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3 er a broad range of frequencies (0.1-30, 000 rad/s), LTM provides a unique ability to noninvasively q
4 horacic radiation therapy consisted of 4,000 rad to the tumor and mediastinum with a 1,000-rad boost.
6 rel (millicurie) injected was 90 Gy/g (9,000 rad/g), of which 64% was from conversion electrons, 16%
12 12 short tandem repeat markers on the 5,000-rad horse x hamster whole-genome radiation hybrid panel
14 The high-resolution Illinois-Texas 5,000-rad RH and comparative maps will facilitate identificati
16 d 0.0020 mGy/MBq (0.0086, 0.0006, and 0.0074 rad/mCi) for the ovaries, testes, and red marrow, respec
19 rrow and spleen were 0.00797 mGy/MBq (0.0295 rad/mCi) and 0.00709 mGy/MBq (0.0262 rad/mCi), respectiv
21 the lipid tail rotation (D(rot_tail) = -0.04 rad(2)/ns) is slower then the head group rotation (D(rot
24 ffusively at an in plane rate of Dphi = 0.07 rad(2)/ps and an out of plane rate of Dtheta = 0.05 rad(
25 ver (mean, 24.78 rad/mCi; range, 15.02-37.07 rad/mCi), with red marrow estimates on the order of 3.32
26 /mCi) to the kidneys, 0.0197 mGy/MBq (0.0728 rad/mCi) to the pancreas, and 0.0186 mGy/MBq (0.0688 rad
30 of the laser trap at frequencies less than 1 rad/s, indicating that at least locally, the gels behave
45 ere the lower large intestine (1.43 +/- 0.19 rad/mCi) and upper large intestine (1.20 +/- 0.38 rad/mC
49 hen the head group rotation (D(rot_hg) = 2.2 rad(2)/ns), which is slower than the overall in plane (D
53 h received an average of 0.062 mGy/MBq (0.23 rad/mCi, range 0.08-0.30 rad/mCi), followed by the kidne
56 ts (n=51) underwent a single, rapid (117-266 rad/s) head rotation in the sagittal (n=13), coronal (n=
60 ntwisting velocity, -2.0+/-0.7 to -5.6+/-2.3 rad/s) that was associated with an increase in IVPG (1.4
62 0.062 mGy/MBq (0.23 rad/mCi, range 0.08-0.30 rad/mCi), followed by the kidneys (0.051 mGy/MBq), liver
63 l mortality included radiation dose >/= 3000 rad ( >/= 30 Gy; supra-diaphragm: HR, 3.8; 95% CI, 1.1-1
66 ap and 37 were positioned on the Roslin 3000-rad radiation hybrid (RH) map, with 20 assignments share
70 y bladder wall dose to 0.0885 mGy/MBq (0.327 rad/mCi) or 0.128 mGy/MBq (0.473 rad/mCi), respectively,
76 was transferred to irradiated ACI rats (400 rad) with either purified T cells (4-10 x 10[7]) or seru
77 myeloma, SCID mice were irradiated with 400 rads and mice were injected either with 10(6) ARH-77 cel
80 /MBq (0.327 rad/mCi) or 0.128 mGy/MBq (0.473 rad/mCi), respectively, and the effective dose to 0.0149
81 ers of magnitude at low frequencies (0.5-1.5 rad/s) but converge at high frequencies (> 10(4) rad/s).
94 ere mapped primarily by genotyping on a 5000-rad horse x hamster radiation hybrid panel, of which 28
98 mCi]), followed by liver (0.14 mGy/MBq [0.52 rad/mCi]); the effective dose is 0.022 mSv/MBq (0.083 re
101 ministered activity was 0.150 mGy/MBq (0.556 rad/mCi) with the realistic void schedule used in our st
105 rils is more mechanically rigid (517 Pa at 6 rad/s) than the gel composed of twisted fibrils (367 Pa
107 ls with peak reorientation speeds of up to 6 rad/s and returning to random after 5 min without stimul
109 e kidney capsule of diabetic irradiated (600 rads), naive C57BL/6 recipients (mean survival time = 48
111 blood (131)I was 0.34 (range, 0.1 6 to 0.63) rad/mCi (0.09 mGy/MBq; range, 0.04 to 0.17 mGy/ MBq).
