119                                              Radiosensitive severe combined immune deficiency in huma
120 oss of ARTEMIS function therefore results in radiosensitive severe combined immunodeficiency (RS-SCID
121         The Artemis nuclease is defective in radiosensitive severe combined immunodeficiency patients
122                                        Human radiosensitive severe combined immunodeficiency results
123 tive in ataxia telangiectasia and a class of Radiosensitive-Severe Combined Immunodeficiency (RS-SCID
124                 Multiple myeloma is a highly radiosensitive skeletal malignancy, but bone-seeking rad
125 on of PAX7 positive cells, we show that this radiosensitive skeletal muscle progenitor pool contribut
126 ase was 1.7- and 1.3-fold for the moderately radiosensitive small cell lung carcinoma 54A and the hig
127        More strikingly, we also can create a radiosensitive state when the select let-7 family of miR
128 um response was more pronounced for the more radiosensitive strain.
129 P, the bladder tumour cell line MGH-U1 and a radiosensitive subclone S40b.
130  population includes genetically predisposed radiosensitive subsets.
131                                      Skin is radiosensitive, suggesting it is well-oxygenated.
132 image but reduced the amount of radiation to radiosensitive superficial structures.
133  their profile in radioresistant (SW480) and radiosensitive (SW48) human colorectal cell lines.
134  discovered as the gene inactivated in human radiosensitive T(-)B(-) severe combined immunodeficiency
135 trating that children are not, in fact, more radiosensitive than adults in the radiologic imaging dos
136 ion, in particular for children who are more radiosensitive than adults.
137 e of the DNA-PKcs variants are slightly more radiosensitive than cells completely deficient in DNA-PK
138 or ataxia telangiectasia (A-T) are much more radiosensitive than cells from unaffected individuals.
139 od) and CFU-GM(blood) were considerably more radiosensitive than femoral progenitors, thereby providi
140 hree SCAN1 lines examined were slightly more radiosensitive than normal cells, but only for fractiona
141 ective in undergoing apoptosis but were more radiosensitive than the WT cells in autophagy.
142 heir DT, i.e. the faster cells grow the more radiosensitive they are.
143  compared with non-stem cells within several radiosensitive tissue niches and culture models.
144 rogeneity of radioactivity in this important radiosensitive tissue.
145        Active bone marrow is one of the more radiosensitive tissues in the human body and, hence, it
146 e potential for complications to nontargeted radiosensitive tissues might be reduced.
147 (177)Lu-DOTA-Bn), that leads to high TIs for radiosensitive tissues such as blood (TI = 73) and kidne
148 tion (IR) induces p53-dependent apoptosis in radiosensitive tissues, suggesting that p53 is a determi
149 nt-related toxicities, based on high TIs for radiosensitive tissues.
150 rpin RNA renders the IR-resistant nu61 cells radiosensitive to IR.
151                                     However, radiosensitive tumor cells and xenografts retained gamma
152 umor xenograft, was selected from a parental radiosensitive tumor SCC-61 by eight serial cycles of pa
153                    Although CTCL is a highly radiosensitive tumor, the complex topography of acral su
154 The loss in effectiveness is most severe for radiosensitive tumors.
155                             Inclusion of the radiosensitive variable improved lasso logistic regressi
156 ass I MHC expression is absent or limited to radiosensitive versus radioresistant cells.
157 significant difference in expression between radiosensitive versus radiotolerant strains, suggesting
158 licular lymphoma has been shown to be highly radiosensitive with responses to doses as low as 4 Gy in

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