113 rgan is gallbladder wall (0.19 mGy/MBq [0.69 rad/mCi]), followed by liver (0.14 mGy/MBq [0.52 rad/mCi
115 nit of administered 131I was 1.0 Gy/GBq (3.7 rad/mCi) for patients with NHL whether in MTD or LD tria
117 treatment absorbed dose limit of 75 cGy (75 rad), the administered 131I activity ranged from 2.1 to
118 lculated in this study of 0.21 mGy/MBq (0.77 rad/mCi) is approximately a factor of 2 less than the va
119 ses were delivered to the liver (mean, 24.78 rad/mCi; range, 15.02-37.07 rad/mCi), with red marrow es
120 ved the highest dose (229.50 muGy/MBq [0.849 rad/mCi]), followed by the small and large intestines (1
122 to amplitudes of approximately 1.5 x 10(-9) rad at the lowest frequency normal mode and the sensitiv
125 e urinary bladder wall, 0.258 mGy/MBq (0.955 rad/mCi), and gallbladder wall, 0.193 mGy/MBq (0.716 rad
128 c and cytological comparisons of Cebrc-2 and rad-51 mutants revealed fundamental phenotypic differenc
129 n DNA repair defects observed in Cebrc-2 and rad-51 mutants, and define mechanistic roles for CeBRC-2
130 that atl-1 (Caenorhabditis elegans ATR) and rad-5/clk-2 prevent mitotic catastrophe, function in the
131 e stress activates ataxia telangiectasia and rad-3-related (ATR) and Chk1 checkpoint kinases that inh
132 ndard prescribed absorbed dose of 7,000 cGy (rad) to the thyroid therefore was reduced by over 50% wi
133 hyperthyroidism, with a standard 7,000-cGy (rad) thyroid absorbed dose generally resulting in an inc
137 s exceeding the MTA safety limit of 200 cGy (rads) to the blood or bone marrow in many patients with
142 9 acts in a process involving the checkpoint rad genes and that the rhp9 mutant is phenotypically ver
143 x fission yeast genes, termed the checkpoint rad genes, which are essential for both the S-M and DNA
145 s complex is dependent on a third checkpoint rad gene, rad9+, suggesting that these three proteins ma
149 in PCMH[Y384F] which produced PchF[Y384F]FAD(rad) x PchC, the mutant enzyme containing the flavin rad
152 )H(-) (E(0)(f) = -1.05 V vs Fc/Fc(+)) and Fl(rad)(*2-) (E(0)(f) = -1.62 V vs Fc/Fc(+)), respectively.
153 y one electron to form the radical anion (Fl(rad)(*-)) at E(0)(f) = -1.22 V versus Fc/Fc(+) (E(0)(f)
154 n rates, the homogeneous reaction between Fl(rad)(*-) and Fl(ox) begins to be outrun, which leads to
155 ciated with the one-electron reduction of Fl(rad)(*-) to form Fl(red)(2-) (E(0)(f) = -1.98 V vs Fc/Fc
156 the starting material (Fl(ox)) to produce Fl(rad)H(*) and Fl(ox)(-), which are both able to undergo f
157 omolog of the S. pombe rad1 checkpoint gene, rad-5, and him-7-block both DNA damage-induced apoptosis
159 r, relocalization appears more frequently in rad-5 mutants, suggesting that RAD-5 plays a role in rep
160 ce tumor-to-nontumor ratios and may increase rad doses to tumor more selectively than directly labele
161 pressure-dependent radiative conductivity, k(rad), from these data is 2-5 times lower than previously
163 nstant alpha to be (-1 +/- 0.34) x 10(-10) N/rad(2); and 3) the ciliary base may be an essential regu
164 calculated to be (4.6 +/- 0.62) x 10(-12) N/rad and nonlinear spring constant alpha to be (-1 +/- 0.
165 ich a torsional spring constant of ~23 pN.nm/rad(2) is estimated on average for all S1 types, similar
167 alternative repair pathway in the absence of rad-51 and independent of nonhomologous end joining (NHE
168 rror-prone DSB repair pathway independent of rad-51 and non-homologous end joining, raising the possi
172 tient-specific mean 90Y dose (cGy/37 MBq, or rad/mCi) was 0.53 (0.32-0.78) to whole body, 3.75 (0.63-
173 cell cycle events and coordinates with other rad/hus checkpoint gene products in responding to radiat
175 al dynein interactions ( approximately 35 pN/rad) to interdoublet sliding resistance in these immobil
176 ibutions of the N-DRCs ( approximately 40 pN/rad) and residual dynein interactions ( approximately 35
179 e identification of homologs of the S. pombe rad checkpoint genes from mammals, arthropods, and nemat
181 over the second-generation EST SSC12 RH7000-rad map of 103 ESTs and 15 framework markers covering ap
186 with defects in the DNA damage aspect of the rad checkpoint control pathway had an increased frequenc
188 course, known to radiology residents as the "rad-path" course, was not a casualty of the BRAC, the Am
190 gnated mec1-srf for synthetic lethality with rad-fifty-two) simultaneously cause two types of phenoty
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